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Semen-Derived Amyloid Fibrils Drastically Enhance HIV Infection
Jan M?nch<sup>1</sup>, Elke R?cker<sup>1</sup>, Ludger St?ndker<sup>2</sup><sup>, </sup><sup>3</sup>, Knut Adermann<sup>2</sup><sup>, </sup><sup>3</sup><sup>, </sup><sup>4</sup>, Christine Goffinet<sup>5</sup>, Michael Schindler<sup>1</sup>, Steffen Wildum<sup>1</sup>, Raghavan Chinnadurai<sup>1</sup>, Devi Rajan<sup>1</sup>, Anke Specht<sup>1</sup>, Guillermo Gim?nez-Gallego<sup>6</sup>, Pedro Cuevas S?nchez<sup>7</sup>, Douglas M. Fowler<sup>8</sup>, Atanas Koulov<sup>8</sup>, Jeffery W. Kelly<sup>8</sup>, Walther Mothes<sup>9</sup>, Jean-Charles Grivel<sup>10</sup>, Leonid Margolis<sup>10</sup>, Oliver T. Keppler<sup>5</sup>, Wolf-Georg Forssmann<sup>2</sup><sup>, </sup><sup>3</sup><sup>, </sup><sup>
</sup><sup>, </sup><sup>
</sup> and Frank Kirchhoff<sup>1</sup><sup>, </sup><sup>
</sup><sup>, </sup><sup>
</sup>
<sup>1</sup>Institute of Virology, University Clinic of Ulm, 89081 Ulm, Germany
<sup>2</sup>IPF PharmaCeuticals GmbH, 30625 Hannover, Germany
<sup>3</sup>Hannover Medical School, Center of Pharmacology, 30625 Hannover, Germany
<sup>4</sup>VIRO Pharmaceuticals GmbH & Co. KG, 30625 Hannover, Germany
<sup>5</sup>Department of Virology, University of Heidelberg, 69120 Heidelberg, Germany
<sup>6</sup>Centro de Investigaciones Biol?gicas (CIB/CSIC), Madrid 28040, Spain
<sup>7</sup>Hospital Ram?n y Cajal, Madrid 28034, Spain
<sup>8</sup>Department of Chemistry and the Skaggs Institute of Chemical Biology, The Scripps Research Institute, La Jolla, CA 92037, USA
<sup>9</sup>Section of Microbial Pathogenesis, Yale University School of Medicine, New Haven, CT 06536, USA
<sup>10</sup>National Institute of Child Health and Human Development, Bethesda, MD 20892, USA
Received 6 February 2007; revised 18 June 2007; accepted 4 October 2007. Published: December 13, 2007. Available online 13 December 2007.
<table class="refersTable" cellpadding="0" cellspacing="0"> <tbody><tr><td class="refersLeftColumn" nowrap="nowrap"> Referred to by:</td><td>
</td><td>A Seminal Finding for Understanding HIV Transmission
Cell, Volume 131, Issue 6, 14 December 2007, Pages 1044-1046
Nadia R. Roan and Warner C. Greene
Abstract | Full Text + Links | PDF (334 K) </td></tr><tr class="refersDivider"><td colspan="3">
</td></tr> </tbody></table>
Summary
Sexual intercourse is the major route of HIV transmission. To identify endogenous factors that affect the efficiency of sexual viral transmission, we screened a complex peptide/protein library derived from human semen. We show that naturally occurring fragments of the abundant semen marker prostatic acidic phosphatase (PAP) form amyloid fibrils. These fibrils, termed Semen-derived Enhancer of Virus Infection (SEVI), capture HIV virions and promote their attachment to target cells, thereby enhancing the infectious virus titer by several orders of magnitude. Physiological concentrations of SEVI amplified HIV infection of T cells, macrophages, ex vivo human tonsillar tissues, and transgenic rats in vivo, as well as trans-HIV infection of T cells by dendritic or epithelial cells. Amyloidogenic PAP fragments are abundant in seminal fluid and boost semen-mediated enhancement of HIV infection. Thus, they may play an important role in sexual transmission of HIV and could represent new targets for its prevention.
Semen-Derived Amyloid Fibrils Drastically Enhance HIV Infection
Jan M?nch<sup>1</sup>, Elke R?cker<sup>1</sup>, Ludger St?ndker<sup>2</sup><sup>, </sup><sup>3</sup>, Knut Adermann<sup>2</sup><sup>, </sup><sup>3</sup><sup>, </sup><sup>4</sup>, Christine Goffinet<sup>5</sup>, Michael Schindler<sup>1</sup>, Steffen Wildum<sup>1</sup>, Raghavan Chinnadurai<sup>1</sup>, Devi Rajan<sup>1</sup>, Anke Specht<sup>1</sup>, Guillermo Gim?nez-Gallego<sup>6</sup>, Pedro Cuevas S?nchez<sup>7</sup>, Douglas M. Fowler<sup>8</sup>, Atanas Koulov<sup>8</sup>, Jeffery W. Kelly<sup>8</sup>, Walther Mothes<sup>9</sup>, Jean-Charles Grivel<sup>10</sup>, Leonid Margolis<sup>10</sup>, Oliver T. Keppler<sup>5</sup>, Wolf-Georg Forssmann<sup>2</sup><sup>, </sup><sup>3</sup><sup>, </sup><sup>
</sup><sup>, </sup><sup>
</sup> and Frank Kirchhoff<sup>1</sup><sup>, </sup><sup>
</sup><sup>, </sup><sup>
</sup> <sup>1</sup>Institute of Virology, University Clinic of Ulm, 89081 Ulm, Germany
<sup>2</sup>IPF PharmaCeuticals GmbH, 30625 Hannover, Germany
<sup>3</sup>Hannover Medical School, Center of Pharmacology, 30625 Hannover, Germany
<sup>4</sup>VIRO Pharmaceuticals GmbH & Co. KG, 30625 Hannover, Germany
<sup>5</sup>Department of Virology, University of Heidelberg, 69120 Heidelberg, Germany
<sup>6</sup>Centro de Investigaciones Biol?gicas (CIB/CSIC), Madrid 28040, Spain
<sup>7</sup>Hospital Ram?n y Cajal, Madrid 28034, Spain
<sup>8</sup>Department of Chemistry and the Skaggs Institute of Chemical Biology, The Scripps Research Institute, La Jolla, CA 92037, USA
<sup>9</sup>Section of Microbial Pathogenesis, Yale University School of Medicine, New Haven, CT 06536, USA
<sup>10</sup>National Institute of Child Health and Human Development, Bethesda, MD 20892, USA
Received 6 February 2007; revised 18 June 2007; accepted 4 October 2007. Published: December 13, 2007. Available online 13 December 2007.
<table class="refersTable" cellpadding="0" cellspacing="0"> <tbody><tr><td class="refersLeftColumn" nowrap="nowrap"> Referred to by:</td><td>
Cell, Volume 131, Issue 6, 14 December 2007, Pages 1044-1046
Nadia R. Roan and Warner C. Greene
Abstract | Full Text + Links | PDF (334 K) </td></tr><tr class="refersDivider"><td colspan="3">
</td></tr> </tbody></table>
Summary
Sexual intercourse is the major route of HIV transmission. To identify endogenous factors that affect the efficiency of sexual viral transmission, we screened a complex peptide/protein library derived from human semen. We show that naturally occurring fragments of the abundant semen marker prostatic acidic phosphatase (PAP) form amyloid fibrils. These fibrils, termed Semen-derived Enhancer of Virus Infection (SEVI), capture HIV virions and promote their attachment to target cells, thereby enhancing the infectious virus titer by several orders of magnitude. Physiological concentrations of SEVI amplified HIV infection of T cells, macrophages, ex vivo human tonsillar tissues, and transgenic rats in vivo, as well as trans-HIV infection of T cells by dendritic or epithelial cells. Amyloidogenic PAP fragments are abundant in seminal fluid and boost semen-mediated enhancement of HIV infection. Thus, they may play an important role in sexual transmission of HIV and could represent new targets for its prevention.