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Isolation and Characterization of Distinct Rotavirus A in Bat and Rodent Hosts.
Kishimoto, Mai; Kajihara, Masahiro; Tabata, Koshiro; Itakura, Yukari; Toba, Shinsuke; Ozono, Seiya; Sato, Yuko; Suzuki, Tadaki; Ito, Naoto; Changula, Katendi; Qiu, Yongjin; Mori-Kajihara, Akina; Eto, Yoshiki; Harima, Hayato; Mwizabi, Daniel; Hang'ombe, Bernard M; Hall, William W; Takada, Ayato; Orba, Yasuko; Sawa, Hirofumi; Sasaki, Michihito.
Afiliación
  • Kishimoto M; Division of Molecular Pathobiology, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
  • Kajihara M; Division of Global Epidemiology, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
  • Tabata K; Division of Molecular Pathobiology, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
  • Itakura Y; Division of Molecular Pathobiology, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
  • Toba S; Division of Molecular Pathobiology, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
  • Ozono S; Drug Discovery and Disease Research Laboratory, Shionogi & Co., Ltd., Osaka, Japan.
  • Sato Y; Department of Pathology, National Institute of Infectious Diseases, Tokyo, Japan.
  • Suzuki T; Department of Pathology, National Institute of Infectious Diseases, Tokyo, Japan.
  • Ito N; Department of Pathology, National Institute of Infectious Diseases, Tokyo, Japan.
  • Changula K; Joint Graduate School of Veterinary Sciences, Gifu University, Gifu, Japan.
  • Qiu Y; Department of Para-clinical Studies, School of Veterinary and Medicine, University of Zambia, Lusaka, Zambia.
  • Mori-Kajihara A; Division of International Research Promotion, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
  • Eto Y; Division of Global Epidemiology, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
  • Harima H; Division of Global Epidemiology, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
  • Mwizabi D; Division of International Research Promotion, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
  • Hang'ombe BM; Laboratory of Veterinary Public Health, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Tokyo, Japan.
  • Hall WW; Department of National Parks and Wildlife, the Ministry of Tourism and Arts, Lusaka, Zambia.
  • Takada A; Department of Para-clinical Studies, School of Veterinary and Medicine, University of Zambia, Lusaka, Zambia.
  • Orba Y; Africa Center of Excellence for Infectious Diseases of Humans and Animals, University of Zambia, Lusaka, Zambia.
  • Sawa H; National Virus Reference Laboratory, School of Medicine, University College Dublin, Dublin, Ireland.
  • Sasaki M; International Collaboration Unit, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
J Virol ; 97(1): e0145522, 2023 01 31.
Article en En | MEDLINE | ID: mdl-36633410
ABSTRACT
Rotavirus A (RVA) causes diarrheal disease in humans and various animals. Recent studies have identified bat and rodent RVAs with evidence of zoonotic transmission and genome reassortment. However, the virological properties of bat and rodent RVAs with currently identified genotypes still need to be better clarified. Here, we performed virus isolation-based screening for RVA in animal specimens and isolated RVAs (representative strains 16-06 and MpR12) from Egyptian fruit bat and Natal multimammate mouse collected in Zambia. Whole-genome sequencing and phylogenetic analysis revealed that the genotypes of bat RVA 16-06 were identical to that of RVA BATp39 strain from the Kenyan fruit bat, which has not yet been characterized. Moreover, all segments of rodent RVA MpR12 were highly divergent and assigned to novel genotypes, but RVA MpR12 was phylogenetically closer to bat RVAs than to other rodent RVAs, indicating a unique evolutionary history. We further investigated the virological properties of the isolated RVAs. In brief, we found that 16-06 entered cells by binding to sialic acids on the cell surface, while MpR12 entered in a sialic acid-independent manner. Experimental inoculation of suckling mice with 16-06 and MpR12 revealed that these RVAs are causative agents of diarrhea. Moreover, 16-06 and MpR12 demonstrated an ability to infect and replicate in a 3D-reconstructed primary human intestinal epithelium with comparable efficiency to the human RVA. Taken together, our results detail the unique genetic and virological features of bat and rodent RVAs and demonstrate the need for further investigation of their zoonotic potential. IMPORTANCE Recent advances in nucleotide sequence detection methods have enabled the detection of RVA genomes from various animals. These studies have discovered multiple divergent RVAs and have resulted in proposals for the genetic classification of novel genotypes. However, most of these RVAs have been identified via dsRNA viral genomes and not from infectious viruses, and their virological properties, such as cell/host tropisms, transmissibility, and pathogenicity, are unclear and remain to be clarified. Here, we successfully isolated RVAs with novel genome constellations from three bats and one rodent in Zambia. In addition to whole-genome sequencing, the isolated RVAs were characterized by glycan-binding affinity, pathogenicity in mice, and infectivity to the human gut using a 3D culture of primary intestinal epithelium. Our study reveals the first virological properties of bat and rodent RVAs with high genetic diversity and unique evolutional history and provides basic knowledge to begin estimating the potential of zoonotic transmission.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones por Rotavirus / Quirópteros / Rotavirus / Murinae Tipo de estudio: Prognostic_studies Límite: Animals País/Región como asunto: Africa Idioma: En Revista: J Virol Año: 2023 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones por Rotavirus / Quirópteros / Rotavirus / Murinae Tipo de estudio: Prognostic_studies Límite: Animals País/Región como asunto: Africa Idioma: En Revista: J Virol Año: 2023 Tipo del documento: Article País de afiliación: Japón