2021
DOI: 10.1007/s00705-021-05053-7
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Isolation and characterization of mammalian orthoreovirus type 3 from a fecal sample from a wild boar in Japan

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Cited by 6 publications
(7 citation statements)
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“…Recombination events in viruses promote adaptation to a novel host species range and increase their pathogenicity [47]. Our previous study revealed a possible intrasegment recombination event in the M2 gene of the Japanese wild boar MRV strain Wild boar/To14/JPN/2018 with a lion strain from the Japanese zoo and bat strains [20]. In the present study, RDP detected crossover points in the M1 gene of Toyama14 with Totto-MoI-6 and Ishi-Ueno-10 (Fig.…”
Section: Discussionmentioning
confidence: 99%
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“…Recombination events in viruses promote adaptation to a novel host species range and increase their pathogenicity [47]. Our previous study revealed a possible intrasegment recombination event in the M2 gene of the Japanese wild boar MRV strain Wild boar/To14/JPN/2018 with a lion strain from the Japanese zoo and bat strains [20]. In the present study, RDP detected crossover points in the M1 gene of Toyama14 with Totto-MoI-6 and Ishi-Ueno-10 (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…However, the S1 gene of Kana-Uchi-15 diverged from that of other strains (≥89.1% and ≥88.3% nucleotide and amino acid sequence identities, respectively; Table 1). Notably, the S1 genes of Kana-Ebina-9 and Kana-Ebina-11 had high sequence identities (98.4% and 98.7% nucleotide and amino acid sequence identities, respectively) with MRV-3 WB/To14 strain isolated from the Japanese wild boar in Toyama prefecture, the central region of the main island, in 2018 [20]. Phylogenetic analysis of the L1 gene showed that Totto-MoI6, Kana-Uchi-15, and Ishi-Ueno-10 branched with porcine MRVs from the USA, Taiwan, and Italy (Fig.…”
Section: Phylogenetic Analysis and Pairwise Nucleotide Comparisonmentioning
confidence: 99%
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“…The viral RNA genome was extracted from the supernatants with the use of a QlAamp Viral RNA Mini Kit (QIAGEN, Hilden, Germany), in accordance with the manufacturer's instructions. The RNA was amplified by using reverse transcription polymerase chain reaction (RT-PCR) for the detection of L1 gene of MRVs with virus-specific primers as shown in Table 1 [40]. Just before RT-PCR assay, 2 μL of extracted RNA was mixed with 1 μL of dimethyl sulfoxide (DMSO) (Wako Pure Chemical Industries, Co., Ltd., Osaka, Japan) and 4.5 μL of redistilled water (dW2), then heated at 98℃ for 5 min.…”
Section: Rt-pcr Testingmentioning
confidence: 99%
“…According to cell‐attachment capability, type‐specific antisera and hemagglutinin activities of σ1 protein encoded by S1 segment, MRVs are assigned to four serotypes: type 1 Lang (T1L), type 2 Jones (T2J), type 3 Dearing (T3D), and putative 4 Ndelle 3 . MRVs have a wide geographic distribution and can infect numerous mammals including humans, bats, and domestic animals such as swine and bovine as well as wild mammals 4–12 . MRV human infections normally cause respiratory 2,13 and enteric diseases 14–16 and neurological signs in some cases 17–19 .…”
Section: Introductionmentioning
confidence: 99%