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1.
Viruses ; 15(9)2023 08 23.
Article in English | MEDLINE | ID: mdl-37766193

ABSTRACT

A new filovirus named Menglà virus was found in bats in southern China in 2015. This species has been assigned to the new genus Dianlovirus and has only been detected in China. In this article, we report the detection of filoviruses in bats captured in Vietnam. We studied 248 bats of 15 species caught in the provinces of Lai Chau and Son La in northern Vietnam and in the province of Dong Thap in the southern part of the country. Filovirus RNA was found in four Rousettus leschenaultii and one Rousettus amplexicaudatus from Lai Chau Province. Phylogenetic analysis of the polymerase gene fragment showed that three positive samples belong to Dianlovirus, and two samples form a separate clade closer to Orthomarburgvirus. An enzyme-linked immunosorbent assay showed that 9% of Rousettus, 13% of Eonycteris, and 10% of Cynopterus bats had antibodies to the glycoprotein of marburgviruses.


Subject(s)
Chiroptera , Filoviridae , Marburgvirus , Animals , Vietnam/epidemiology , Phylogeny
2.
Pathogens ; 12(7)2023 Jul 06.
Article in English | MEDLINE | ID: mdl-37513761

ABSTRACT

The prevalence of the tick-borne spotted fever group rickettsioses pathogens in ticks collected in Barnaul, the administrative center of Altai Krai, Western Siberia, was studied. The causative agent of tick-borne lymphadenopathy (TIBOLA) Rickettsia raoultii was revealed to be present in 61.9% of the samples from Dermacentor ticks. Moreover, Rickettsia helvetica has been identified in 5.1% of Ixodes ticks.

3.
Viruses ; 14(9)2022 08 29.
Article in English | MEDLINE | ID: mdl-36146715

ABSTRACT

Members of the jingmenviruses group have been found in arthropods and mammals on all continents except Australia and Antarctica. Two viruses of this group were isolated from patients with fever after a tick bite. Using a nested RT-PCR assay targeting a jingmenvirus polymerase gene fragment, we screened ticks collected in seven regions of Russia and found that the abundant jingmenvirus-positive were of Ixodes ricinus species, with the prevalence ranging from 19.8% to 34.3%. In all cases, DNase/RNase treatment suggested that the detected molecule was DNA and subsequent next generation sequencing (NGS) proved that the viral polymerase gene was integrated in the I. ricinus genome. The copy number of the integrated polymerase gene was quantified by qPCR relative to the ITS2 gene and estimated as 1.32 copies per cell. At least three different genetic variants of the integrated polymerase gene were found in the territory of Russia. Phylogenetic analysis of the integrated jingmenvirus polymerase gene showed the highest similarity with the sequence of the correspondent gene obtained in Serbia from I. ricinus.


Subject(s)
Ixodes , Animals , Deoxyribonucleases , Genome, Insect , Humans , Mammals , Phylogeny , Polymerase Chain Reaction , Ribonucleases
4.
Infect Genet Evol ; 102: 105295, 2022 08.
Article in English | MEDLINE | ID: mdl-35526822

ABSTRACT

Haemorrhagic fever with renal syndrome (HFRS) is the most widespread natural-focal human disease in the Russian Federation. In this study, we report virological assessment of a fatal case of HFRS-PUUV (Puumala virus) in the Kursk Region. The infection caused severe multiorgan failure and the maximum viral load was detected in the tissue of the spleen. Viral sequences were obtained from the patient's autopsy material and lung tissues of bank voles captured in the region. These sequences formed a new clade in the PUUV phylogenetic tree, an outgroup to all known Russian (RUS) lineage sequences. On the other hand viruses collected in the Kursk Region grouped with the RUS lineage and are separated from all other PUUV linages. We propose to nominate this novel group as W-RUS as the identified viruses were collected near the western Russian boundary. The recombination signals between their ancestors and RUS lineage representatives from the Volga region were revealed. The strain Samara_94/CG/2005 suggestively emerged as the result of reassortment between the ancestors of W-RUS and DTK-Ufa-97.


Subject(s)
Hemorrhagic Fever with Renal Syndrome , Puumala virus , Viruses , Animals , Arvicolinae , Humans , Phylogeny , Puumala virus/genetics , Russia
5.
Ticks Tick Borne Dis ; 11(2): 101333, 2020 03.
Article in English | MEDLINE | ID: mdl-31787560

ABSTRACT

Kemerovo virus (KEMV) is a member of the Great Island virus genetic group, belonging to the tick-borne arboviruses of the genus Orbivirus within the family Reoviridae. Nine strains of KEMV, which were isolated from various locations in Russia, were sequenced by high-throughput sequencing to study their intraspecific diversity and the interspecific relationships of viruses within the Great Island genetic group. For the first time, multiple reassortment within KEMV was reliably demonstrated. Different types of independently emerged alternative reading frames in segment 9 and heterogeneity of the viral population in one of the KEMV strains were found. The hypothesis of the role of an alternative open reading frame (ORF) in segment 9 in KEMV cellular tropism was not confirmed in this study.


Subject(s)
Genetic Variation , Genome, Viral , Orbivirus/genetics , Phylogeny , Russia , Sequence Analysis, DNA
6.
Infect Genet Evol ; 34: 160-72, 2015 Aug.
Article in English | MEDLINE | ID: mdl-26190451

ABSTRACT

Influenza A(H1N1)pdm09 virus caused about 2000 laboratory confirmed lethal cases in Russia during 2009-2010 and 1302, 135 and 29 cases in the 2010-2011, 2012-2013 and 2013-2014 seasons respectively. The on average short duration (7.8±5 days) of lethal cases of Influenza A(H1N1)pdm09 infections in Russia suggests primary viral rather than secondary bacterial pneumonia. Hemorrhagic syndrome was recorded in 36.6% of patients. An examination of 221 lung samples from lethal influenza cases for the presence of bacterial DNA that could cause pneumonia did not reveal bacterial superinfections in 86% of cases. Molecular-genetic analyses of Influenza A(H1N1)pdm09 viruses from lethal and recovered cases were performed. Amino acids G and N at position 222 of the influenza virus hemagglutinin, which increase the affinity for the lower respiratory tract receptors, were detected more often in the lungs of patients who died than in respiratory swabs collected from recovered patients (p<0.0001 and p=0.007). Viruses harboring various mutations (222D/G/N/S) was significantly associated with lung samples compared with respiratory swabs from recovered patients (p<0.0001). Amino acid 222E, which increases the affinity for upper respiratory tract receptors, was found more frequently in recovered patients than in patients with lethal disease (27% versus 3%, p=0.005). Phylogenetic analysis identified an isolated cluster of viruses in the 2009-2010 season that harbored amino acid 222E, which could explain the high transmissibility of the virus at the beginning of the pandemic. Bayesian skyline plot implied a decline in the effective population size of Influenza A(H1N1)pdm09 viruses in Russia from 2010-2011 to 2011-2012, followed by an increase in 2012-2013; this trend was accompanied by the increased genetic diversity of the hemagglutinin antigenic sites. Mutations of viral RNA leading to oseltamivir resistance were found in 2.8% of tested patients during only 2010-2011 season. Deletions in the nucleoprotein cDNA were found in influenza viruses from two patients.


Subject(s)
Influenza, Human/virology , Nucleoproteins/genetics , Viral Proteins/genetics , Adolescent , Adult , Aged , Child , Child, Preschool , DNA Mutational Analysis , Female , Humans , Infant , Influenza A Virus, H1N1 Subtype/genetics , Influenza, Human/mortality , Lung/virology , Male , Middle Aged , Mutation, Missense , Phylogeny , Sequence Deletion , Young Adult
7.
Vector Borne Zoonotic Dis ; 14(11): 808-16, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25409272

ABSTRACT

During arbovirus surveillance in Ixodes ricinus ticks in South Ukraine, two strains of Tribec virus were isolated using an in vivo method and characterized using the complement fixation text (CFT), hemagglutination assay (HA), electron microscopy, and molecular methods. Both strains replicated well in the BHK-21, PEC, and Vero cell lines and demonstrated 95% nucleotide identity in their VP3 sequences compared with the reference VP3 sequence for Tribec virus. These two strains of Tribec virus were named Tr35 and Tr19. Also, segment reassortment involving Tr35, Tr19, TRBV, and LIPV strains was shown.


Subject(s)
Genome, Viral/genetics , Ixodes/virology , Orbivirus/isolation & purification , Reoviridae Infections/virology , Animals , Animals, Newborn , Base Sequence , Cell Line , Chlorocebus aethiops , Cricetinae , Dogs , Female , Geese , Geography , Humans , Male , Mice , Orbivirus/classification , Orbivirus/genetics , Orbivirus/ultrastructure , Phylogeny , RNA, Viral/chemistry , RNA, Viral/genetics , Reoviridae Infections/epidemiology , Sequence Alignment , Sequence Analysis, RNA , Sheep , Swine , Ukraine/epidemiology , Vero Cells , Viral Proteins/genetics
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