The Challenges of Using Oropharyngeal Samples To Measure Pneumococcal Carriage in Adults

被引:11
作者
Boelsen, Laura K. [1 ,2 ]
Dunne, Eileen M. [1 ,2 ,9 ]
Gould, Katherine A. [3 ,4 ]
Ratu, F. Tupou [5 ]
Vidal, Jorge E. [6 ]
Russell, Fiona M. [1 ,2 ]
Mulholland, E. Kim [1 ,2 ,7 ]
Hinds, Jason [3 ,4 ]
Satzke, Catherine [1 ,2 ,8 ]
机构
[1] Royal Childrens Hosp, Murdoch Childrens Res Inst, Infect & Immun, Parkville, Vic, Australia
[2] Univ Melbourne, Dept Paediat, Parkville, Vic, Australia
[3] St Georges Univ London, Inst Infect & Immun, London, England
[4] London Biosci Innovat Ctr, BUGS Biosci, London, England
[5] Minist Hlth & Med Serv, Suva, Fiji
[6] Univ Mississippi, Med Ctr, Dept Microbiol & Immunol, Jackson, MS 39216 USA
[7] London Sch Hyg & Trop Med, London, England
[8] Univ Melbourne, Dept Microbiol & Immunol, Peter Doherty Inst Infect & Immun, Parkville, Vic, Australia
[9] Ctr Dis Control & Prevent, Atlanta, GA USA
来源
MSPHERE | 2020年 / 5卷 / 04期
基金
比尔及梅琳达.盖茨基金会; 英国医学研究理事会; 澳大利亚国家健康与医学研究理事会; 美国国家卫生研究院;
关键词
PCR; Streptococcus pneumoniae; carriage; genotypic; identification; nasopharyngeal; oropharyngeal; serotyping; UPPER RESPIRATORY-TRACT; STREPTOCOCCUS-PNEUMONIAE; NASOPHARYNGEAL CARRIAGE; HAEMOPHILUS-INFLUENZAE; CONJUGATE VACCINES; LYTA; COLONIZATION; CHILDREN; SEROTYPE; DISEASE;
D O I
10.1128/mSphere.00478-20
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Streptococcus pneumoniae (the pneumococcus) carriage is commonly used to measure effects of pneumococcal vaccines. Based on findings from culture-based studies, the World Health Organization recommends both nasopharyngeal (NP) and oropharyngeal (OP) sampling for detecting adult carriage. Given evidence of potential confounding by other streptococci, we evaluated molecular methods for pneumococcal identification and serotyping from 250 OP samples collected from adults in Fiji, using paired NP samples for comparison. Samples were screened using lytA quantitative PCR (qPCR), as well as pneumococcal identification and serotyping conducted by DNA microarray. A subset of OP samples were characterized by latex sweep agglutination and multiplex PCR. Alternate qPCR assays (piaB and bguR) for pneumococcal identification were evaluated. The lytA qPCR was less specific and had poor positive predictive value (PPV) in OP samples (88% and 26%, respectively) compared with NP samples (95% and 64%, respectively). Using additional targets piaB and/or bguR improved qPCR specificity in OP, although the PPV (42 to 53%) was still poor. Using microarray, we found that 102/107 (95%) of OP samples contained nonpneumococcal streptococci with partial or divergent complements of pneumococcal capsule genes. We explored 91 colonies isolated from 11 OP samples using various techniques, including multiplex PCR, latex agglutination, and microarray. We found that nonpneumococcal streptococci contribute to false positives in pneumococcal serotyping and may also contribute to spurious identification by qPCR. Our results highlight that molecular approaches should include multiple loci to minimize false-positive results when testing OP samples. Regardless of method, pneumococcal identification and serotyping results from OP samples should be interpreted with caution. IMPORTANCE Streptococcus pneumoniae (the pneumococcus) is a significant global pathogen. Accurate identification and serotyping are vital. In contrast with World Health Organization recommendations based on culture methods, we demonstrate that pneumococcal identification and serotyping with molecular methods are affected by sample type. Results from oropharyngeal samples from adults were often inaccurate. This is particularly important for assessment of vaccine impact using carriage studies, particularly in low- and middle-income countries where there are significant barriers for disease surveillance.
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页数:15
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