The vertebrate immune system includes numerous proteins involved in the recognition and elimination of parasitic organisms. The general goals of this research are to understand the origin and evolution of key molecular components of this system, especially the molecules encoded by the genes of the major histocompatibility complex (MHC), and to understand the evolution of molecular adaptations in parasitic organisms that evade recognition and elimination by the host's immune system. The MHC is a multi-gene family encoding cell-surface glycoproteins, which play an important role in the immune system, binding foreign proteins and presenting them to T cells. Several of the MHC loci are highly polymorphic, and there is evidence that this polymorphism is maintained by balancing selection relating to most host immune surveillance. The methods used in this research involve statistical analysis of published DNA sequence data, of which a large amount is now available both for immune system genes and for genes of major human pathogens (particularly viruses). The purposes of these analyses are as follows: (1) to understand the evolutionary origin of MHC class I peptide-binding specificities; (2) to understand the evolutionary origin of MHC-related molecules that have assumed other functions; (3) to test the hypothesis that selection exerted by the host class I MHC and cytotoxic T cell (CTL) recognition system has played a role in the long-term evolution of viruses infecting vertebrates (including human immunodeficiency virus 1, hepatitis B virus, and papilloma viruses); (4) to understand the evolution of overlapping reading frames in viral genomes, with particular emphasis on the role of natural selection exerted by the host class I MHC/CTL recognition system on genes encoded by overlapping reading frames; (5) to understand the process by which the genomes of large DNA viruses (including adenoviruses, herpes viruses, poxviruses and baculoviruses) have """"""""captured"""""""" host genes over the course of their evolution, a process which has enabled these viruses to obtain genes encoding immuno-modulating proteins which can interfere with host immune processes; and (6) to understand the evolution of repeat-containing proteins, which are believed to enable parasites to evade the highly specific recognition mechanisms of the host MHC and T cell system, in the genomes of the malaria parasites and DNA viruses.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM043940-16
Application #
6868880
Study Section
Genetics Study Section (GEN)
Program Officer
Eckstrand, Irene A
Project Start
1990-09-01
Project End
2007-03-31
Budget Start
2005-04-01
Budget End
2006-03-31
Support Year
16
Fiscal Year
2005
Total Cost
$158,088
Indirect Cost
Name
University of South Carolina at Columbia
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
111310249
City
Columbia
State
SC
Country
United States
Zip Code
29208
Putaporntip, C; Kuamsab, N; Kosuwin, R et al. (2016) Natural selection of K13 mutants of Plasmodium falciparum in response to artemisinin combination therapies in Thailand. Clin Microbiol Infect 22:285.e1-8
Hughes, Austin L (2015) Adaptive amino acid composition in collagens of parasitic nematodes. Infect Genet Evol 31:277-83
Hughes, Austin L (2014) Evolutionary diversification of aminopeptidase N in Lepidoptera by conserved clade-specific amino acid residues. Mol Phylogenet Evol 76:127-33
Hughes, Austin L; Friedman, Robert (2014) Evolutionary diversification of the vertebrate transferrin multi-gene family. Immunogenetics 66:651-61
Hughes, Austin L (2013) Origin of Ecdysosteroid UDP-glycosyltransferases of Baculoviruses through Horizontal Gene Transfer from Lepidoptera. Coevolution 1:1-7
Putaporntip, Chaturong; Hughes, Austin L; Jongwutiwes, Somchai (2013) Low level of sequence diversity at merozoite surface protein-1 locus of Plasmodium ovale curtisi and P. ovale wallikeri from Thai isolates. PLoS One 8:e58962
Hughes, Austin L (2013) Accumulation of slightly deleterious mutations in the mitochondrial genome: a hallmark of animal domestication. Gene 515:28-33
Mudd, Philip A; Ericsen, Adam J; Burwitz, Benjamin J et al. (2012) Escape from CD8(+) T cell responses in Mamu-B*00801(+) macaques differentiates progressors from elite controllers. J Immunol 188:3364-70
Hughes, Austin L; Becker, Ericka A; Lauck, Michael et al. (2012) SIV genome-wide pyrosequencing provides a comprehensive and unbiased view of variation within and outside CD8 T lymphocyte epitopes. PLoS One 7:e47818
Hughes, Austin L (2012) Amino acid sequence coevolution in the insect bursicon ligand-receptor system. Mol Phylogenet Evol 63:617-24

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