Cargando…
Population genetics of group B Streptococcus from maternal carriage in an ethnically diverse community in London
INTRODUCTION: Maternal immunization against Group B Streptococcus (GBS) has the potential to significantly reduce the burden of neonatal GBS infections. Population genetics of GBS from maternal carriage can offer key insights into vaccine target distribution. METHODS: In this study we characterized...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233156/ https://www.ncbi.nlm.nih.gov/pubmed/37275158 http://dx.doi.org/10.3389/fmicb.2023.1185753 |
_version_ | 1785052176127623168 |
---|---|
author | Jamrozy, Dorota Gopal Rao, Guduru Feltwell, Theresa Lamagni, Theresa Khanna, Priya Efstratiou, Androulla Parkhill, Julian Bentley, Stephen D. |
author_facet | Jamrozy, Dorota Gopal Rao, Guduru Feltwell, Theresa Lamagni, Theresa Khanna, Priya Efstratiou, Androulla Parkhill, Julian Bentley, Stephen D. |
author_sort | Jamrozy, Dorota |
collection | PubMed |
description | INTRODUCTION: Maternal immunization against Group B Streptococcus (GBS) has the potential to significantly reduce the burden of neonatal GBS infections. Population genetics of GBS from maternal carriage can offer key insights into vaccine target distribution. METHODS: In this study we characterized the population structure of GBS isolates from maternal carriage (n = 535) in an ethnically diverse community in London, using whole genome sequencing. RESULTS: The isolates clustered into nine clonal complexes (CCs) but the majority (95%) belonged to five lineages: CC1 (26%), CC19 (26%), CC23 (20%), CC17 (13%) and CC8/10 (10%). Nine serotypes were identified, the most common were serotypes III (26%), V (21%), II (19%) and Ia (19%). Other serotypes (Ib, IV, VI, VII, IX) represented less than 10% of all isolates each. Intra-lineage serotype diversity was observed in all major CCs but was highest in CC1, which revealed nine serotypes. Nearly all isolates (99%) carried at least one of the four alpha family protein genes (alpha, alp1, alp23, and rib). All isolates were susceptible to penicillin. We found 21% and 13% of isolates to be resistant to clarithromycin and clindamycin, respectively. Prevalence of macrolide-lincosamide-streptogramin B (MLS(B)) resistance genes was 22% and they were most common in CC19 (37%) and CC1 (28%), and isolates with serotypes V (38%) and IV (32%). We identified some associations between maternal ethnicity and GBS population structure. Serotype Ib was significantly less common among the South Asian compared to Black women (S. Asian: 3/142, Black: 15/135, p = 0.03). There was also a significantly lower proportion of CC1 isolates among the White other (24/142) in comparison to Black (43/135) and S. Asian (44/142) women (p = 0.04). We found a significantly higher proportion of CC17 isolates among the White other compared to S. Asian women (White other: 32/142, S. Asian: 10/142, p = 0.004). CONCLUSION: Our study showed high prevalence of GBS vaccine targets among isolates from pregnant women in London. However, the observed serotype diversity in CC1 and high prevalence of MLS(B) resistance genes in CC19 demonstrates presence of high risk lineages, which might act as a reservoir of non-vaccine strains and antimicrobial resistance determinants. |
format | Online Article Text |
id | pubmed-10233156 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102331562023-06-02 Population genetics of group B Streptococcus from maternal carriage in an ethnically diverse community in London Jamrozy, Dorota Gopal Rao, Guduru Feltwell, Theresa Lamagni, Theresa Khanna, Priya Efstratiou, Androulla Parkhill, Julian Bentley, Stephen D. Front Microbiol Microbiology INTRODUCTION: Maternal immunization against Group B Streptococcus (GBS) has the potential to significantly reduce the burden of neonatal GBS infections. Population genetics of GBS from maternal carriage can offer key insights into vaccine target distribution. METHODS: In this study we characterized the population structure of GBS isolates from maternal carriage (n = 535) in an ethnically diverse community in London, using whole genome sequencing. RESULTS: The isolates clustered into nine clonal complexes (CCs) but the majority (95%) belonged to five lineages: CC1 (26%), CC19 (26%), CC23 (20%), CC17 (13%) and CC8/10 (10%). Nine serotypes were identified, the most common were serotypes III (26%), V (21%), II (19%) and Ia (19%). Other serotypes (Ib, IV, VI, VII, IX) represented less than 10% of all isolates each. Intra-lineage serotype diversity was observed in all major CCs but was highest in CC1, which revealed nine serotypes. Nearly all isolates (99%) carried at least one of the four alpha family protein genes (alpha, alp1, alp23, and rib). All isolates were susceptible to penicillin. We found 21% and 13% of isolates to be resistant to clarithromycin and clindamycin, respectively. Prevalence of macrolide-lincosamide-streptogramin B (MLS(B)) resistance genes was 22% and they were most common in CC19 (37%) and CC1 (28%), and isolates with serotypes V (38%) and IV (32%). We identified some associations between maternal ethnicity and GBS population structure. Serotype Ib was significantly less common among the South Asian compared to Black women (S. Asian: 3/142, Black: 15/135, p = 0.03). There was also a significantly lower proportion of CC1 isolates among the White other (24/142) in comparison to Black (43/135) and S. Asian (44/142) women (p = 0.04). We found a significantly higher proportion of CC17 isolates among the White other compared to S. Asian women (White other: 32/142, S. Asian: 10/142, p = 0.004). CONCLUSION: Our study showed high prevalence of GBS vaccine targets among isolates from pregnant women in London. However, the observed serotype diversity in CC1 and high prevalence of MLS(B) resistance genes in CC19 demonstrates presence of high risk lineages, which might act as a reservoir of non-vaccine strains and antimicrobial resistance determinants. Frontiers Media S.A. 2023-05-18 /pmc/articles/PMC10233156/ /pubmed/37275158 http://dx.doi.org/10.3389/fmicb.2023.1185753 Text en Copyright © 2023 Jamrozy, Gopal Rao, Feltwell, Lamagni, Khanna, Efstratiou, Parkhill and Bentley. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Jamrozy, Dorota Gopal Rao, Guduru Feltwell, Theresa Lamagni, Theresa Khanna, Priya Efstratiou, Androulla Parkhill, Julian Bentley, Stephen D. Population genetics of group B Streptococcus from maternal carriage in an ethnically diverse community in London |
title | Population genetics of group B Streptococcus from maternal carriage in an ethnically diverse community in London |
title_full | Population genetics of group B Streptococcus from maternal carriage in an ethnically diverse community in London |
title_fullStr | Population genetics of group B Streptococcus from maternal carriage in an ethnically diverse community in London |
title_full_unstemmed | Population genetics of group B Streptococcus from maternal carriage in an ethnically diverse community in London |
title_short | Population genetics of group B Streptococcus from maternal carriage in an ethnically diverse community in London |
title_sort | population genetics of group b streptococcus from maternal carriage in an ethnically diverse community in london |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233156/ https://www.ncbi.nlm.nih.gov/pubmed/37275158 http://dx.doi.org/10.3389/fmicb.2023.1185753 |
work_keys_str_mv | AT jamrozydorota populationgeneticsofgroupbstreptococcusfrommaternalcarriageinanethnicallydiversecommunityinlondon AT gopalraoguduru populationgeneticsofgroupbstreptococcusfrommaternalcarriageinanethnicallydiversecommunityinlondon AT feltwelltheresa populationgeneticsofgroupbstreptococcusfrommaternalcarriageinanethnicallydiversecommunityinlondon AT lamagnitheresa populationgeneticsofgroupbstreptococcusfrommaternalcarriageinanethnicallydiversecommunityinlondon AT khannapriya populationgeneticsofgroupbstreptococcusfrommaternalcarriageinanethnicallydiversecommunityinlondon AT efstratiouandroulla populationgeneticsofgroupbstreptococcusfrommaternalcarriageinanethnicallydiversecommunityinlondon AT parkhilljulian populationgeneticsofgroupbstreptococcusfrommaternalcarriageinanethnicallydiversecommunityinlondon AT bentleystephend populationgeneticsofgroupbstreptococcusfrommaternalcarriageinanethnicallydiversecommunityinlondon |