EID Journal Home > Volume 14, Number 10–October 2008

Volume 14, Number 10–October 2008

Research CME

Microbial Interactions during Upper Respiratory Tract Infections

Melinda M. Pettigrew, Janneane F. Gent, Krystal Revai, Janak A. Patel, and Tasnee Chonmaitree
Author affiliations: Yale School of Public Health, New Haven, Connecticut, USA (M. Pettigrew, J. Gent); and University of Texas Medical Branch, Galveston, Texas, USA (K. Revai, J. Patel, T. Chonmaitree)

Suggested citation for this article

Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis, and Staphylococcus aureus often asymptomatically colonize the nasopharynx of young children and are also associated with disease. S. pneumoniae, H. influenzae, and M. catarrhalis are the 3 most common otitis media pathogens (1,2). S. pneumoniae are also common causes of pneumonia, sepsis, and meningitis in young children (3). The proportion of young children colonized with any of these 3 bacteria species can be >50% in certain populations (4–6). S. aureus strains colonize up to 35% of young children and are associated with a wide range of diseases including soft tissue infections, sepsis, and pneumonia (7,8). Increases in the incidence of disease caused by community-acquired methicillin-resistant S. aureus are of great concern (9).

Host factors have been shown to influence colonization with S. pneumoniae, H. influenzae, M. catarrhalis, and S. aureus. These include host immunity, age, gender, race, out-of-home daycare, breastfeeding, and environmental exposure to tobacco smoke (10). The magnitude of host effects may differ by bacteria species.

Interactions between bacteria influence which species persist in the nasopharynx (11–13). Bacteria species may be positively associated; this occurs when they are found together more often than would be expected by chance. A negative association could occur when bacteria compete within same environment. Several studies have described a negative association between S. pneumoniae and S. aureus (12–16). Understanding of interactions between S. pneumoniae, H. influenzae, M. catarrhalis, and S. aureus is limited.

The nasopharyngeal flora change over time; the level of bacteria colonization is higher during upper respiratory infection (URI) (6,17). Knowledge is lacking regarding S. pneumoniae, H. influenzae, M. catarrhalis, and S. aureus interactions during URI because colonization studies either do not examine competitive interactions among all 4 pathogens or focus on healthy children (5,11,16,18). Children are susceptible to secondary bacterial infections during and after URI (19–21).

A better understanding of polymicrobial interactions in the nasopharynx is important for several reasons. Colonization is the initial step in the disease process (22,23). Colonized children serve as reservoirs for bacterial transmission to others in the community (24). Additionally, antibimicrobial drugs or vaccines, which target specific bacteria species, may alter polymicrobial interactions in the nasopharynx and have unanticipated consequences (25,26). The goals of our study were to 1) describe the prevalence of colonization with S. pneumoniae, H. influenzae, M. catarrhalis, and S. aureus; 2) evaluate interactions between S. pneumoniae, H. influenzae, M. catarrhalis, and S. aureus; and 3) estimate the effect of host factors on colonization with S. pneumoniae, H. influenzae, M. catarrhalis, and S. aureus after a URI in a prospective cohort of young children.

Methods

Study Design and Participants

We used data from a prospective study of otitis media complications of URI in children at the University of Texas Medical Branch (UTMB) at Galveston (19,26). The study was reviewed and approved by the UTMB Institutional Review Board. The parents of healthy children 6 months through 3 years of age, who were receiving medical care at UTMB from January 2003 through March 2007, were invited to enroll their children. Children with chronic medical problems and anatomic or physiologic defects of the ear or nasopharynx were excluded.

At enrollment, we collected information about demographic and UTI risk factors. Parents were asked to describe their child's race and ethnicity. We also obtained information regarding the number of weeks the child had been breast-fed and the number of hours and days/week the child currently attended day care. We ascertained environmental exposure to tobacco smoke based on self-reports of whether any household members smoked cigarettes in the home.

The children in our study were followed up for 1 year. We requested that parents notify study staff when the child began to exhibit URI symptoms including nasal congestion, rhinorrhea, cough, sore throat, or fever. A study physician saw children as soon as possible after the onset of URI symptoms. At each study visit, the study physician obtained information regarding specific URI symptoms and examined the child's ears. The children were then monitored closely for 3 weeks for the development of otitis media. The study physician collected a nasopharyngeal swab during the visit for each URI episode and when acute otitis media or sinusitis was diagnosed. URI episodes were categorized as the same episode if symptoms persisted. An episode of URI was considered new when symptoms of the previous episode subsided and the parents noted new symptoms of URI as described above. Given our prospective study design, many children had >1 URI episode and some had >1 visit/URI episode. We collected 1 swab/physician visit. Data regarding antimicrobial drug therapy during the past 7 days were collected by medical record review. A description of the methods is provided elsewhere (19,26).

A total of 294 children were enrolled in the original study (19,26). Included in these analyses are data from 212 (72%) children who experienced at least 1 URI, were seen by a study physician, and had a nasopharyngeal swab collected for bacterial culture. Thus, we excluded 82 children who did not have a URI and a swab for bacterial culture. Of these 82 children without URI visits, 35 (59%) were lost to follow-up in the first 6 months, 13 (38%) were lost to follow-up in months 7–11, and 34 (17%) completed 1 year of follow up.

Mini-Tip Culturette kits (Becton Dickinson Microbiology Systems, Cockeysville, MD, USA) were used for sample collection. Each swab was streaked onto 1 blood and 1 chocolate agar plate. We subcultured and identified suspected isolates of each species as follows: S. pneumoniae isolates were identified by using the optochin disk susceptibility test (Taxo P, Becton Dickinson Microbiology Systems), H. influenzae isolates were identified by the Haemophilus ID Quad Plate with Growth Factors (Becton Dickinson Microbiology Systems), M. catarrhalis isolates were identified by the API QuadFerm assay (bioMérieux, Inc., Hazelwood, MO, USA), and S. aureus isolates were identified by coagulase, catalase, and latex agglutination test (Staphaurex Plus, Remel, Lenexa, KS, USA).

Statistical Methods

The main outcomes of interest were the relationships between bacteria during URI. All statistical analyses were conducted by using SAS version 9.1 (SAS Institute, Inc., Cary, NC, USA). We examined colonization by S. pneumoniae, H. influenzae, M. catarrhalis, and S. aureus by using repeated measures logistic regression with generalized estimating equations and an autoregressive correlation structure (AR1) using the procedure PROC GENMOD (SAS Institute, Inc.). Because each child could potentially have multiple URI episodes and contribute multiple bacterial swabs to the analysis, we used a repeated measures design to take into account variability of multiple samples from each child. To examine the effect of covariates on each bacteria species, we modeled colonization by S. pneumoniae, H. influenzae, and M. catarrhalis separately. We did not separately model the outcome of colonization by S. aureus because of low numbers of isolates obtained. Each model included the presence or absence of other bacteria species, as well as potential sampling-time confounders comprising time of swab collection after URI onset, antimicrobial drug therapy within the past 7 days, and age of the child at the time of swab collection. Host factors included in the model were gender, race, day care, breast-fed for >4 months, and environmental exposure to tobacco smoke.

Results

Characteristics of the study participants are shown in Table 1. The median age of study participants was 12.0 months; mean age was 14.1 (SD 7.4) months. Most children were white, were cared for at home, and had not been breast-fed for >4 months. Children were followed up for a median of 12 months and a mean of 10.7 (SD 2.8) months.

Individual children contributed between 1 and 20 swab specimens each (mean [SD] and median of 4.6 [3.8] and 3.0 swabs, respectively) from 1 to 18 URI episodes each (mean [SD] and median of 4.0 [3.3] and 3.0 episodes, respectively). Overall, at least 1 of the 4 species was isolated from 841 of 968 swab samples (86.9%) from 212 children. Of the 968 swabs, S. pneumoniae was present in 441 (45.6%), H. influenzae was present in 314 (32.4%), and M. catarrhalis was the most common bacteria species identified in 611 (63.1%) swabs. S. aureus was relatively rare in comparison; 69 swabs (7.1%) were positive for this species. The distribution and colonization patterns of the 4 bacteria species by swab and number of URI visits are shown in Table 2.

Most swabs (849 [87.7%]) were collected within 7 days of URI onset; 119 (12.3%) were taken 8–30 days after URI onset. Of the 968 swab samples, only 54 (5.6%) were collected from children who had taken antimicrobial drugs within the past 7 days. Therefore, most swabs were collected from children who were not taking antimicrobial drugs at the time of swab collection (94.5%). Of the 212 children, 205 (>96%) had received at least 1 dose of the 7-valent pneumococcal conjugate vaccine (PCV7) at the time of enrollment. Most of the children had received all age-appropriate scheduled PCV7 vaccinations at their URI visit, 666 (69%) of samples were collected from children who had received the age-appropriate number of PCV7 doses at the time of swab collection. There was no association between being up to date with PCV7 vaccination and colonization with S. pneumoniae (p = 0.71). We did not further examine the effect of the pneumococcal vaccine further because of the high level of coverage in our study population.

Repeated measures logistic regression models predicting colonization by S. pneumoniae, H. influenzae, or M. catarrhalis are shown in Table 3. A positive association between bacteria is indicated by an odds ratio (OR) >1; a negative association is indicated by an OR <1. An OR of 1.0, or any 95% confidence interval that includes 1.0 indicates no significant association. The model predicting colonization by S. pneumoniae indicated that colonization by H. influenzae was negatively associated with S. pneumoniae. However, when H. influenzae and M. catarrhalis colonized together, they were positively associated with S. pneumoniae colonization. Colonization by S. aureus resulted in a 40% reduction in the odds of S. pneumoniae colonization. Older children were less likely to be colonized with S. pneumoniae; each 1-month increase in age was associated with a 2% decrease in the odds of S. pneumoniae colonization (Table 3). Antimicrobial drug therapy in the past 7 days was associated with decreased odds of S. pneumoniae colonization. The timing of swab collection after onset of URI symptoms and host characteristics such as gender, race, daycare, breastfeeding, and environmental exposure to tobacco smoke were not associated with colonization by S. pneumoniae.

In our model examining H. influenzae colonization as the outcome, H. influenzae was negatively associated with S. pneumoniae, M. catarrhalis, and S. aureus (Table 3). In contrast to their association with S. pneumoniae colonization, age and antimicrobial drug therapy during the past 7 days were not significantly associated with colonization by H. influenzae. Host characteristics were associated with colonization by H. influenzae. Male gender and out-of-home daycare were associated with increased odds of H. influenzae colonization. White race was associated with decreased odds of H. influenzae colonization.

Our third model examined factors associated with colonization by M. catarrhalis (Table 3). H. influenzae was negatively associated with colonization by M. catarrhalis, but when H. influenzae and S. pneumoniae colonized together, they were positively associated with colonization by M. catarrhalis. Older children were less likely to be colonized with M. catarrhalis; each 1-month increase in age was associated with a 2% decrease in the odds of M. catarrhalis colonization (Table 3). Antimicrobial drug therapy in the past 7 days was associated with decreased odds of M. catarrhalis colonization. The timing of swab collection after onset of URI symptoms and host characteristics such as gender, race, daycare, breastfeeding, and environmental exposure to tobacco smoke were not associated with colonization by M. catarrhalis.

Discussion

We describe nasopharyngeal colonization of children with S. pneumoniae, H. influenzae, M. catarrhalis, and S. aureus alone or in combination during URI. Our models predicting S. pneumoniae colonization indicated that H. influenzae is negatively associated with S. pneumoniae. However, when H. influenzae was present with M. catarrhalis, odds of S. pneumoniae colonization increased by >2-fold. Models predicting H. influenzae colonization indicated a negative association with S. pneumoniae, M. catarrhalis, and S. aureus. Competitive interactions between bacteria are complex after URI and may shift from negative to positive when additional bacteria species are present. Modeling S. pneumoniae, H. influenzae, and M. catarrhalis colonization separately showed that gender, race, and daycare were associated with colonization by H. influenzae, but not with colonization by either S. pneumoniae or M. catarrhalis.

Jacoby et al. used a multivariate random effects model to examine S. pneumoniae colonization in Aboriginal and non-Aboriginal children in Australia (11). Their study differed from ours in that they examined the relationship between S. pneumoniae, H. influenzae, M. catarrhalis, and S. aureus in pairwise combinations. These researchers also examined healthy children; we examined children who had a URI. Jacoby et al. observed positive associations between pairwise combinations of S. pneumoniae and H. influenzae and between S. pneumoniae and M. catarrhalis. They did not identify an association between S. pneumoniae and S. aureus or between H. influenzae and S. aureus (11).

Our results confirm a recent report describing a negative association between H. influenzae and S. aureus in HIV-negative children (12). Our data also support a growing body of literature describing negative associations between S. pneumoniae and S. aureus (12–15). For example, a cross-sectional study of 790 children younger than 40 months identified a negative association between S. pneumoniae colonization and S. aureus (OR 0.47; 95% confidence interval 0.28–0.78) (13).

An in vivo mouse model of competitive interactions between S. pneumoniae and H. influenzae has suggested mechanisms to explain our observations (27). Both S. pneumoniae and H. influenzae successfully colonized BALBc/SCID mice when each bacteria species was injected separately. However, S. pneumoniae was cleared rapidly when H. influenzae was present in a co-colonization model. The competitive interaction between H. influenzae and S. pneumoniae was dependent on complement and neutrophils (27). These researchers proposed that H. influenzae cellular components activate the host innate immune response, thus killing S. pneumoniae (27). M. catarrhalis was not examined in this model, but our data suggest that the additional presence of M. catarrhalis might alter the competitive balance between S. pneumoniae and H. influenzae and that all 3 bacteria species would successfully colonize.

In vitro studies have also demonstrated competition between H. influenzae and S. pneumoniae but predicted that S. pneumoniae should inhibit the growth of H. influenzae. Neuraminidase A is produced by S. pneumoniae and cleaves sialic acid. It has been shown to remove sialic acid from lipopolysaccharides of H. influenzae strains (28), potentially giving pneumococci a competitive advantage by making H. influenzae more susceptible to complement-mediated clearance. Furthermore, in vitro co-culture experiments indicate that S. pneumoniae can inhibit H. influenzae through the action of hydrogen peroxide (29). Interference between S. pneumoniae and S. aureus may also be caused by hydrogen peroxide production by S. pneumoniae (30).

Our results indicate that antimicrobial drug therapy in the past 7 days was associated with a lower prevalence of colonization with S. pneumoniae or M. catarrhalis. In contrast, antimicrobial drug therapy in the past 7 days was not associated with colonization by H. influenzae. Varon et al. studied the effect of antimicrobial drugs on colonization with S. pneumoniae, H. influenzae, and M. catarrhalis in a cohort of young children with URI (31). Children in this study received antimicrobial drugs for a mean treatment period of 8 days. Swab samples were taken before treatment and on days 2 through 6 after treatment. Results showed that colonization by S. pneumoniae, H. influenzae, and M. catarrhalis decreased after antimicrobial drug therapy (31). The magnitude of the effect differed by bacteria species and the specific antimicrobial drug prescribed. In general, antimicrobial drugs were less effective for reducing colonization with H. influenzae than with S. pneumoniae and M. catarrhalis (31).

The effect of age, gender, race, and breastfeeding on colonization differs by population studied (10). Daycare has consistently been associated with increased levels of colonization with S. pneumoniae, H. influenzae, and M. catarrhalis (10), as has exposure to other children in the household (32,33). Our study was limited by lack of data on age and number of siblings or other potential confounders such as household crowding and socioeconomic status.

Our study had additional limitations. A cross-sectional study of S. aureus and S. pneumoniae colonization indicated a negative association between PCV7 vaccine serotypes and S. aureus (15). No association was found between S. pneumoniae nonvaccine types and S. aureus. We were unable to examine the association between S. pneumoniae serotype and colonization. Along these lines, we did not have data regarding H. influenzae type B vaccination status and did not serotype our H. influenzae strains. Therefore, we were also unable to evaluate the effect of this vaccination on polymicrobial colonization.

Nasopharyngeal colonization likely involves a complex combination of factors including host characteristics that influence exposure to specific bacterial species, host immune responses that may result in killing the bacteria, and direct competitive interactions between bacteria species. In addition to the inhibiting effects of neuraminidase A and hydrogen peroxide already described, competitive interactions between bacteria may also include the secretion of small peptide inhibitors, competition for nutrients, and competition for receptor binding sites. It is also possible that the presence of 1 bacteria species could create a more hospitable niche for another bacteria species. We were unable to evaluate the precise molecular mechanisms that mediate these complex polymicrobial interactions, an important area for future research.

Our study had several strengths, including its longitudinal, prospective design. We examined nasopharyngeal carriage during URI, a time when children are at risk for secondary bacterial infections. In addition, we took advantage of repeated measures analytic techniques to examine microbe-level factors influencing bacterial colonization while controlling for host factors.

Results from our study have public health implications. Scientists have debated whether they should seek to eradicate disease by preventing nasopharyngeal colonization (34). Vaccines targeting nasopharyngeal carriage of S. pneumoniae, H. influenzae, and M. catarrhalis may be needed to prevent otitis media because simultaneous carriage of these 3 bacteria may increase risk for otitis media (35). Our data indicate that the elimination of nasopharyngeal colonization with bacteria such as S. pneumoniae and H. influenzae may increase risk for colonization with S. aureus. Scientists conducting a randomized trial of the effectiveness of pneumococcal vaccines noted an increase in S. aureus when spontaneously draining infected middle ears of vaccinated children (25). Factors that may increase the risk of colonization with S. aureus are of special concern given the spread of methicillin-resistant S. aureus (9). Researchers are attempting to develop an S. pneumoniae vaccine containing pneumococcal choline binding protein A, which would protect against sepsis and pneumonia without interfering with pneumococcal colonization (36). Although this type of vaccination strategy may eventually decrease the incidence of potentially fatal invasive pneumococcal disease, it is unlikely to prevent otitis media. Thus, the public health impact of a given intervention strategy may be hard to predict, and caution should be used when designing control strategies that target nasopharyngeal colonization.

Acknowledgments

The authors thank M. Lizette Rangel, Kyralessa B. Ramirez, Syed Ahmad, Michelle Tran, Liliana Najera, Rafael Serna, and Carolina Pillion for assistance with study participants. We also thank Sangeeta Nair and Nahed Ismail for assistance in the laboratory.

This work was supported by grants R01 DC005841 and DC 005841-02S1 from the National Institutes of Health. The study was conducted at the General Clinical Research Center at the University of Texas Medical Branch, which is funded by National Center for Research Resources (National Institutes of Health, US Public Health Service), grant M01 RR 00073.

Dr Pettigrew is on the faculty at the Yale School of Public Health. Her research interests include the epidemiology and molecular epidemiology of pediatric infectious diseases.

References

1. Giebink G. The microbiology of otitis media. Pediatr Infect Dis J. 1989;8:S18–20. PubMed DOI
2. Casey JR, Pichichero ME. Changes in the frequency and pathogens causing acute otitis media in 1995–2003. Pediatr Infect Dis J. 2004;23:824–8. PubMed DOI
3. Hausdorff WP. Invasive pneumococcal disease in children: geographic and temporal variations in incidence and serotype distribution. Eur J Pediatr. 2002;161:S135–9. PubMed DOI
4. Watson K, Carville K, Bowman J, Jacoby P, Riley TV, Leach AJ, et al. Upper respiratory tract bacterial carriage in Aboriginal and non-Aboriginal children in a semi-arid area of Western Australia. Pediatr Infect Dis J. 2006;25:782–90. PubMed DOI
5. St Sauver J, Marrs CF, Foxman B, Somsel P, Madera R, Gilsdorf JR. Risk factors for otitis media and carriage of multiple strains of Haemophilus influenzae and Streptococcus pneumoniae. Emerg Infect Dis. 2000;6:622–30.
6. Faden H, Duffy L, Wasielewski R, Wolf J, Krystofik D, Tung Y, et al. Relationship between nasopharyngeal colonization and the development of otitis media in children. J Infect Dis. 1997;175:1440–5.
7. Shopsin B, Mathema B, Martinez J, Ha E, Campo ML, Fierman A, et al. Prevalence of methicillin-resistant and methicillin-susceptible Staphylococcus aureus in the community. J Infect Dis. 2000;182:359–62. PubMed DOI
8. Zetola N, Francis JS, Nuermberger EL, Bishai WR. Community-acquired meticillin-resistant Staphylococcus aureus: an emerging threat. Lancet Infect Dis. 2005;5:275–86. PubMed DOI
9. Crum NF, Lee RU, Thornton SA, Stine OC, Wallace MR, Barrozo C, et al. Fifteen-year study of the changing epidemiology of methicillin-resistant Staphylococcus aureus. Am J Med. 2006;119:943–51. PubMed DOI
10. Garcia-Rodriguez JA, Fresnadillo Martinez MJ. Dynamics of nasopharyngeal colonization by potential respiratory pathogens. J Antimicrob Chemother. 2002;50:59–73. PubMed DOI
11. Jacoby P, Watson K, Bowman J, Taylor A, Riley TV, Smith DW, et al. Modelling the co-occurrence of Streptococcus pneumoniae with other bacterial and viral pathogens in the upper respiratory tract. Vaccine. 2007;25:2458–64. PubMed DOI
12. Madhi SA, Adrian P, Kuwanda L, Cutland C, Albrich WC, Klugman KP. Long-term effect of pneumococcal conjugate vaccine on nasopharyngeal colonization by Streptococcus pneumoniae and associated interactions with Staphylococcus aureus and Haemophilus influenzae colonization in HIV-infected and HIV-uninfected children. J Infect Dis. 2007;196:1662–6. PubMed DOI
13. Regev-Yochay G, Dagan R, Raz M, Carmeli Y, Shainberg B, Derazne E, et al. Association between carriage of Streptococcus pneumoniae and Staphylococcus aureus in children. JAMA. 2004;292:716–20. PubMed DOI
14. Veenhoven R, Bogaert D, Uiterwaal C, Brouwer C, Kiezebrink H, Bruin J, et al. Effect of conjugate pneumococcal vaccine followed by polysaccharide pneumococcal vaccine on recurrent acute otitis media: a randomised study. Lancet. 2003.28;361:2189–95.
15. Bogaert D, van Belkum A, Sluijter M, Luijendijk A, de Groot R, Rumke HC, et al. Colonisation by Streptococcus pneumoniae and Staphylococcus aureus in healthy children. Lancet. 2004;363:1871–2. PubMed DOI
16. Zemlickova H, Urbaskova P, Adamkova V, Motlova J, Lebedova V, Prochazka B. Characteristics of Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis and Staphylococcus aureus isolated from the nasopharynx of healthy children attending day-care centres in the Czech Republic. Epidemiol Infect. 2006;134:1179–87. PubMed DOI
17. Syrjanen RK, Kilpi TM, Kaijalainen TH, Herva EE, Takala AK. Nasopharyngeal carriage of Streptococcus pneumoniae in Finnish children younger than 2 years old. J Infect Dis. 2001;184:451–9. PubMed DOI
18. Aniansson G, Alm B, Andersson B, Larsson P, Nylen O, Peterson H, et al. Nasopharyngeal colonization during the first year of life. J Infect Dis. 1992;165 (Suppl1):S38–42.
19. Chonmaitree T, Revai K, Grady JJ, Clos A, Patel JA, Nair S, et al. Viral upper respiratory tract infection and otitis media complication in young children. Clin Infect Dis. 2008;46:815–23. PubMed DOI
20. Brundage JF. Interactions between influenza and bacterial respiratory pathogens: Implications for pandemic preparedness. Lancet Infect Dis. 2006;6:303–12. PubMed DOI
21. Revai K, Dobbs L, Nair S, Patel J, Grady J, Chonmaitree T. Incidence of acute otitis media and sinusitis complicating upper respiratory tract infection: the effect of age. Pediatrics. 2007;119:e1408–12. PubMed DOI
22. von Eiff C, Becker K, Machka K, Stammer H, Peters G. Nasal carriage as a source of Staphylococcus aureus bacteremia. N Engl J Med. 2001;344:11–6. PubMed DOI
23. Gray BM, Converse GM, Dillon HC. Epidemiologic studies of Streptococcus pneumoniae in infants: acquisition, carriage, and infection during the first 24 months of life. J Infect Dis. 1980;142:923–33.
24. Givon-Lavi N, Fraser D, Porat N, Dagan R. Spread of Streptococcus pneumoniae and antibiotic-resistant S. pneumoniae from day-care center attendees to their younger siblings. J Infect Dis. 2002;186:1608–14. PubMed DOI
25. Veenhoven R, Bogaert D, Uiterwaal C, Brouwer C, Kiezebrink HH, Bruin J, et al. Effect of conjugate pneumococcal vaccine followed by polysaccharide pneumococcal vaccine on recurrent acute otitis media: a randomised study. Lancet. 2003;361:2189–95. PubMed DOI
26. Revai K, Mamidi D, Chonmaitree T. Association of nasopharyngeal bacterial colonization during upper respiratory tract infection and the development of acute otitis media. Clin Infect Dis. 2008;46:e34–7. PubMed DOI
27. Lysenko ES, Ratner AJ, Nelson AL, Weiser JN. The role of innate immune responses in the outcome of interspecies competition for colonization of mucosal surfaces. PLoS Pathog. 2005;1:e1. PubMed DOI
28. Shakhnovich EA, King SJ, Weiser JN. Neuraminidase expressed by Streptococcus pneumoniae desialylates the lipopolysaccharide of Neisseria meningitidis and Haemophilus influenzae: a paradigm for interbacterial competition among pathogens of the human respiratory tract. Infect Immun. 2002;70:7161–4. PubMed DOI
29. Pericone CD, Overweg K, Hermans PW, Weiser JN. Inhibitory and bactericidal effects of hydrogen peroxide production by Streptococcus pneumoniae on other inhabitants of the upper respiratory tract. Infect Immun. 2000;68:3990–7. PubMed DOI
30. Regev-Yochay G, Trzcinski K, Thompson CM, Malley R, Lipsitch M. Interference between Streptococcus pneumoniae and Staphylococcus aureus: in vitro hydrogen peroxide-mediated killing by Streptococcus pneumoniae. J Bacteriol. 2006;188:4996–5001. PubMed DOI
31. Varon E, Levy C, De La Rocque F, Boucherat M, Deforche D, Podglajen I, et al. Impact of antimicrobial therapy on nasopharyngeal carriage of Streptococcus pneumoniae, Haemophilus influenzae, and Branhamella catarrhalis in children with respiratory tract infections. Clin Infect Dis. 2000;31:477–81. PubMed DOI
32. Vives M, Garcia ME, Saenz P, Mora MA, Mata L, Sabharwal H, et al. Nasopharyngeal colonization in Costa Rican children during the first year of life. Pediatr Infect Dis J. 1997;16:852–8. PubMed DOI
33. Principi N, Marchisio P, Schito GC, Mannelli S. Risk factors for carriage of respiratory pathogens in the nasopharynx of healthy children. Pediatr Infect Dis J. 1999;18:517–23. PubMed DOI
34. Bogaert D, De Groot R, Hermans PW. Streptococcus pneumoniae colonisation: the key to pneumococcal disease. Lancet Infect Dis. 2004;4:144–54. PubMed DOI
35. Leach AJ, Boswell JB, Asche V, Nienhuys TG, Mathews JD. Bacterial colonization of the nasopharynx predicts very early onset and persistence of otitis media in Australian Aboriginal infants. Pediatr Infect Dis J. 1994;13:983–9. PubMed DOI
36. Glover DT, Hollingshead SK, Briles DE. Streptococcus pneumoniae surface protein PcpA elicits protection against lung infection and fatal sepsis. Infect Immun. 2008;76:2767–76. PubMed DOI

Tables

Table 1. Characteristics of study participants enrolled through the University of Texas Medical Branch, Galveston, Texas, USA, 2003–2007
Table 2. Distribution of bacteria on nasopharyngeal swabs collected from children with URI, University of Texas Medical Branch, Galveston, Texas, USA, 2003–2007
Table 3. Predicted outcome of colonization with Stretococcus pneumoniae, Haemophilus influenzae, or Moraxella catarrhalis in young children after upper respiratory tract infection (968 swabs from 212 children; see Table 2)

Suggested Citation for this Article

Pettigrew MM, Gent JF, Revai K, Patel JA, Chonmaitree T. Microbial interactions during upper respiratory tract infections. Emerg Infect Dis [serial on the Internet]. 2008 Oct [date cited]. Available from http://www.cdc.gov/EID/content/14/10/1584.htm

DOI: 10.3201/eid1410.080119

The opinions expressed by authors contributing to this journal do not necessarily reflect the opinions of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.

This page posted September 25, 2008

• Home
• Expedited
• Current Issue
• Ahead of Print
• Past Issues
• Announcements

• About Us
• Instructions to Authors
• Submit Manuscript
• Subscribe
• Contact Us

Safer Healthier People

Centers for Disease Control and Prevention, 1600 Clifton Rd, Atlanta, GA 30333, U.S.A
Tel: (404) 639-3311 / Public Inquiries: (404) 639-3534 / (800) 311-3435