• We are sorry, but NCBI web applications do not support your browser and may not function properly. More information
Logo of cmrPermissionsJournals.ASM.orgJournalCMR ArticleJournal InfoAuthorsReviewers
Clin Microbiol Rev. Jan 2007; 20(1): 39–48.
PMCID: PMC1797631

Global Dissemination of Vibrio parahaemolyticus Serotype O3:K6 and Its Serovariants


Vibrio parahaemolyticus is recognized as a cause of food-borne gastroenteritis, particularly in the Far East, where raw seafood consumption is high. An unusual increase in admissions of V. parahaemolyticus cases was observed at the Infectious Diseases Hospital in Calcutta, a city in the northeastern part of India, beginning February 1996. Analysis of the strains revealed that a unique serotype, O3:K6, not previously isolated during the surveillance in Calcutta accounted for 50 to 80% of the infections in the following months. After this report, O3:K6 isolates identical to those isolated in Calcutta were reported from food-borne outbreaks and from sporadic cases in Bangladesh, Chile, France, Japan, Korea, Laos, Mozambique, Peru, Russia, Spain, Taiwan, Thailand, and the United States. Other serotypes, such as O4:K68, O1:K25, and O1:KUT (untypeable), that had molecular characteristics identical to that of the O3:K6 serotype were subsequently documented. These serotypes appeared to have diverged from the O3:K6 serotype by alteration of the O:K antigens and were defined as “serovariants” of the O3:K6 isolate. O3:K6 and its serovariants have now spread into Asia, America, Africa, and Europe. This review traces the genesis, virulence features, molecular characteristics, serotype variants, environmental occurrence, and global spread of this unique clone of V. parahaemolyticus.


Vibrio parahaemolyticus, a gram-negative halophilic bacterium, is recognized as a worldwide cause of food-borne gastroenteritis, particularly in the Far East, where seafood consumption is high. The halophile was first identified as a cause of food-borne illness in Japan in 1950, when 272 individuals became ill and 20 died after the consumption of semidried juvenile sardines (27). V. parahaemolyticus causes three major syndromes of clinical illness, i.e., gastroenteritis, wound infections, and septicemia. The most common syndrome is gastroenteritis; the symptoms include diarrhea with abdominal cramps, nausea, vomiting, headache, and low-grade fever (34). Sometimes the diarrhea is bloody, with stools described as “meat washed” since the stool is reddish watery stool (77) but unlike that seen in dysentery caused by Shigella species or in amebiasis. The mean incubation period for V. parahaemolyticus infection is 15 h (range, 4 to 96 h). The illness is self-limiting and of moderate severity and lasts an average of 3 days in immunocompetent patients.

V. parahaemolyticus strains that are isolated from diarrheal patients produce either the thermostable direct hemolysin (TDH), the TDH-related hemolysin (TRH), or both, while hardly any isolates from the environment have these properties (34, 83, 87). An isolate producing TDH is referred to as Kanagawa positive and can be identified by β hemolysis on a special agar known as Wagatsuma blood agar (87, 93). TDH has been shown to have hemolytic, enterotoxic, cardiotoxic, and cytotoxic activities (34, 68, 83, 93). A strong correlation between urease production (an unusual phenotype for V. parahaemolyticus) and the trh gene exists (38). Enteroinvasiveness of the bacterium has been reported for a rabbit model, in which the organism invaded, colonized, and produced inflammation in the small intestine (13). In patients in the acute stage of V. parahaemolyticus infection, the inflammatory response in the gut and in the circulation is less severe than that observed in patients with shigellosis but more severe than that seen in patients with cholera (77). It has been shown that gastroenteritis caused by V. parahaemolyticus results in strong systemic and mucosal B-cell responses to TDH and lipopolysaccharide; both antigens also induce an increase in the presence of immunoglobulin M antibody-secreting cells, which suggests that this is a primary response to the antigen (77). In a recent study, it was shown that irrespective of TDH production, V. parahaemolyticus profoundly disturbs epithelial barrier function in Caco-2 cells due to the involvement of another virulence factor(s) (53). The overall mechanism of pathogenesis by V. parahaemolyticus, however, remains unclear.

Most gram-negative pathogens disrupt the normal physiology of the intestinal mucosa by inducing cytoskeleton rearrangements, proinflammatory responses, and/or cell death. Many of these cellular events are caused by bacterial effector proteins, which are delivered into intestinal cells that directly modulate the activities of host cell proteins and are secreted and translocated into host cells through the bacterial type III secretion systems (TTSSs). The TTSS macromolecular assembly is a needle-like complex composed of more than 20 proteins, and its components are highly conserved among bacteria. Genes encoding the TTSS apparatus are generally found on the chromosomal pathogenicity islands or plasmids (35, 99). In several bacteria, the genes encoding TTSS-secreted proteins are located outside the gene clusters encoding the TTSS apparatus (35). The specific properties of the effectors and their symptomatic effects on the host vary widely (35). Based on the assembly and functions of different proteins, the TTSSs in animal pathogens are classified into the following three major groups: (i) the Ysc-plus-Psc system, (ii) the 1-plus-Mxi/Spe system of the Salmonella pathogenicity island, and (iii) the enterohemorrhagic Escherichia coli system (22).

In V. parahaemolyticus, two sets of genes, for TTSS1 and TTSS2, were identified on the large and small chromosomes, respectively (54, 76). V. parahaemolyticus TTSS1 is a Ysc-plus-Psc system and is similar to the TTSSs of Yersinia spp. and Pseudomonas aeruginosa in the number of genes, their order, and the identity of each protein (54, 61, 73). However, no homologue of the effector protein genes has been found in the TTSS1 region. Four new TTSS1-secreted proteins were identified in V. parahaemolyticus, and one was located in the small chromosome (73). TTSS2 is detected only in Kanagawa-positive V. parahaemolyticus strains and is not similar to any particular TTSS of other bacteria (76). The G+C contents of the DNA regions of TTSS1 and TTSS2 suggest that the former is intrinsic in V. parahaemolyticus while the latter has a feature of laterally transferred DNA (54). Both TTSSs in V. parahaemolyticus may act as effectors during infections, as mutational studies and an adenylate cyclase fusion assay with TTSS1 showed it to be involved in the cytotoxicity in HeLa cells, while TTSS2 has a role in enterotoxicity in a rabbit model (73, 76). It was assumed that both TTSSs might act synergistically in the pathogenesis of V. parahaemolyticus (73).

V. parahaemolyticus is widely disseminated in estuarine, marine, and coastal environments throughout the world (42) and has been detected as far north as Alaska (91). Water temperature, salinity, zooplankton blooms, tidal flushing, and dissolved oxygen play an important role in dictating its spatial and temporal distribution (45). This pathogen is typically not recovered from estuarine waters during winter months in temperate zones, when the water temperature is too low for its existence. Water temperatures have been shown to influence the growth of V. parahaemolyticus (44, 46, 47, 88), and the importance of water temperature in the epidemiology of infections is reflected by the fact that most outbreaks occur during the warmer months. In tropical countries, in contrast, the seasonality of V. parahaemolyticus is less defined, with infection occurring throughout the year. Studies in Calcutta have shown that both marine and freshwater fishes provide ideal substrates for the survival and proliferation of V. parahaemolyticus. The isolation of V. parahaemolyticus from market samples of freshwater fishes was attributed to cross-contamination due to mishandling at fishmongers' stalls (81). Most V. parahaemolyticus outbreaks that occurred between 1973 and 1998 in the United States occurred during the warmer months and were attributed to seafood, particularly oysters and other shellfish, and the median attack rate among persons who consumed the implicated seafood was 56% (63). Many investigations have shown that marine mollusks are associated with the spread of toxigenic V. parahaemolyticus (10, 15, 24, 32, 59).

The primary basis of classification of strains of V. parahaemolyticus is a serotyping scheme, which depends on the antigenic properties of the somatic (O) and capsular (K) antigens. The serotyping scheme for V. parahaemolyticus is a combination of O and K antigens, and serotyping is done using commercially available antisera that include 11 different O antigens and 71 different K types (37). The serotyping scheme was developed using strains of clinical origin. Early investigations carried out by Baross et al. (6) with 20 bacteriophages against V. parahaemolyticus showed no correlation between O and K serotypes in the lytic pattern, and hence they were assumed to have a wide host range. The first phage typing scheme for V. parahaemolyticus was formulated in 1992 with 46 phages belonging to morphological groups II, IV, and V (49). However, for these phages the specificities for the serotypes have also not been established. Libinzon et al. (51) tested 34 V. parahaemolyticus phages isolated from the Black Sea. Except for one, which was specific for O5:K15, the majority of the phages were also found to lyse Vibrio alginolyticus strains. Phage typing studies conducted during an O3:K6 outbreak in Vladivostok showed types 1, 2, 7, and 10 with V. parahaemolyticus strains and phage types 2, 4, 5, and 7 with V. alginolyticus strains (85). Due to the lack of specificity, the phage typing scheme for V. parahaemolyticus is not customary in international practice. In recent years, a variety of molecular typing techniques, such as ribotyping, pulsed-field gel electrophoresis (PFGE), and multilocus sequence typing (MLST) techniques, as alluded to later in this review, have been used successfully to study the molecular epidemiology of the organism.


During active surveillance of diarrheal etiologies among hospitalized patients in Calcutta, a city in the northeastern part of India, an increase in hospital admissions of patients with V. parahaemolyticus gastroenteritis was observed beginning in February 1996. Analysis of the strains revealed that a unique serotype, O3:K6, which was not previously isolated during surveillance in Calcutta, accounted for 50 to 80% of infections in the following months (69). The O3:K6 isolates had identical genotypes (tdh positive, trh and urease negative) and nearly identical arbitrarily primed PCR (AP-PCR) profiles and shared similar antibiotic sensitivity patterns (69).

From the literature, it seems that the first O3:K6 isolate was isolated from a traveler returning from Indonesia to Japan in 1995 (69). Curiously, the seventh pandemic strain of Vibrio cholerae O1, which is of the El Tor biotype, also had its origin in the island of Sulawesi in Indonesia (43). However, based on hospital admissions, the first localized cluster of cases of O3:K6 occurred in Calcutta starting in February 1996. Thus, the epidemiological setting in Calcutta at that time was conducive to infecting a larger population. Food-borne outbreak statistics for Taiwan revealed that the O3:K6 serotype could have emerged as early as October 1995, when it was responsible for a single outbreak with three isolates (15). Four tdh-negative O3:K6 isolates obtained in Japan between 1983 and 1988 grouped with the unique O3:K6 cluster (>75% similarity) when recently examined by AP-PCR and showed toxRS sequences identical to that of an O3:K6 clone, leading Okura et al. (70) to speculate that the O3:K6 isolates might have originated from these nonpathogenic strains after acquisition of the tdh gene. Therefore, at this point it appears that the progenitors of the O3:K6 isolate might have originated in the environs of Japan.

The regional dominance of a specific serotype of V. parahaemolyticus has occasionally been reported. Early investigations in Calcutta revealed the dominance of serotype O1:K56 among diarrheal cases (12) and in index cases and carriers (75, 84). Along the western coasts of Mexico and the United States, V. parahaemolyticus O4:K12 was the dominant serotype causing infections (1). The O3:K6 clustering of cases, however, differs from the previously reported clustering of single V. parahaemolyticus serotypes in possessing additional attributes. One is the ability to rapidly increase hospitalizations in areas where it prevails and the other is to become the dominant serotype, supplanting other serotypes of V. parahaemolyticus in the given area. Both of these attributes were not observed before for V. parahaemolyticus. For example, in the Aichi Prefecture in Japan, the percentage of outbreaks by V. parahaemolyticus O3:K6 increased from 3% for the period 1988 to 1995 to 75% for the period 1996 to 2001 (104).


The development of a specific method to facilitate the rapid identification of O3:K6 isolates (57) led to the serendipitous finding of other serotypes, such as O4:K68, O1:K25, and O1:KUT (untypeable), that had toxRS sequences, AP-PCR profiles, ribotypes, and PFGE profiles identical to those of the O3:K6 serotype (17, 18, 57). The discovery of the filamentous phage designated f237 in O3:K6 isolates (62) led to the development of another specific PCR method, which targeted ORF8 of f237, claimed to be a specific genetic marker of O3:K6 isolates. Later, it was found that other serotypes that were not like the O3:K6 isolates also carried ORF8 (39). In addition to O4:K68, O1:K25, and O1:KUT, another serotype, O6:K18, which shared high molecular identity with an O3:K6 isolate, was detected in Taiwan (102). Therefore, from a single O3:K6 serotype, other serotypes that had identical genotypes and molecular profiles to those of O3:K6 isolates emerged, and these were collectively referred to as “serovariants” of O3:K6 isolates (57). These serotypes appeared to have diverged from the O3:K6 isolates by alteration of the O:K antigens and were postulated to be clonal derivatives of the O3:K6 serotype. MLST data have further confirmed the finding that multiple serotypes occur in a single genetic lineage (18, 19, 57). The acquisition of additional serotypes of the pandemic strain may be a selected response to host immunological pressure (19). Eleven O:K serotypes were detected among the strains isolated during a survey of diarrhea patients in Khanh Hoa Province, Vietnam, and all were found to be closely related to O3:K6 (16). To date, 21 serotypes that are similar to the O3:K6 serotype have been identified (Table (Table1)1) by a variety of molecular typing techniques.

Chronology of appearance of Vibrio parahaemolyticus O3:K6 and its serovariants in different countries

Table Table22 shows the chronology of appearance of the various serotypes in Calcutta that are similar to the O3:K6 isolates recorded from February 1996. Clearly, the vigor with which the O3:K6 isolates appeared in the beginning of 1996 is on the wane. This matches the epidemiology of cholera, which generally settles into an endemic pattern of seasonal outbreaks separated by periods of quiescence after passage of a pandemic wave through a geographic region (62). The more recent serotypes, which have molecular traits similar to those of O3:K6, do not seem to have the propensity for elevating hospital admissions due to V. parahaemolyticus gastroenteritis observed with O3:K6 and the earlier serovariants of O3:K6. Some kind of decay in the epidemic process seems to be evident.

Emergence of O3:K6 serotype of Vibrio parahaemolyticus and its serovariants in Calcutta from January 1994 to December 2004a


When the Calcutta O3:K6 isolates were compared with an archived collection of O3:K6 strains isolated between 1982 and 1996 from travelers returning to Japan, it was found that the Calcutta O3:K6 isolates were identical to the isolates obtained from travelers from 1995 onwards but differed from O3:K6 strains isolated prior to 1993. This comparison also fortuitously revealed that isolates of O3:K6 like those found in Calcutta were already prevalent in Indonesia, Thailand, and Singapore, since travelers returning from these countries were infected (69). Evidence supporting the hypothesis that the O3:K6 serotype emerged only recently was furnished by Matsumoto et al. (57), who showed that O3:K6 isolates from clinical sources in Taiwan, Laos, Japan, Thailand, Korea, and the United States in 1997 and 1998 were identical to the Calcutta O3:K6 strains. Based on this evidence, they concluded that the unique O3:K6 isolate and its serovariants were causing a pandemic. Such a widespread occurrence of one clonal type of V. parahaemolyticus was unprecedented and spurred great interest.

In retrospect and following the trend of the spread of O3:K6 isolates over the past decade, it seems that use of the word “pandemic” is somewhat misleading and might be a bit of a strong term in a true epidemiological sense. The Webster's dictionary definition of pandemic describes it as “occurring over wide geographic areas and afflicting an exceptionally high proportion of the population.” Although the O3:K6 serotype of V. parahaemolyticus has been isolated over a wide geographic area, supplanting the other serotypes of V. parahaemolyticus in the process, it has not affected an exceptionally high proportion of the population, and it apparently has caused little, if any, mortality. In fact, compared to the seventh pandemic El Tor biotype V. cholerae O1 (80) or compared to V. cholerae O139 (65), V. parahaemolyticus is a pretty rare disease. In this review, we use the term “pandemic” only to allude to the description investigators have used in their publications, but as explained above, we are of the opinion that the spread of O3:K6 and its serovariants is not a pandemic in the real sense.


Starting with AP-PCR (17, 18, 57, 69), a variety of molecular techniques, including ribotyping and pulsed-field gel electrophoresis (18, 25, 101, 105), revealed that O3:K6 isolates from widely different geographic areas were genetically similar to each other and distinct from O3:K6 isolates obtained before 1995 and from non-O3:K6 serotypes. The O3:K6 isolates appearing after 1995 carried the tdh but not the trh gene, did not produce urease, and were defined by a positive group-specific PCR (GS-PCR) based on the mismatched nucleotides at seven base positions of the toxRS gene sequences and ORF8 from the f237 phage. Ribotyping revealed a certain degree of instability in the early Calcutta O3:K6 isolates, reflected as genomic reassortment during their initial period of existence (5). According to biochemical fingerprinting by a PhenePlate system (PhP-48; PhenePlate Microplate Techniques, Stockholm, Sweden) based on the kinetic measurement of the fermentation of selected reagents, the pandemic strains belonged to the same biochemical phenotype, whereas the nonpandemic strains were heterogeneous (79). Thirty-five isolates of V. parahaemolyticus from different countries and belonging to different serotypes (O3:K6, O4:K68, and O1:KUT) showed identical ribotypes and PFGE patterns, with some exceptions, including a Japanese tdh-negative O3:K6 strain and a U.S. clinical O3:K6 isolate (18). At least two different ribotype patterns were observed among O3:K6 isolates from the United States and Asia, and most of the strains from the 1998 Galveston Bay outbreak were different from those isolated in New York and parts of Asia (28). The 11 serotypes of V. parahaemolyticus obtained from surveillance in Vietnam were shown to be closely related, regardless of the ORF8 genotype, using AP-PCR and PFGE (16).

MLST provided strong molecular evidence for the clonal origin of V. parahaemolyticus O3:K6 and revealed that isolates within such a clonal group may acquire previously identified serotypes of V. parahaemolyticus. The MLST study also confirmed genetic diversity among the V. parahaemolyticus strains that prevailed before O3:K6 and genetic uniformity between O3:K6 and its serovariants in spite of their serotype diversity (16). All of the O3:K6 isolates collected from 1983 to 1993 from diverse countries around the Indian Ocean were related. However, the sequence types (STs) of all 11 other serotypes were distinct. In contrast, the four distinct serotypes O3:K6, O4:K68, O1:KUT, and O1:K25 were clonally related. Fifty-one of 54 isolates had the ST 1,1,1,1 (19).


At about the same time as the Calcutta occurrence, information on steadily increasing numbers of V. parahaemolyticus infection in Japan was documented. The number of food-borne infections caused by this pathogen in 1998 in Japan doubled compared to that in 1997 and exceeded the number of infections by Salmonella, which previously was the dominant cause of food-borne infections in Japan (103). An increase in food-borne disease outbreaks was recorded in Taiwan in 1996, and this increase correlated with the high rate of isolation of V. parahaemolyticus O3:K6 (15, 100). During 1995 in Taiwan, the O3:K6 serotype accounted for only 0.6% of V. parahaemolyticus infections, and this level abruptly increased to 50.1% in 1996 and reached a peak of 83.8% in 1997 (15). From 1996 onwards, the O3:K6 serotype was isolated from diarrhea patients admitted to the ICDDR,B hospital in Dhaka, Bangladesh (7, 15, 57). Between May and June 1998, 416 persons in 13 states reported having gastroenteritis after eating oysters harvested from Galveston Bay, Tex. All 28 available stool samples yielded V. parahaemolyticus O3:K6 isolates which closely resembled the Asian O3:K6 isolates by PFGE (23). During July to September 1998, an outbreak of V. parahaemolyticus O3:K6 infections associated with the consumption of oysters and clams harvested from Long Island Sound occurred among residents of Connecticut, New Jersey, and New York (10, 11). Significantly, before this series of outbreaks in the United States, V. parahaemolyticus serotype O3:K6 was not reported in this country (23). Subsequently, O3:K6 isolates obtained in 1997 and 1998 from clinical sources in Taiwan, Laos, Japan, Thailand, Korea, and the United States were found to share nearly identical AP-PCR profiles (57).

Outbreaks caused by the O3:K6 serotype occurred in the northern city of Antofagasta, Chile, from November 1997 to March 1998, and other outbreaks occurred during the summer months of 2004 and 2005, mainly in Puerto Montt, a region with usually cold waters (21, 26, 30). Interestingly, a recent retrospective analysis of V. parahaemolyticus strains isolated from several places in Peru showed the prevalence of the O3:K6 serotype and other pandemic serovariants of V. parahaemolyticus, with the earliest O3:K6 isolate being recovered as early as 1996, the same year that the pandemic O3:K6 serotype was identified in Calcutta, India (29). The majority of the V. parahaemolyticus strains isolated during an outbreak of acute enteric disease in Vladivostok, Russia, in 1997 belonged to serotype O3:K6 (85). More recently, the O3:K6 serotype was isolated from hospitalized diarrhea patients in Mozambique, ushering its spread into the African continent (3). V. parahaemolyticus O3:K6 strains similar to the pandemic clone have been isolated from the coasts of Spain and France (55, 78). A diarrheal outbreak caused by serotype O3:K6 was reported from Calcutta, India (82). The incidence of tdh-positive strains of V. parahaemolyticus in patients in Hangzhou, China (107), has been reported, but the molecular traits of the isolates were not examined. Clearly, global dissemination of a specific clone of V. parahaemolyticus is apparent, and at the time of writing of this review, this clone has spread into Asia, America, Africa, and Europe (Fig. (Fig.11).

FIG. 1.
Global dissemination of the unique O3:K6 isolate of Vibrio parahaemolyticus and its serovariants.


Since the discovery of the unique O3:K6 serotype of V. parahaemolyticus, efforts have been made to determine the factor that endows these isolates with the ability to rapidly increase hospitalizations and to become the dominant serotype. The initial efforts were centered on whether the O3:K6 isolates produced more TDH than the other existing serotypes of V. parahaemolyticus. Such a difference in production of TDH was not evident (69, 101), but later studies revealed one amino acid polymorphism in the tdh open reading frame (ORF) that appeared to differentiate the O3:K6 isolates (Gly109) from non-O3:K6 strains (Asp109) (105). Interestingly, sequence polymorphisms were also observed in the putative tdh promoter region of these isolates (99), but the significance of these differences was not clear given that there was no discernible difference in the amounts of TDH produced by O3:K6 and non-O3:K6 strains of V. parahaemolyticus (69). These findings match well with an early report from Calcutta indicating that the clinical symptoms of patients infected by O3:K6 isolates did not differ significantly from those of patients infected by non-O3:K6 serotypes. O3:K6 isolates compared to non-O3:K6 strains that were tdh positive were shown to demonstrate an enhanced ability to swarm over agar surface plates, and the presence of magnesium appeared to further stimulate swarming (105). There were, however, no significant differences between survival rates under the same environmental stresses, such as extreme temperatures, low pH, and high salinity, for O3:K6 and non-O3:K6 strains of V. parahaemolyticus (69, 101).

The V. parahaemolyticus phage f237 is similar to the CTX filamentous phage of V. cholerae O1 (94), but instead of the ctxAB genes, f237 has ORF8, and therefore it was thought that ORF8 may play a significant role (like the profound role that cholera toxin has in the disease cholera) in increasing the virulence of O3:K6 isolates. Based on the similarity of the motifs of the predicted amino acid sequence of ORF8 to those of the plx gene of Drosophila, which encodes a novel adhesion molecule (106), Nasu et al. (67) speculated that ORF8 encodes an adherence protein and that strains possessing this gene could be more adhesive to host intestinal cells or to the surfaces of marine plankton. In vitro adherence and cytotoxicity studies with human epithelial cells showed that O3:K6 isolates exhibited statistically higher levels of adherence and cytotoxicity to host cells than did non-O3:K6 isolates (105). Studies in Bangladesh, however, showed that ORF8 could not be detected in several O3:K6 isolates from hospitalized diarrhea patients (7).

Recently, Okura et al. (71) identified, cloned, and sequenced a 930-bp AP-PCR fragment that was unique to the O3:K6 isolates and their serovariants; the sequence of this fragment was found to be 80% homologous to the Mn2+ and Fe2+ transporter of the NRAMP family of Vibrio vulnificus. Again, a specific function was not attributed to this fragment. In O3:K6 isolates of V. parahaemolyticus, a histone-like DNA-binding protein, HU-α, with a C-terminal amino acid sequence different from those in other strains of V. parahaemolyticus, has been identified (72, 98). Further study has revealed that the gene encoding this protein has a 16-kb insert at the 3′ terminus of the ORF, but the effect of this insertion sequence on the activity of the HU-α protein in relation to a change in pathogenicity is unknown at this time (72, 98). The functional role of a histone-like protein in streptococci was shown to be associated with tissue inflammation (86). The 16-kb insertion sequence might have evolved from a phage, as it includes a gene encoding a putative phage protein and has the insertion gene sequence TTCTTCAG at its 5′ and 3′ ends (54, 72). Bioinformatic study of the whole genome sequence of an O3:K6 isolate (RIMD2210633) revealed the exclusive presence of four genomic islands, termed V. parahaemolyticus islands (VPaIs), in the pandemic group, which may represent DNAs acquired by the pandemic group that increased its fitness either in the aquatic environment or in the ability to infect humans (36). The direct repeats present in VPaIs 1, 4, and 5 and those in VPaI 6 are located in the large and small chromosomes, respectively. Moreover, the phage-like integrases show that these VPaIs were acquired by horizontal gene transfer (36). Clearly, O3:K6 isolates seem to have acquired some attributes that are not seen in non-O3:K6 isolates, but so far the determining factor(s) remains elusive. A methyltransferase gene carried by a 23-kb novel pathogenicity island-like element was identified among pandemic V. parahaemolyticus strains (95). However, its specific advantages in virulence traits among pandemic strains have not yet been established.


The detection of virulent V. parahaemolyticus organisms against a background of numerically greater numbers of avirulent V. parahaemolyticus organisms has remained a daunting problem. Undifferentiated total V. parahaemolyticus counts are therefore used as an indicator for the control of food contamination and the prevention of infection. Clearly, this is inadequate, as reflected in the outbreaks caused in the United States, where despite bacteriologic monitoring at harvest sites and despite the number of V. parahaemolyticus organisms being lower than the permissible most probable number of 10,000, the outbreaks could not be prevented (23). Attempts to isolate O3:K6 from the environment and from seafood have not met with much success.

An immunomagnetic separation technique targeting different K antigens was established for food poisoning investigations of V. parahaemolyticus (89). Application of this technique, targeting the K6 antigen for the identification of O3:K6 isolates, was successfully demonstrated using clinical and environmental samples (31, 92). An extensive environmental study in Japan combining a tdh-specific PCR method, chromogenic agar medium, and the most-probable-number method showed that isolates similar to the Calcutta O3:K6 isolates were widely distributed throughout the Japanese coastal environment. Of the 19 strains examined, 14 were tdh and GS-PCR positive and showed the same AP-PCR profile as the reference O3:K6 isolates (32). Studies conducted at Kii Channel, Tokushima, Japan, further confirmed this finding (33). However, neither the O3:K6 serotype nor any of the ribogroups associated with the O3:K6 serotype was found among any of the environmental or food isolates examined, suggesting that the O3:K6 serotype has not become established in the United States (25). It was felt that the O3:K6 serotype did not have an environmental reservoir in the United States and that the origin and spread of this organism may have occurred via ship ballast water. Cargo ships entering the Gulf of Mexico were thought to be responsible for the introduction of the Latin American epidemic strain of V. cholerae O1 into Gulf Coast waters in 1991 (58). O3:K6 isolates have also been isolated from the aquatic environs of Bangladesh (40) and from the east coast of India (24). O3:K6 and other serovariants seem to have established an ecological niche in Asia (4). It appears that, in some regions, aquatic birds act as reservoirs of V. parahaemolyticus during the winter (60). However, more information should be generated in identifying the pandemic strains from such nonhuman reservoirs. Environmental surveys have shown that the application of sensitive techniques is essential for isolating specific pathogenic strains, such as O3:K6 isolates, from environmental and seafood samples.


The origin and subsequent spread of the O3:K6 isolates of V. parahaemolyticus must be the consequence of coincidental events occurring at the right time and at the right place. Is the emergence of O3:K6 isolates and their serovariants the consequence of the effects of global warming? For several of the reported outbreaks, especially during the period 1996 to 1998, elevated environmental temperatures have been ascribed as a cause (23, 59). The year 1998 was part of the El Niño years, when elevated seawater temperatures were shown to influence the incidence of V. cholerae (20) and other diarrheal diseases (14). In 2005, serotype O6:K18 caused a diarrheal outbreak in Alaska (59); however, its genetic relatedness with the O3:K6 isolate was not established. The Alaskan outbreak was associated with warming of ocean waters (59). Among the food-borne disease outbreaks in 13 provinces of China during 2003, about 40% of the patients were infected with V. parahaemolyticus (52). Are environmental conditions becoming conducive for the proliferation of pathogens like V. parahaemolyticus? It would at least seem so because V. parahaemolyticus has been recognized since the 1950s, and raw oysters and seafood have been consumed from time immemorial. Yet 1996 to 1998 seemed to be particularly unpleasant years for humans, especially for those who had an inclination for oysters, which is the most important source of infection of V. parahaemolyticus in the United States and the Far East. We still do not understand the epidemiology of V. parahaemolyticus infections. In Vietnam, the incidence of V. parahaemolyticus stopped abruptly without meteorological changes or changes in water supply and sanitation, and the reasons for this abrupt interruption in transmission are not clear (90). In recent times, there have been occurrences of other extraordinary events in relation to pathogenic Vibrio species. In the summer of 1996, a major outbreak of systemic V. vulnificus infections started among Israeli fish market workers and fish consumers (8). Molecular analysis showed that this strain evolved by hybridization of the genomes of two existing nonpathogenic forms of V. vulnificus, which apparently led to the emergence of an epidemic caused by the newly evolved pathogenic variant (9). Similarly, the appearance of new hybrids between the classical and El Tor biotypes of V. cholerae O1 has been reported from Matlab, Bangladesh (66), and from Mozambique (2).

The transmission and epidemiology of V. parahaemolyticus infections in places such as Calcutta, India, and Bangladesh are entirely different because seafood is never eaten raw and freshwater fish is preferred over seawater fish by the local population. Contamination of freshwater fish by seawater fish at the fish market and secondary contamination of other foods in the kitchen by V. parahaemolyticus-contaminated fish brought from markets are thought to be the most likely routes of transmission in this setting (75). Early ecological studies have shown the occurrence of V. parahaemolyticus in freshwater plankton and in freshwater fishes (81). The survival of V. parahaemolyticus in freshwater ecosystems has been shown to be transient and dependent on a biological host (81).


The emergence of the O3:K6 serotype and its serovariants and its widespread distribution have necessitated the development of specific methods to detect such strains. Serotyping enabled the detection of the O3:K6 isolates in Calcutta. Although serotyping is a relatively easy technique for identifying clusters of cases caused by a specific serotype and also for tracking their spread, the cost of antisera is prohibitive and therefore limits their availability and applicability. In the Calcutta episode, the identification of the clustering of the O3:K6 serotype did not occur in real time because a V. parahaemolyticus antiserum kit was not available at that time at the National Institute of Cholera and Enteric Diseases in Calcutta, and the strains were confirmed and serotyped later at the Osaka Prefecture Institute of Public Health, Osaka, Japan.

The API-20 E identification system is used in many laboratories for the identification of enteric bacteria. For the identification of V. parahaemolyticus, it appears that the use of specific concentrations of NaCl makes a considerable difference in the identification of clinical (0.85%) and environmental (2.0%) strains (56). Over the past few years, PCR-based detection techniques, including GS-PCR (52) and orf8 PCR (57, 64, 67), have been developed to specifically detect the O3:K6 serotype and its serovariants. The development of GS-PCR was a milestone in simplifying the identification of the O3:K6 isolate and also for detecting other serotypes that share identical molecular traits (57). Inconsistencies between the results of the toxRS and ORF8 PCRs related to serotypes that were not like the O3:K6 isolates or their serovariants and that were toxRS negative but positive by ORF8 PCR were reported (74). Additionally, some of the O3:K6 isolates from Bangladesh isolated between 1998 and 2000 (7) and from Vietnam (16) were negative by orf8 PCR, indicating that neither the toxRS nor the ORF8 sequence is a reliable gene marker for the definite identification of the pandemic group. A real-time PCR assay targeting the orf8 gene was shown to be specific and sensitive for the detection of pandemic O3:K6 strains (97). However, this assay may not be useful for the detection of pandemic strains that are devoid of orf8. Pyrolysis metastable atom bombardment mass spectrometry was shown to identify various phenotypic characteristics of V. parahaemolyticus (96). By targeting specific phenotypic markers, this technique may differentiate pandemic and nonpandemic V. parahaemolyticus strains.

Okura et al. (70) developed a novel multiplex PCR assay specific for the O3:K6 isolates and their serovariants that successfully distinguished these stains from other V. parahaemolyticus strains by yielding two distinct PCR products, for tdh (263 bp) and the toxRS/new sequence (651 bp). A PCR-based assay was developed, employing an oligonucleotide primer pair derived from the group-specific sequence of an arbitrarily primed PCR fragment which was located in the genome encoding a hypothetical protein. The assay distinguished the O3:K6 isolates and their serovariants from other V. parahaemolyticus strains by yielding a 235-bp specific amplicon (70). Khan et al. (48) reported that all of the O3:K6 strains isolated from the Texas and New York outbreaks yielded an 850-bp DNA fragment along with other amplicons in enterobacterial repetitive intergenic consensus PCR. The primers designed from this 850-bp gene sequence were specifically identified in O3:K6 isolates with a 327-bp amplicon, whose function and homology remain unknown. However, this PCR method was not validated. Using the detection of an insertion mutation in the HU-α ORF, a PCR technique was reported for the identification of not only the O3:K6 serotype but also other serovariants, such as O1:K25, O1:KUT, and O4:K68 (72, 98), which had molecular traits identical to those of the O3:K6 isolate. Genes located on VPaIs 4, 5, and 6 (36) can be targeted for the specific detection of pandemic strains by PCR. However, the specificity and sensitivity are not yet established for routine use in the laboratory. Use of microarray technology with specific amplification and oligonucleotides was shown to be useful for the detection and identification of pathogenic bacteria, including V. parahaemolyticus (41). Targeting specific genes in this microarray technique will differentiate pandemic and nonpandemic strains.


The emergence and spread of the O3:K6 isolate and its serovariants offer an invaluable opportunity to examine factors that abet and perpetuate events like this. Many aspects of O3:K6 and its serovariants are still unknown. For example, we do not know the factors that triggered the genesis of the O3:K6 serotype and the bacterial factors that are involved. We also do not know the mechanism of formation of serovariants and those extraneous factors that drive this event.


The core donors to the International Centre for Diarrheal Disease Research, Bangladesh (ICDDR,B) supported this work. Current donors providing unrestricted support include the aid agencies of the Governments of Australia, Bangladesh, Belgium, Canada, Japan, Kingdom of Saudi Arabia, The Netherlands, Sweden, Sri Lanka, Switzerland, and the United States. The funding sources had no involvement in the study design, interpretation, or decision to submit the manuscript.


1. Abbott, S. L., C. Powers, C. A. Kaysner, Y. Takeda, M. Ishibashi, S. W. Joseph, and J. M. Janda. 1998. Emergence of a restricted bioserovar of Vibrio parahaemolyticus as the predominant cause of Vibrio-associated gastroenteritis on the West Coast of the United States and Mexico. J. Clin. Microbiol. 27:2891-2893. [PMC free article] [PubMed]
2. Ansaruzzaman, M., N. A. Bhuiyan, G. B. Nair, D. A. Sack, M. Lucas, J. L. Deen, J. Ampuero, C. L. Chaignat, and The Mozambique Cholera Vaccine Demonstration Project Coordination Group. 2004. Cholera in Mozambique, variant of Vibrio cholerae. Emerg. Infect. Dis. 10:2057-2059. [PMC free article] [PubMed]
3. Ansaruzzaman, M., M. Lucas, J. L. Deen, N. A. Bhuiyan, A. Safa, M. Sultana, A. Chowdhury, G. B. Nair, D. A. Sack, L. V. Seidlein, C. L. Chaignat, J. D. Clemens, and A. Barreto. 2005. Pandemic serovars (O3:K6 and O4:K68) of Vibrio parahaemolyticus associated with diarrhea in Mozambique: spread of the pandemic into the African continent. J. Clin. Microbiol. 43:2559-2562. [PMC free article] [PubMed]
4. Arakawa, E., T. Murase, T. Shimada, T. Okitsu, S. Yamai, and H. Watanabe. 1999. Emergence and prevalence of a novel Vibrio parahaemolyticus O3:K6 in Japan. Jpn. J. Infect. Dis. 52:246-247. [PubMed]
5. Bag, P. K., S. Nandi, R. K. Bhadra, T. Ramamurthy, S. K. Bhattacharya, M. Nishibuchi, T. Hamabata, S. Yamasaki, Y. Takeda, and G. B. Nair. 1999. Clonal diversity among recently emerged strains of Vibrio parahaemolyticus O3:K6 associated with pandemic spread. J. Clin. Microbiol. 37:2354-2357. [PMC free article] [PubMed]
6. Baross, J. A., J. Liston, and R. Y. Morita. 1978. Ecological relationship between Vibrio parahaemolyticus and agar-digesting vibrios as evidenced by bacteriophage susceptibility patterns. Appl. Environ. Microbiol. 36:500-505. [PMC free article] [PubMed]
7. Bhuiyan, N. A., M. Ansaruzzaman, M. Kamruzzaman, K. Alam, N. R. Chowdhury, M. Nishibuchi, S. M. Faruque, D. A. Sack, Y. Takeda, and G. B. Nair. 2002. Prevalence of the pandemic genotype of Vibrio parahaemolyticus in Dhaka, Bangladesh, and significance of its distribution across different serotypes. J. Clin. Microbiol. 40:284-286. [PMC free article] [PubMed]
8. Bisharat, N., and R. Raz. 1996. Vibrio infection in Israel due to changes in fish marketing. Lancet 348:1585-1586. [PubMed]
9. Bisharat, N., D. I. Cohen, R. M. Harding, D. Falush, D. W. Crook, T. Peto, and M. C. Maiden. 2005. Hybrid Vibrio vulnificus. Emerg. Infec. Dis. 11:30-35. [PMC free article] [PubMed]
10. Centers for Disease Control and Prevention. 1998. Outbreak of Vibrio parahaemolyticus infection associated with eating raw oysters—Pacific Northwest, 1997. Morb. Mortal. Wkly. Rep. 47:457-462. [PubMed]
11. Centers for Disease Control and Prevention. 1999. Outbreak of Vibrio parahaemolyticus infection associated with eating raw oysters and clams harvested from Long Island Sound—Connecticut, New Jersey, and New York, 1998. Morb. Mortal. Wkly. Rep. 48:48-51. [PubMed]
12. Chatterjee, B. D., and T. Sen. 1974. Vibrio parahaemolyticus serotypes in Calcutta, India. Bull. W. H. O. 50:559-561. [PMC free article] [PubMed]
13. Chatterjee, B. D., A. Mukherjee, and S. N. Sanyal. 1984. Enteroinvasive model of Vibrio parahaemolyticus. Indian J. Med. Res. 79:151-158. [PubMed]
14. Checkley, W., L. D. Epstein, R. H. Gilman, D. Figueroa, R. I. Cama, J. A. Patz, and R. E. Black. 2000. Effect of El Nino and ambient temperature on hospital admissions for diarrhoeal diseases in Peruvian children. Lancet 355:442-450. [PubMed]
15. Chiou, C. S., S. Y. Hsu, S. I. Chiu, T. K. Wang, and C. S. Chao. 2000. Vibrio parahaemolyticus serovar O3:K6 as cause of unusually high incidence of food-borne disease outbreaks in Taiwan from 1996 to 1999. J. Clin. Microbiol. 38:4621-4625. [PMC free article] [PubMed]
16. Chowdhury, A., M. Ishibashi, V. D. Thiem, D. T. N. Tuyet, T. V. Tung, B. T. Chien, L. V. Seidlein, D. G. Canh, J. Clements, D. D. Trach, and M. Nishibuchi. 2004. Emergence and serovar transition of Vibrio parahaemolyticus pandemic strains isolated during a diarrhea outbreak in Vietnam between 1997 and 1999. Microbiol. Immunol. 48:319-327. [PubMed]
17. Chowdhury, N. R., S. Chakraborty, B. Eampokalap, W. Chaicumpa, M. Chongsa-Nguan, P. Moolasart, R. Mitra, T. Ramamurthy, S. K. Bhattacharya, M. Nishibuchi, Y. Takeda, and G. B. Nair. 2000. Clonal dissemination of Vibrio parahaemolyticus displaying similar DNA fingerprint but belonging to two different serovars (O3:K6 and O4:K68) in Thailand and India. Epidemiol. Infect. 125:17-25. [PMC free article] [PubMed]
18. Chowdhury, N. R., S. Chakraborty, T. Ramamurthy, M. Nishibuchi, S. Yamasaki, Y. Takeda, and G. B. Nair. 2000. Molecular evidence of clonal Vibrio parahaemolyticus pandemic strains. Emerg. Infect. Dis. 6:631-636. [PMC free article] [PubMed]
19. Chowdhury, N. R., O. C. Stine, J. G. Morris, and G. B. Nair. 2004. Assessment of evolution of pandemic Vibrio parahaemolyticus by multilocus sequencing typing. J. Clin. Microbiol. 42:1280-1282. [PMC free article] [PubMed]
20. Colwell, R. R. 1996. Global climate and infectious diseases: the cholera paradigm. Science 274:2025-2031. [PubMed]
21. Cordova, J. L., J. Astorga, W. Silva, and C. Riquelme. 2002. Characterization by PCR of Vibrio parahaemolyticus isolates collected during the 1997-1998 Chilean outbreak. Biol. Res. 35:433-440. [PubMed]
22. Cornelis, G. R., and F. Van Gijsegem. 2000. Assembly and function of type III secretory systems. Annu. Rev. Microbiol. 54:735-774. [PubMed]
23. Daniels, N. A., L. MacKinnon, R. Bishop, S. Altekruse, B. Ray, R. M. Hammond, S. Thompson, S. Wilson, N. H. Bean, P. M. Griffin, and L. Slutsker. 2000. Vibrio parahaemolyticus infections in the United States, 1973-1998. J. Infect. Dis. 181:1661-1666. [PubMed]
24. Deepanjali, H., S. Kumar, I. Karuasagar, and I. Karunasagar. 2005. Seasonal variation in abundance of total and pathogenic Vibrio parahaemolyticus bacteria in oysters along the southwest coast of India. Appl. Environ. Microbiol. 71:3575-3580. [PMC free article] [PubMed]
25. DePaola, A., J. Ulaszek, C. A. Kaysner, B. J. Tenge, J. L. Nordstrom, J. Wells, N. Puhr, and S. M. Gendel. 2003. Molecular, serological, and virulence characteristics of Vibrio parahaemolyticus isolated from environmental, food, and clinical sources in North America and Asia. Appl. Environ. Microbiol. 69:3999-4005. [PMC free article] [PubMed]
26. Fuenzalida, L., C. Hernandez, J. Toro, M. L. Rioseco, J. Romero, and R. T. Espejo. 2006. Vibrio parahaemolyticus in shellfish and clinical samples during two large epidemics of diarrhoea in southern Chile. Environ. Microbiol. 8:675-683. [PubMed]
27. Fujino, T., Y. Okuno, D. Nakada, A. Aoyama, K. Fukai, T. Mukai, and T. Uebo. 1953. On the bacteriological examination of Shirasu food poisoning. Med. J. Osaka Univ. 4:299-304.
28. Gendel, S. M., J. Ulazek, M. Nishibuchi, and A. DePaola. 2001. Automated ribotyping differentiates Vibrio parahaemolyticus O3:K6 strains associated with the Texas outbreak from other clinical strains. J. Food Prot. 64:1617-1620. [PubMed]
29. Gil, A. I., H. Miranda, C. F. Lanata, A. Prada, E. R. Hall, C. M. Barreno, S. Nusrin, N. A. Bhuiyan, D. A. Sack, and G. B. Nair. Serotype of Vibrio parahaemolyticus identical to the global pandemic clone associated with diarrhea in Peru. Int. J. Infect. Dis., in press. [PubMed]
30. González-Escalona, N., V. Cachicas, C. Acevedo, M. L. Rioseco, J. A. Vergara, F. Cabello, J. Romero, and R. T. Espejo. 2005. Vibrio parahaemolyticus diarrhea, Chile, 1998 and 2004. Emerg. Infect. Dis. 11:129-131. [PMC free article] [PubMed]
31. Hara-Kudo, Y., K. Sugiyama, T. Nishina, A. Saitoh, H. Nakagawa, T. Ichihara, H. Konuma, J. Hasegawa, and S. Kumagai. 2001. Detection of TDH-producing Vibrio parahaemolyticus O3:K6 from naturally contaminated shellfish using an immunomagnetic separation method and chromogenic agar medium. Kansenshogaku Zasshi 75:955-960. (In Japanese.) [PubMed]
32. Hara-Kudo, Y., K. Sugiyama, M. Nishibuchi, A. Chowdhury, J. Yatsuyanagi, Y. Ohtomo, A. Saito, H. Nagano, T. Nishina, H. Nakagawa, H. Konuma, M. Miyahara, and S. Kumagai. 2003. Prevalence of thermostable direct hemolysin-producing Vibrio parahaemolyticus O3:K6 in seafood and coastal environment in Japan. Appl. Environ. Microbiol. 69:3883-3891. [PMC free article] [PubMed]
33. Hayat Mahmud, Z., A. Kassu, A. Mohammad, M. Yamato, N. A. Bhuiyan, G. B. Nair, and F. Ota. 2006. Isolation and molecular characterization of toxigenic Vibrio parahaemolyticus from the Kii Channel, Japan. Microbiol. Res. 161:25-37. [PubMed]
34. Honda, T., and T. Iida. 1993. The pathogenicity of Vibrio parahaemolyticus and the role of the thermostable direct haemolysin and related haemolysins. Rev. Med. Microbiol. 4:106-113.
35. Hueck, C. J. 1998. Type III protein secretion systems in bacterial pathogens of animals and plants. Microbiol. Mol. Biol. Rev. 62:379-433. [PMC free article] [PubMed]
36. Hurley, C. C., A. M. Quirke, F. J. Reen, and E. F. Boyd. 2006. Four genomic islands that mark post-1995 pandemic Vibrio parahaemolyticus isolates. BMC Genomics 7:104-122. [PMC free article] [PubMed]
37. Iguchi, T., S. Kondo, and K. Hisatune. 1995. Vibrio parahaemolyticus O serotypes from O1 to O13 all produce R-type lipopolysaccharide: SDS PAGE and compositional sugar analysis. FEMS Microbiol. Lett. 130:287-292. [PubMed]
38. Iida, T., O. Suthienkul, K. S. Park, G. Q. Tang, R. K. Yamamoto, M. Ishibashi, K. Yamamoto, and T. Honda. 1997. Evidence for genetic linkage between the ure and trh genes in Vibrio parahaemolyticus. J. Med. Microbiol. 46:639-645. [PubMed]
39. Iida, T., A. Hattori, K. Tagomori, R. Nasu, R. Naim, and T. Honda. 2001. Filamentous phage associated with recent pandemic strains of Vibrio parahaemolyticus. Emerg. Infect. Dis. 7:477-478. [PMC free article] [PubMed]
40. Islam, M. S., R. Tasmin, S. I. Khan, H. B. Bakht, Z. H. Mahmood, M. Z. Rahman, N. A. Bhuiyan, M. Nishibuchi, G. B. Nair, R. B. Sack, A. Huq, R. R. Colwell, and D. A. Sack. 2004. Pandemic strains of O3:K6 Vibrio parahaemolyticus in the aquatic environment of Bangladesh. Can. J. Microbiol. 50:827-834. [PubMed]
41. Jin, L., J. W. Li, S. Q. Wang, F. H. Chao, X. W. Wang, and Z. Q. Yuan. 2005. Detection and identification of intestinal pathogenic bacteria by hybridization to oligonucleotide microarrays. World J. Gastroenterol. 11:7615-7619. [PubMed]
42. Joseph, S. W., R. R. Colwell, and J. B. Kaper. 1982. Vibrio parahaemolyticus and related halophilic vibrios. Crit. Rev. Microbiol. 10:77-124. [PubMed]
43. Kamal, A. M. 1994. The seventh pandemic of cholera, p. 1-9. In D. Barua and W. Burrows (ed.), Cholera. W. B. Saunders, Philadelphia, PA.
44. Kaneko, T., and R. R. Colwell. 1975. Incidence of Vibrio parahaemolyticus in Chesapeake Bay. Appl. Microbiol. 30:251-257. [PMC free article] [PubMed]
45. Kaneko, T., and R. R. Colwell. 1978. The annual cycle of Vibrio parahaemolyticus in Chesapeake Bay. Microb. Ecol. 4:135-155. [PubMed]
46. Kaneko, T., and R. R. Colwell. 1973. Ecology of Vibrio parahaemolyticus in Chesapeake Bay. J. Bacteriol. 113:24-32. [PMC free article] [PubMed]
47. Kelly, M. T., and E. M. D. Stroh. 1981. Occurrence of Vibrionaceae in natural and cultivated oyster populations in the Pacific Northwest. Diagn. Microbiol. Infect. Dis. 9:1-5. [PubMed]
48. Khan, A. A., S. McCarthy, R. F. Wang, and C. E. Cerniglia. 2002. Characterization of United States outbreak isolates of Vibrio parahaemolyticus using enterobacterial repetitive intergenic consensus (ERIC) PCR and development of a rapid PCR method for detection of O3:K6 isolates. FEMS Microbiol. Lett. 206:209-214. [PubMed]
49. Kudriakova, T. A., L. D. Makedonova, O. S. Dudkina, B. M. Degtiarev, A. B. Khaitovich, B. I. Savchenko, G. A. Riabchinskaia, Z. I. Us, and P. A. Serova. 1992. The phages of halophilic vibrios and its use. Zh. Mikrobiol. Epidemiol. Immunobiol. 9-10:5-7. (In Russian.) [PubMed]
50. Laohaprertthisan, V., A. Chowdhury, U. Kongmuang, S. Kalnauwakul, M. Ishibashi, C. Matsumoto, and M. Nishibuchi. 2000. Prevalence of serodiversity of the pandemic clone among the clinical strains of Vibrio parahaemolyticus isolated from Thailand. Epidemiol. Infect. 130:395-406. [PMC free article] [PubMed]
51. Libinzon, A. E., Z. I. Us, G. V. Galtseva, B. M. Degtiareva, and G. M. Golkovskii. 1995. Phages of halophilic vibrios. Zh. Mikrobiol. Epidemiol. Immunobiol. 1:15-18. (In Russian.) [PubMed]
52. Liu, X. M., Y. Chen, Y. X. Fan, and M. Q. Wang. 2006. Foodborne disease occurred in 2003—report of the National Foodborne Diseases Surveillance System. Wei Sheng Yan Jiu 35:201-204. (In Chinese.) [PubMed]
53. Lynch, T., S. Livingstone, E. Buenaventura, E. Lutter, J. Fedwick, A. G. Buret, D. Graham, and R. DeViney. 2005. Vibrio parahaemolyticus disruption of epithelial cell tight junctions occurs independently of toxin production. Infect. Immun. 73:1275-1283. [PMC free article] [PubMed]
54. Makino, K., K. Oshima, K. Kurokawa, K. Yokoyama, T. Uda, K. Tagomori, Y. Iijima, N. Najima, M. Nakano, A. Yamashita, Y. Kubota, S. Kimura, Y. Yasunaga, T. Honda, H. Shinagawa, M. Hottori, and I. Iida. 2003. Genome sequence of Vibrio parahaemolyticus: a pathogenic mechanism distinct from that of V. cholerae. Lancet 361:743-749. [PubMed]
55. Martinez-Urtaza, J., A. Lozano-Leon, A. DePaola, M. Ishibashi, K. Shimada, M. Nishibuchi, and E. Liebana. 2004. Characterization of pathogenic Vibrio parahaemolyticus isolates from clinical sources in Spain and comparison with Asian and North American pandemic isolates. J. Clin. Microbiol. 42:4672-4678. [PMC free article] [PubMed]
56. Martinez-Urtaza, J., A. Lozano-Leon, A. Vina-Feas, J. de Nova, and O. Garcia-Martin. 2006. Differences in the API 20E biochemical patterns of clinical and environmental Vibrio parahaemolyticus isolates. FEMS Microbiol. Lett. 255:75-81. [PubMed]
57. Matsumoto, C., J. Okuda, M. Ishibashi, M. Iwanaga, P. Garg, T. Ramamurthy, H. C. Wong, A. Depaola, Y. B. Kim, M. J. Albert, and M. Nishibuchi. 2000. Pandemic spread of an O3:K6 clone of Vibrio parahaemolyticus and emergence of related strains evidenced by arbitrarily primed PCR and toxRS sequence analysis. J. Clin. Microbiol. 38:578-585. [PMC free article] [PubMed]
58. McCarthy, S. A., and F. M. Khambaty. 1994. International dissemination of epidemic Vibrio cholerae by cargo ship ballast and other nonpotable waters. Appl. Environ. Microbiol. 60:2597-2601. [PMC free article] [PubMed]
59. McLaughlin, J. B., A. DePaola, C. A. Bopp, K. A. Martinek, N. P. Napolilli, C. G. Allison, S. L. Murray, E. C. Thompson, M. M. Bird, and J. P. Middaugh. 2005. Outbreak of Vibrio parahaemolyticus gastroenteritis associated with Alaskan oysters. N. Engl. J. Med. 353:1463-1470. [PubMed]
60. Miyasaka, J., S. Yahiro, Y. Arahira, H. Tokunaga, K. Katsuki, and Y. Hara-Kudo. 2006. Isolation of Vibrio parahaemolyticus and Vibrio vulnificus from wild aquatic birds in Japan. Epidemiol. Infect. 134:780-785. [PMC free article] [PubMed]
61. Monack, D. M., J. Mecsas, N. Ghori, and S. Falkow. 1997. Yersinia signals macrophages to undergo apoptosis and YopJ is necessary for this cell death. Proc. Natl. Acad. Sci. USA 94:10385-10390. [PMC free article] [PubMed]
62. Morris, J. G., Jr. 2003. Cholera and other types of vibriosis: a story of human pandemics and oysters on the half shell. Clin. Infect. Dis. 37:272-280. [PubMed]
63. Morris, J. G., Jr., R. Wilson, B. R. Davis, I. K. Wachsmuth, C. F. Riddle, H. G. Wathen, R. A. Pollard, and P. A. Blake. 1981. Non-O group 1 Vibrio cholerae gastroenteritis in the United States: clinical, epidemiologic, and laboratory characteristics of sporadic cases. Ann. Intern. Med. 94:656-658. [PubMed]
64. Myers, M. L., G. Panicker, and A. K. Bej. 2003. PCR detection of a newly emerged pandemic Vibrio parahaemolyticus O3:K6 pathogen in pure cultures and seeded waters from the Gulf of Mexico. Appl. Environ. Microbiol. 69:2194-2200. [PMC free article] [PubMed]
65. Nair, G. B., T. Ramamurthy, S. K. Bhattacharya, A. K. Mukhopadhyay, S. Garg, M. K. Bhattacharya, T. Takeda, T. Shimada, Y. Takeda, and B. C. Deb. 1994. Spread of Vibrio cholerae O139 Bengal in India. J. Infect. Dis. 169:1029-1034. [PubMed]
66. Nair, G. B., S. M. Faruque, N. A. Bhuiyan, M. Kamruzzaman, A. K. Siddique, and D. A. Sack. 2002. New variants of Vibrio cholerae biotype O1 El Tor with attributes of the classical biotype from hospitalized patients with acute diarrhea in Bangladesh. J. Clin. Microbiol. 40:3296-3299. [PMC free article] [PubMed]
67. Nasu, H., T. Iida, T. Sugahara, Y. Yamaichi, K. S. Park, K. Yokoyama, K. Makino, H. Shinagawa, and T. Honda. 2000. A filamentous phage associated with recent pandemic Vibrio parahaemolyticus O3:K6 strains. J. Clin. Microbiol. 38:2156-2161. [PMC free article] [PubMed]
68. Nishibuchi, M., A. Fasano, R. G. Russel, and J. B. Kaper. 1992. Enterotoxigenicity of Vibrio parahaemolyticus with and without genes encoding thermostable direct hemolysin. Infect. Immun. 60:3539-3545. [PMC free article] [PubMed]
69. Okuda, J., M. Ishibashi, E. Hayakawa, T. Nishino, Y. Takeda, A. K. Mukhopadhyay, S. Garg, S. K. Bhattacharya, G. B. Nair, and M. Nishibuchi. 1997. Emergence of a unique O3:K6 clone of Vibrio parahaemolyticus in Calcutta, India, and isolation of strains from the same clonal group from Southeast Asian travelers arriving in Japan. J. Clin. Microbiol. 35:3150-3155. [PMC free article] [PubMed]
70. Okura, M., R. Osawa, A. Iguchi, E. Arakawa, J. Terajima, and H. Watanabe. 2003. Genotypic analyses of Vibrio parahaemolyticus and development of a pandemic group-specific multiplex PCR assay. J. Clin. Microbiol. 41:4676-4682. [PMC free article] [PubMed]
71. Okura, M., R. Osawa, A. Iguchi, M. Takagi, E. Arakawa, J. Terajima, and H. Watanabe. 2004. PCR-based identification of pandemic group of Vibrio parahaemolyticus with a novel group-specific primer pair. Microbiol. Immunol. 48:787-790. [PubMed]
72. Okura, M., R. Osawa, E. Arakawa, J. Terajima, and H. Watanabe. 2005. Identification of Vibrio parahaemolyticus pandemic group-specific DNA sequence by genomic subtraction. J. Clin. Microbiol. 43:3533-3536. [PMC free article] [PubMed]
73. Ono, T., K. S. Park, M. Ueta, T. Iida, and T. Honda. 2006. Identification of proteins secreted via Vibrio parahaemolyticus type III secretion system I. Infect. Immun. 74:1032-1042. [PMC free article] [PubMed]
74. Osawa, R., A. Iguchi, E. Arakawa, and H. Watanabe. 2002. Genotyping of pandemic Vibrio parahaemolyticus O3:K6 still open to question. J. Clin. Microbiol. 40:2708-2709. [PMC free article] [PubMed]
75. Pal, S. C., B. K. Sircar, G. B. Nair, and B. C. Deb. 1984. Epidemiology of bacterial diarrhoeal diseases in India with special reference to Vibrio parahaemolyticus infections, p. 65-73. In Y. Takeda and T. Miwatani (ed.), Bacterial diarrhoeal disease. KTK Scientific Publishers, Tokyo, Japan.
76. Park, S.-M., T. Ono, M. Rokuda, M.-H. Jang, K. Okada, T. Iida, and T. Honda. 2004. Functional characterization of two type III secretion systems of Vibrio parahaemolyticus. Infect. Immun. 72:6659-6665. [PMC free article] [PubMed]
77. Qadri, F., M. S. Alam, M. Nishibuchi, T. Rahman, N. H. Alam, J. Chisti, S. Kondo, J. Sugiyama, N. A. Bhuiyan, M. M. Mathan, D. A. Sack, and G. B. Nair. 2003. Adaptive and inflammatory immune response in patients infected with strains of Vibrio parahaemolyticus. J. Infect. Dis. 187:1085-1096. [PubMed]
78. Quilici, M.-L., A. R. Pillot, J. Picart, and J.-M. Fournier. 2005. Pandemic Vibrio parahaemolyticus O3:K6 spread, France. Emerg. Infect. Dis. 11:1148-1149. [PMC free article] [PubMed]
79. Rahman, M., N. A. Bhuiyan, I. Kuhn, T. Ramamurthy, M. Rahman, R. Mollby, and G. B. Nair. 2006. Biochemical fingerprinting of Vibrio parahaemolyticus by the PhenePlate system: comparison between pandemic and non-pandemic serotypes. Epidemiol. Infect. 28:1-5. [PMC free article] [PubMed]
80. Sack, D. A., R. B. Sack, G. B. Nair, and A. K. Siddique. 2004. Cholera. Lancet 363:223-233. [PubMed]
81. Sarkar, B. L., G. B. Nair, A. K. Banerjee, and S. C. Pal. 1985. Seasonal distribution of Vibrio parahaemolyticus in fresh water environs and in association with freshwater fishes in Calcutta. Appl. Environ. Microbiol. 49:132-136. [PMC free article] [PubMed]
82. Sen, B., B. Dutta, S. Chatterjee, M. K. Bhattacharya, R. K. Nandy, A. K. Mukhopadhyay, D. N. Gangopadhyay, S. K. Bhattacharya, and T. Ramamurthy. The first outbreak of acute diarrhea due to pandemic strain of Vibrio parahaemolyticus O3:K6 in Kolkata, India. Int. J. Infect. Dis., in press. [PubMed]
83. Shirai, H., H. Ito, T. Hirayama, Y. Nakamoto, N. Nakabayashi, K. Kumagai, Y. Takeda, and M. Nishibuchi. 1990. Molecular epidemiologic evidence for association of thermostable direct hemolysin (TDH) and TDH-related hemolysin of Vibrio parahaemolyticus with gastroenteritis. Infect. Immun. 58:3568-3573. [PMC free article] [PubMed]
84. Sircar, B. K., B. C. Deb, S. P. De, A. Ghosh, and S. C. Pal. 1976. Clinical and epidemiological studies on Vibrio parahaemolyticus infection in Calcutta (1975). Indian J. Med. Res. 64:576-580. [PubMed]
85. Smolikova, L. M., I. M. Lomov, T. V. Khomenko, G. P. Murnachev, T. A. Kudriakova, O. P. Fetsailova, E. M. Sanamiants, L. D. Makedonova, G. V. Kachkina, and E. N. Golenishcheva. 2001. Studies on halophilic vibrios causing a food poisoning outbreak in the city of Vladivostok. Zh. Mikrobiol. Epidemiol. Immunobiol. 63:3-7. [PubMed]
86. Stinson, M. W., R. McLaughlin, S. H. Choi, Z. E. Juarez, and J. Barnard. 1998. Streptococcal histone-like protein: primary structure of hlpA and protein binding to lipoteichoic acid and epithelial cells. Infect. Immun. 66:259-265. [PMC free article] [PubMed]
87. Takeda, Y. 1983. Thermostable direct hemolysin of Vibrio parahaemolyticus. Pharmacol. Ther. 19:123-146. [PubMed]
88. Thompson, C. A., C. Vanderzant, and S. M. Ray. 1976. Serological and hemolytic characteristics of Vibrio parahaemolyticus from marine sources. J. Food Sci. 41:204-205.
89. Tomoyasu, T. 1992. Development of immunomagnetic enrichment method selective for Vibrio parahaemolyticus serotype K and its application to food poisoning study. Appl. Environ. Microbiol. 58:2679-2682. [PMC free article] [PubMed]
90. Tuyet, D. T., V. D. Thiem, L. V. Seidlein, A. Chowdhury, E. Park, D. G. Canh, B. T. Chien, T. V. Tung, A. Naficy, M. R. Rao, M. Ali, H. Lee, T. H. Sy, M. Nichibuchi, J. Clemens, and D. D. Trach. 2002. Clinical, epidemiological, and socioeconomic analysis of an outbreak of Vibrio parahaemolyticus in Khanh Hoa province, Vietnam. J. Infect. Dis. 186:1615-1620. [PubMed]
91. Vasconcelos, F. J., W. J. Stang, and R. H. Laidlaw. 1975. Isolation of Vibrio parahaemolyticus and Vibrio alginolyticus from estuarine areas of Southeastern Alaska. Appl. Microbiol. 29:557-559. [PMC free article] [PubMed]
92. Vuddhakul, V., A. Chowdhury, V. Laohaprertthisan, P. Pungrasamee, N. Patararungrong, P. Thianmontri, M. Ishibashi, C. Matsumoto, and M. Nishibuchi. 2000. Isolation of a pandemic O3:K6 clone of a Vibrio parahaemolyticus strain from environmental and clinical sources in Thailand. Appl. Environ. Microbiol. 66:2685-2689. [PMC free article] [PubMed]
93. Wagatsuma, S. 1974. Ecological studies on Kanagawa phenomenon positive strains of Vibrio parahaemolyticus, p. 91-96. In T. Fujino, G. Sakaguchi, R. Sakazaki, and Y. Takeda (ed.), International symposium on Vibrio parahaemolyticus. Saikon Publishing Co., Ltd., Tokyo, Japan.
94. Waldor, M. K., and J. J. Mekalanos. 1996. Lysogenic conversion by a filamentous phage encoding cholera toxin. Science 272:1910-1914. [PubMed]
95. Wang, H. Z., M. M. Wang, D. O'Toole, M. M. Mak, R. S. Wu, and R. Y. Kong. 2006. Identification of a DNA methyltransferase gene carried on a pathogenicity island-like element (VPAI) in Vibrio parahaemolyticus and its prevalence among clinical and environmental isolates. Appl. Environ. Microbiol. 72:4455-4460. [PMC free article] [PubMed]
96. Ward, L. N., and A. K. Bej. 2006. Detection of Vibrio parahaemolyticus in shellfish by use of multiplexed real-time PCR with Taqman fluorescent probes. Appl. Environ. Microbiol. 72:2031-2042. [PMC free article] [PubMed]
97. Wilkes, J. G., L. G. Rushing, J. F. Gagnon, S. A. McCarthy, F. Rafii, A. A. Khan, C. A. Kaysner, T. M. Heinze, and J. B. Sutherland. 2005. Rapid phenotypic characterization of Vibrio isolates by pyrolysis metastable atom bombardment mass spectrometry. Antonie Leeuwenhoek 88:151-161. [PubMed]
98. Williams, T. L., S. M. Musser, J. L. Nordstrom, A. D. Paola, and S. R. Monday. 2004. Identification of a protein biomarker unique to the pandemic O3:K6 clone of Vibrio parahaemolyticus. J. Clin. Microbiol. 42:1657-1665. [PMC free article] [PubMed]
99. Winstanley, C., and C. A. Hart. 2001. Type III secretion systems and pathogenicity islands. J. Med. Microbiol. 50:116-126. [PubMed]
100. Wong, H. C., S. H. Liu, L. W. Ku, I. Y. Lee, T. K. Wang, Y. S. Lee, C. L. Lee, L. P. Kuo, and D. Y. Shih. 2000. Characterization of Vibrio parahaemolyticus isolates obtained from food-borne illness outbreaks during 1992 through 1995 in Taiwan. J. Food Prot. 63:900-906. [PubMed]
101. Wong, H. C., S. H. Liu, T. K. Wang, C. L. Lee, C. S. Chiou, D. P. Liu, M. Nishibuchi, and B. K. Lee. 2000. Characteristics of Vibrio parahaemolyticus O3:K6 from Asia. Appl. Environ. Microbiol. 66:3981-3986. [PMC free article] [PubMed]
102. Wong, H. C., C. H. Chen, Y. J. Chung, S. H. Liu, T. K. Wang, C. L. Lee, C. S. Chiou, M. Nishibuchi, and B. K. Lee. 2005. Characterization of new O3:K6 strains and phylogenetically related strains of Vibrio parahaemolyticus isolated in Taiwan and other countries. J. Appl. Microbiol. 98:572-580. [PubMed]
103. World Health Organization. 1999. Vibrio parahaemolyticus, Japan, 1996-1998. Wkly. Epidemiol. Rec. 74:361-363. [PubMed]
104. Yamasaki, M., D. M. Meng, J. C. Pan, F. Y. Zhu, and K. Chen. 2003. Epidemiological study of outbreaks and sporadic cases due to Vibrio parahaemolyticus-serotype O3:K6 in Aichi Prefecture, Japan during 1998 and 2001. Kansenshogaku Zasshi 77:1015-1023. (In Japanese.) [PubMed]
105. Yeung, P. S., M. C. Hayes, A. DePaola, C. A. Kaysner, L. Kornstein, and K. J. Boor. 2002. Comparative phenotypic, molecular, and virulence characterization of Vibrio parahaemolyticus O3:K6 isolates. Appl. Environ. Microbiol. 68:2901-2909. [PMC free article] [PubMed]
106. Zhang, S. D., J. Kassis, B. Olde, D. M. Mellerick, and W. F. Odenwald. 1996. Pollux, a novel Drosophila adhesion molecule, belongs to a family of proteins expressed in plants, yeast, nematodes, and man. Genes Dev. 10:1108-1119. [PubMed]
107. Zhang, W., D. M. Meng, J. C. Pan, F. Y. Zhu, and K. Chen. 2004. Characteristics of virulence gene in Vibrio parahaemolyticus strains isolated from clinical patients and environment in Hangzhou, China. Zhonghua Yu Fang Yi Xue Za Zhi 38:200-203. (In Chinese.) [PubMed]

Articles from Clinical Microbiology Reviews are provided here courtesy of American Society for Microbiology (ASM)
PubReader format: click here to try


Related citations in PubMed

See reviews...See all...

Cited by other articles in PMC

See all...


Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...