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Malcolm A. Martin, M.D.
Building 4, Room 315
4 Memorial Drive
Bethesda, MD 20892-0460
Phone: 301-496-4012
Fax: 301-480-2716
mmartin@niaid.nih.gov

Laboratory of Molecular Microbiology

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Malcolm A. Martin, M.D.

Photo of Malcolm A. Martin, M.D.

Chief, Laboratory of Molecular Microbiology
Chief, Viral Pathogenesis and Vaccine Section, LMM

Major Areas of Research

  • Studies of primate and murine retroviral biology and genetics in cell culture systems and animal models
  • Assessment of the SIV and SIV/HIV chimeric virus (SHIV) acute infections in macaque monkeys
  • Development of R5-tropic SHIVs as challenge viruses in vaccine experiments
  • Use of R5-tropic SHIVs to investigate the development of cross-reacting anti-HIV-1 neutralizing antibodies in virus-infected and vaccinated nonhuman primate models of HIV/AIDS
 

Program Description

The Viral Pathogenesis and Vaccine Section (VPVS) develops and uses SIV and SIV/HIV chimeric viruses (SHIVs) as surrogates of HIV-1 to investigate virus-induced immunopathogenesis and to develop effective prophylactic vaccines in nonhuman primate models. Toward this end, we have constructed X4- and R5-tropic SHIVs that durably infect macaques and cause systemic depletion of CD4+ T cells in rhesus monkeys, resulting in clinical disease. Recent work has focused on 1) recombination-mediated changes in co-receptor utilization that confer an augmented pathogenic phenotype and 2) the development of cross-reacting neutralizing antibodies directed against the HIV-1 envelope glycoproteins in animals inoculated with the R5-tropic SHIVAD8.

Recent Results

Intermolecular recombination between HIV‑1 strains circulating in an infected individual is now recognized to be a major mechanism involved in the emergence of drug-resistant and immunological escape variants. HIV‑1 recombination has been studied in vivo by inoculating individual rhesus macaques with X4- and R5-tropic SHIVs. In one of the infected monkeys, both SHIVs were potently suppressed by week 12 post-inoculation, but a burst of viremia at week 51 was accompanied by an unrelenting loss of total CD4+ T cells and the development of clinical disease (Fig. 1A). PCR analyses of plasma viral RNA indicated an env gene segment, containing the V3 region from the inoculated X4 SHIV, had been transferred into the genetic background of the input R5 SHIV by intergenomic recombination, creating an X4 virus with novel replicative, serological, and pathogenic properties (Fig. 1B). These results indicate that the effects of retrovirus recombination in vivo can be functionally profound and may even occur when one of the recombination participants is undetectable in the circulation as cell-free virus.

Rhesus monkey following the inoculation of X4 and R5 SHIVs
Figure 1A
Composition of envelope genes in the plasma virus
Figure 1B
Figure 1: Timeline of recombination events occurring in a rhesus monkey following the inoculation of X4 and R5 SHIVs. A. Levels of plasma viral RNA and CD4+ T cells in the dually infected animal. B. Composition of envelope genes in the plasma virus(es) present following infection.

An R5-tropic SHIV that causes gradual losses of both memory and naïve CD4+ T lymphocytes, generates anti-viral CD4+ and CD8+ T-cell responses, and generates sustained chronic immune activation while maintaining variable levels of plasma viremia (102 to 105 RNA copies/ml for up to three years post-innoculation) and death from immunodeficiency has been generated (Fig 2). 

Levels of plasma viremiaHIVs
Rhesus macaques inoculated intravenously
Figure 2: The levels of plasma viremia (a) and absolute numbers of peripheral CD4+ T lymphocytes (b) in rhesus macaques inoculated intravenously with the R5-tropic SHIVAD8.

SHIVs express the HIV envelope glycoprotein and can therefore be used to evaluate HIV-1 Env specific neutralizing antibody (NAb) responses. Developing an SHIV that is capable of eliciting broad and potent NAb responses and tracking the evolution of this immune response might provide unprecedented insight into the factors associated with the development of bNAbs. Plasma from 14 R5-tropic SHIV-infected macaques was therefore screened for the presence of high-titered broadly reacting neutralizing activity, and a single macaque (Rh CE8J) with potent cross-clade plasma NAb response was identified (Fig. 3). Neutralization assays were carried out using samples taken at serial time points and indicated that the development of broad plasma neutralization was unusually rapid and coincided with the development of autologous NAbs. Furthermore, serum mapping studies suggested that the bNAbs interact with carbohydrates and are critically dependent on the N332 glycan (Fig. 4).

Chart of development of potent broadly cross-clade neutralizing a
Figure 3: Development of potent broadly cross-clade neutralizing antibodies directed against heterologous HIV-1 strains by a macaque (Rh CE8J) inoculated with the R5-tropic SHIVAD8. Titers in each cell are color coded as follows: gray, IC50 <1:100; green, 1:100< IC50 <1:300; yellow, 1:300< IC50 <1:500; orange, 1:500< IC50 <1:1000; red, IC50 >1:1000.
Chart of the cross-reacting anti-HIV-1 neutralizing activity generated in macaque CE8J
Figure 4: The cross-reacting anti-HIV-1 neutralizing activity generated in macaque CE8J is directed against the gp120 N332 glycan epitope. Plasma samples collected at serial time points were tested for neutralizing activity against JR-CSF, MGRM-C26, and SHIVAD8 pseudovirus variants containing an N332A mutation. Cells are color coded as follows: gray, IC50 <1:100; green, 1:100< IC50 <1:300; yellow, 1:300< IC50 <1:600; orange, 1:600< IC50 <1:1000; red, IC50 >1:1000.

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Biography

Dr. Martin received an M.D. from Yale University School of Medicine in 1962 and, following two years of clinical training in internal medicine at the University of Rochester, joined NIH as a research associate. He initially investigated the replication and gene regulation of SV40 and polyomaviruses and subsequently studied endogenous murine and human retroviral sequences. Since 1984, his research program has focused on HIV. Dr. Martin was appointed chief of the Laboratory of Molecular Microbiology when it was established in 1981. He is a member of the National Academy of Sciences and the recipient of numerous scientific awards.

Memberships

  • Elected to The National Academy of Sciences, 1998
  • Elected to The American Academy of Microbiology, 1998
  • ISI Highly Cited Researcher

Editorial Boards

  • Journal of Virology
  • Associate Editor, Fields Virology, Fourth, Fifth and Sixth Editions, 2001-2012
  • Scientific Advisory Committee, New England Regional Primate Center

 

Research Group

Yoshiaki Nishimura, Ph.D., Staff Scientist
Bernard Lafont, Ph.D., Staff Scientist
Rajeev Gautam, Ph.D., Staff Scientist
Masashi Shingai, Ph.D., Research Fellow
Wendy Lee, B.S., Biologist
Olivia Donau, B.A., Biologist
Reza Sadjadpour, M.S., Biologist

Selected Publications

Gautam R, Nishimura Y, Lee WR, Donau O, Buckler-White A, Shingai M, Sadjadpour R, Schmidt SD, LaBranche CC, Keele BF, Montefiori D, Mascola JR, Martin MA. Pathogenicity and mucosal transmissibility of the R5-tropic simian/human immunodeficiency virus SHIV(AD8) in rhesus macaques: implications for use in vaccine studies. J Virol. 2012 Aug;86(16):8516-26.

Walker LM, Sok D, Nishimura Y, Donau O, Sadjadpour R, Gautam R, Shingai M, Pejchal R, Ramos A, Simek MD, Geng Y, Wilson IA, Poignard P, Martin MA, Burton DR. Rapid development of glycan-specific, broad, and potent anti-HIV-1 gp120 neutralizing antibodies in an R5 SIV/HIV chimeric virus infected macaque. Proc Natl Acad Sci U S A. 2011 Dec 13;108(50):20125-9.

Shingai M, Yoshida T, Martin MA, Strebel K. Some human immunodeficiency virus type 1 Vpu proteins are able to antagonize macaque BST-2 in vitro and in vivo: Vpu-negative simian-human immunodeficiency viruses are attenuated in vivo. J Virol. 2011 Oct;85(19):9708-15.

Nishimura Y, Martin MA. The acute HIV infection: implications for intervention, prevention and development of an effective AIDS vaccine. Curr Opin Virol. 2011 Sep;1(3):204-10.

Nishimura Y, Shingai M, Lee WR, Sadjadpour R, Donau OK, Willey R, Brenchley JM, Iyengar R, Buckler-White A, Igarashi T, Martin MA. Recombination-mediated changes in coreceptor usage confer an augmented pathogenic phenotype in a nonhuman primate model of HIV-1-induced AIDS. J Virol. 2011 Oct;85(20):10617-26.

Nishimura Y, Shingai M, Willey R, Sadjadpour R, Lee WR, Brown CR, Brenchley JM, Buckler-White A, Petros R, Eckhaus M, Hoffman V, Igarashi T, Martin MA. Generation of the pathogenic R5-tropic simian/human immunodeficiency virus SHIVAD8 by serial passaging in rhesus macaques. J Virol. 2010 May;84(9):4769-81.

Visit PubMed for a complete publication listing.

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Patents

Martin MA, Willey R, inventors; The United States of America as represented by the Department of Health, assignee. Non-infectious mutant clone of HIV. United States patent US 4,931,393. 5 Jun 1990.

Folks TM, Powell D, Malcolm MA, inventors; The United States of America as represented by the Department of Health, assignee. Cell line producing AIDS viral antigens without producing infectious virus particles. United States patents US 4,752,565. 21 Jun 1988.

 

Last Updated March 14, 2014