Common evolutionary features of the envelope glycoprotein of HIV-1 in patients belonging to a transmission chain
The diversity of the HIV-1 envelope glycoproteins (Env) is largely a consequence of the pressure exerted by the adaptive immune response to infection. While it was generally assumed that the neutralizing antibody (NAb) response depended mainly on the infected individual, the concept that virus-relat...
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Published in | Scientific reports Vol. 10; no. 1; p. 16744 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Nature Publishing Group UK
07.10.2020
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Abstract | The diversity of the HIV-1 envelope glycoproteins (Env) is largely a consequence of the pressure exerted by the adaptive immune response to infection. While it was generally assumed that the neutralizing antibody (NAb) response depended mainly on the infected individual, the concept that virus-related factors could be important in inducing this response has recently emerged. Here, we analyzed the influence of the infecting viral strain in shaping NAb responses in four HIV-1 infected subjects belonging to a transmission chain. We also explored the impact of NAb responses on the functional evolution of the viral quasispecies. The four patients developed a strong autologous neutralizing antibody response that drove viral escape and coincided with a parallel evolution of their infecting quasispecies towards increasing infectious properties, increasing susceptibility to T20 and increasing resistance to both CD4 analogs and V3 loop-directed NAbs. This evolution was associated with identical Env sequence changes at several positions in the V3 loop, the fusion peptide and the HR2 domain of gp41. The common evolutionary pattern of Env in different hosts suggests that the capacity of a given Env to adapt to changing environments may be restricted by functional constraints that limit its evolutionary landscape. |
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AbstractList | The diversity of the HIV-1 envelope glycoproteins (Env) is largely a consequence of the pressure exerted by the adaptive immune response to infection. While it was generally assumed that the neutralizing antibody (NAb) response depended mainly on the infected individual, the concept that virus-related factors could be important in inducing this response has recently emerged. Here, we analyzed the influence of the infecting viral strain in shaping NAb responses in four HIV-1 infected subjects belonging to a transmission chain. We also explored the impact of NAb responses on the functional evolution of the viral quasispecies. The four patients developed a strong autologous neutralizing antibody response that drove viral escape and coincided with a parallel evolution of their infecting quasispecies towards increasing infectious properties, increasing susceptibility to T20 and increasing resistance to both CD4 analogs and V3 loop-directed NAbs. This evolution was associated with identical Env sequence changes at several positions in the V3 loop, the fusion peptide and the HR2 domain of gp41. The common evolutionary pattern of Env in different hosts suggests that the capacity of a given Env to adapt to changing environments may be restricted by functional constraints that limit its evolutionary landscape.The diversity of the HIV-1 envelope glycoproteins (Env) is largely a consequence of the pressure exerted by the adaptive immune response to infection. While it was generally assumed that the neutralizing antibody (NAb) response depended mainly on the infected individual, the concept that virus-related factors could be important in inducing this response has recently emerged. Here, we analyzed the influence of the infecting viral strain in shaping NAb responses in four HIV-1 infected subjects belonging to a transmission chain. We also explored the impact of NAb responses on the functional evolution of the viral quasispecies. The four patients developed a strong autologous neutralizing antibody response that drove viral escape and coincided with a parallel evolution of their infecting quasispecies towards increasing infectious properties, increasing susceptibility to T20 and increasing resistance to both CD4 analogs and V3 loop-directed NAbs. This evolution was associated with identical Env sequence changes at several positions in the V3 loop, the fusion peptide and the HR2 domain of gp41. The common evolutionary pattern of Env in different hosts suggests that the capacity of a given Env to adapt to changing environments may be restricted by functional constraints that limit its evolutionary landscape. The diversity of the HIV-1 envelope glycoproteins (Env) is largely a consequence of the pressure exerted by the adaptive immune response to infection. While it was generally assumed that the neutralizing antibody (NAb) response depended mainly on the infected individual, the concept that virus-related factors could be important in inducing this response has recently emerged. Here, we analyzed the influence of the infecting viral strain in shaping NAb responses in four HIV-1 infected subjects belonging to a transmission chain. We also explored the impact of NAb responses on the functional evolution of the viral quasispecies. The four patients developed a strong autologous neutralizing antibody response that drove viral escape and coincided with a parallel evolution of their infecting quasispecies towards increasing infectious properties, increasing susceptibility to T20 and increasing resistance to both CD4 analogs and V3 loop-directed NAbs. This evolution was associated with identical Env sequence changes at several positions in the V3 loop, the fusion peptide and the HR2 domain of gp41. The common evolutionary pattern of Env in different hosts suggests that the capacity of a given Env to adapt to changing environments may be restricted by functional constraints that limit its evolutionary landscape. |
ArticleNumber | 16744 |
Author | Goujard, Cécile Moreau, Alain Chaix, Marie-Laure Barin, Francis Braibant, Martine Meyer, Laurence Migraine, Julie Beretta, Maxime Bouvin-Pley, Mélanie Essat, Asma Drouin, Aurélie |
Author_xml | – sequence: 1 givenname: Maxime surname: Beretta fullname: Beretta, Maxime organization: Université de Tours et CHRU de Tours, Inserm U1259, Laboratory of Humoral Immunology, Department of Immunology, Institut Pasteur – sequence: 2 givenname: Julie surname: Migraine fullname: Migraine, Julie organization: Université de Tours et CHRU de Tours, Inserm U1259 – sequence: 3 givenname: Alain surname: Moreau fullname: Moreau, Alain organization: Université de Tours et CHRU de Tours, Inserm U1259 – sequence: 4 givenname: Asma surname: Essat fullname: Essat, Asma organization: Université Paris Sud, Université Paris Saclay, CESP Inserm U1018 – sequence: 5 givenname: Cécile surname: Goujard fullname: Goujard, Cécile organization: Université Paris Sud, Université Paris Saclay, CESP Inserm U1018, AP-HP Hôpital de Bicêtre – sequence: 6 givenname: Marie-Laure surname: Chaix fullname: Chaix, Marie-Laure organization: Université de Paris, Inserm U944, Laboratoire de Virologie, AP-HP, Hôpital Saint Louis – sequence: 7 givenname: Aurélie surname: Drouin fullname: Drouin, Aurélie organization: Université de Tours et CHRU de Tours, Inserm U1259 – sequence: 8 givenname: Mélanie surname: Bouvin-Pley fullname: Bouvin-Pley, Mélanie organization: Université de Tours et CHRU de Tours, Inserm U1259 – sequence: 9 givenname: Laurence surname: Meyer fullname: Meyer, Laurence organization: Université Paris Sud, Université Paris Saclay, CESP Inserm U1018, AP-HP Hôpital de Bicêtre – sequence: 10 givenname: Francis surname: Barin fullname: Barin, Francis organization: Université de Tours et CHRU de Tours, Inserm U1259, CHRU de Tours, CNR VIH – sequence: 11 givenname: Martine surname: Braibant fullname: Braibant, Martine email: braibant@med.univ-tours.fr organization: Université de Tours et CHRU de Tours, Inserm U1259 |
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Title | Common evolutionary features of the envelope glycoprotein of HIV-1 in patients belonging to a transmission chain |
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