Pandemic HIV-1 Vpu overcomes intrinsic herd immunity mediated by tetherin

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作者
Shingo Iwami
Kei Sato
Satoru Morita
Hisashi Inaba
Tomoko Kobayashi
Junko S. Takeuchi
Yuichi Kimura
Naoko Misawa
Fengrong Ren
Yoh Iwasa
Kazuyuki Aihara
Yoshio Koyanagi
机构
[1] Faculty of Sciences,Mathematical Biology Laboratory, Department of Biology
[2] Kyushu University,Department of Mathematical and Systems Engineering
[3] Fukuoka,Laboratory for Animal Health, Department of Animal Science
[4] PRESTO,Department of Bioinformatics
[5] JST,undefined
[6] CREST,undefined
[7] JST,undefined
[8] Laboratory of Viral Pathogenesis,undefined
[9] Institute for Virus Research,undefined
[10] Kyoto University,undefined
[11] Kyoto,undefined
[12] Shizuoka University,undefined
[13] Hamamatsu,undefined
[14] Graduate School of Mathematical Sciences,undefined
[15] The University of Tokyo,undefined
[16] Meguro-ku,undefined
[17] Faculty of Agriculture,undefined
[18] Tokyo University of Agriculture,undefined
[19] Medical Research Institute,undefined
[20] Tokyo Medical and Dental University,undefined
[21] Institute of Industrial Science,undefined
[22] The University of Tokyo,undefined
[23] Meguro-ku,undefined
[24] Graduate School of Information Science and Technology,undefined
[25] The University of Tokyo,undefined
[26] Meguro-ku,undefined
来源
Scientific Reports | / 5卷
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摘要
Among the four groups of HIV-1 (M, N, O and P), HIV-1M alone is pandemic and has rapidly expanded across the world. However, why HIV-1M has caused a devastating pandemic while the other groups remain contained is unclear. Interestingly, only HIV-1M Vpu, a viral protein, can robustly counteract human tetherin, which tethers budding virions. Therefore, we hypothesize that this property of HIV-1M Vpu facilitates human-to-human viral transmission. Adopting a multilayered experimental-mathematical approach, we demonstrate that HIV-1M Vpu confers a 2.38-fold increase in the prevalence of HIV-1 transmission. When Vpu activity is lost, protected human populations emerge (i.e., intrinsic herd immunity develops) through the anti-viral effect of tetherin. We also reveal that all Vpus of transmitted/founder HIV-1M viruses maintain anti-tetherin activity. These findings indicate that tetherin plays the role of a host restriction factor, providing ‘intrinsic herd immunity’, whereas Vpu has evolved in HIV-1M as a tetherin antagonist.
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