Skip to main content
New Microbes and New Infections logoLink to New Microbes and New Infections
letter
. 2019 Jul 3;31:100584. doi: 10.1016/j.nmni.2019.100584

Multi-locus sequence analysis reveals a novel sequence type of Chlamydia trachomatis in Saratov Region, Russia

VA Feodorova 1,, SS Zaitsev 1, YV Saltykov 1, SS Ulyanov 1,2, VL Motin 3,∗∗
PMCID: PMC6658990  PMID: 31372233

Abstract

Chlamydia trachomatis is the causative agent of a variety of chlamydial infections in humans with a predominantly (up to 80%) asymptomatic course of disease. In this study, a potentially novel C. trachomatis sequence type (ST) was detected in an asymptomatic man who has sex with a man among the nine STs revealed in urogenital swabs from individuals with chlamydia (n = 18). Phylogenetically this ST270 clustered separately as a single clade to an ST13-founded group of C. trachomatis strains and differed from the latter by a single allele, hflX. This finding emphasizes the importance of careful investigation of individuals with asymptomatic chlamydia infections.

Keywords: Chlamydia trachomatis, men-who-have-sex-with-men, multilocus sequence typing, ompA, sequence type


Chlamydia trachomatis is one of the most successful pathogens worldwide. It can cause a variety of chlamydial infections in humans, for instance trachoma, urogenital infection and lymphogranuloma venereum [1]. Chlamydial infection is a leading cause of serious complications such as pelvic inflammatory disease, ectopic pregnancy, inflammation, scarring and infertility [2]. Most chlamydial infections in humans could be asymptomatic (up to 80%) with no clinical manifestations, but the rate of transmission could remain extremely high [2], [3], [4], [5]. Here, we describe a 38-year-old man, single who has sex with a man with an asymptomatic chlamydial genital infection. Sexual debut had occurred by age 16 years. He declared few additional irregular sexual contacts during the last 6 months in parallel with his regular sex partner. He denied any pernicious habits, except smoking, and had no addiction to alcohol. Previous regular annual physical and laboratory examinations by a family physician found neither clinically apparent genital manifestations of chlamydial infection nor any other sexually transmitted infections. However, there were chlamydial IgG titres in serum of 1:160, registered with an ELISA kit. Therefore, he was referred to our Diagnostic Centre for laboratory confirmation of сhlamydia infection. Indeed, further routine diagnostic PCR demonstrated that his clinical sample (urethral swab) contained C. trachomatis DNA. Molecular analysis based on ompA and multilocus sequence typing (MLST), conducted as we described recently [6], assigned this DNA to the C. trachomatis genovar G, and a novel ST270 of C. trachomatis that was previously absent in the PubMLST database (http://pubmlst.org/chlamydiales/). Then, we studied other chlamydial clinical specimens to identify the frequency of occurrence of this novel ST270 in our region. DNA obtained from cervical and urethral swabs from women and men (n = 18) was analysed for the presence of major C. trachomatis genovars and sequence types (ST). The ompA-based genotyping revealed seven variants (Fig. 1a), while MLST analysis identified nine well-known STs, including the novel ST270, which was assigned as SaratovG/61.21-M156 (Fig. 1b).

Fig. 1.

Fig. 1

Phylogenetic analyses of Chlamydia trachomatis strains identified in the Saratov Region (highlighted in grey) combined with the reference strains. Novel sequence type (ST) strain SaratovG/61.21-M156 is marked with an asterisk. The trees were constructed using the UPGMA hierarchical clustering method model based on (a) polymorphism in ompA sequences; (b) concatenated partial sequences of seven housekeeping gene fragments, such as gatA, oppA, hfiX, gitA, enoA, hemN and fumC. The concatenated sequences were aligned and analysed in MEGA 7 [8]. Thick branches, subtending all large clades, represent 100% bootstrap support; and (c) GrapeTree clustering of 14 STs available in the Chlamydiales PubMLST database (https://pubmlst.org/chlamydiales/). Each node corresponds to a single ST marked with an individual colour. The numbers in square brackets indicate C. trachomatis representatives in the MLST database. The novel ST270 belongs to Group I with ST13 as founder.

The GrapeTree analysis of our strains with those obtained from the PubMLST/Chlamydiales database grouped the Saratov variants into three different clonal complexes (Fig. 1c). The first complex consisted of ST6, ST9, ST10, ST270 and ST13 (ST13 as the founder) and the second one included ST4, ST12, ST38 and ST118 (ST4 as the founder). Both of the complexes consisted of international C. trachomatis strains and were assigned earlier as Group I and Group III, respectively [7]. The strains from each Group differed in four alleles (oppA, hplX, gidA and enoA) (see Supplementary material, Table S1). SaratovG/61.21-M156 demonstrated identical alleles with six out of the seven loci found in ST13 and differed from the latter by a single allele hflX (see Supplementary material, Table S1). This C. trachomatis strain on ompA-typing formed a single additional clade to the Group I C. trachomatis strains and was located in an intermediate position between Groups 1/3 and Group 2 (Fig. 1b).

In conclusion, individuals with asymptomatic chlamydia infections should be systematically tested independently of their sexual behaviour. Molecular methods including MLST typing are effective approaches to support identification and differentiation of existing and novel C. trachomatis variants. This will provide new insights into the molecular evolution and phylogenetic relationships of C. trachomatis worldwide.

PubMLST sequences accession number. The ST sequence was deposited in PubMLST/Chlamydiales database under accession numbers 4434–4450 (https://pubmlst.org/).

Acknowledgements

This work was supported by the Russian Science Foundation, Russia, Project No. 17-16-01099.

Footnotes

Appendix A

Supplementary data to this article can be found online at https://doi.org/10.1016/j.nmni.2019.100584.

Contributor Information

V.A. Feodorova, Email: feodorovav@mail.ru.

V.L. Motin, Email: vlmotin@utmb.edu.

Conflicts of interest

None declared.

Appendix A. Supplementary data

The following is the Supplementary data to this article:

Multimedia component 1
mmc1.doc (87KB, doc)

References

  • 1.Garland S.M., Malatt A., Tabrizi S., Grando D., Lees M.I., Andrew J.H. Chlamydia trachomatis conjunctivitis. Prevalence and association with genital tract infection. Med J Aust. 1995;162:363–366. [PubMed] [Google Scholar]
  • 2.Menon S., Timms P., Allan J.A., Alexander K., Rombauts L., Horner P. Human and pathogen factors associated with Chlamydia trachomatis related infertility in women. Clin Microbiol Rev. 2015;28:969–985. doi: 10.1128/CMR.00035-15. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Korenromp E.L., Sudaryo M.K., de Vlas S.J., Gray R.H., Sewankambo N.K., Serwadda D. What proportion of episodes of gonorrhoea and chlamydia becomes symptomatic? Int J STD AIDS. 2002;13:91–101. doi: 10.1258/0956462021924712. [DOI] [PubMed] [Google Scholar]
  • 4.Farley T.A., Cohen D.A., Elkins W. Asymptomatic sexually transmitted diseases: the case for screening. Prev Med. 2003;36:502–509. doi: 10.1016/s0091-7435(02)00058-0. [DOI] [PubMed] [Google Scholar]
  • 5.Ljubin-Sternak S., Mestrovic T. Chlamydia trachomatis and genital mycoplasmas: pathogens with an impact on human reproductive health. J Pathog. 2014:183167. doi: 10.1155/2014/183167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Feodorova V.A., Konnova S.S., Saltykov Y.V., Zaitsev S.S., Subbotina I.A., Polyanina T.I. One urogenital Chlamydia trachomatis multilocus sequence types and genovar distribution in chlamydia infected patients in a multi-ethnic region of Saratov, Russia. PLoS One. 2018;13(4) doi: 10.1371/journal.pone.0195386. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Pannekoek Y., Morelli G., Kusecek B., Morré S.A., Ossewaarde J.M., Langerak A.A. Multi locus sequence typing of Chlamydiales: clonal groupings within the obligate intracellular bacteria Chlamydia trachomatis. BMC Microbiol. 2008;8:42. doi: 10.1186/1471-2180-8-42. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Kumar S., Stecher G., Tamura K. MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol. 2016;33:1870–1874. doi: 10.1093/molbev/msw054. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Multimedia component 1
mmc1.doc (87KB, doc)

Articles from New Microbes and New Infections are provided here courtesy of Elsevier

RESOURCES