Abstract

Syphilis, which is caused by the sexually transmitted bacterium Treponema pallidum subsp. pallidum, has an estimated 6.3 million cases worldwide per annum. In the past ten years, the incidence of syphilis has increased by more than 150% in some high-income countries, but the evolution and epidemiology of the epidemic are poorly understood. To characterize the global population structure of T. pallidum, we assembled a geographically and temporally diverse collection of 726 genomes from 626 clinical and 100 laboratory samples collected in 23 countries. We applied phylogenetic analyses and clustering, and found that the global syphilis population comprises just two deeply branching lineages, Nichols and SS14. Both lineages are currently circulating in 12 of the 23 countries sampled. We subdivided T. p.pallidum into 17 distinct sublineages to provide further phylodynamic resolution. Importantly, two Nichols sublineages have expanded clonally across 9 countries contemporaneously with SS14. Moreover, pairwise genome analyses revealed examples of isolates collected within the last 20 years from 14 different countries that had genetically identical core genomes, which might indicate frequent exchange through international transmission. It is striking that most samples collected before 1983 are phylogenetically distinct from more recently isolated sublineages. Using Bayesian temporal analysis, we detected a population bottleneck occurring during the late 1990s, followed by rapid population expansion in the 2000s that was driven by the dominant T. pallidum sublineages circulating today. This expansion may be linked to changing epidemiology, immune evasion or fitness under antimicrobial selection pressure, since many of the contemporary syphilis lineages we have characterized are resistant to macrolides.

Highlights

  • Syphilis, caused by the bacterium Treponema pallidum subsp. pallidum (TPA), is a prevalent sexually transmitted infection that can cause severe long-term sequelae when left untreated

  • SS14-lineage strains represent the vast majority of published genomes[4], and phylogenetic analysis showed that the origins of the SS14 lineage can be traced back to the 1950s3, followed by subsequent expansion of sublineages occurring during the 1990s4

  • We show that this genetic homogeneity is the result of a rapid and global expansion of TPA sublineages occurring within the last 30 years following a population bottleneck

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Summary

Discussion

Previous attempts to understand the origins of the original syphilis pandemic[3,6,21], as well as the dynamics of the current one[3,4], have been constrained by the technical difficulty in sequencing TPA genomes, as well as relatively small datasets with limited geographical diversity and sampling biases. Because of limited sampling before 2000, historic lineages that lack extant descendants (for example due to extinction) would not be modelled by our Bayesian Skyline, and this could limit our estimates of historic population diversity Despite these limitations, our data show that the T. pallidum infecting patients today is not the same T. pallidum infecting patients even 30 years ago – ancestral sublineages may have become extinct, being replaced by new sublineages that have swept to dominance across the globe with the dramatic upswing in syphilis cases in the USA, the UK and other Western European countries, which were heavily sampled in our study. It would be interesting to integrate epidemiological evidence of sexual networks in purpose-designed cohort studies to explore this further

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