Kidd Alana, Casteriano Andrea, Krockenberger Mark B, Higgins Damien P, Wright Belinda R
Sydney School of Veterinary Science, University of Sydney, Camperdown, NSW, 2006, Australia.
Sci Rep. 2024 Dec 28;14(1):31074. doi: 10.1038/s41598-024-82217-w.
Chlamydiosis is a common infectious disease impacting koalas and is a major cause of population decline due to resulting mortality and infertility. Polymorphisms of major histocompatibility complex (MHC) genes influence chlamydial disease outcomes in several species but koala studies have produced variable results. We aimed to identify the MHC II DAB and DBB repertoire of koalas from Liverpool Plains, NSW, a population heavily impacted by chlamydiosis. We compared variants between two studies, age cohorts and chlamydial infertility groups. Four DBB and eight DAB alleles were identified. The mean number of DAB alleles per individual increased and allele frequencies differed relative to a previous study, however the mean number of DBB alleles per individual decreased generationally, between age cohorts. DAB allele frequencies differed among fertility groups but contributing alleles could not be identified. While there is a likely role of MHCII in the complex pathogenesis of chlamydiosis, this study suggests that single gene association studies are not appropriate for understanding the impact of host genetics on koala chlamydiosis. A shift to larger multivariate studies is required to yield functional information on complex immunological interactions, and to inform targeted koala conservation across its diverse range and host-pathogen-environment contexts.
衣原体病是一种影响考拉的常见传染病,由于其导致的死亡率和不育症,是考拉种群数量下降的主要原因。主要组织相容性复合体(MHC)基因的多态性影响了几种物种的衣原体病发病情况,但对考拉的研究结果却不尽相同。我们旨在确定新南威尔士州利物浦平原考拉的MHC II DAB和DBB基因库,该种群受到衣原体病的严重影响。我们比较了两项研究、不同年龄组和衣原体不育组之间的变异情况。共鉴定出4个DBB等位基因和8个DAB等位基因。与之前的研究相比,每个个体的DAB等位基因平均数增加,且等位基因频率有所不同,然而,不同年龄组之间,每个个体的DBB等位基因平均数呈世代下降趋势。不同生育组的DAB等位基因频率不同,但无法确定其贡献等位基因。虽然MHCII可能在衣原体病的复杂发病机制中起作用,但本研究表明,单基因关联研究并不适合理解宿主遗传学对考拉衣原体病的影响。需要转向更大规模的多变量研究,以获取关于复杂免疫相互作用的功能信息,并为在考拉分布广泛的不同区域以及宿主-病原体-环境背景下进行有针对性的考拉保护提供依据。