Article Text
Abstract
Introduction Lymphogranuloma venereum (LGV) is a sexually transmitted infection caused by Chlamydia trachomatis genotypes L1–L3. A combination of techniques with high discriminatory capacity such as multilocus sequence typing (MLST) and the analysis of the ompA gene may be useful to determine the greater penetration of certain strains in transmission networks and their relationship with certain tropisms.
Aim The aim of this study was to investigate the molecular epidemiology of LGV isolates from different regions of Spain.
Methods Genetic characterisation of LGV isolates detected in six hospitals from Spain between 2018 and 2019 was performed. MLST (five variable regions: hctB, CT058, CT144, CT172 and pbpB) and ompA sequence determination were used to study the LGV strains.
Results Most of the 161 LGV isolates (93.8%) were detected in men who have sex with men (MSM). At least 43.5% of the patients presented with HIV coinfection and 53.4% were symptomatic, with proctitis being the most prevalent symptom (73.3%). Most isolates were detected in Barcelona (n=129).
The distribution of ompA genovariants was as follows: 56.1% belonged to L2, 24.3% to L2b, 5.4% to L2bV1, 4.7% to L2bV4, 4.1% to L1, 2.7% to L2b/D-Da, 2.0% to L2bV2 and 0.7% to L2bV7. MLST was successfully performed in 81 samples and 9 different sequence types (STs) were detected. The ompA and MLST combination obtained 17 different genetic profiles, with L2-ST53 and L2-ST58 being the most prevalent (29.5% and 14.1%, respectively). L1 genotype strains belonged to ST23 (n=3) and ST2 (n=3).
Conclusion LGV infections were mainly found in MSM living with HIV and with proctitis. The joint analysis of ompA and MLST genetic characterisation techniques showed a high discriminatory capacity. Our findings suggest a cocirculation of L2 and L2b ompA genotypes, and with the inclusion of MLST characterisation, the most prevalent profiles were ompA genotype L2-MLST ST53 and L2-MLST ST58.
- LYMPHOGRANULOMA VENEREUM
- Chalmydia Trachomatis
- Sexual Behavior
Data availability statement
Data are available on reasonable request. The datasets generated and analysed during the current study are available from the corresponding author on reasonable request.
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Data availability statement
Data are available on reasonable request. The datasets generated and analysed during the current study are available from the corresponding author on reasonable request.
Footnotes
Handling editor Anna Maria Geretti
X @Luis_Pineiro_V
Contributors LP is the guarantor and conceived and led the design of this project. All authors performed data collection. PS carried out the molecular characterisation analysis, analysed the results and wrote the initial draft with JS-P and LP. All authors reviewed and approved the final draft.
Funding This study was funded by Instituto de Salud Carlos III (ISCIII) through the project ‘PI17/01886’ and cofunded by the European Union.
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Competing interests None declared.
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