Genecology Research Centre, University of the Sunshine Coast, 90 Sippy Downs Drive, Sippy Downs, QLD, 4556, Australia.
Lone Pine Koala Sanctuary, Fig Tree Pocket, QLD, Australia.
Immunogenetics. 2020 Dec;72(9-10):499-506. doi: 10.1007/s00251-020-01181-7. Epub 2020 Oct 20.
Characterizing the allelic diversity within major histocompatibility complex (MHC) genes is an important way of determining the potential genetic resilience of a population to infectious and ecological pressures. For the koala (Phascolarctos cinereus), endemic diseases, anthropogenic factors and climate change are all placing increased pressure on this vulnerable marsupial. To increase the ability of researchers to study MHC genetics in koalas, this study developed and tested a high-throughput immunogenetic profiling methodology for targeting MHC class I UA and UC genes and MHC class II DAB, DBB, DCB and DMB genes in a population of 82 captive koalas. This approach was validated by comparing the determined allelic profiles from 36 koala family units (18 dam-sire-joey units and 18 parent-joey pairs), finding 96% overall congruence within family profiles. Cancers are a significant cause of morbidity in koalas and the risk factors remain undetermined. Our analysis of this captive population revealed several novel MHC alleles, including a potential link between the DBB*03 allele and a risk of developing cancer. This method offers a reliable, high-throughput protocol for expanded study into koala immunogenetics.
对主要组织相容性复合体 (MHC) 基因的等位基因多样性进行特征分析是确定一个种群对感染和生态压力的潜在遗传弹性的重要方法。对于树袋熊(Phascolarctos cinereus)来说,地方性疾病、人为因素和气候变化都给这种脆弱的有袋类动物带来了更大的压力。为了提高研究人员在树袋熊中研究 MHC 遗传学的能力,本研究开发并测试了一种高通量免疫遗传分析方法,用于针对 82 只圈养树袋熊中的 MHC Ⅰ类 UA 和 UC 基因和 MHC Ⅱ类 DAB、DBB、DCB 和 DMB 基因进行靶向分析。通过比较 36 个树袋熊家庭单位(18 个母-父-幼崽单位和 18 个亲-幼崽对)的确定的等位基因谱,该方法在家族谱中得到了 96%的总体一致性验证。癌症是树袋熊发病率的一个重要原因,但其风险因素仍未确定。我们对这一圈养种群的分析揭示了几个新的 MHC 等位基因,包括 DBB*03 等位基因与癌症发病风险之间的潜在联系。该方法为进一步研究树袋熊免疫遗传学提供了一种可靠的高通量方案。