Materniak-Kornas Magdalena, Ropka-Molik Katarzyna, Piórkowska Katarzyna, Kowalik Joanna, Szmatoła Tomasz, Sikora Jacek, Kawęcka Aldona, Kuźmak Jacek
Department of Biochemistry, National Veterinary Research Institute, 24-100 Pulawy, Poland.
Department of Animal Molecular Biology, National Research Institute of Animal Production, Krakowska 1, 32-083 Balice, Poland.
Pathogens. 2024 Sep 25;13(10):830. doi: 10.3390/pathogens13100830.
Small ruminant lentivirus (SRLV) infections are spread in the flocks of sheep and goats all over the world, causing economic loss. Although only a fraction of infected animals develop disease symptoms, all of them may shed the virus, causing uncontrolled spread of the infection. Antibodies against the virus can be detected in the blood of infected animals and are the main marker of infection. Additionally, in most infected animals, proviral DNA can also be detected, but at different levels. Due to the lack of treatment or vaccines, the most effective strategy to prevent SRLV infections are control programmes introduced by several countries based on the elimination of seropositive individuals from the flock. An alternative approach, which has currently become the rationale, is an identification of host factors which may predispose certain individuals or breeds to resistance or susceptibility to small ruminant lentivirus infection. In our work, attention was paid to goats of the Carpathian breed infected with SRLV. Available RNA-seq results from the blood of 12 goats with a determined level of SRLV proviral load were used to analyse single nucleotide polymorphisms (SNPs) by the variant calling method. Six SNPs within five genes (, , , , ) were selected for genotyping to determine their association with the level of small ruminant lentivirus proviral DNA in a group of 60 goats. Interestingly, in seronegative individuals, only the TT genotype of the gene was observed, while the CC genotype was found only in seropositive goats. Both genes may be considered potential markers for resistance/susceptibility to SRLV infection. In contrast, polymorphisms identified in and genes seemed to be deleterious for respective protein functions; therefore, these genes are less likely to be recognised as resistance/susceptibility markers of SRLV infection.
小反刍兽疫病毒(SRLV)感染在世界各地的绵羊和山羊群体中传播,造成经济损失。尽管只有一小部分受感染动物会出现疾病症状,但所有受感染动物都可能排毒,导致感染不受控制地传播。在受感染动物的血液中可以检测到针对该病毒的抗体,这些抗体是感染的主要标志物。此外,在大多数受感染动物中,也可以检测到前病毒DNA,但水平不同。由于缺乏治疗方法或疫苗,预防SRLV感染的最有效策略是一些国家实施的控制计划,即从羊群中清除血清阳性个体。一种目前已成为基本原理的替代方法是识别可能使某些个体或品种对小反刍兽疫病毒感染具有抗性或易感性的宿主因素。在我们的研究中,重点关注了感染SRLV的喀尔巴阡山羊品种。利用12只已确定SRLV前病毒载量水平的山羊血液中的现有RNA测序结果,通过变异检测方法分析单核苷酸多态性(SNP)。选择五个基因(,,,,)中的六个SNP进行基因分型,以确定它们与一组60只山羊中小反刍兽疫病毒前病毒DNA水平的关联。有趣的是,在血清阴性个体中,仅观察到基因的TT基因型,而CC基因型仅在血清阳性山羊中发现。这两个基因都可被视为对SRLV感染具有抗性/易感性的潜在标志物。相比之下,在基因和中鉴定出的多态性似乎对各自的蛋白质功能有害;因此,这些基因不太可能被识别为SRLV感染的抗性/易感性标志物。