Molecular Characterisation and Phylogeny of Tula Virus in Kazakhstan.


Journal

Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722

Informations de publication

Date de publication:
09 06 2022
Historique:
received: 14 04 2022
revised: 03 06 2022
accepted: 07 06 2022
entrez: 24 6 2022
pubmed: 25 6 2022
medline: 28 6 2022
Statut: epublish

Résumé

Orthohantaviruses are zoonotic pathogens that play a significant role in public health. These viruses can cause haemorrhagic fever with renal syndrome in Eurasia. In the Republic of Kazakhstan, the first human cases were registered in the year 2000 in the West Kazakhstan region. Small mammals can be reservoirs of orthohantaviruses. Previous studies showed orthohantavirus antigens in wild-living small mammals in four districts of West Kazakhstan. Clinical studies suggested that there might be further regions with human orthohantavirus infections in Kazakhstan, but genetic data of orthohantaviruses in natural foci are limited. The aim of this study was to investigate small mammals for the presence of orthohantaviruses by molecular biological methods and to provide a phylogenetic characterization of the circulating strains in Kazakhstan. Small mammals were trapped at 19 sites in West Kazakhstan, four in Almaty region and at seven sites around Almaty city during all seasons of 2018 and 2019. Lung tissues of small mammals were homogenized and RNA was extracted. Orthohantavirus RT-PCR assays were applied for detection of partial S and L segment sequences. Results were compared to published fragments. In total, 621 small mammals from 11 species were analysed. Among the collected small mammals, 2.4% tested positive for orthohantavirus RNA, one sample from West Kazakhstan and 14 samples from Almaty region. None of the rodents caught in Almaty city were infected. Sequencing parts of the small (S) and large (L) segments specified Tula virus (TULV) in these two regions. Our data show that geographical distribution of TULV is more extended as previously thought. The detected sequences were found to be split in two distinct genetic clusters of TULV in West Kazakhstan and Almaty region. TULV was detected in the common vole (

Identifiants

pubmed: 35746729
pii: v14061258
doi: 10.3390/v14061258
pmc: PMC9230364
pii:
doi:

Substances chimiques

RNA 63231-63-0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Nur Tukhanova (N)

Center for International Health, University Hospital, Ludwig Maximilians University, 80336 Munich, Germany.
Aikimbayev's National Scientific Center for Especially Dangerous Infections, Almaty 050054, Kazakhstan.

Anna Shin (A)

Center for International Health, University Hospital, Ludwig Maximilians University, 80336 Munich, Germany.
Aikimbayev's National Scientific Center for Especially Dangerous Infections, Almaty 050054, Kazakhstan.

Nurkeldi Turebekov (N)

Aikimbayev's National Scientific Center for Especially Dangerous Infections, Almaty 050054, Kazakhstan.

Talgat Nurmakhanov (T)

Aikimbayev's National Scientific Center for Especially Dangerous Infections, Almaty 050054, Kazakhstan.

Karlygash Abdiyeva (K)

Almaty Branch National Center for Biotechnology, Almaty 050054, Kazakhstan.

Alexandr Shevtsov (A)

National Center for Biotechnology, Nur Sultan 010000, Kazakhstan.

Toktasyn Yerubaev (T)

Aikimbayev's National Scientific Center for Especially Dangerous Infections, Almaty 050054, Kazakhstan.

Gulnara Tokmurziyeva (G)

Aikimbayev's National Scientific Center for Especially Dangerous Infections, Almaty 050054, Kazakhstan.

Almas Berdibekov (A)

Taldykorgan Antiplague Station, Branch Aikimbayev's National Scientific Center for Especially Dangerous Infections, Taldykorgan 040000, Kazakhstan.

Vitaliy Sutyagin (V)

Taldykorgan Antiplague Station, Branch Aikimbayev's National Scientific Center for Especially Dangerous Infections, Taldykorgan 040000, Kazakhstan.

Nurbek Maikanov (N)

Oral Antiplague Station, Branch Aikimbayev's National Scientific Center for Especially Dangerous Infections, Oral 09002, Kazakhstan.

Andrei Zakharov (A)

Oral Antiplague Station, Branch Aikimbayev's National Scientific Center for Especially Dangerous Infections, Oral 09002, Kazakhstan.

Ilmars Lezdinsh (I)

Taldykorgan Antiplague Station, Branch Aikimbayev's National Scientific Center for Especially Dangerous Infections, Taldykorgan 040000, Kazakhstan.

Lyazzat Yeraliyeva (L)

National Scientific Center of Phthisiopulmonology, Almaty 050010, Kazakhstan.

Guenter Froeschl (G)

Center for International Health, University Hospital, Ludwig Maximilians University, 80336 Munich, Germany.
Division of Infectious Diseases and Tropical Medicine, University Hospital, Ludwig Maximilians University, 80802 Munich, Germany.

Michael Hoelscher (M)

Division of Infectious Diseases and Tropical Medicine, University Hospital, Ludwig Maximilians University, 80802 Munich, Germany.

Stefan Frey (S)

Bundeswehr Research Institute for Protective Technologies and CBRN Protection, 29633 Munster, Germany.

Edith Wagner (E)

Section of Experimental Virology, Institute of Medical Microbiology, Jena University Hospital, 07745 Jena, Germany.
German Centre for Infection Research, Department Virology and Intracellular Agents, Munich Partner Site Bundeswehr Institute of Microbiology, 80937 Munich, Germany.

Lukas Peintner (L)

German Centre for Infection Research, Department Virology and Intracellular Agents, Munich Partner Site Bundeswehr Institute of Microbiology, 80937 Munich, Germany.

Sandra Essbauer (S)

German Centre for Infection Research, Department Virology and Intracellular Agents, Munich Partner Site Bundeswehr Institute of Microbiology, 80937 Munich, Germany.

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