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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptNIH Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
Clin Infect Dis. Author manuscript; available in PMC Apr 15, 2009.
Published in final edited form as:
PMCID: PMC2613645
NIHMSID: NIHMS82424

Epidemiology of Pneumocystis Colonization in Families

Abstract

Whether Pneumocystis colonization is transmitted in families with HIV-infected members is unknown. Using nested polymerase chain reaction of oropharyngeal or nasopharyngeal samples, we detected colonization in 11.4% of HIV-infected adults and 3.3% of their children, but there was no evidence of clustering.

Keywords: Pneumocystis, colonization, HIV, children

Introduction

The development of sensitive molecular techniques has led to the discovery of a colonization or carrier state of Pneumocystis jirovecii in which low levels of the organism are detected in subjects without clinical Pneumocystis pneumonia (PCP)[1]. Colonization may be an important step in the organism's life cycle, and transmission of disease could occur via colonized individuals. In addition, Pneumocystis (Pc) colonization might increase risk of developing PCP in a susceptible host. Pneumocystis colonization has been detected in HIV-infected adults and in non-immunosuppressed children [2-4], but whether transmission of Pneumocystis colonization occurs in families with HIV-infected members is unknown.

We examined a cohort of HIV-infected adults and their HIV-infected and HIV-negative children to determine the prevalence and risk factors for Pneumocystis colonization in families.

Methods

Subjects

Subjects were recruited from the Maternal, Child, and Adolescent clinic at the University of Southern California from September 2004 through August 2005. This clinic consists of HIV-infected adults, primarily women, and their HIV-infected and HIV-negative offspring. Subjects were enrolled at routinely scheduled and urgent care medical appointments. Informed consent was obtained from all subjects, and the Institutional Review Board of the University of Southern California approved the study.

Data collection

Clinical data were collected by subject interview and medical record review. Demographic data consisted of age, gender, and race/ethnicity. Medical history obtained included previous episodes of PCP or other opportunistic infections, smoking history or smoke exposure (in children), current respiratory symptoms, and use of Pneumocystis prophylaxis and antiretroviral medications. Laboratory data for the HIV-infected subjects included most recent CD4 cell count and serum HIV viral RNA level.

Specimen collection

Nasopharyngeal aspirates were obtained from children less than three years of age with 3cc of sterile saline using a 6.0 or 8.0 French suction catheter. Oropharyngeal washes were obtained from older children and adults by a one-minute gargle with 10cc of sterile saline.

DNA extraction and PCR amplification

DNA was extracted from oropharyngeal washes or nasopharyngeal aspirates using the DNeasy kit (Qiagen, Valencia, CA). Pneumocystis colonization was determined by nested PCR of the mitochondrial large subunit rRNA (mtLSU) as previously described [2]. In order to prevent contamination, all steps of DNA extraction and PCR amplification were carried out in separate rooms. Negative and positive controls (DNA from lung tissue known to contain human Pneumocystis) were included in all reactions. PCR products were purified and sequenced as previously described and determined to be human Pneumocystis [2]. PCR for the human beta-globin gene was performed to test for the presence of DNA and lack of PCR inhibitors [5].

Statistical analysis

Data were double-entered and analyzed using SAS version 9.1 (SAS Institute Inc., Cary, NC). Continuous variables were described using mean and standard deviation or median and range depending on normality of data. Univariate analyses were performed to determine clinical variables related to Pc colonization using either t-tests/Wilcoxon ranksum or chi-square/Fisher's exact test. Significance was determined for a p-value of less than 0.05.

Results

Forty-four HIV-infected adults were enrolled. Pc colonization was detected in 5 of 44 (11.3%) adults. There were no significant differences between the colonized and non-colonized adults in terms of demographic or clinical characteristics (Table 1). Most were females (93.2%) and of a minority ethnic group or race (86.4%). The mean years since HIV diagnosis was 5.7 and 34.1% had ever had an AIDS diagnosis. Only 11.4% had a CD4 cell count below 200 cells/μl and many (63.6%) had a serum HIV viral RNA level below 400 copies/ml.

Table 1
Characteristics of adult subjects by Pneumocystis colonization status.

Sixty children, ages 2 weeks to 17.6 years, were enrolled. Colonization was detected in two (3.3%) pediatric subjects (Table 2). These subjects were HIV-negative females less than six months of age with HIV-infected mothers. Neither had a mother with a history of PCP. One mother was receiving PCP prophylaxis. Both subjects had upper respiratory tract symptoms at the time of colonization. Colonized children were significantly more likely to be less than one year of age (p=0.04). None of the colonized adults or children were members of the same family. Interestingly, all colonized adults and children were Hispanic (p=0.04 for comparison to all other race/ethnicities).

Table 2
Characteristics of pediatric subjects by Pneumocystis colonization status.

Discussion

This study is one of the first to examine Pneumocystis colonization in HIV-infected children and in families with an HIV-infected member. Somewhat surprisingly, we found no evidence of transmission in families and a low prevalence of colonization in HIV-infected adults and their offspring. There were also no clinical characteristics that distinguished colonized from non-colonized subjects in the adult population, but when examining the adult and pediatric cohorts together, colonized subjects were more likely to be Hispanic. Colonization in the pediatric population was associated with age less than one year, and there was a tendency for colonized children to have upper respiratory symptoms.

We found no evidence of clustering of colonization within families despite previous work demonstrating that person-to-person transmission of Pneumocystis likely occurs. Other studies have found that health care workers caring for patients with PCP can develop Pneumocystis colonization [14,15], and there has been a reported case of probable maternal-infant transmission of PCP from an HIV-infected mother [16]. Animal studies support the theory that transmission of colonization to a normal adult host can result from exposure to an infected one [17-19], and newborn mice rapidly acquire Pneumocystis colonization after birth, suggesting transmission from a maternal source [20]. Our results indicate that if person-to-person transmission is occurring, it may be transient or the burden of organisms in asymptomatic individuals may be quite low.

The prevalence of colonization we found in HIV-infected adults is much lower than previously reported. In an autopsy study, 46.2% of subjects were colonized and another study of HIV-infected subjects with pneumonia found that 68.8% were colonized [2,3]. Other studies have reported prevalence of colonization in HIV-infected adults ranging from 10.0% to 43.8% [1].

In the pediatric HIV-infected population, only one previous study has reported prevalence of colonization and found that 9 of 45 (20.0%) HIV-infected children were colonized when examined at autopsy after dying of a respiratory illness [6]. In the non-HIV-infected pediatric population, Pneumocystis colonization prevalence ranges from 15.9% to 32.0% using nasopharyngeal and/or oropharyngeal samples in children with bronchiolitis or acute respiratory syndromes [1]. Colonization in autopsy series of children has found a range of colonization from 25% to 100% [21,22]. The colonization prevalence we found was much lower than in any of these populations.

There are several possible explanations for our low prevalence of colonization. First, geographic variation might contribute to a lower level of colonization. We have previously shown that colonization risk varies by city, with Los Angeles, our study site, having a lower prevalence than other cities [2]. Therefore, our results might be different if repeated in a different area. Season might also affect colonization as has previously been shown with PCP [7], although we did not find variation in colonization throughout the study period. In addition, our population was fairly healthy and consisted entirely of outpatients. Many previous studies have examined subjects with advanced HIV or with lower respiratory tract symptoms. Colonization in a relatively healthy population might be rapidly cleared by the immune system. Finally, nasopharyngeal and oral washes might lack sufficient sensitivity. More invasive samples such as bronchoalveolar lavage might have detected evidence of colonization, but were not feasible in this outpatient study. However, other studies using similar PCR techniques have shown that oropharyngeal washes and nasopharyngeal aspirates adequately detect colonization [4,8-10], and there was no evidence of PCR inhibitors. Collection of serial samples might also have increased our ability to detect colonization or clustering in families.

We found no clinical risk factors that were associated with colonization in adults. We have previously reported that cigarette smoking increases the risk of colonization, but this result was not duplicated in the current study [2]. Interestingly, both current and previous work demonstrate that CD4 cell count, history of PCP, and use of PCP prophylaxis do not impact colonization [2,3]. In the non-HIV-infected population, underlying lung disease and pregnancy have been shown to increase colonization risk [11-13], but these subject groups were not included in the current cohort. Previously reported risk factors in non-HIV-infected children include presence of respiratory symptoms and young age [4], similar to our pediatric population. Interestingly, when we examined the cohort as a whole, colonized subjects were more likely to be Hispanic and in fact, there were no colonized adults or children who were not Hispanic. Race or ethnicity has not been previously demonstrated to influence Pneumocystis colonization risk, and it is unclear if this finding is due to environmental or biologic causes. Because the number of colonized subjects was low, we may have lacked sufficient power to detect all clinical characteristics associated with colonization.

In conclusion, this study demonstrates that Pneumocystis colonization is relatively uncommon in healthy HIV-infected outpatient adults and their children. Transmission of colonization does not seem to be occurring within families. Colonization was more common in Hispanic adult and pediatric subjects, but no other clinical characteristics were associated with colonization in the adult population. The pediatric subjects who were colonized were young HIV-negative infants who had respiratory symptoms at the time of colonization.

Acknowledgments

Supported by NIH HL072837 and HL083461 (AM).

Footnotes

None of the authors has a conflict of interest.

Reference List

1. Morris A, Wei K, Afshar K, Huang L. Epidemiology and significance of Pneumocystis colonization. J Inf Dism. in press.
2. Morris A, Kingsley LA, Groner G, Lebedeva IP, Beard CB, Norris KA. Prevalence and clinical predictors of Pneumocystis colonization among HIV-infected men. AIDS. 2004;18:793–8. [PubMed]
3. Huang L, Crothers K, Morris A, et al. Pneumocystis colonization in HIV-infected patients. J Eukaryot Microbiol. 2003;50S:616–7. [PubMed]
4. Vargas SL, Hughes WT, Santolaya ME, et al. Search for primary infection by Pneumocystis carinii in a cohort of normal, healthy infants. Clin Infect Dis. 2001;32:855–61. [PubMed]
5. Saiki RK, Scharf S, Faloona F, et al. Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. 1985. Biotechnology. 1992;24:476–80. [PubMed]
6. Kasolo F, Lishimpi K, Chintu C, et al. Identification of Pneumocystis carinii DNA by polymerase chain reaction in necropsy lung samples from children dying of respiratory tract illnesses. J Pediatr. 2002;140:367–9. [PubMed]
7. Miller RF, Grant AD, Foley NM. Seasonal variation in presentation of Pneumocystis carinii pneumonia. Lancet. 1992;339:747–8. [PubMed]
8. Nevez G, Totet A, Pautard JC, Raccurt C. Pneumocystis carinii detection using nested-PCR in nasopharyngeal aspirates of immunocompetent infants with bronchiolitis. J Eukaryot Microbiol. 2001;(Suppl):122S–3S. [PubMed]
9. Totet A, Meliani L, Lacube P, et al. Immunocompetent infants as a human reservoir for Pneumocystis jirovecii: rapid screening by non-invasive sampling and real-time PCR at the mitochondrial large subunit rRNA gene. J Eukaryot Microbiol. 2003;50S:668–9. [PubMed]
10. Larsen HH, von Linstow ML, Lundgren B, Hogh B, Westh H, Lundgren JD. Primary Pneumocystis infection in infants hospitalized with acute respiratory tract infection. Emerg Infect Dis. 2007;13:66–72. [PMC free article] [PubMed]
11. Vargas SL, Ponce CA, Sanchez CA, Ulloa AV, Bustamante R, Juarez G. Pregnancy and asymptomatic carriage of Pneumocystis jiroveci. Emerg Infect Dis. 2003;9:605–6. [PMC free article] [PubMed]
12. Calderon EJ, Varela JM, Medrano FJ, et al. Epidemiology of Pneumocystis carinii pneumonia in southern Spain. Clin Microbiol Infect. 2004;10:673–6. [PubMed]
13. Morris A, Sciurba FC, Lebedeva IP, et al. Association of chronic obstructive pulmonary disease severity and Pneumocystis colonization. Am J Respir Crit Care Med. 2004;170:408–13. [PubMed]
14. Vargas SL, Ponce CA, Gigliotti F, et al. Transmission of Pneumocystis carinii DNA from a patient with P. carinii pneumonia to immunocompetent contact health care workers. J Clin Microbiol. 2000;38:1536–8. [PMC free article] [PubMed]
15. Miller RF, Ambrose HE, Wakefield AE. Pneumocystis carinii f. sp. hominis DNA in immunocompetent health care workers in contact with patients with P. carinii pneumonia. J Clin Microbiol. 2001;39:3877–82. [PMC free article] [PubMed]
16. Miller RF, Ambrose HE, Novelli V, Wakefield AE. Probable mother-to-infant transmission of Pneumocystis carinii f. sp. hominis infection. J Clin Microbiol. 2002;40:1555–7. [PMC free article] [PubMed]
17. Dumoulin A, Mazars E, Seguy N, et al. Transmission of Pneumocystis carinii disease from immunocompetent contacts of infected hosts to susceptible hosts. Eur J Clin Microbiol Infect Dis. 2000;19:671–8. [PubMed]
18. An CL, Gigliotti F, Harmsen AG. Exposure of immunocompetent adult mice to Pneumocystis carinii f. sp. muris by cohousing: growth of P. carinii f. sp. muris and host immune response. Infect Immun. 2003;71:2065–70. [PMC free article] [PubMed]
19. Gigliotti F, Harmsen AG, Wright TW. Characterization of transmission of Pneumocystis carinii f. sp. muris through immunocompetent BALB/c mice. Infect Immun. 2003;71:3852–6. [PMC free article] [PubMed]
20. Icenhour CR, Rebholz SL, Collins MS, Cushion MT. Early acquisition of Pneumocystis carinii in neonatal rats as evidenced by PCR and oral swabs. Eukaryot Cell. 2002;1:414–9. [PMC free article] [PubMed]
21. Vargas SL, Ponce CA, Hughes WT, et al. Association of primary Pneumocystis carinii infection and sudden infant death syndrome. Clin Infect Dis. 1999;29:1489–93. [PubMed]
22. Beard CB, Fox MR, Lawrence GG, et al. Genetic differences in Pneumocystis isolates recovered from immunocompetent infants and from adults with AIDS: Epidemiological implications. J Inf Dis. 2005;192:1815–18. [PubMed]

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