Endosymbionts in Trichomonas Vaginalis Pathogenicity

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-80
SponsorMedical University of Vienna

About this trial

With this project, the investigators aim to expand knowledge on the molecular epidemiology of Trichomonas vaginalis, thereby also evaluating the endosymbionts (Mycoplasma hominis and Trichomonas vaginalis virus) and their impact on T. vaginalis virulence. A key aspect of the study is the direct comparison between identical T. vaginalis isolates harbouring endosymbionts and those from which the endosymbionts have been removed or inhibited. For this purpose T. vaginalis clinical isolates collected in Outpatients' Centre for Infectious Venereal and Dermatological Diseases, Vienna from patients specimens (vaginal swabs or urine) will be tested. Mycoplasma hominis isolates already collected from patients samples will also be analyzed and compared with M. hominis, which are T. vaginalis endosymbionts.

In addition, 700 samples from female sex workers in Austria, who undergo regular medical check-ups, will be examined. The prevalence of sexually transmitted diseases (STDs) will be evaluated using DNA extracted from vaginal swabs, with a particular focus on parasite Trichomonas vaginalis and bacterium M. hominis. Of particular interest is the study of the prevalence of these organisms in a cohort of women who are at increased risk of infection with these pathogens due to their occupation. Moreover, the study will provide detailed information on possible co-infections, as data from routine screenings are available.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Trichomonas vaginalis positive samples (vaginal swabs/urine) from Outpatients' Centre for Infectious Venereal and Dermatological Diseases

female sex-workers subjected to routine testing at Austrian Agency for Health and Food Safety

Disqualifiers

samples negative for Trichomonas vaginalis from Outpatients' Centre for Infectious Venereal and Dermatological Diseases

Trial population

Outpatients' Centre for Infectious Venereal and Dermatological Diseases: T. vaginalis positive samples (routine control) Austrian Agency for Health and Food Safety: sex-workers

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Characterisation of T. vaginalis isolates and evaluation of the proportion of sexually transmitted agents in vaginal swabs of Austrian sex workers

Clinical isolates of T. vaginalis or vaginal swabs taken from sex workers will be used in the study. Researchers will not have access to any patient information. The results of the experiments conducted on samples from sex workers will be evaluated by sequencing the products obtained by PCR (with primers detecting different sexually transmitted pathogens) and comparing them with the Gene Bank data. In addition, the researchers will assess the percentage of samples positive for T. vaginalis, M. hominis, Ureaplasma spp. among a random group of samples obtained from anonymous sex workers. Clinical isolates of T. vaginalis will be tested by PCR for the presence of endosymbionts (M. hominis, T. vaginalis virus). PCR products will also be sequenced and results will be compared with those present in the Gene Bank.

Time frame
2 years

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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