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

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 evide...

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Autores principales: Boelsen, Laura K., Dunne, Eileen M., Gould, Katherine A., Ratu, F. Tupou, Vidal, Jorge E., Russell, Fiona M., Mulholland, E. Kim, Hinds, Jason, Satzke, Catherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392543/
https://www.ncbi.nlm.nih.gov/pubmed/32727860
http://dx.doi.org/10.1128/mSphere.00478-20
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author Boelsen, Laura K.
Dunne, Eileen M.
Gould, Katherine A.
Ratu, F. Tupou
Vidal, Jorge E.
Russell, Fiona M.
Mulholland, E. Kim
Hinds, Jason
Satzke, Catherine
author_facet Boelsen, Laura K.
Dunne, Eileen M.
Gould, Katherine A.
Ratu, F. Tupou
Vidal, Jorge E.
Russell, Fiona M.
Mulholland, E. Kim
Hinds, Jason
Satzke, Catherine
author_sort Boelsen, Laura K.
collection PubMed
description 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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spelling pubmed-73925432020-07-31 The Challenges of Using Oropharyngeal Samples To Measure Pneumococcal Carriage in Adults Boelsen, Laura K. Dunne, Eileen M. Gould, Katherine A. Ratu, F. Tupou Vidal, Jorge E. Russell, Fiona M. Mulholland, E. Kim Hinds, Jason Satzke, Catherine mSphere Research Article 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. American Society for Microbiology 2020-07-29 /pmc/articles/PMC7392543/ /pubmed/32727860 http://dx.doi.org/10.1128/mSphere.00478-20 Text en Copyright © 2020 Boelsen et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Boelsen, Laura K.
Dunne, Eileen M.
Gould, Katherine A.
Ratu, F. Tupou
Vidal, Jorge E.
Russell, Fiona M.
Mulholland, E. Kim
Hinds, Jason
Satzke, Catherine
The Challenges of Using Oropharyngeal Samples To Measure Pneumococcal Carriage in Adults
title The Challenges of Using Oropharyngeal Samples To Measure Pneumococcal Carriage in Adults
title_full The Challenges of Using Oropharyngeal Samples To Measure Pneumococcal Carriage in Adults
title_fullStr The Challenges of Using Oropharyngeal Samples To Measure Pneumococcal Carriage in Adults
title_full_unstemmed The Challenges of Using Oropharyngeal Samples To Measure Pneumococcal Carriage in Adults
title_short The Challenges of Using Oropharyngeal Samples To Measure Pneumococcal Carriage in Adults
title_sort challenges of using oropharyngeal samples to measure pneumococcal carriage in adults
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392543/
https://www.ncbi.nlm.nih.gov/pubmed/32727860
http://dx.doi.org/10.1128/mSphere.00478-20
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