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Conceived and designed the experiments: RJS KG PCV ACC PSM AJL HSV GR MIM NB PJT ABC KH . Performed the experiments: RJS GR ABC KH ALR GBM LC . Analyzed the data: KH ACC MC KG ABC. Contributed reagents/materials/analysis tools: KH RJS PSM ALR GBM LC ABC. Wrote the paper: KH KG ABC ACC PSM AJL RJS HSV MC.
Indigenous children in Australia and Alaska have very high rates of chronic suppurative lung disease (CSLD)/bronchiectasis. Antibiotics, including frequent or long-term azithromycin in Australia and short-term beta-lactam therapy in both countries, are often prescribed to treat these patients. In the Bronchiectasis Observational Study we examined over several years the nasopharyngeal carriage and antibiotic resistance of respiratory bacteria in these two PCV7-vaccinated populations.
Indigenous children aged 0.5–8.9 years with CSLD/bronchiectasis from remote Australia (n=79) and Alaska (n=41) were enrolled in a prospective cohort study during 2004–8. At scheduled study visits until 2010 antibiotic use in the preceding 2-weeks was recorded and nasopharyngeal swabs collected for culture and antimicrobial susceptibility testing. Analysis of respiratory bacterial carriage and antibiotic resistance was by baseline and final swabs, and total swabs by year.
Streptococcus pneumoniae carriage changed little over time. In contrast, carriage of Haemophilus influenzae declined and Staphylococcus aureus increased (from 0% in 2005–6 to 23% in 2010 in Alaskan children); these changes were associated with increasing age. Moraxella catarrhalis carriage declined significantly in Australian, but not Alaskan, children (from 64% in 2004–6 to 11% in 2010). While beta-lactam antibiotic use was similar in the two cohorts, Australian children received more azithromycin. Macrolide resistance was significantly higher in Australian compared to Alaskan children, while H. influenzae beta-lactam resistance was higher in Alaskan children. Azithromycin use coincided significantly with reduced carriage of S. pneumoniae, H. influenzae and M. catarrhalis, but increased carriage of S. aureus and macrolide-resistant strains of S. pneumoniae and S. aureus (proportion of carriers and all swabs), in a ‘cumulative dose-response’ relationship.
Over time, similar (possibly age-related) changes in nasopharyngeal bacterial carriage were observed in Australian and Alaskan children with CSLD/bronchiectasis. However, there were also significant frequency-dependent differences in carriage and antibiotic resistance that coincided with azithromycin use.
Indigenous children in Australia, Alaska and New Zealand have amongst the world's highest recorded rates of chronic suppurative lung disease (CSLD), including bronchiectasis unrelated to cystic fibrosis (CF) . Antibiotics play a key role in managing persistent respiratory symptoms and acute exacerbations associated with bronchiectasis . However, few longitudinal data exist on the impact of antibiotics upon the airway bacteriology of these patients. This is an important knowledge gap as Indigenous children have high rates of nasopharyngeal bacterial carriage  and microaspiration of upper airway bacteria may contribute to both the pathogenesis and on-going morbidity of bronchiectasis .
Based upon the clinical impression that patients receiving azithromycin have fewer acute respiratory exacerbations, there is anecdotal evidence that many clinicians in Australia routinely prescribe azithromycin (frequently long-term) for children with bronchiectasis, while in Alaska such practice is uncommon. In contrast, both sites utilize short-term intermittent therapy with beta-lactam antibiotics (e.g. amoxicillin or amoxicillin-clavulanate) for acute pulmonary exacerbations associated with bronchiectasis. The Bronchiectasis Observational Study was established in Australia and Alaska to study prospectively the clinical course of CSLD/bronchiectasis in Indigenous children . Using the opportunity thus provided, we examined the nasopharyngeal carriage of respiratory bacteria and their antibiotic resistance patterns in children. We hypothesised that the two populations would differ in their nasopharyngeal carriage of potential respiratory bacterial pathogens and antibiotic resistance in these organisms as a result of differences in prescribing practices between the two settings.
Children 0.5–8.9 years of age with a diagnosis of non-CF bronchiectasis (confirmed on high-resolution computerized tomography) or chronic (>3-months) daily wet (or productive) cough were enrolled in a prospective cohort study during 2004–8 . Children were recruited opportunistically while attending an outpatient clinic or in hospital undergoing bronchoscopy for suspected CSLD/bronchiectasis or for respiratory exacerbations. Subsequently, enrolled children were examined and nasopharyngeal swabs collected by research staff at scheduled study visits until 2010. These visits were scheduled quarterly in Australia (to ensure at least one annual review in highly mobile enrolled children) and annually in Alaska. Such visits were planned independently of the children's health status. Only visits where swabs were collected were included in this analysis. Children's vaccination status at baseline was recorded from immunisation registers. Antibiotic use in the 2-weeks preceding swab collection (to capture recent antibiotic events and allow comparison with other studies in this population  and studies using parent recall) was recorded from clinic notes.
The study was approved by the Human Research Ethics Committee of the Northern Territory Department of Health and Menzies School of Health Research in Australia (HREC 04/46) and the Alaska Area Institutional Review Board (which acts under the Indian Health Service Institutional Review Board FWA number 0008894). At enrolment written informed consent was obtained from the carer of each child and when appropriate assent was also provided by the older children in the cohort. The process of obtaining consent, and the information sheets and consent forms used (stored securely at each research institute), were approved by the respective ethics bodies.
Nasopharyngeal swabs collected at study visits were transported and processed according to published methods , , unless otherwise noted. Swabs stored in skim-milk tryptone glucose glycerol broth at −80°C were thawed and 10 µL aliquots plated on selective media and incubated overnight at 37°C and 5% CO2. In Australia, four colonies each (including any with differing morphologies) of presumptive Streptococcus pneumoniae and Haemophilus influenzae, two of Moraxella catarrhalis and one of Staphylococcus aureus were isolated and identified using standard methods . In Alaska, multiple colonies were picked when differing morphologies were observed. When multiple isolates underwent antibiotic susceptibility testing, the child was reported as carrying a resistant strain if one or more of the isolates proved resistant. S. pneumoniae serotypes were determined by the Quellung reaction using antisera from Statens Serum Institute (Denmark).
Antimicrobial sensitivities for S. pneumoniae, H. influenzae and S. aureus isolates were determined by disk diffusion (Australia ; Alaska ). Minimum inhibitory concentrations (MICs) were determined for resistant S. pneumoniae and H. influenzae isolates using Etest strips (AB bioMérieux, France) in Australia. In Alaska, erythromycin and penicillin MICs for S. pneumoniae were determined by microbroth dilution and ampicillin MICs for H. influenzae were determined using Etest strips. MIC breakpoints from the European Committee on Antimicrobial Susceptibility Testing (EUCAST, http://www.eucast.org) were used to define resistance for S. pneumoniae (penicillin resistance MIC>2 mg/L, intermediate resistance MIC>0.06–2 mg/L; macrolide [azithromycin or erythromycin] resistance MIC>0.5 mg/L) and H. influenzae (ampicillin resistance MIC>1 mg/L; macrolide resistance MIC>4 mg/L, intermediate resistance MIC>0.12–4 mg/L). A nitrocephin-based test detected beta-lactamase activity in H. influenzae and M. catarrhalis isolates.
Carriage data are reported as the proportion of children at baseline (first swab) and as they left the study (last swab), and also presented graphically as the proportion of total swabs collected per study year. As storage of 29 swabs from Central Australia during 2004–6 was at −20°C, which is suboptimal for recovery of H. influenzae , these samples were excluded from analyses involving this pathogen and the first subsequent swab for each child was included for H. influenzae baseline data. Also, as only 20 swabs were collected from both cohorts in 2004–5, their data were combined with those from 2006.
Antibiotic resistance data are reported as the proportion of carriers as children entered and left the study, proportion of total isolates for each bacterial species, and graphically as the proportion of all positive swabs by study year. Multiple strains detected in the same swab (differing serotype or antibiotype for S. pneumoniae and H. influenzae, differing beta-lactamase status for M. catarrhalis) were counted as additional isolates where results for total isolates are presented.
Confidence intervals (CIs) were calculated using the exact binomial method for first and last swabs from each child and where numbers were small (<5), and otherwise adjusted for repeated sampling using the clustered sandwich estimator for estimating the variance-covariance matrix, implemented as vce(cluster id) in Stata. We used Stata's logistic command for bivariate and multivariate analyses, and nptrend to test for trend across ordered groups. Statistical tests were performed using Stata 12 (College Station, Texas).
To investigate the cumulative effect of repeated and sustained long-term azithromycin exposure on bacterial carriage and resistance, Australian children were divided into three groups based on frequency of azithromycin use during the study period: Azi-None = no azithromycin in the 2-weeks preceding swab collection at any of the study visits; Azi-Infrequent = azithromycin preceding 1–50% of study visits; Azi-Frequent = azithromycin preceding >50% of study visits. Tables and figures are presented as Supporting Information.
A total of 120 children were enrolled and 597 swabs collected (Table 1). At enrolment, 24% of Alaskan and 30% of Australian children had respiratory exacerbations. At subsequent visits the numbers were 8% and 17% respectively. The mean number of swabs collected per child per year enrolled (person-years of follow-up) was 2.5 in Australia and 1.3 in Alaska. Most (88%) children had received ≥3 doses of the 7-valent pneumococcal conjugate vaccine (PCV7). In addition, two Australian children received ≥1 dose of the pneumococcal Haemophilus influenzae protein D conjugate vaccine introduced in 2009. No Alaskan children received PCV13, introduced in 2010. Australian children were more likely to receive azithromycin in the 2-weeks preceding swab collection, while beta-lactam antibiotic use was similar in the two cohorts (Table 1). There were no clear temporal trends in antibiotic use; peaks were observed in beta-lactam antibiotic and azithromycin use in 2007 and 2008 (preceding 18% and 55% of swabs collected respectively) in Australian children, and in beta-lactam antibiotic use in Alaskan children in 2008 (preceding 25% of swabs collected).
Nasopharyngeal bacterial carriage as children entered and left the study is shown in Table 2. Australian children were at significantly lower risk than Alaskan children of M. catarrhalis carriage at the study's end, and this finding persisted after adjusting for carriage at baseline. When all data were analysed as a proportion of swabs by year (Figure 1), S. pneumoniae carriage remained relatively stable, H. influenzae carriage declined in both Australian (nptrend P=0.007) and Alaskan (P=0.033) children, M. catarrhalis carriage in Australian children showed a marked decline from 64% (95% CI 47–81) in 2004–6 to 11% (95% CI 2–21) in 2010 (P<0.001), and S. aureus carriage in Alaskan children increased from 0% (95% CI 0–9) in 2005–6 to 23% (95% CI 6–40) in 2010 (P=0.010).
The number of children and time in the study were comparable when Australian children were grouped by azithromycin exposure (Table S1). However, there was a significant difference in the frequency of visits by group: Azi-None: median 3.5 (range 1–10); Azi-Infrequent: median 5 (range 2–14); Azi-Frequent: median 7 (range 1–15); nptrend P=0.014. The median proportion of visits at which children had received azithromycin was 33% (range 12–50) in the Azi-Infrequent group and 75% (range 57–100) in the Azi-Frequent group. Differences in bacterial carriage among these groups were apparent at baseline. These differences were accentuated by the end of the study and were significant for all four bacteria (Table S1). A ‘cumulative dose-response’ relationship was observed: increasing azithromycin use coincided with decreasing carriage of S. pneumoniae, H. influenzae and M. catarrhalis, and increasing carriage of S. aureus. The same trends were apparent when data from all swabs were included (Figure S1, nptrend P<0.001 for all four bacteria).
Since azithromycin use coincided with carriage differences in the Australian children, carriage in the Alaskan children was compared with carriage in the Australian Azi-None group. Carriage of S. pneumoniae was higher in the Australian children, while S. aureus carriage was higher in Alaskan children. These differences were significant when all data were included; S. pneumoniae and S. aureus carriage were 79% (95% CI 71–87) and 2% (95% CI 0–6) respectively in the Australian Azi-None group compared to 60% (95% CI 52–67) and 15% (95% CI 9–21) respectively in Alaskan children.
Resistance of bacterial pathogens as children entered and left the study is shown in Table 3 and as a proportion of positive swabs by year in Figure 2. No penicillin resistant S. pneumoniae isolates (MIC>2 mg/L) were detected in either cohort. Macrolide resistance in S. pneumoniae and S. aureus carriers was significantly higher in Australian compared to Alaskan children. However, beta-lactam antibiotic resistance was higher in Alaskan H. influenzae carriers. Macrolide-resistant strains of S. pneumoniae and S. aureus were also more prevalent in Australian children when all swabs were included in analysis, isolated from 30% (95% CI 24–36) and 14% (95% CI 9–20) of swabs respectively, compared to 4.5% (95% CI 1–8) and 4% (95% CI 0–8) respectively in Alaskan children. H. influenzae and M. catarrhalis beta-lactam antibiotic resistance were both higher in Alaskan children as a proportion of all swabs: 19% (95% CI 13–26) had ampicillin-resistant H. influenzae and 65% (95% CI 56–74) had beta-lactamase positive M. catarrhalis strains compared to 4% (95% CI 2–6) and 29% (95% CI 23–35) respectively in Australian children.
Resistance as a proportion of all isolates is reported in Table 4. All H. influenzae isolates from Alaskan children and 80% from Australian children were macrolide-susceptible by disk diffusion. Since most H. influenzae possess an intrinsic macrolide efflux mechanism  which confers intermediate resistance by EUCAST criteria, MICs were determined for all Australian isolates.
Differences in bacterial resistance in the first and last swabs from Australian children grouped by azithromycin exposure are shown in Table S2. Macrolide resistance tended to be highest in the Azi-Frequent group for S. pneumoniae, H. influenzae and S. aureus carriers, but increased in S. pneumoniae in all three groups from the beginning to the end of the study. When all swabs were included, macrolide-resistant S. pneumoniae and S. aureus strains were found in 21% (95% CI 14–28) and 1% (95% CI 0–5) respectively from the Azi-None group, 28% (95% CI 17–38) and 14% (95% CI 6–22) from the Azi-Infrequent group, and 38% (95% CI 26–49) and 23% (95% CI 14–33) from the Azi-Frequent group (nptrend P=0.002 and P<0.001 respectively). There were no trends for beta-lactam antibiotic resistance in any of the four pathogens. Trends by study year are shown in Figure S2.
Of 285 S. pneumoniae isolates serotyped from the Australian children, PCV7 serotypes 19F and 23F were among the top 10 (Figure 3). The most prevalent serotype (8% of isolates) was 23B, followed by 6A, 19A and 6C (each 7%), and 16F, 17F, 19F and 23F (each 6.5%). Of 96 isolates serotyped from the Alaskan children the most prevalent serotype was 19A (15% of isolates) followed by 23B (9%) and 3, 15A and 34 (each 6.5%). The serotype hierarchy in Australian children appeared to coincide with azithromycin use; serotypes that were prevalent in the Azi-Frequent group also had the highest prevalence of azithromycin resistance. Commonly carried macrolide-resistant serotypes in the Australian group were 23B, 6A, 6C, 17F, 23F, 22F, 9N, 15A and 33D. In Alaskan children, azithromycin resistance was found in only 7 isolates (5 different serotypes). Intermediate penicillin resistance (MIC>0.06–2 mg/L) was most prevalent in serotypes 19A (100%), 19F, 23B (70% were both macrolide and intermediate penicillin resistant) and 16F in Australian children, and serotypes 19A (67%) and 35B in Alaskan children. Multiple strains were detected in 30 (12%) positive specimens (two had three serotypes) from Australian children and four (4%) from Alaskan children; this difference was likely due to more colonies being selected in Australia. Overall, PCV7 serotypes comprised 13% of Australian and 3% of Alaskan isolates.
Most H. influenzae isolates from both cohorts were nontypeable (NTHi) (Australia 89% of 191 isolates, Alaska 83% of 100 isolates). Capsular type b (Hib) was isolated from four children in both cohorts (2% and 4% of isolates respectively); three (75%) Hib isolates from Alaskan children were ampicillin resistant, but none from Australian children. Using EUCAST criteria, three isolates from Australian and eight from Alaskan children (three and seven NTHi respectively, no Hib) were beta-lactamase negative, but ampicillin resistant (BLNAR). However, only one BLNAR NTHi isolate from an Alaskan child had ampicillin MIC≥4 mg/L. Multiple strains (different serotype and/or antibiotype) were detected in 14% of Australian and 11% of Alaskan children.
In bivariate analyses adjusted for repeated sampling of children, age was significantly associated with carriage. Older children were less likely to carry H. influenzae (Odds Ratio (OR) 0.91 per additional year of age, 95% CI 0.83–0.99), but more likely to carry S. aureus (OR 1.13 per additional year of age, 95% CI 1.01–1.25). These associations largely remained when study year was included in the analysis: OR 0.94 (95% CI 0.86–1.02) for H. influenzae and OR 1.11 (95% CI 0.99–1.25) for S. aureus.
In multivariate analyses adjusted for the presence of other respiratory bacteria and for repeated sampling of children, similar associations were seen in both cohorts for S. pneumoniae colonization, which was positively associated with H. influenzae (OR 3.18, 95% CI 2.07–4.88) and M. catarrhalis (OR 3.86, 95% CI 2.41–6.19) and negatively associated with S. aureus (OR 0.38, 95% CI 0.21–0.70). Similar associations were also seen for H. influenzae which was positively associated with the presence of M. catarrhalis (OR 3.27, 95% CI 2.21–4.81), and for M. catarrhalis which was negatively associated with S. aureus (OR 0.55, 95% CI 0.31–0.99).
This is the first longitudinal study reporting nasopharyngeal carriage in children with CSLD/bronchiectasis. While the two patient populations described are distinct and geographically dispersed, they share surprisingly similar environmental risk factors . Carriage of respiratory pathogens in these two populations receiving different antibiotic treatment strategies showed similarities, but also important differences. S. pneumoniae carriage was similar overall and relatively stable in both Alaskan and Australian children during the study period. Carriage of H. influenzae declined in both cohorts over time, while S. aureus carriage increased. Carriage of M. catarrhalis in Alaskan children remained high throughout the study period, while carriage in Australian children started at the same level, but declined dramatically. Despite broadly similar carriage of three of the four main bacteria in the two populations, azithromycin use in the Australian cohort coincided with significant differences in the carriage of all four organisms, with an apparent ‘cumulative dose-response’ effect.
In the Australian Azi-None group, carriage of S. pneumoniae (79% of all swabs) was equivalent to that previously reported in this population . Carriage of S. pneumoniae has been reported in several populations to peak at 2–3 years of age and decline thereafter , . However, in Indigenous children and children from developing countries, carriage is higher than in developed countries and remains common up to 10-years of age , . In the Azi-None group, carriage of H. influenzae was lower (60%) than the 85% reported in a younger cohort of Indigenous children , but similar to that reported for Aboriginal children 5–8 years of age . The observed decline in carriage in both cohorts may therefore be age-related (as we found in bivariate analysis) as children grew older during the study. M. catarrhalis carriage (63%) in the Australian Azi-None group was lower than previously reported, even in older Indigenous children . Nevertheless, M. catarrhalis carriage in this group and the Alaskan children was higher than generally reported in healthy children or children with upper respiratory tract infections .
S. aureus carriage has not been reported previously in this Australian population, and Alaskan reports are from a community with high rates of methicillin-resistant S. aureus infection . In other populations, S. aureus carriage is high in infants <3-months of age, but declines rapidly as carriage of the other three bacteria increases, reaching a low point at 1–2 years , . Carriage then increases again to reach its highest prevalence in children 6–11 years of age , . If these trends apply to Australian and Alaskan children, then S. aureus carriage could be expected to be near its lowest point at the age when most of the children in this study were enrolled and highest at the age when their last swabs were collected. This would explain the observed increase in S. aureus carriage over the study period in both cohorts.
Consistent with other studies , , we found that azithromycin use coincided with significant reductions in carriage of S. pneumoniae, H. influenzae and M. catarrhalis in the Australian children. Our study also found an apparent ‘cumulative dose response’ effect on carriage and resistance. However, a potential confounding factor was attendance at clinic, as children who did not take azithromycin had fewer clinic attendances (fewer swabs collected). While we cannot exclude the possibility that they only attended clinic when they were sick and therefore more likely to be carrying bacteria, most swabs were collected at scheduled visits that were arranged independently of the child's health status. Factors other than azithromycin may also be involved in the decline of M. catarrhalis carriage in Australian children, since this decline was also seen in the Azi-None group. Conversely, while the increase in S. aureus carriage in Alaskan children is most likely age-related, the increase in Australian children may also be partly attributable to azithromycin since no such increase was seen in the Azi-None group (where S. pneumoniae carriage remained high).
Levels of macrolide resistance in bacteria colonizing the Australian children were not only higher than in the Alaskan children, but also higher than previously reported for most S. pneumoniae and H. influenzae paediatric respiratory tract isolates worldwide , , , and similar to the high levels of macrolide resistance in S. aureus often found in CF patients treated with azithromycin , . Levels of beta-lactam antibiotic resistance in Alaskan children were similar to previous reports from North America , , and higher than H. influenzae and M. catarrhalis (but not S. pneumoniae) beta-lactam antibiotic resistance in Australian children. Beta-lactamase produced by one organism may protect co-colonizing bacteria from beta-lactam antibiotics , . However, we found conflicting evidence using simple multivariate analyses (data not shown). The higher rates of intermediate resistance to penicillin in Australian S. pneumoniae isolates may be due to other factors, e.g. co-occurrence of macrolide and intermediate penicillin resistance in prevalent serotypes such as 23B.
As with other observational studies, it is possible that the associations observed may be confounded by factors not measured. Patients who took azithromycin consistently may differ from those who did not. Antibiotics taken before enrolment likely affected baseline carriage. Additionally, biases may have been introduced if the carriage status of children for whom we achieved good follow-up was systemically different to those for whom our follow-up was less successful. The different swabbing schedules (quarterly in Australia and annually in Alaska) may also have led to bias, e.g. if carriage varied seasonally and children were mostly seen at a particular time of year, or if resistant strains were persistently carried by the same child. However, children from both cohorts were seen in all months of the year, and a recent Kenyan study found the mean duration of S. pneumoniae carriage to be just over 30-days . Thus swabbing every 3-months is unlikely to detect the same S. pneumoniae carriage episode, and this was confirmed by inspection of our serotype data by child visit. However, without further strain discrimination we cannot comment on carriage duration in other species. Finally, while changes in H. influenzae and S. aureus carriage over time appeared to be age-related, differences could also be explained by other temporal changes.
In conclusion, this study adds important new information on long-term carriage and antibiotic resistance trends in Indigenous children with CSLD/bronchiectasis from two environmentally diverse regions of the world. While similar, possibly age-related, changes in carriage were observed over time in both patient populations, azithromycin use was associated with a ‘cumulative dose-dependent’ pattern of carriage and resistance in the Australian children. Moreover, while two recent randomised controlled trials showed that adults with non-CF bronchiectasis had fewer respiratory exacerbations after receiving azithromycin continuously for 6–12 month periods , , this was accompanied by increased macrolide resistance amongst respiratory pathogens . Such studies need to be repeated in children and, in light of these findings in adults and our own studies in children, special attention should be paid to monitoring antibiotic resistance as this may ultimately offset any clinical benefit derived from this important class of antibiotics.
Pathogen carriage (proportion of swabs) by study year in Australian and Alaskan children.1 1Australian children were grouped by proportion of study visits with azithromycin use <2-weeks before swab collection at: Azi-None = no study visits; Azi-Infreq(uent) =1–50% of study visits; Azi-Freq(uent) =51–100% of study visits.
Pathogen resistance (proportion of carriers) by study year in Australian and Alaskan children.1 1Australian children were grouped by proportion of study visits with azithromycin use <2-weeks before swab collection at: Azi-None = no study visits; Azi-Infreq(uent) =1–50% of study visits; Azi-Freq(uent) =51–100% of study visits.
Nasopharyngeal carriage of respiratory bacteria from Australian children, grouped by azithromycin exposure1, at baseline and end of study. 1Australian children were grouped by proportion of study visits with azithromycin use <2-weeks before swab collection at: Azi-None = no study visits; Azi-Infreq(uent) =1–50% of study visits; Azi-Freq(uent) =51–100% of study visits.
Antibiotic resistance (proportion of carriers) in respiratory bacteria from Australian children, grouped by azithromycin exposure1, at baseline and end of study. 1Australian children were grouped by proportion of study visits with azithromycin use <2-weeks before swab collection at: Azi-None = no study visits; Azi-Infreq(uent) = 1–50% of study visits; Azi-Freq(uent) =51–100% of study visits.
We wish to thank the children and their families for participating in the study. We also thank the paid research personnel including Valerie Logan and Abbey Diaz for their help with data management and cleaning. In Australia, we wish to thank Emma Tilley, Stacey Svenson, Kobi Schutz, Clare Wilson and Lesley Versteegh (clinical staff), and Estelle Carter, Vanya Hampton, Joanna Bugg and Nerida Liddle (laboratory staff). In Alaska, we wish to thank research personnel Nicolette Nick, Bessie Francis, and Mary Jackson and Debra Parks. We also thank the Menzies Child Health Indigenous Reference Group for oversight of this study.
This work was supported by the National Health and Medical Research Council of Australia (http://www.nhmrc.gov.au/, National Health and Medical Research Council (NHMRC) project grants 389837 (clinical component) and 545223 (microbiology component), and Centre for Research Excellence in Lung Health of Aboriginal and Torres Strait Islanders grant 1040830). The Alaskan study site received funding from the National Institutes of Health (http://www.nih.gov/) and the National Heart Lung and Blood Institute (http://www.nhlbi.nih.gov/, No.U26IHS3000001/01). KMH is supported by the NHMRC Gustav Nossal Postgraduate Scholarship 1038072 and the Australian Academy of Science's (http://science.org.au/) Douglas and Lola Douglas Scholarship; PCV is supported by an Australian Research Council (http://www.arc.gov.au/) Future Fellowship No.100100511; ACC and HSV are funded by NHMRC Career Development Fellowships 1009945 and 1024175; AJL is supported by the NHMRC Elizabeth Blackburn Research Fellowship 1020561; and ABC is supported by a NHMRC Practitioner Fellowship 545216. The findings and conclusions in this article are those of the authors and do not necessarily represent the official position of the funding agencies. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.