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Detection and molecular characterization of double-stranded RNA viruses in Philippine Trichomonas vaginalis isolates

Authors :
Windell L. Rivera
Christine Aubrey C. Justo
Mary Ann Cielo V. Relucio-San Diego
Lorenz M. Loyola
Source :
Journal of Microbiology, Immunology and Infection, Vol 50, Iss 5, Pp 669-676 (2017)
Publication Year :
2017
Publisher :
Elsevier, 2017.

Abstract

Background/Purpose: The flagellated protozoon Trichomonas vaginalis that parasitizes the urogenital tract of humans was reported to harbor double-stranded RNA (dsRNA) viruses. These viruses, identified as Trichomonas vaginalis virus (TVV), belong to the genus Trichomonasvirus of the family Totiviridae. Four species, formally recognized by the International Committee on Taxonomy of Viruses (ICTV), have been reported and distinguished by pairwise comparisons of the sequences of genes coding for major capsid protein (CP) and RNA-dependent RNA polymerase (RdRp). Methods: Reverse transcription polymerase chain reaction (RT-PCR) was used to amplify the complimentary DNA of target virus genes coding for CP and RdRp. Sequence analyses confirmed the identity of the TVV isolates from T. vaginalis cultures. Results: A total of 35 dsRNA viruses were identified from 18 (19%) T. vaginalis isolates. Multiple TVV species were observed in six of the 18 T. vaginalis cultures. Phylogenetic analyses show monophyly in TVV1 and TVV2 whereas TVV3 and TVV4 appear paraphyletic. The phylogeny of Philippine Trichomonasvirus reflects the global distribution of its host. Conclusion: This is the first study in the Philippines and one of the two reports worldwide to detect the four TVVs and their concurrent infection in a single T. vaginalis isolate.

Details

Language :
English
ISSN :
16841182
Volume :
50
Issue :
5
Database :
Directory of Open Access Journals
Journal :
Journal of Microbiology, Immunology and Infection
Publication Type :
Academic Journal
Accession number :
edsdoj.5369b25884924ac4bc239ac12574e63c
Document Type :
article
Full Text :
https://doi.org/10.1016/j.jmii.2015.07.016