lymphogranuloma venereum
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2022 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Angeliki N. Georgopoulou ◽  
Evangelia Skoura ◽  
Eleftheria Lakiotaki ◽  
Nikolaos V. Sipsas ◽  
Theodoros P. Vassilakopoulos

2021 ◽  
Vol 193 (49) ◽  
pp. E1889-E1889
Author(s):  
Eric J. Eckbo ◽  
Malcolm Hedgcock ◽  
Troy Grennan

Author(s):  
Aws Waleed M. Al-Hayani ◽  
Iris Martínez Alemany ◽  
Carlos Santonja ◽  
Alfonso Cabello Úbeda ◽  
Laura Prieto Pérez ◽  
...  

2021 ◽  
Vol 27 (10) ◽  
pp. 2695-2699
Author(s):  
Mateo Prochazka ◽  
Hannah Charles ◽  
Hester Allen ◽  
Michelle Cole ◽  
Gwenda Hughes ◽  
...  

Author(s):  
J. Riera‐Monroig ◽  
F. Alamon‐Reig ◽  
P. Giavedoni ◽  
Y. Zboromyrska ◽  
N. Castrejón ◽  
...  

Author(s):  
Evonne N. Woodson ◽  
Samantha S. Katz ◽  
Sheree S. Mosley ◽  
Damien C. Danavall ◽  
Katherine E. Bowden ◽  
...  

PLoS ONE ◽  
2021 ◽  
Vol 16 (7) ◽  
pp. e0254233
Author(s):  
Chloe Manning ◽  
Colette O’Neill ◽  
Ian N. Clarke ◽  
Monica Rebec ◽  
Penelope R. Cliff ◽  
...  

Background Lymphogranuloma venereum (LGV) is caused by Chlamydia trachomatis strains with ompA genotypes L1 to L3. An LGV epidemic associated with the L2b genotype has emerged in the past few decades amongst men who have sex with men (MSM). C. trachomatis genotypes can be discriminated by outer membrane protein A gene (ompA) sequencing, however this method has limited resolution. This study employed a high-resolution genotyping method, namely, multi-locus tandem repeat (VNTR) analysis with ompA sequencing (MLVA-ompA), to assess the distribution of LGV MLVA-ompA genotypes amongst individuals attending genitourinary medicine (GUM) clinics in London. Methods Clinical specimens were collected from individuals attending eight London-based GUM clinics. Specimens that tested positive for C. trachomatis by commercial nucleic acid amplification test (NAAT) were confirmed as LGV by pmpH real-time PCR. LGV-positive DNA extracts were subsequently genotyped using MLVA-ompA. Results Two hundred and thirty DNA extracts were confirmed as LGV, and 162 (70%) yielded complete MLVA-ompA genotypes. Six LGV MLVA-ompA genotypes were identified: 1.9.2b-L2, 1.9.3b-L2b, 1.9.2b-L2b, 1.9.2b-L2b/D, 1.4a.2b-L2b, and 5.9.2b-L1. The following LGV ompA genotypes were identified (in descending order of abundance): L2, L2b, L2b/D, and L1. Eight ompA sequences with the hybrid L2b/D profile were detected. The hybrid sequence was identical to the ompA of a recombinant L2b/D strain detected in Portugal in 2017. Conclusions The L2 ompA genotype was found to predominate in the London study population. The study detected an unusual hybrid L2b/D ompA profile that was previously reported in Portugal. We recommend further monitoring and surveillance of LGV strains within the UK population.


2021 ◽  
Vol 21 (7) ◽  
pp. 1049
Author(s):  
Andrew Kapoor ◽  
Simi Padival

2021 ◽  
Author(s):  
D Richardson ◽  
J Devlin ◽  
Z Buss ◽  
C Fitzpatrick ◽  
N Pinto-Sander

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