Detection of Leishmania RNA virus 2 in Leishmania species from Turkey.


Journal

Transactions of the Royal Society of Tropical Medicine and Hygiene
ISSN: 1878-3503
Titre abrégé: Trans R Soc Trop Med Hyg
Pays: England
ID NLM: 7506129

Informations de publication

Date de publication:
01 07 2019
Historique:
received: 21 01 2019
revised: 08 03 2019
accepted: 26 03 2019
pubmed: 30 4 2019
medline: 25 7 2020
entrez: 30 4 2019
Statut: ppublish

Résumé

Leishmania RNA virus (LRV) is a double-stranded RNA (dsRNA) virus infecting some Leishmania strains and triggering a destructive hyperinflammatory response in mammalian hosts in the New World. There is limited knowledge of the presence of this virus in Old World Leishmania species and its role in the outcome of the disease. We aimed to investigate the presence of LRV in Leishmania species/strains from Turkey. Twenty-nine previously identified Leishmania isolates (24 L. tropica, 2 L. infantum, 3 L. major) were examined for LRV positivity using dsRNA visualization in agarose gel after total nucleic acid extraction and RQ-deoxyribonuclease treatment and amplification of a 526 bp fragment of the LRV2-specific RNA-dependent RNA polymerase gene by reverse transcription polymerase chain reaction. Ten (7 L. tropica [24.13%], 3 L. major [10.34%]) of the 29 Leishmania strains gave positive results for LRV. Basic Local Alignment Search Tool analysis showed that all these viruses are LRV2-1. LRV2 was detected for the first time in L. tropica strains in the present study. The clinical manifestation and resistance status of the disease can be different depending on the host and parasite species/strains. The presence of LRV2 may be one of the factors contributing the course of disease. Further studies are needed to elucidate the specific role of LRV2, as it may be a potential target for effective treatment strategies.

Sections du résumé

BACKGROUND
Leishmania RNA virus (LRV) is a double-stranded RNA (dsRNA) virus infecting some Leishmania strains and triggering a destructive hyperinflammatory response in mammalian hosts in the New World. There is limited knowledge of the presence of this virus in Old World Leishmania species and its role in the outcome of the disease. We aimed to investigate the presence of LRV in Leishmania species/strains from Turkey.
METHODS
Twenty-nine previously identified Leishmania isolates (24 L. tropica, 2 L. infantum, 3 L. major) were examined for LRV positivity using dsRNA visualization in agarose gel after total nucleic acid extraction and RQ-deoxyribonuclease treatment and amplification of a 526 bp fragment of the LRV2-specific RNA-dependent RNA polymerase gene by reverse transcription polymerase chain reaction.
RESULTS
Ten (7 L. tropica [24.13%], 3 L. major [10.34%]) of the 29 Leishmania strains gave positive results for LRV. Basic Local Alignment Search Tool analysis showed that all these viruses are LRV2-1. LRV2 was detected for the first time in L. tropica strains in the present study.
CONCLUSIONS
The clinical manifestation and resistance status of the disease can be different depending on the host and parasite species/strains. The presence of LRV2 may be one of the factors contributing the course of disease. Further studies are needed to elucidate the specific role of LRV2, as it may be a potential target for effective treatment strategies.

Identifiants

pubmed: 31034027
pii: 5481342
doi: 10.1093/trstmh/trz023
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

410-417

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of Royal Society of Tropical Medicine and Hygiene. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Muhammed Nalçacı (M)

Ege University, Institute of Science, Division of Biology, Department of Zoology, Bornova, İzmir, Turkey.

Mehmet Karakuş (M)

University of Health Sciences, Health Sciences Institute, Biotechnology Department, Üsküdar, İstanbul, Turkey.

Bahtiyar Yılmaz (B)

Ege University, Institute of Science, Division of Biology, Department of Microbiology, Bornova, İzmir, Turkey.

Samiye Demir (S)

Ege University, Institute of Science, Division of Biology, Department of Zoology, Bornova, İzmir, Turkey.

Ahmet Özbilgin (A)

Manisa Celal Bayar University, Medical Faculty, Department of Parasitology, Manisa, Turkey.

Yusuf Özbel (Y)

Ege University, Medical Faculty, Department of Parasitology, Bornova, İzmir, Turkey.

Seray Töz (S)

Ege University, Medical Faculty, Department of Parasitology, Bornova, İzmir, Turkey.

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Classifications MeSH