This proposal in response to RFA-RR-10-005 leverages a new collaboration between Dr. Skip Virgin and Dr. Dan Barouch to define the role of the enteric microbiome, virome, and metagenome in the health of SIV-infected and uninfected macaques. Little is known about the metagenome of the macaque intestine and its relationship to disease, yet understanding intestinal 'ecology'is essential for defining the basic biology and immunology of the intestine. This is critical for understanding how to diagnose precious animals, vaccinate against mucosal lentivirus challenge, and the mechanisms driving progression to AIDS. In a cross-sectional study of 39 macaques we used deep sequencing and metagenomic analysis to find at least 19 new enteric macaque viruses (indicating that the macaque 'virome'is extensive) and significant differences in the microbiome and virome in SIV-infected compared to uninfected animals. Thus we have a unique opportunity to analyze interactions between lentivirus infection and the enteric microbiome/virome in macaques. The significance of this proposal will be defining: (i) the fundamental nature of, and effects of SIV on, the microbiome/virome;(ii) the role of many newly discovered viruses and changes in the microbiome in disease, and (iii) whether the microbiome/virome contributes to intestinal leakage and systemic immune activation during SIV infection. We will address these cross-disciplinary questions by linking expertise in macaque health and lentivirus infection and vaccination (Barouch/Carville/Mansfeild) with expertise in relating the microbiome/virome to intestinal pathology, virus discovery, and metagenomics (Virgin/Wang/ Zhao/Handley). This team can rapidly generate data that may fundamentally change approaches to the use of primates in biomedical research. Since little is known about macaque metagenomics, we will combine unbiased longitudinal discovery experiments with testing of our primary hypothesis that vaccination will block the effects of SIV on the microbiome and virome. The impact of our studies could come from: (i) changes in veterinary care, (ii) a new paradigm for the source of systemic immune activation during SIV infection, and (iii) improved fundamental understanding of the relationship between intestinal ecology and the immune system. We will therefore address the following Aims:
Aim 1) Define the relationship between the macaque microbiome and virome and enteric disease.
Aim 2) Define the impact of SIV infection on the enteric microbiome/virome.
Macaques are precious non-human primates used in biomedical research. Of special importance, macaques are used to study AIDS since infection of these animals with simian immunodeficiency virus (SIV) mimics infection of people with human immunodeficiency virus 1 (HIV). One of the most common diseases seen in both SIV-infected and uninfected macaques is diarrhea- but the causes of this are not completely understood. In addition, it now appears that intestinal damage in SIV-infected macaques may contribute to the development of AIDS via release of materials from the lumen of the intestine into the circulation that stimulate the immune system. Thus there are important unknowns about enteric viruses and bacteria that, if answered, could improve macaque health and disease diagnosis, and perhaps also shed light on the progression of SIV infection. We approached this problem using next-generation sequencing and new computational methods to define the bacteria and viruses (microbiome and virome) present in the macaque intestine. Remarkably we discovered more than 19 new enteric viruses, mostly present in SIV-infected macaques that progress rapidly to AIDS. Our data also suggest that SIV progression to AIDS is accompanied by substantial changes in the microbiome and the virome- these might well contribute to intestinal damage and diarrheal disease. This proposal is to study the macaque microbiome and virome in health and disease. We expect to develop a better understanding of the viruses, and changes in bacterial populations, that cause disease in macaques, to develop new diagnostic tests whose application will improve macaque health, and to leverage these cutting edge sequencing and computational methods to better understand AIDS.
|Monaco, Cynthia L; Gootenberg, David B; Zhao, Guoyan et al. (2016) Altered Virome and Bacterial Microbiome in Human Immunodeficiency Virus-Associated Acquired Immunodeficiency Syndrome. Cell Host Microbe 19:311-22|
|Handley, Scott A; Desai, Chandni; Zhao, Guoyan et al. (2016) SIV Infection-Mediated Changes in Gastrointestinal Bacterial Microbiome and Virome Are Associated with Immunodeficiency and Prevented by Vaccination. Cell Host Microbe 19:323-35|
|Reese, Tiffany A; Bi, Kevin; Kambal, Amal et al. (2016) Sequential Infection with Common Pathogens Promotes Human-like Immune Gene Expression and Altered Vaccine Response. Cell Host Microbe 19:713-9|
|Krishnamurthy, Siddharth R; Janowski, Andrew B; Zhao, Guoyan et al. (2016) Hyperexpansion of RNA Bacteriophage Diversity. PLoS Biol 14:e1002409|
|Stephenson, Kathryn E; D'Couto, Helen T; Barouch, Dan H (2016) New concepts in HIV-1 vaccine development. Curr Opin Immunol 41:39-46|
|Abbink, Peter; Maxfield, Lori F; Ng'ang'a, David et al. (2015) Construction and evaluation of novel rhesus monkey adenovirus vaccine vectors. J Virol 89:1512-22|
|Norman, Jason M; Handley, Scott A; Baldridge, Megan T et al. (2015) Disease-specific alterations in the enteric virome in inflammatory bowel disease. Cell 160:447-60|
|Moon, Clara; Baldridge, Megan T; Wallace, Meghan A et al. (2015) Vertically transmitted faecal IgA levels determine extra-chromosomal phenotypic variation. Nature 521:90-3|
|Barouch, Dan H; Alter, Galit; Broge, Thomas et al. (2015) Protective efficacy of adenovirus/protein vaccines against SIV challenges in rhesus monkeys. Science 349:320-4|
|Virgin, Herbert W (2014) The virome in mammalian physiology and disease. Cell 157:142-50|
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