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Two-step evolution of HIV-1 budding system leading to pandemic in the human population.
Konno, Yoriyuki; Uriu, Keiya; Chikata, Takayuki; Takada, Toru; Kurita, Jun-Ichi; Ueda, Mahoko Takahashi; Islam, Saiful; Yang Tan, Benjy Jek; Ito, Jumpei; Aso, Hirofumi; Kumata, Ryuichi; Williamson, Carolyn; Iwami, Shingo; Takiguchi, Masafumi; Nishimura, Yoshifumi; Morita, Eiji; Satou, Yorifumi; Nakagawa, So; Koyanagi, Yoshio; Sato, Kei.
Affiliation
  • Konno Y; Division of Systems Virology, Department of Microbiology and Immunology, The Institute of Medical Science, The University of Tokyo, Tokyo 1088639, Japan.
  • Uriu K; Division of Systems Virology, Department of Microbiology and Immunology, The Institute of Medical Science, The University of Tokyo, Tokyo 1088639, Japan; Graduate School of Medicine, the University of Tokyo, Tokyo 1130033, Japan; Department of Biochemistry and Molecular Biology, Faculty of Agricultu
  • Chikata T; Joint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto 8608556, Japan.
  • Takada T; Department of Biology, Faculty of Sciences, Kyushu University, Fukuoka 8128581, Japan.
  • Kurita JI; Graduate School of Medical Life Science, Yokohama City University, Kanagawa 2300045, Japan.
  • Ueda MT; Department of Molecular Life Science, Tokai University School of Medicine, Kanagawa 2591193, Japan.
  • Islam S; Joint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto 8608556, Japan.
  • Yang Tan BJ; Joint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto 8608556, Japan.
  • Ito J; Division of Systems Virology, Department of Microbiology and Immunology, The Institute of Medical Science, The University of Tokyo, Tokyo 1088639, Japan.
  • Aso H; Division of Systems Virology, Department of Microbiology and Immunology, The Institute of Medical Science, The University of Tokyo, Tokyo 1088639, Japan; Institute for Frontier Life and Medical Sciences, Kyoto University, Kyoto 6068507, Japan; Graduate School of Pharmaceutical Sciences, Kyoto Univer
  • Kumata R; Division of Systems Virology, Department of Microbiology and Immunology, The Institute of Medical Science, The University of Tokyo, Tokyo 1088639, Japan.
  • Williamson C; Institute of Infectious Diseases and Molecular Medicine, University of Cape Town, Cape Town 7925, South Africa.
  • Iwami S; Department of Biology, Faculty of Sciences, Kyushu University, Fukuoka 8128581, Japan; MIRAI, Japan Science and Technology Agency, Kawaguchi 3320012, Japan.
  • Takiguchi M; Joint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto 8608556, Japan.
  • Nishimura Y; Graduate School of Medical Life Science, Yokohama City University, Kanagawa 2300045, Japan.
  • Morita E; Department of Biochemistry and Molecular Biology, Faculty of Agriculture and Life Science, Hirosaki University, Aomori 0368561, Japan.
  • Satou Y; Joint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto 8608556, Japan.
  • Nakagawa S; Department of Molecular Life Science, Tokai University School of Medicine, Kanagawa 2591193, Japan.
  • Koyanagi Y; Institute for Frontier Life and Medical Sciences, Kyoto University, Kyoto 6068507, Japan; Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto 6068501, Japan.
  • Sato K; Division of Systems Virology, Department of Microbiology and Immunology, The Institute of Medical Science, The University of Tokyo, Tokyo 1088639, Japan; Graduate School of Medicine, the University of Tokyo, Tokyo 1130033, Japan; International Research Center for Infectious Diseases, The Institute o
Cell Rep ; 43(2): 113697, 2024 Feb 27.
Article in En | MEDLINE | ID: mdl-38294901
ABSTRACT
The pandemic HIV-1, HIV-1 group M, emerged from a single spillover event of its ancestral lentivirus from a chimpanzee. During human-to-human spread worldwide, HIV-1 diversified into multiple subtypes. Here, our interdisciplinary investigation mainly sheds light on the evolutionary scenario of the viral budding system of HIV-1 subtype C (HIV-1C), a most successfully spread subtype. Of the two amino acid motifs for HIV-1 budding, the P(T/S)AP and YPxL motifs, HIV-1C loses the YPxL motif. Our data imply that HIV-1C might lose this motif to evade immune pressure. Additionally, the P(T/S)AP motif is duplicated dependently of the level of HIV-1 spread in the human population, and >20% of HIV-1C harbored the duplicated P(T/S)AP motif. We further show that the duplication of the P(T/S)AP motif is caused by the expansion of the CTG triplet repeat. Altogether, our results suggest that HIV-1 has experienced a two-step evolution of the viral budding process during human-to-human spread worldwide.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: HIV-1 / HIV Seropositivity Limits: Animals / Humans Language: En Journal: Cell Rep Year: 2024 Document type: Article Affiliation country: Japón

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: HIV-1 / HIV Seropositivity Limits: Animals / Humans Language: En Journal: Cell Rep Year: 2024 Document type: Article Affiliation country: Japón