Sin Yung Wa, Newman Chris, Dugdale Hannah L, Buesching Christina, Mannarelli Maria-Elena, Annavi Geetha, Burke Terry, Macdonald David W
Wildlife Conservation Research Unit, Department of Zoology, University of Oxford, Recanati-Kaplan Centre, Tubney House, Abingdon Road, Tubney, Abingdon, Oxfordshire, OX13 5QL, United Kingdom.
NERC Biomolecular Analysis Facility, Department of Animal and Plant Sciences, University of Sheffield, Sheffield, S10 2TN, United Kingdom.
PLoS One. 2016 Oct 3;11(10):e0163773. doi: 10.1371/journal.pone.0163773. eCollection 2016.
The innate immune system provides the primary vertebrate defence system against pathogen invasion, but it is energetically costly and can have immune pathological effects. A previous study in sticklebacks found that intermediate major histocompatibility complex (MHC) diversity correlated with a lower leukocyte coping capacity (LCC), compared to individuals with fewer, or many, MHC alleles. The organization of the MHC genes in mammals, however, differs to the highly duplicated MHC genes in sticklebacks by having far fewer loci. Using European badgers (Meles meles), we therefore investigated whether innate immune activity, estimated functionally as the ability of an individual's leukocytes to produce a respiratory burst, was influenced by MHC diversity. We also investigated whether LCC was influenced by factors such as age-class, sex, body condition, season, year, neutrophil and lymphocyte counts, and intensity of infection with five different pathogens. We found that LCC was not associated with specific MHC haplotypes, MHC alleles, or MHC diversity, indicating that the innate immune system did not compensate for the adaptive immune system even when there were susceptible MHC alleles/haplotypes, or when the MHC diversity was low. We also identified a seasonal and annual variation of LCC. This temporal variation of innate immunity was potentially due to physiological trade-offs or temporal variation in pathogen infections. The innate immunity, estimated as LCC, does not compensate for MHC diversity suggests that the immune system may function differently between vertebrates with different MHC organizations, with implications for the evolution of immune systems in different taxa.
先天性免疫系统是脊椎动物抵御病原体入侵的主要防御系统,但它耗能巨大,且可能产生免疫病理效应。先前一项对棘鱼的研究发现,与拥有较少或较多主要组织相容性复合体(MHC)等位基因的个体相比,中等MHC多样性与较低的白细胞应对能力(LCC)相关。然而,哺乳动物的MHC基因组织与棘鱼高度重复的MHC基因不同,其基因座要少得多。因此,我们利用欧洲獾(Meles meles)研究了功能性评估为个体白细胞产生呼吸爆发能力的先天性免疫活性是否受MHC多样性影响。我们还研究了LCC是否受年龄组、性别、身体状况、季节、年份、中性粒细胞和淋巴细胞计数以及五种不同病原体感染强度等因素的影响。我们发现LCC与特定的MHC单倍型、MHC等位基因或MHC多样性无关,这表明即使存在易感的MHC等位基因/单倍型,或MHC多样性较低时,先天性免疫系统也无法补偿适应性免疫系统。我们还发现了LCC的季节性和年度变化。先天性免疫的这种时间变化可能是由于生理权衡或病原体感染的时间变化。以LCC评估的先天性免疫无法补偿MHC多样性,这表明在具有不同MHC组织的脊椎动物中,免疫系统的功能可能不同,这对不同分类群免疫系统的进化具有启示意义。