• We are sorry, but NCBI web applications do not support your browser and may not function properly. More information
Logo of eidLink to Publisher's site
Emerg Infect Dis. Jan 2008; 14(1): 155–157.
PMCID: PMC2600150

Human Case of Streptococcus suis Serotype 16 Infection

Abstract

Streptococcus suis infection is an emerging zoonosis in Southeast Asia. We report a fatal case of S. suis serotype 16 infection in a Vietnamese man in 2001.

Keywords: Streptococcus suis, serotype 16, typing, dispatch

Streptococcus suis is a gram-positive, facultatively anaerobic coccus that may cause pneumonia, meningitis, septicemia, and arthritis in pigs. The pig can also be a healthy carrier of S. suis in the upper respiratory tract (particularly the tonsils and nasal cavities), the genital tract, and the alimentary tract (1,2). The first case of S. suis infection in humans was reported in Denmark in 1968. Since then, increasing numbers of cases have been reported in many countries, including the Netherlands; the United Kingdom; France; Hong Kong Special Administrative Region, People’s Republic of China; Thailand; Taiwan; and the United States (37). A recent outbreak of S. suis infections in Sichuan Province, People’s Republic of China, emphasized the importance of S. suis as an emerging zoonosis (8). S. suis is also the most important cause of bacterial meningitis in adults at the Hospital for Tropical Diseases (HTD) in Ho Chi Minh City, Vietnam (N.T.H Mai et al., unpub. data). The number of cases is likely underreported and will likely increase further with increased awareness and enhanced capacity to culture and identify S. suis.

The Patient

A 57-year-old unemployed man from Long An Province, southern Vietnam, who had a history of alcohol abuse, had a 10-day history of abdominal pain, jaundice, anorexia, and weight loss. At the time of admission to HTD in 2001, the patient was lethargic, his vital signs were stable, and his neck was not stiff. Physical examination showed cutaneous spider naevi, jaundice, hepatosplenomegaly, and ascites. Leukocyte count was 15.3 ×103 cells/μL (70% neutrophils), blood urea nitrogen 12.1 mmol/L (reference range 3.57–7.14 mmol/L), creatinine 150 μmol/L (<115 mmol/L), sodium 127 mmol/L (135–145 mmol/L), potassium 6.67 mmol/L (3.5–5.1 mmol/L), serum aspartate aminotransferase 87 IU/L (12–30 IU/L), serum alamine aminotransferase 41 IU/L (13–40 IU/L), and albumin 20 g/L (35–52 g/L). An abdominal ultrasound examination showed hepatosplenomegaly and ascites. Ascitic fluid was cloudy and contained 5 g/L protein. Results of Gram stain and culture of ascitic fluid were negative. A diagnosis of spontaneous bacterial peritonitis associated with alcoholic liver cirrhosis was made, and the patient was treated with 2 g/day of ceftriaxone.

Twenty-four hours after admission, acute respiratory distress developed. The patient’s family decided to take him home because they were unable to pay for further treatment; the patient died on the same day. The blood culture (BACTEC 9050 system; Becton Dickinson Microbiology Systems, Sparks, MD, USA), which was taken at the time of admission, grew S. suis 24 hours after collection. Further inquiries into potential pig exposure, after the blood culture results were reported, indicated that the patient kept pigs near his house and was known to regularly consume portions of the pig that had a high risk of being contaminated, such as the intestine.

S. suis was identified on the basis of colony morphology, negative katalase reaction, optochin resistance, and APIStrep (bioMérieux, Marcy l’Etoile, France). Serotyping was performed by slide agglutination using specific antisera (Statens Serum Institute, Copenhagen, Denmark) and was positive for serotype 16. Confirmation of the serotype was performed at the International Reference Laboratory for S. suis Serotyping, Quebec City, Quebec, Canada (M. Gottschalk). This strain was susceptible to penicillin (MIC 0.032 mg/L), ceftriaxone (0.064 mg/L), rifampin (0.032 mg/L), chloramphenicol (2 mg/L), erythromycin (0.064 mg/L), levofloxacin (0.38 mg/L), and vancomycin (0.5 mg/L) but resistant to tetracycline (64 mg/L) by Etest (AB-Biodisk, Solna, Sweden) when Clinical Laboratory Standard Institute breakpoints were used. On pulsed-field gel electrophoresis (PFGE) that used restriction enzyme SmaI, this strain showed little similarity with a representative set of serotype 2 isolates from Vietnam (Figure). Multilocus sequence typing (MLST) (www.mlst.net) showed that the sequence of 5 of 7 alleles of the included housekeeping genes had not been previously described. Thus, this strain was assigned the new sequence type 106. On eBURST analysis (www.mlst.net), this sequence type does not belong to any of the clonal complexes but is a singleton. PCR for detection of the genes encoding the putative virulence factors extracellular protein factor (EF) and suilysin were negative. Results of Western blot for detection of muramidase-released protein (MRP) and EF, using rabbit polyclonal antibody against MRP and EF (provided by H. Smith, the Netherlands), were also negative. S. suis serotype 2 strains 31533 and 89-1591 (provided by M. Gottschalk, Canada) were used as positive and negative controls, respectively.

Figure
Pulsed-field gel electrophoresis after SmaI digestion of Streptococcus suis serotype 16 strain SS07 and a representative set of S. suis serotype 2 strains isolated from patients with meningitis in southern Vietnam. A dendrogram was generated by Dice analysis ...

The total number of human S. suis infections reported until August 2006 was ≈400, and nearly 90% of these cases occurred in China, Thailand, Hong Kong, Taiwan, and the Netherlands (4). These data did not include at least 200 cases of S. suis infection in Vietnam (C. Schultsz, unpub. data). At present, 33 capsular serotypes of S. suis have been recognized (1,4). S. suis serotype 2 is considered to be the most pathogenic to pigs and humans. All human cases of S. suis infection for which serotyping was available were caused by S. suis serotype 2, except for 1 case of serotype 1 (9), 1 case of serotype 4 (3), and 1 case of serotype 14 (6). Among 116 cases of S. suis meningitis seen at HTD from 1997 through 2005, 115 were caused by serotype 2 and 1 by serotype 14.

S. suis serotype 2 can cause meningitis, septicemia and septic shock, arthritis, endocarditis, pneumonia, endophthalmitis, and cellulitis in humans (3,5,8). The mortality rate for S. suis serotype 2 meningitis is <10% (10), but it can reach 70% among patients with septicemia and septic shock (11). The exact route of infection for humans is not known. Cases have been linked to accidental inoculation through skin injuries, for example, during occupational exposure to pigs and pork, but inhalation of aerosols and ingestion of contaminated food have also been suggested (3,9,11,12). Preexisting medical conditions, such as alcoholism and liver cirrhosis, as was present in our patient, or a prior splenectomy may predispose to severe infection.

Serotype 16 has never been isolated from humans and, to our knowledge, has also rarely been reported as a cause of invasive disease in pigs. One isolate of S. suis serotype 16 was reported from a diseased pig in Germany and 4 isolates from slaughter pigs in South Korea (13,14). The S. suis serotype 16 strain was sensitive to all antimicrobial agents tested except tetracycline, as has been reported for serotype 2 isolates (5). PFGE results showed that this human serotype 16 isolate was unrelated to human serotype 2 isolates. On MLST, this isolate had a new sequence type that did not belong to any of the clonal complexes. In contrast, most serotype 2 isolates reported so far belong to clonal complex 1 (www.mlst.net). Taken together, these results suggest that capsule switch, such as has been observed for S. pneumoniae, does not explain the emergence of invasive isolates of a different serotype. In addition, the PCR and Western blot analyses indicate that the serotype 2 capsule, EF, MRP, or suilysin is not required for virulence of S. suis in humans, as has also been shown in pigs.

Conclusions

S. suis infection is an emerging zoonosis in Asia. Strains with serotype 16 are among those capable of infecting humans.

Acknowledgments

This study was supported by The Wellcome Trust.

Biography

• 

Dr Nghia is an infectious disease specialist. His research interests include the epidemiology, diagnosis, clinical manifestations, and treatment of Streptococcus suis infection in Vietnam.

Footnotes

Suggested citation for this article: Nghia HDT, Hoa NT, Linh LD, Campbell J, Diep TS, Chau NVV, et al. Human case of Streptococcus suis serotype 16 infection. Emerg Infect Dis [serial on the Internet]. 2008 Jan [date cited]. Available from http://www.cdc.gov/EID/content/14/1/155.htm

References

1. Gottschalk M, Segura M The pathogenesis of the meningitis caused by Streptococcus suis: the unresolved questions. Vet Microbiol 2000;76:259–72 10.1016/S0378-1135(00)00250-9 [PubMed] [Cross Ref]
2. Staats JJ, Feder I, Okwumabua O, Chengappa MM Streptococcus suis: past and present. Vet Res Commun 1997;21:381–407 10.1023/A:1005870317757 [PubMed] [Cross Ref]
3. Arends JP, Zanen HC Meningitis caused by Streptococcus suis in humans. Rev Infect Dis 1988;10:131–7 [PubMed]
4. Lun ZR, Wang QP, Chen XG, Li AX, Zhu XQ Streptococcus suis: an emerging zoonotic pathogen. Lancet Infect Dis 2007;7:201–9 10.1016/S1473-3099(07)70001-4 [PubMed] [Cross Ref]
5. Wangkaew S, Chaiwarith R, Tharavichitkul P, Supparatpinyo K Streptococcus suis infection: a series of 41 cases from Chiang Mai University Hospital. J Infect 2006;52:455–60 10.1016/j.jinf.2005.02.012 [PubMed] [Cross Ref]
6. Watkins EJ, Brooksby P, Schweiger MS, Enright SM Septicaemia in a pig-farm worker. Lancet 2001;357:38 10.1016/S0140-6736(00)03570-4 [PubMed] [Cross Ref]
7. Willenburg KS, Sentochnik DE, Zadoks RN Human Streptococcus suis meningitis in the United States. N Engl J Med 2006;354:1325 10.1056/NEJMc053089 [PubMed] [Cross Ref]
8. Yu H, Jing H, Chen Z, Zheng H, Zhu X, Wang H, et al. Human Streptococcus suis outbreak, Sichuan, China. Emerg Infect Dis 2006;12:914–20 [PMC free article] [PubMed]
9. Vilaichone RK, Vilaichone W, Nunthapisud P, Wilde H Streptococcus suis infection in Thailand. J Med Assoc Thai 2002;85(Suppl 1):S109–17 [PubMed]
10. Suankratay C, Intalapaporn P, Nunthapisud P, Arunyingmongkol K, Wilde H Streptococcus suis meningitis in Thailand. Southeast Asian J Trop Med Public Health 2004;35:868–76 [PubMed]
11. Tang J, Wang C, Feng Y, Yang W, Song H, Chen Z, et al. Streptococcal toxic shock syndrome caused by Streptococcus suis serotype 2. PLoS Med 2006;3:e151 10.1371/journal.pmed.0030151 [PMC free article] [PubMed] [Cross Ref]
12. Sriskandan S, Slater JD Invasive disease and toxic shock due to zoonotic Streptococcus suis: an emerging infection in the East? PLoS Med 2006;3:e187 10.1371/journal.pmed.0030187 [PMC free article] [PubMed] [Cross Ref]
13. Han DU, Choi C, Ham HJ, Jung JH, Cho WS, Kim J, et al. Prevalence, capsular type and antimicrobial susceptibility of Streptococcus suis isolated from slaughter pigs in Korea. Can J Vet Res 2001;65:151–5 [PMC free article] [PubMed]
14. Wisselink HJ, Smith HE, Stockhofe-Zurwieden N, Peperkamp K, Vecht U Distribution of capsular types and production of muramidase-released protein (MRP) and extracellular factor (EF) of Streptococcus suis strains isolated from diseased pigs in seven European countries. Vet Microbiol 2000;74:237–48 10.1016/S0378-1135(00)00188-7 [PubMed] [Cross Ref]

Articles from Emerging Infectious Diseases are provided here courtesy of Centers for Disease Control and Prevention
PubReader format: click here to try

Formats:

Related citations in PubMed

See reviews...See all...

Cited by other articles in PMC

See all...

Links

Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...