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Lymphogranuloma venereum (LGV) ompA-subvariants of the Portuguese collection of Chlamydia trachomatis, 2007–2023

dc.contributor.authorLodhia, Zohra
dc.contributor.authorCordeiro, Dora
dc.contributor.authorCorreia, Cristina
dc.contributor.authorJoão, Inês
dc.contributor.authorCarreira, Teresa
dc.contributor.authorNunes, Alexandra
dc.contributor.authorFerreira, Rita
dc.contributor.authorSchäfer, Sandra
dc.contributor.authorAliyeva, Elzara
dc.contributor.authorPortugal, Clara
dc.contributor.authorMonge, Isabel
dc.contributor.authorGonçalves, Elsa
dc.contributor.authorMatos, Susana
dc.contributor.authorDias, Ana Paula
dc.contributor.authorCorte-Real, Rita
dc.contributor.authorVieira, Luís
dc.contributor.authorGomes, Joao Paulo
dc.contributor.authorBorges, Vítor
dc.contributor.authorJose Borrego, Maria
dc.date.accessioned2025-11-14T10:28:48Z
dc.date.available2025-11-14T10:28:48Z
dc.date.issued2025-02-06
dc.description.abstractBackground: Lymphogranuloma venereum (LGV) is a sexually transmitted infection caused by Chlamydia trachomatis ompA-genotypes L1–L3, with increasing numbers of detected cases across Europe. Here, we analysed diversity and temporal distribution of the LGV ompA-subvariants detected in Portugal between 2007 and 2023, in order to better understand the dissemination and diversification landscape of LGV strains. Methods: The collection of the Portuguese National Reference Laboratory includes 1188 LGV ompA-genotyped samples between 2007 and 2023. In-depth analysis of the diversity of LGV ompA-subvariants circulating in Portugal across the years was performed, identifying newly described subvariants and integrating this data in a comprehensive compilation with all representative LGV ompA-subvariants described globally. Results: L2 ompA-variant (L2/434/Bu) was consistently the most frequently detected in our collection, with annual proportions ranging from 34.0% to 82.9%, between 2016 and 2023. L2bV5 was the second most frequent followed by L2b, ranging from 5.0% to 27.9% and 2.6% to 23.7% across the years, respectively, from 2017 to 2023. We highlighted the emergence and considerable increase in circulation of L1-like ompA-subvariants in recent years, representing 13.7% of LGV sequences in 2023. We also identified 13 novel LGV ompA-subvariants that had not been described before, differing by up to three mutations from the respective genotype reference sequences. Conclusions: This study contributes to the worldwide picture of the LGV molecular epidemiology, highlighting the importance of long-term molecular surveillance to monitor the circulation and geographical spread of LGV and to timely identify and track new strains, such as the recently emerging L1-like ompA-subvariants.eng
dc.identifier.citationSex Transm Infect. 2025 Aug 28;101(6):374-379. doi: 10.1136/sextrans-2024-056427
dc.identifier.doi10.1136/sextrans-2024-056427
dc.identifier.eissn1368-4973
dc.identifier.issn1368-4973
dc.identifier.pmid39915233
dc.identifier.urihttp://hdl.handle.net/10400.18/10611
dc.language.isoeng
dc.peerreviewedyes
dc.publisherBMJ Publishing Group
dc.relation.hasversionhttps://sti.bmj.com/content/101/6/374.long
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectChlamydia trachomatis
dc.subjectLymphogranuloma venereum
dc.subjectMolecular Typing
dc.subjectGenetic Variation
dc.subjectGenotype
dc.subjectGenetics
dc.subjectEpidemiology
dc.subjectMicrobiology
dc.subjectInfecções Sexualmente Transmissíveis
dc.subjectPortugal
dc.titleLymphogranuloma venereum (LGV) ompA-subvariants of the Portuguese collection of Chlamydia trachomatis, 2007–2023eng
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage379
oaire.citation.issue6
oaire.citation.startPage374
oaire.citation.titleSexually Transmitted Infections
oaire.citation.volume101
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85

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