Abstract

Trachoma is a blinding disease caused by repeated conjunctival infection with different Chlamydia trachomatis (Ct) genovars. Ct B genovars have been associated with more severe trachoma symptoms. Here, we investigated associations between Ct genovars and bacterial loads in ocular samples from two distinct geographical locations in Africa, which are currently unclear. We tested ocular swabs from 77 Moroccan children (28 with trachomatous inflammation-follicular (TF) and 49 healthy controls), and 96 Sudanese children (54 with TF and 42 healthy controls) with a Ct-specific real-time polymerase chain reaction (PCR) assay. To estimate bacterial loads, Ct-positive samples were further processed by multiplex real-time qPCR to amplify the chromosomal outer membrane complex B and plasmid open reading frame 2 of Ct. Genotyping was performed by PCR-based amplification of the outer membrane protein A gene (~1120 base pairs) of Ct and Sanger sequencing. Ct-positivities among the Moroccan and Sudanese patient groups were 60·7% and 31·5%, respectively. Significantly more Sudanese patients than Moroccan patients were genovar A-positive. In contrast, B genovars were significantly more prevalent in Moroccan patients than in Sudanese patients. Significantly higher Ct loads were found in samples positive for B genovars (598596) than A genovar (51005). Geographical differences contributed to the distributions of different ocular Ct genovars. B genovars may induce a higher bacterial load than A genovars in trachoma patients. Our findings emphasize the importance of conducting broader studies to elucidate if the noted difference in multiplication abilities are genovar and/or endemicity level dependent.

Highlights

  • Trachoma is an infectious ocular disease caused by repeated infection of the conjunctiva with Chlamydia trachomatis (Ct) [1]

  • We investigated the association between different Ct genovars, the approximate load of infection, and the distribution of Chlamydia genovars by comparing samples from one trachoma-endemic area and one previously endemic area, currently considered as nonendemic

  • This study is the first to reveal a significant difference between the genome copy numbers of Ct genovar A and B/Ba in children with TF

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Summary

Introduction

Trachoma is an infectious ocular disease caused by repeated infection of the conjunctiva with Chlamydia trachomatis (Ct) [1]. Ct is the most prominent pathogen in the Chlamydiae phylum [4,5]. Differences between 19 serological variants (serovars) of Ct have been identified using monoclonal antibodies that react to epitopes on the major outer membrane protein (MOMP) [6,7]. Serovars A–C mainly cause trachoma, serovars D–K are major causes of sexually transmitted infections, and serovars L1–L3 mainly cause lymphogranuloma venereum, an invasive infection of lymph nodes [1,8,9]. Sequence heterogenicity in the outer membrane protein A (ompA) gene, which encodes MOMP, corresponds to 19 Ct genovars that reflect previously established serologic variants [10,11]

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