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Evaluation of procedures for typing of group B Streptococcus: a retrospective study
BACKGROUND: This study evaluates two procedures for typing of Streptococcus agalactiae (group B streptococci; GBS) isolates, using retrospective typing data from the period 2010 to 2014 with a commercial latex agglutination test (latex test) and the Lancefield precipitation test (LP test). Furthermo...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357338/ https://www.ncbi.nlm.nih.gov/pubmed/28321367 http://dx.doi.org/10.7717/peerj.3105 |
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author | Slotved, Hans-Christian Hoffmann, Steen |
author_facet | Slotved, Hans-Christian Hoffmann, Steen |
author_sort | Slotved, Hans-Christian |
collection | PubMed |
description | BACKGROUND: This study evaluates two procedures for typing of Streptococcus agalactiae (group B streptococci; GBS) isolates, using retrospective typing data from the period 2010 to 2014 with a commercial latex agglutination test (latex test) and the Lancefield precipitation test (LP test). Furthermore, the genotype distribution of phenotypically non-typable (NT) GBS isolates is presented. We also raise the awareness, that the difference in typing results obtained by phenotypical methods and genotype based methods may have implications on vaccine surveillance in case a GBS vaccine is introduced. METHODS: A total of 616 clinical GBS isolates from 2010 to 2014 were tested with both a latex test and the LP test. Among these, 66 isolates were genotyped by PCR, including 41 isolates that were phenotypically NT. RESULTS: The latex test provided a serotype for 83.8% of the isolates (95% CI [80.7–86.6]) compared to 87.5% (95% CI [84.6–90.0]) obtained by the LP method. The two assays provided identical capsular identification for all sero-typeable isolates (excluding NT isolates). The PCR assay provided a genotype designation to the 41 isolates defined as phenotypically NT isolates. DISCUSSION: We found that the latex test showed a slightly lower identification percentage than the LP test. Our recommendation is to use the latex agglutination as the routine primary assay for GBS surveillance, and then use the more labour intensive precipitation test on the NT isolates to increase the serotyping rate. A genotype could be assigned to all the phenotypically NT isolates, however, as a consequence genotyping will overestimate the coverage from possible future capsular polysaccharide based GBS vaccines. |
format | Online Article Text |
id | pubmed-5357338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53573382017-03-20 Evaluation of procedures for typing of group B Streptococcus: a retrospective study Slotved, Hans-Christian Hoffmann, Steen PeerJ Microbiology BACKGROUND: This study evaluates two procedures for typing of Streptococcus agalactiae (group B streptococci; GBS) isolates, using retrospective typing data from the period 2010 to 2014 with a commercial latex agglutination test (latex test) and the Lancefield precipitation test (LP test). Furthermore, the genotype distribution of phenotypically non-typable (NT) GBS isolates is presented. We also raise the awareness, that the difference in typing results obtained by phenotypical methods and genotype based methods may have implications on vaccine surveillance in case a GBS vaccine is introduced. METHODS: A total of 616 clinical GBS isolates from 2010 to 2014 were tested with both a latex test and the LP test. Among these, 66 isolates were genotyped by PCR, including 41 isolates that were phenotypically NT. RESULTS: The latex test provided a serotype for 83.8% of the isolates (95% CI [80.7–86.6]) compared to 87.5% (95% CI [84.6–90.0]) obtained by the LP method. The two assays provided identical capsular identification for all sero-typeable isolates (excluding NT isolates). The PCR assay provided a genotype designation to the 41 isolates defined as phenotypically NT isolates. DISCUSSION: We found that the latex test showed a slightly lower identification percentage than the LP test. Our recommendation is to use the latex agglutination as the routine primary assay for GBS surveillance, and then use the more labour intensive precipitation test on the NT isolates to increase the serotyping rate. A genotype could be assigned to all the phenotypically NT isolates, however, as a consequence genotyping will overestimate the coverage from possible future capsular polysaccharide based GBS vaccines. PeerJ Inc. 2017-03-16 /pmc/articles/PMC5357338/ /pubmed/28321367 http://dx.doi.org/10.7717/peerj.3105 Text en ©2017 Slotved and Hoffmann http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Microbiology Slotved, Hans-Christian Hoffmann, Steen Evaluation of procedures for typing of group B Streptococcus: a retrospective study |
title | Evaluation of procedures for typing of group B Streptococcus: a retrospective study |
title_full | Evaluation of procedures for typing of group B Streptococcus: a retrospective study |
title_fullStr | Evaluation of procedures for typing of group B Streptococcus: a retrospective study |
title_full_unstemmed | Evaluation of procedures for typing of group B Streptococcus: a retrospective study |
title_short | Evaluation of procedures for typing of group B Streptococcus: a retrospective study |
title_sort | evaluation of procedures for typing of group b streptococcus: a retrospective study |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357338/ https://www.ncbi.nlm.nih.gov/pubmed/28321367 http://dx.doi.org/10.7717/peerj.3105 |
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