Experimental Adaptive Evolution of Simian Immunodeficiency Virus SIVcpz to Pandemic Human Immunodeficiency Virus Type 1 by Using a Humanized Mouse Model
Human immunodeficiency virus type 1 (HIV-1), the causative agent of AIDS, originated from simian immunodeficiency virus from chimpanzees (SIVcpz), the precursor of the human virus, approximately 100 years ago. This indicates that HIV-1 has emerged through the cross-species transmission of SIVcpz fro...
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creator | Sato, Kei Misawa, Naoko Takeuchi, Junko S Kobayashi, Tomoko Izumi, Taisuke Aso, Hirofumi Nagaoka, Shumpei Yamamoto, Keisuke Kimura, Izumi Konno, Yoriyuki Nakano, Yusuke Koyanagi, Yoshio |
description | Human immunodeficiency virus type 1 (HIV-1), the causative agent of AIDS, originated from simian immunodeficiency virus from chimpanzees (SIVcpz), the precursor of the human virus, approximately 100 years ago. This indicates that HIV-1 has emerged through the cross-species transmission of SIVcpz from chimpanzees to humans. However, it remains unclear how SIVcpz has evolved into pandemic HIV-1 in humans. To address this question, we inoculated three SIVcpz strains (MB897, EK505, and MT145), four pandemic HIV-1 strains (NL4-3, NLCSFV3, JRCSF, and AD8), and two nonpandemic HIV-1 strains (YBF30 and DJO0131). Humanized mice infected with SIVcpz strain MB897, a virus phylogenetically similar to pandemic HIV-1, exhibited a peak viral load comparable to that of mice infected with pandemic HIV-1, while peak viral loads of mice infected with SIVcpz strain EK505 or MT145 as well as nonpandemic HIV-1 strains were significantly lower. These results suggest that SIVcpz strain MB897 is preadapted to humans, unlike the other SIVcpz strains. Moreover, viral RNA sequencing of MB897-infected humanized mice identified a nonsynonymous mutation in
, a G413R substitution in gp120. The infectivity of the gp120 G413R mutant of MB897 was significantly higher than that of parental MB897. Furthermore, we demonstrated that the gp120 G413R mutant of MB897 augments the capacity for viral replication in both
cell cultures and humanized mice. Taken together, this is the first experimental investigation to use an animal model to demonstrate a gain-of-function evolution of SIVcpz into pandemic HIV-1.
From the mid-20th century, humans have been exposed to the menace of infectious viral diseases, such as severe acute respiratory syndrome coronavirus, Ebola virus, and Zika virus. These outbreaks of emerging/reemerging viruses can be triggered by cross-species viral transmission from wild animals to humans, or zoonoses. HIV-1, the causative agent of AIDS, emerged by the cross-species transmission of SIVcpz, the HIV-1 precursor in chimpanzees, around 100 years ago. However, the process by which SIVcpz evolved to become HIV-1 in humans remains unclear. Here, by using a hematopoietic stem cell-transplanted humanized-mouse model, we experimentally recapitulate the evolutionary process of SIVcpz to become HIV-1. We provide evidence suggesting that a strain of SIVcpz, MB897, preadapted to infect humans over other SIVcpz strains. We further demonstrate a gain-of-function evolution of SIVcpz in infecte |
doi_str_mv | 10.1128/jvi.01905-17 |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5790958</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1974013131</sourcerecordid><originalsourceid>FETCH-LOGICAL-c450t-77410c683567126ef2df11e0fe89f61c965920d9a48d53855523b4ec8cd533663</originalsourceid><addsrcrecordid>eNp1kUFP3DAQha2qFSzb3nqufOyhoR7HTuJLJYS2sIiKSsCqN8trT6hRYqdxsuryS_pzG1hA7QFZGsuaT2_G7xHyHtghAK8-3278IQPFZAblKzIDpqpMShCvyYwxzjOZVz_2yUFKt4yBEIXYI_tcceAqL2fkz-J3h71vMQymoUfOdIPfIF1sYjMOPgYaa3rpW28CXbbtGKLD2luPwW7pyvdjopfLle3u6BDpdxMctt7S07F9mb_adkiBrrf0OvlwQ80O93fo6Lc4Jpyqw-YteVObJuG7x3tOrr8uro5Ps_OLk-Xx0XlmhWRDVpYCmC2qXBYl8AJr7moAZDVWqi7AqkIqzpwyonKTE1JKnq8F2spOz7wo8jn5stPtxnWLzk5G9KbR3eSJ6bc6Gq__7wT_U9_EjZalYkpWk8DHR4E-_hoxDbr1yWLTmIDTdzSoUjDI78-cfNqhto8p9Vg_jwGm78PUZ6ulfghTQznhH_5d7Rl-Si__C5XbnQc</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1974013131</pqid></control><display><type>article</type><title>Experimental Adaptive Evolution of Simian Immunodeficiency Virus SIVcpz to Pandemic Human Immunodeficiency Virus Type 1 by Using a Humanized Mouse Model</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Sato, Kei ; Misawa, Naoko ; Takeuchi, Junko S ; Kobayashi, Tomoko ; Izumi, Taisuke ; Aso, Hirofumi ; Nagaoka, Shumpei ; Yamamoto, Keisuke ; Kimura, Izumi ; Konno, Yoriyuki ; Nakano, Yusuke ; Koyanagi, Yoshio</creator><contributor>Kirchhoff, Frank</contributor><creatorcontrib>Sato, Kei ; Misawa, Naoko ; Takeuchi, Junko S ; Kobayashi, Tomoko ; Izumi, Taisuke ; Aso, Hirofumi ; Nagaoka, Shumpei ; Yamamoto, Keisuke ; Kimura, Izumi ; Konno, Yoriyuki ; Nakano, Yusuke ; Koyanagi, Yoshio ; Kirchhoff, Frank</creatorcontrib><description>Human immunodeficiency virus type 1 (HIV-1), the causative agent of AIDS, originated from simian immunodeficiency virus from chimpanzees (SIVcpz), the precursor of the human virus, approximately 100 years ago. This indicates that HIV-1 has emerged through the cross-species transmission of SIVcpz from chimpanzees to humans. However, it remains unclear how SIVcpz has evolved into pandemic HIV-1 in humans. To address this question, we inoculated three SIVcpz strains (MB897, EK505, and MT145), four pandemic HIV-1 strains (NL4-3, NLCSFV3, JRCSF, and AD8), and two nonpandemic HIV-1 strains (YBF30 and DJO0131). Humanized mice infected with SIVcpz strain MB897, a virus phylogenetically similar to pandemic HIV-1, exhibited a peak viral load comparable to that of mice infected with pandemic HIV-1, while peak viral loads of mice infected with SIVcpz strain EK505 or MT145 as well as nonpandemic HIV-1 strains were significantly lower. These results suggest that SIVcpz strain MB897 is preadapted to humans, unlike the other SIVcpz strains. Moreover, viral RNA sequencing of MB897-infected humanized mice identified a nonsynonymous mutation in
, a G413R substitution in gp120. The infectivity of the gp120 G413R mutant of MB897 was significantly higher than that of parental MB897. Furthermore, we demonstrated that the gp120 G413R mutant of MB897 augments the capacity for viral replication in both
cell cultures and humanized mice. Taken together, this is the first experimental investigation to use an animal model to demonstrate a gain-of-function evolution of SIVcpz into pandemic HIV-1.
From the mid-20th century, humans have been exposed to the menace of infectious viral diseases, such as severe acute respiratory syndrome coronavirus, Ebola virus, and Zika virus. These outbreaks of emerging/reemerging viruses can be triggered by cross-species viral transmission from wild animals to humans, or zoonoses. HIV-1, the causative agent of AIDS, emerged by the cross-species transmission of SIVcpz, the HIV-1 precursor in chimpanzees, around 100 years ago. However, the process by which SIVcpz evolved to become HIV-1 in humans remains unclear. Here, by using a hematopoietic stem cell-transplanted humanized-mouse model, we experimentally recapitulate the evolutionary process of SIVcpz to become HIV-1. We provide evidence suggesting that a strain of SIVcpz, MB897, preadapted to infect humans over other SIVcpz strains. We further demonstrate a gain-of-function evolution of SIVcpz in infected humanized mice. Our study reveals that pandemic HIV-1 has emerged through at least two steps: preadaptation and subsequent gain-of-function mutations.</description><identifier>ISSN: 0022-538X</identifier><identifier>EISSN: 1098-5514</identifier><identifier>DOI: 10.1128/jvi.01905-17</identifier><identifier>PMID: 29212937</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Animals ; Animals, Wild - virology ; Disease Models, Animal ; Evolution, Molecular ; Female ; HEK293 Cells ; HIV-1 - genetics ; Humans ; Male ; Mice ; Mice, Knockout ; Pan troglodytes - virology ; Phylogeny ; RNA, Viral - genetics ; Simian Acquired Immunodeficiency Syndrome - virology ; Simian Immunodeficiency Virus - genetics ; Viral Load ; Virus Replication ; Virus-Cell Interactions ; Zoonoses - transmission</subject><ispartof>Journal of virology, 2018-02, Vol.92 (4)</ispartof><rights>Copyright © 2018 American Society for Microbiology.</rights><rights>Copyright © 2018 American Society for Microbiology. 2018 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c450t-77410c683567126ef2df11e0fe89f61c965920d9a48d53855523b4ec8cd533663</citedby><cites>FETCH-LOGICAL-c450t-77410c683567126ef2df11e0fe89f61c965920d9a48d53855523b4ec8cd533663</cites><orcidid>0000-0003-4431-1380</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790958/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790958/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,315,728,781,785,886,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29212937$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Kirchhoff, Frank</contributor><creatorcontrib>Sato, Kei</creatorcontrib><creatorcontrib>Misawa, Naoko</creatorcontrib><creatorcontrib>Takeuchi, Junko S</creatorcontrib><creatorcontrib>Kobayashi, Tomoko</creatorcontrib><creatorcontrib>Izumi, Taisuke</creatorcontrib><creatorcontrib>Aso, Hirofumi</creatorcontrib><creatorcontrib>Nagaoka, Shumpei</creatorcontrib><creatorcontrib>Yamamoto, Keisuke</creatorcontrib><creatorcontrib>Kimura, Izumi</creatorcontrib><creatorcontrib>Konno, Yoriyuki</creatorcontrib><creatorcontrib>Nakano, Yusuke</creatorcontrib><creatorcontrib>Koyanagi, Yoshio</creatorcontrib><title>Experimental Adaptive Evolution of Simian Immunodeficiency Virus SIVcpz to Pandemic Human Immunodeficiency Virus Type 1 by Using a Humanized Mouse Model</title><title>Journal of virology</title><addtitle>J Virol</addtitle><description>Human immunodeficiency virus type 1 (HIV-1), the causative agent of AIDS, originated from simian immunodeficiency virus from chimpanzees (SIVcpz), the precursor of the human virus, approximately 100 years ago. This indicates that HIV-1 has emerged through the cross-species transmission of SIVcpz from chimpanzees to humans. However, it remains unclear how SIVcpz has evolved into pandemic HIV-1 in humans. To address this question, we inoculated three SIVcpz strains (MB897, EK505, and MT145), four pandemic HIV-1 strains (NL4-3, NLCSFV3, JRCSF, and AD8), and two nonpandemic HIV-1 strains (YBF30 and DJO0131). Humanized mice infected with SIVcpz strain MB897, a virus phylogenetically similar to pandemic HIV-1, exhibited a peak viral load comparable to that of mice infected with pandemic HIV-1, while peak viral loads of mice infected with SIVcpz strain EK505 or MT145 as well as nonpandemic HIV-1 strains were significantly lower. These results suggest that SIVcpz strain MB897 is preadapted to humans, unlike the other SIVcpz strains. Moreover, viral RNA sequencing of MB897-infected humanized mice identified a nonsynonymous mutation in
, a G413R substitution in gp120. The infectivity of the gp120 G413R mutant of MB897 was significantly higher than that of parental MB897. Furthermore, we demonstrated that the gp120 G413R mutant of MB897 augments the capacity for viral replication in both
cell cultures and humanized mice. Taken together, this is the first experimental investigation to use an animal model to demonstrate a gain-of-function evolution of SIVcpz into pandemic HIV-1.
From the mid-20th century, humans have been exposed to the menace of infectious viral diseases, such as severe acute respiratory syndrome coronavirus, Ebola virus, and Zika virus. These outbreaks of emerging/reemerging viruses can be triggered by cross-species viral transmission from wild animals to humans, or zoonoses. HIV-1, the causative agent of AIDS, emerged by the cross-species transmission of SIVcpz, the HIV-1 precursor in chimpanzees, around 100 years ago. However, the process by which SIVcpz evolved to become HIV-1 in humans remains unclear. Here, by using a hematopoietic stem cell-transplanted humanized-mouse model, we experimentally recapitulate the evolutionary process of SIVcpz to become HIV-1. We provide evidence suggesting that a strain of SIVcpz, MB897, preadapted to infect humans over other SIVcpz strains. We further demonstrate a gain-of-function evolution of SIVcpz in infected humanized mice. Our study reveals that pandemic HIV-1 has emerged through at least two steps: preadaptation and subsequent gain-of-function mutations.</description><subject>Animals</subject><subject>Animals, Wild - virology</subject><subject>Disease Models, Animal</subject><subject>Evolution, Molecular</subject><subject>Female</subject><subject>HEK293 Cells</subject><subject>HIV-1 - genetics</subject><subject>Humans</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Pan troglodytes - virology</subject><subject>Phylogeny</subject><subject>RNA, Viral - genetics</subject><subject>Simian Acquired Immunodeficiency Syndrome - virology</subject><subject>Simian Immunodeficiency Virus - genetics</subject><subject>Viral Load</subject><subject>Virus Replication</subject><subject>Virus-Cell Interactions</subject><subject>Zoonoses - transmission</subject><issn>0022-538X</issn><issn>1098-5514</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUFP3DAQha2qFSzb3nqufOyhoR7HTuJLJYS2sIiKSsCqN8trT6hRYqdxsuryS_pzG1hA7QFZGsuaT2_G7xHyHtghAK8-3278IQPFZAblKzIDpqpMShCvyYwxzjOZVz_2yUFKt4yBEIXYI_tcceAqL2fkz-J3h71vMQymoUfOdIPfIF1sYjMOPgYaa3rpW28CXbbtGKLD2luPwW7pyvdjopfLle3u6BDpdxMctt7S07F9mb_adkiBrrf0OvlwQ80O93fo6Lc4Jpyqw-YteVObJuG7x3tOrr8uro5Ps_OLk-Xx0XlmhWRDVpYCmC2qXBYl8AJr7moAZDVWqi7AqkIqzpwyonKTE1JKnq8F2spOz7wo8jn5stPtxnWLzk5G9KbR3eSJ6bc6Gq__7wT_U9_EjZalYkpWk8DHR4E-_hoxDbr1yWLTmIDTdzSoUjDI78-cfNqhto8p9Vg_jwGm78PUZ6ulfghTQznhH_5d7Rl-Si__C5XbnQc</recordid><startdate>20180215</startdate><enddate>20180215</enddate><creator>Sato, Kei</creator><creator>Misawa, Naoko</creator><creator>Takeuchi, Junko S</creator><creator>Kobayashi, Tomoko</creator><creator>Izumi, Taisuke</creator><creator>Aso, Hirofumi</creator><creator>Nagaoka, Shumpei</creator><creator>Yamamoto, Keisuke</creator><creator>Kimura, Izumi</creator><creator>Konno, Yoriyuki</creator><creator>Nakano, Yusuke</creator><creator>Koyanagi, Yoshio</creator><general>American Society for Microbiology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-4431-1380</orcidid></search><sort><creationdate>20180215</creationdate><title>Experimental Adaptive Evolution of Simian Immunodeficiency Virus SIVcpz to Pandemic Human Immunodeficiency Virus Type 1 by Using a Humanized Mouse Model</title><author>Sato, Kei ; Misawa, Naoko ; Takeuchi, Junko S ; Kobayashi, Tomoko ; Izumi, Taisuke ; Aso, Hirofumi ; Nagaoka, Shumpei ; Yamamoto, Keisuke ; Kimura, Izumi ; Konno, Yoriyuki ; Nakano, Yusuke ; Koyanagi, Yoshio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c450t-77410c683567126ef2df11e0fe89f61c965920d9a48d53855523b4ec8cd533663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Animals, Wild - virology</topic><topic>Disease Models, Animal</topic><topic>Evolution, Molecular</topic><topic>Female</topic><topic>HEK293 Cells</topic><topic>HIV-1 - genetics</topic><topic>Humans</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Pan troglodytes - virology</topic><topic>Phylogeny</topic><topic>RNA, Viral - genetics</topic><topic>Simian Acquired Immunodeficiency Syndrome - virology</topic><topic>Simian Immunodeficiency Virus - genetics</topic><topic>Viral Load</topic><topic>Virus Replication</topic><topic>Virus-Cell Interactions</topic><topic>Zoonoses - transmission</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sato, Kei</creatorcontrib><creatorcontrib>Misawa, Naoko</creatorcontrib><creatorcontrib>Takeuchi, Junko S</creatorcontrib><creatorcontrib>Kobayashi, Tomoko</creatorcontrib><creatorcontrib>Izumi, Taisuke</creatorcontrib><creatorcontrib>Aso, Hirofumi</creatorcontrib><creatorcontrib>Nagaoka, Shumpei</creatorcontrib><creatorcontrib>Yamamoto, Keisuke</creatorcontrib><creatorcontrib>Kimura, Izumi</creatorcontrib><creatorcontrib>Konno, Yoriyuki</creatorcontrib><creatorcontrib>Nakano, Yusuke</creatorcontrib><creatorcontrib>Koyanagi, Yoshio</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sato, Kei</au><au>Misawa, Naoko</au><au>Takeuchi, Junko S</au><au>Kobayashi, Tomoko</au><au>Izumi, Taisuke</au><au>Aso, Hirofumi</au><au>Nagaoka, Shumpei</au><au>Yamamoto, Keisuke</au><au>Kimura, Izumi</au><au>Konno, Yoriyuki</au><au>Nakano, Yusuke</au><au>Koyanagi, Yoshio</au><au>Kirchhoff, Frank</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Experimental Adaptive Evolution of Simian Immunodeficiency Virus SIVcpz to Pandemic Human Immunodeficiency Virus Type 1 by Using a Humanized Mouse Model</atitle><jtitle>Journal of virology</jtitle><addtitle>J Virol</addtitle><date>2018-02-15</date><risdate>2018</risdate><volume>92</volume><issue>4</issue><issn>0022-538X</issn><eissn>1098-5514</eissn><abstract>Human immunodeficiency virus type 1 (HIV-1), the causative agent of AIDS, originated from simian immunodeficiency virus from chimpanzees (SIVcpz), the precursor of the human virus, approximately 100 years ago. This indicates that HIV-1 has emerged through the cross-species transmission of SIVcpz from chimpanzees to humans. However, it remains unclear how SIVcpz has evolved into pandemic HIV-1 in humans. To address this question, we inoculated three SIVcpz strains (MB897, EK505, and MT145), four pandemic HIV-1 strains (NL4-3, NLCSFV3, JRCSF, and AD8), and two nonpandemic HIV-1 strains (YBF30 and DJO0131). Humanized mice infected with SIVcpz strain MB897, a virus phylogenetically similar to pandemic HIV-1, exhibited a peak viral load comparable to that of mice infected with pandemic HIV-1, while peak viral loads of mice infected with SIVcpz strain EK505 or MT145 as well as nonpandemic HIV-1 strains were significantly lower. These results suggest that SIVcpz strain MB897 is preadapted to humans, unlike the other SIVcpz strains. Moreover, viral RNA sequencing of MB897-infected humanized mice identified a nonsynonymous mutation in
, a G413R substitution in gp120. The infectivity of the gp120 G413R mutant of MB897 was significantly higher than that of parental MB897. Furthermore, we demonstrated that the gp120 G413R mutant of MB897 augments the capacity for viral replication in both
cell cultures and humanized mice. Taken together, this is the first experimental investigation to use an animal model to demonstrate a gain-of-function evolution of SIVcpz into pandemic HIV-1.
From the mid-20th century, humans have been exposed to the menace of infectious viral diseases, such as severe acute respiratory syndrome coronavirus, Ebola virus, and Zika virus. These outbreaks of emerging/reemerging viruses can be triggered by cross-species viral transmission from wild animals to humans, or zoonoses. HIV-1, the causative agent of AIDS, emerged by the cross-species transmission of SIVcpz, the HIV-1 precursor in chimpanzees, around 100 years ago. However, the process by which SIVcpz evolved to become HIV-1 in humans remains unclear. Here, by using a hematopoietic stem cell-transplanted humanized-mouse model, we experimentally recapitulate the evolutionary process of SIVcpz to become HIV-1. We provide evidence suggesting that a strain of SIVcpz, MB897, preadapted to infect humans over other SIVcpz strains. We further demonstrate a gain-of-function evolution of SIVcpz in infected humanized mice. Our study reveals that pandemic HIV-1 has emerged through at least two steps: preadaptation and subsequent gain-of-function mutations.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>29212937</pmid><doi>10.1128/jvi.01905-17</doi><orcidid>https://orcid.org/0000-0003-4431-1380</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Animals, Wild - virology Disease Models, Animal Evolution, Molecular Female HEK293 Cells HIV-1 - genetics Humans Male Mice Mice, Knockout Pan troglodytes - virology Phylogeny RNA, Viral - genetics Simian Acquired Immunodeficiency Syndrome - virology Simian Immunodeficiency Virus - genetics Viral Load Virus Replication Virus-Cell Interactions Zoonoses - transmission |
title | Experimental Adaptive Evolution of Simian Immunodeficiency Virus SIVcpz to Pandemic Human Immunodeficiency Virus Type 1 by Using a Humanized Mouse Model |
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