Rapid dissemination of SIV follows multisite entry after rectal inoculation

Patricia Ribeiro Dos Santos1, Magali Rancez, Jean-Luc Prétet

  • 1Laboratoire de Transmission et Dissémination Virales, Université Paris Diderot, Sorbonne Paris Cité, Paris, France.

Plos One
|May 17, 2011
PubMed

Insights

Rectal HIV transmission is poorly understood. This study in macaques shows Simian Immunodeficiency Virus (SIV) rapidly enters and spreads through the rectum within hours, highlighting the need for specific prevention strategies.

Area of Science:

  • Virology
  • Immunology
  • Gastroenterology

Background:

  • Receptive anal intercourse is a primary HIV transmission route for men who have sex with men and heterosexual individuals.
  • Current understanding of rectal HIV entry and spread mechanisms is limited, hindering the development of effective prevention strategies.
  • Investigating early rectal infection dynamics is crucial for designing targeted interventions.

Purpose of the Study:

  • To elucidate the early mechanisms of rectal infection and Simian Immunodeficiency Virus (SIV) dissemination in a primate model.
  • To identify the initial cellular targets and pathways involved in SIV rectal transmission.
  • To inform the development of specific microbicides and vaccines for preventing rectal HIV transmission.

Main Methods:

  • Rhesus macaques were inoculated with the pathogenic SIVmac251 isolate.
  • Animals were necropsied at various time points (4 hours to 9 days post-infection).
  • Techniques included nested PCR for viral DNA, immunohistofluorescence for antigen detection, and nested RT-PCR for viral mRNA.

Main Results:

  • SIV DNA was detected in rectal lymphoid aggregates and lamina propria as early as 4 hours post-infection.
  • Infectious virus and viral replication (Env mRNA) were confirmed in rectal tissues and colic lymph nodes within 4 hours.
  • SIV-infected cells included T cells, macrophages, and dendritic cells, but not epithelial cells; DC-SIGN+ cells harbored infectious virus.

Conclusions:

  • Rapid SIV entry and dissemination occur via trans-epithelial transport across both digestive and follicle-associated epithelia.
  • Viral replication appears more efficient within lymphoid aggregates.
  • The distinct early events in rectal infection necessitate rectal-specific microbicides and vaccines targeting both rectal tissues and lymph nodes.