Insights into the phylogeny, resistome, virulome and host adaptation from Gardnerella genome analysis
Autor(a) principal: | |
---|---|
Data de Publicação: | 2023 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://doi.org/10.48797/sl.2023.50 |
Resumo: | Background: Gardnerella spp. is often seen as evidence of vaginal pathologies, although members of this genus can also be found in the urinary and vaginal microbiota of asymptomatic women [1,2], making its role in the urogenital tract unclear. Objective: To assess phylogenomic and functional analysis of Gardnerella genus. Resistance (ARGs) and virulence genes (Vg) was also explored to unveil their role in health and urogenital disease development. Methods:Twenty-nine Gardnerella isolates from urine (U, n=22) and vaginal swabs (VSn=7) of women [24 asymptomatic, 5 with overactive bladder (OAB)] were identified by cpn60 and WGS (NovaSeq 6000; Illumina). Together with118 genomes from public databases (from U (n=35), VS (n=82) blood (n=1), and unknown samples (n=2)), we used TYGS platform and fastANI for species identification. Phylogenomic and pangenome analyses were performed using anvi’o v7.1 and Roary. Vg were annotated with COG and KEGG databases, and ARGs with AMRFinder Plus. Vg presence/absence outoputs were analyzed with R. Results: 4 species and 10 genomic species were identified, 41% of the collection being comprised by G. vaginalis. ANI and dDDH values are insufficient for distinguishing Gardnerella species. Pangenome was composed by4537 gene clusters and the core genome of by 514. Differences in carbohydrates and amino acid metabolism and absence of correlation of functions with human body sites or disease were observed. The virulome and Gardnerellaspecies/genomospecies exhibit are intertwined. ARG to aminoglycosides (aph(3')-Ia), macrolides (mefA, msrD, ermX), tetracyclines (tetM, tetL), lincosamide and streptogramins (lsaC) were detected in several isolates. Open pangenomes were observed in G. vaginalis, G. leopoldii, G. swidsinskii and GG3. Conclusions: Gardnerella comprises 4 species and 10 genomic species. Core genome analysis, ANI and dDDH are recommended for appropriate species assignment. Gardnerella species/genomospecies are associated with a particular set of VFs and metabolic functions. ARGs with clinical relevance were also observed in different Gardnerella species. |
id |
RCAP_06393974389c86d648aac22a0f3717c2 |
---|---|
oai_identifier_str |
oai:publicacoes.cespu.pt:article/50 |
network_acronym_str |
RCAP |
network_name_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository_id_str |
7160 |
spelling |
Insights into the phylogeny, resistome, virulome and host adaptation from Gardnerella genome analysisSelected Oral CommunicationBackground: Gardnerella spp. is often seen as evidence of vaginal pathologies, although members of this genus can also be found in the urinary and vaginal microbiota of asymptomatic women [1,2], making its role in the urogenital tract unclear. Objective: To assess phylogenomic and functional analysis of Gardnerella genus. Resistance (ARGs) and virulence genes (Vg) was also explored to unveil their role in health and urogenital disease development. Methods:Twenty-nine Gardnerella isolates from urine (U, n=22) and vaginal swabs (VSn=7) of women [24 asymptomatic, 5 with overactive bladder (OAB)] were identified by cpn60 and WGS (NovaSeq 6000; Illumina). Together with118 genomes from public databases (from U (n=35), VS (n=82) blood (n=1), and unknown samples (n=2)), we used TYGS platform and fastANI for species identification. Phylogenomic and pangenome analyses were performed using anvi’o v7.1 and Roary. Vg were annotated with COG and KEGG databases, and ARGs with AMRFinder Plus. Vg presence/absence outoputs were analyzed with R. Results: 4 species and 10 genomic species were identified, 41% of the collection being comprised by G. vaginalis. ANI and dDDH values are insufficient for distinguishing Gardnerella species. Pangenome was composed by4537 gene clusters and the core genome of by 514. Differences in carbohydrates and amino acid metabolism and absence of correlation of functions with human body sites or disease were observed. The virulome and Gardnerellaspecies/genomospecies exhibit are intertwined. ARG to aminoglycosides (aph(3')-Ia), macrolides (mefA, msrD, ermX), tetracyclines (tetM, tetL), lincosamide and streptogramins (lsaC) were detected in several isolates. Open pangenomes were observed in G. vaginalis, G. leopoldii, G. swidsinskii and GG3. Conclusions: Gardnerella comprises 4 species and 10 genomic species. Core genome analysis, ANI and dDDH are recommended for appropriate species assignment. Gardnerella species/genomospecies are associated with a particular set of VFs and metabolic functions. ARGs with clinical relevance were also observed in different Gardnerella species. IUCS-CESPU Publishing2023-04-21info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://doi.org/10.48797/sl.2023.50https://doi.org/10.48797/sl.2023.50Scientific Letters; Vol. 1 No. Sup 1 (2023)2795-5117reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPenghttps://publicacoes.cespu.pt/index.php/sl/article/view/50https://publicacoes.cespu.pt/index.php/sl/article/view/50/103Copyright (c) 2023 P. Teixeira, M. Sousa, F. Grosso, T. Ribeiro, L. Peixeinfo:eu-repo/semantics/openAccessTeixeira, P.Sousa, M.Grosso, F.Ribeiro, T.Peixe, L.2023-04-29T08:46:00Zoai:publicacoes.cespu.pt:article/50Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:50:21.970702Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Insights into the phylogeny, resistome, virulome and host adaptation from Gardnerella genome analysis |
title |
Insights into the phylogeny, resistome, virulome and host adaptation from Gardnerella genome analysis |
spellingShingle |
Insights into the phylogeny, resistome, virulome and host adaptation from Gardnerella genome analysis Teixeira, P. Selected Oral Communication |
title_short |
Insights into the phylogeny, resistome, virulome and host adaptation from Gardnerella genome analysis |
title_full |
Insights into the phylogeny, resistome, virulome and host adaptation from Gardnerella genome analysis |
title_fullStr |
Insights into the phylogeny, resistome, virulome and host adaptation from Gardnerella genome analysis |
title_full_unstemmed |
Insights into the phylogeny, resistome, virulome and host adaptation from Gardnerella genome analysis |
title_sort |
Insights into the phylogeny, resistome, virulome and host adaptation from Gardnerella genome analysis |
author |
Teixeira, P. |
author_facet |
Teixeira, P. Sousa, M. Grosso, F. Ribeiro, T. Peixe, L. |
author_role |
author |
author2 |
Sousa, M. Grosso, F. Ribeiro, T. Peixe, L. |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Teixeira, P. Sousa, M. Grosso, F. Ribeiro, T. Peixe, L. |
dc.subject.por.fl_str_mv |
Selected Oral Communication |
topic |
Selected Oral Communication |
description |
Background: Gardnerella spp. is often seen as evidence of vaginal pathologies, although members of this genus can also be found in the urinary and vaginal microbiota of asymptomatic women [1,2], making its role in the urogenital tract unclear. Objective: To assess phylogenomic and functional analysis of Gardnerella genus. Resistance (ARGs) and virulence genes (Vg) was also explored to unveil their role in health and urogenital disease development. Methods:Twenty-nine Gardnerella isolates from urine (U, n=22) and vaginal swabs (VSn=7) of women [24 asymptomatic, 5 with overactive bladder (OAB)] were identified by cpn60 and WGS (NovaSeq 6000; Illumina). Together with118 genomes from public databases (from U (n=35), VS (n=82) blood (n=1), and unknown samples (n=2)), we used TYGS platform and fastANI for species identification. Phylogenomic and pangenome analyses were performed using anvi’o v7.1 and Roary. Vg were annotated with COG and KEGG databases, and ARGs with AMRFinder Plus. Vg presence/absence outoputs were analyzed with R. Results: 4 species and 10 genomic species were identified, 41% of the collection being comprised by G. vaginalis. ANI and dDDH values are insufficient for distinguishing Gardnerella species. Pangenome was composed by4537 gene clusters and the core genome of by 514. Differences in carbohydrates and amino acid metabolism and absence of correlation of functions with human body sites or disease were observed. The virulome and Gardnerellaspecies/genomospecies exhibit are intertwined. ARG to aminoglycosides (aph(3')-Ia), macrolides (mefA, msrD, ermX), tetracyclines (tetM, tetL), lincosamide and streptogramins (lsaC) were detected in several isolates. Open pangenomes were observed in G. vaginalis, G. leopoldii, G. swidsinskii and GG3. Conclusions: Gardnerella comprises 4 species and 10 genomic species. Core genome analysis, ANI and dDDH are recommended for appropriate species assignment. Gardnerella species/genomospecies are associated with a particular set of VFs and metabolic functions. ARGs with clinical relevance were also observed in different Gardnerella species. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-04-21 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://doi.org/10.48797/sl.2023.50 https://doi.org/10.48797/sl.2023.50 |
url |
https://doi.org/10.48797/sl.2023.50 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://publicacoes.cespu.pt/index.php/sl/article/view/50 https://publicacoes.cespu.pt/index.php/sl/article/view/50/103 |
dc.rights.driver.fl_str_mv |
Copyright (c) 2023 P. Teixeira, M. Sousa, F. Grosso, T. Ribeiro, L. Peixe info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2023 P. Teixeira, M. Sousa, F. Grosso, T. Ribeiro, L. Peixe |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
IUCS-CESPU Publishing |
publisher.none.fl_str_mv |
IUCS-CESPU Publishing |
dc.source.none.fl_str_mv |
Scientific Letters; Vol. 1 No. Sup 1 (2023) 2795-5117 reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
|
_version_ |
1799131583700008960 |