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Identifying genome-wide immune gene variation underlying infectious disease in wildlife populations - a next generation sequencing approach in the gopher tortoise
被引:21
|作者:
Elbers, Jean P.
[1
]
Brown, Mary B.
[2
]
Taylor, Sabrina S.
[1
]
机构:
[1] Louisiana State Univ, Sch Renewable Nat Resources, 227 RNR Bldg, Baton Rouge, LA 70803 USA
[2] AgCenter, Baton Rouge, LA 70803 USA
来源:
基金:
美国国家卫生研究院;
美国食品与农业研究所;
美国国家科学基金会;
关键词:
Genome-wide association study;
Target enrichment;
Sequence capture;
Next-generation sequencing;
Immunogenetics;
Gopherus polyphemus;
Immunomes;
RESPIRATORY-TRACT DISEASE;
MYCOPLASMA-AGASSIZII;
TARGETED CAPTURE;
INNATE IMMUNITY;
UNITED-STATES;
NK CELLS;
RESISTANCE;
ASSOCIATION;
PROTEIN;
TOOL;
D O I:
10.1186/s12864-018-4452-0
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Background: Infectious disease is the single greatest threat to taxa such as amphibians (chytrid fungus), bats (white nose syndrome), Tasmanian devils (devil facial tumor disease), and black-footed ferrets (canine distemper virus, plague). Although understanding the genetic basis to disease susceptibility is important for the long-term persistence of these groups, most research has been limited to major-histocompatibility and Toll-like receptor genes. To better understand the genetic basis of infectious disease susceptibility in a species of conservation concern, we sequenced all known/predicted immune response genes (i.e., the immunomes) in 16 Florida gopher tortoises, Gopherus polyphemus. All tortoises produced antibodies against Mycoplasma agassizii (an etiologic agent of infectious upper respiratory tract disease; URTD) and, at the time of sampling, either had (n = 10) or lacked (n = 6) clinical signs. Results: We found several variants associated with URTD clinical status in complement and lectin genes, which may play a role in Mycoplasma immunity. Thirty-five genes deviated from neutrality according to Tajima's D. These genes were enriched in functions relating to macromolecule and protein modifications, which are vital to immune system functioning. Conclusions: These results are suggestive of genetic differences that might contribute to disease severity, a finding that is consistent with other mycoplasmal diseases. This has implications for management because tortoises across their range may possess genetic variation associated with a more severe response to URTD. More generally: 1) this approach demonstrates that a broader consideration of immune genes is better able to identify important variants, and; 2) this data pipeline can be adopted to identify alleles associated with disease susceptibility or resistance in other taxa, and therefore provide information on a population's risk of succumbing to disease, inform translocations to increase genetic variation for disease resistance, and help to identify potential treatments.
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