Abstract

Syphilis is a global, re-emerging sexually transmitted infection and congenital syphilis remains a major cause of adverse pregnancy outcomes due to bacterial infection in developing nations with a high rate of fetus loss. The molecular mechanisms involved in pathogenesis of the causative agent, Treponema pallidum subsp. pallidum remain poorly understood due to the difficulties of working with this pathogen, including the inability to grow it in pure culture. To reduce the spread of syphilis, we must first increase our knowledge of the virulence factors of T. pallidum and their contribution to syphilis manifestations. Tp0954 was predicted to be a surface lipoprotein of T. pallidum. Therefore, we experimentally demonstrated that Tp0954 is indeed a surface protein and further investigated its role in mediating bacterial attachment to various mammalian host cells. We found that expression of Tp0954 in a poorly adherent, but physiologically related derivative strain of the Lyme disease causing spirochete Borrelia burgdorferi B314 strain promotes its binding to epithelial as well as non-epithelial cells including glioma and placental cell lines. We also found that Tp0954 expression facilitates binding of this strain to purified dermatan sulfate and heparin, and also that bacterial binding to mammalian cell lines is mediated by the presence of heparan sulfate and dermatan sulfate in the extracellular matrix of the specific cell lines. These results suggest that Tp0954 may be involved not only in initiating T. pallidum infection by colonizing skin epithelium, but it may also contribute to disseminated infection and colonization of distal tissues. Significantly, we found that Tp0954 promotes binding to the human placental choriocarcinoma BeWo cell line, which is of trophoblastic endocrine cell type, as well as human placental tissue sections, suggesting its role in placental colonization and possible contribution to transplacental transmission of T. pallidum. Altogether, these novel findings offer an important step toward unraveling syphilis pathogenesis, including placental colonization and T. pallidum vertical transmission from mother to fetus during pregnancy.

Highlights

  • Syphilis is a chronic, systemic disease that is caused by the spirochete Treponema pallidum subspecies pallidum (T. pallidum)

  • We demonstrate here that Tp0954 is indeed a surface-exposed adhesin that mediates binding of spirochetes to the host epithelial, neuronal, and placental cells

  • Such results will suggest that prevention of transplacental mother to child transmission could be facilitated by Tp0954-based vaccine when used alone, or with other protective antigenic candidates to prevent vertical transmission of T. pallidum, inhibiting congenital syphilis in countries with limited resources to reach different regions for prenatal care

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Summary

Introduction

Systemic disease that is caused by the spirochete Treponema pallidum subspecies pallidum (T. pallidum) This pathogen is transmitted by sexual contact and vertically during pregnancy from mother to fetus. A few other pathogens, such as Plasmodium falciparum and Trypanosoma cruzi can be transmitted through the vertical, transplacental route from mother to fetus (Carlier et al, 2012) Among these infectious diseases, the molecular basis of mother to child transmission that results in congenital syphilis remains almost completely unexplored. It is essential to reveal the mechanisms used by T. pallidum to colonize and cross placental syncytiotrophoblast cell barrier to infect the fetus Such an understanding will lead to the development of an effective vaccine to prevent congenital transmission of this pathogen similar to that undergoing testing for malaria (Fried and Duffy, 2015)

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