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The protozoan Trichomonas vaginalis targets bacteria with laterally-acquired NlpC/P60 peptidoglycan hydrolases

Jully Pinheiro, Jacob Biboy, Waldemar Vollmer, View ORCID ProfileRobert P. Hirt, Jeremy R. Keown, View ORCID ProfileAnastasiia Artuyants, View ORCID ProfileDavid C. Goldstone, View ORCID ProfileAugusto Simoes-Barbosa
doi: https://doi.org/10.1101/320382
Jully Pinheiro
1School of Biological Sciences, University of Auckland, New Zealand
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Jacob Biboy
2Centre for Bacterial Cell Biology, Institute for Cell and Molecular Biosciences, Newcastle University, Newcastle upon Tyne, NE2 4AX, UK
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Waldemar Vollmer
2Centre for Bacterial Cell Biology, Institute for Cell and Molecular Biosciences, Newcastle University, Newcastle upon Tyne, NE2 4AX, UK
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Robert P. Hirt
3Institute for Cell and Molecular Biosciences, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK
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Jeremy R. Keown
1School of Biological Sciences, University of Auckland, New Zealand
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Anastasiia Artuyants
1School of Biological Sciences, University of Auckland, New Zealand
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David C. Goldstone
1School of Biological Sciences, University of Auckland, New Zealand
4Maurice Wilkins Centre for Molecular Biodiscovery, New Zealand
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Augusto Simoes-Barbosa
1School of Biological Sciences, University of Auckland, New Zealand
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  • ORCID record for Augusto Simoes-Barbosa
  • For correspondence: d.goldstone@auckland.ac.nz a.barbosa@auckland.ac.nz
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Abstract

Trichomonas vaginalis is a human eukaryotic pathogen and the causative agent of trichomoniasis, the most prevalent non-viral sexually transmitted infection worldwide. This extracellular protozoan parasite is intimately associated with the human vaginal mucosa and microbiota but key aspects of the complex interactions between the parasite and the vaginal bacteria remain elusive. We report that T. vaginalis has acquired, by lateral gene transfer from bacteria, genes encoding peptidoglycan hydrolases of the NlpC/P60 family. Two of the T. vaginalis enzymes were active against bacterial peptidoglycan, retaining the active site fold and specificity as DL-endopeptidases. The endogenous NlpC/P60 genes are transcriptionally up regulated in T. vaginalis when in the presence of bacteria. The over-expression of an exogenous copy produces a remarkable phenotype where the parasite is capable of competing out bacteria from mixed cultures, consistent with the biochemical activity of the enzyme in vitro. Our study highlights the relevance of the interactions of this eukaryotic pathogen with bacteria, a poorly understood aspect on the biology of this important human parasite.

Author summary Trichomonas vaginalis is a protozoan parasite that causes a very common sexually transmitted disease known as trichomoniasis. This extracellular parasite resides in the vagina where it is in close association with the mucosa and the local microbiota. Very little is known about the nature of the parasite-bacteria interactions. Here, we report that this parasite had acquired genes from bacteria which retained their original function producing active enzymes capable of degrading peptidoglycan, a polymer that is chemically unique to the cell envelope of bacteria. Our results indicate that these enzymes help the parasite compete out bacteria in mixed cultures. These observations suggest that these enzymes may be critical for the parasite to establish infection in the vagina, a body site that is densely colonised with bacteria. Our study further highlights the importance of understanding the interactions between pathogens and microbiota, as the outcomes of these interactions are increasingly understood to have important implications on health and disease.

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Posted May 11, 2018.
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The protozoan Trichomonas vaginalis targets bacteria with laterally-acquired NlpC/P60 peptidoglycan hydrolases
Jully Pinheiro, Jacob Biboy, Waldemar Vollmer, Robert P. Hirt, Jeremy R. Keown, Anastasiia Artuyants, David C. Goldstone, Augusto Simoes-Barbosa
bioRxiv 320382; doi: https://doi.org/10.1101/320382
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The protozoan Trichomonas vaginalis targets bacteria with laterally-acquired NlpC/P60 peptidoglycan hydrolases
Jully Pinheiro, Jacob Biboy, Waldemar Vollmer, Robert P. Hirt, Jeremy R. Keown, Anastasiia Artuyants, David C. Goldstone, Augusto Simoes-Barbosa
bioRxiv 320382; doi: https://doi.org/10.1101/320382

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