Pervin Shahnaj, Islam Md Shafiqul, Tada Naomi, Tsutsui Toshihiko, Rahman Mohammad Mahbubur, Yabuki Akira, Tacharina Martia Rani, Rakib Tofazzal Md, Maki Shinichiro, Yamato Osamu
Laboratory of Clinical Pathology, Joint Faculty of Veterinary Medicine, Kagoshima University, 1-21-24 Korimoto, Kagoshima 890-0065, Japan.
Department of Pathology and Parasitology, Faculty of Veterinary Medicine, Chattogram Veterinary and Animal Sciences University, Khulshi, Chattogram 4225, Bangladesh.
Animals (Basel). 2022 May 7;12(9):1210. doi: 10.3390/ani12091210.
Neuronal ceroid lipofuscinosis (NCL) is a group of rare lethal neurodegenerative lysosomal storage diseases that occur in a range of dog breeds, including Chihuahuas. Recently, a homozygous single base-pair deletion (c.846delT), which causes a frame shift generating a premature stop codon (p.Phe282Leufs13*) in the canine / gene, has been identified as a causative mutation for NCL in Chihuahuas. The objective of this study was to determine the frequency of the mutant allele and/or carrier rate of NCL in Chihuahuas in Japan using a newly designed real-time PCR assay. Samples of saliva were randomly collected from 1007 Chihuahua puppies during physical examinations prior to the transportation to pet shops. Screening results revealed a carrier rate of 1.29%, indicating a mutant allele frequency (0.00645) that is considered sufficiently high to warrant measures for the control and prevention of this lethal disease. The genotyping assay designed in this study could make a valuable contribution to the control and prevention of NCL.
神经元蜡样脂褐质沉积症(NCL)是一组罕见的致死性神经退行性溶酶体贮积病,发生于包括吉娃娃犬在内的多种犬种。最近,一个纯合单碱基对缺失(c.846delT),它导致犬/基因中产生移码,生成一个提前终止密码子(p.Phe282Leufs13*),已被确定为吉娃娃犬NCL的致病突变。本研究的目的是使用新设计的实时PCR检测法确定日本吉娃娃犬中NCL突变等位基因的频率和/或携带率。在运往宠物店之前的体检期间,从1007只吉娃娃幼犬中随机采集唾液样本。筛查结果显示携带率为1.29%,表明突变等位基因频率(0.00645)被认为足够高,有必要采取措施控制和预防这种致死性疾病。本研究设计的基因分型检测法可为NCL的控制和预防做出宝贵贡献。