Nath Tilak Chandra, Lee Dongmin, Park Hansol, Choe Seongjun, Ndosi Barakaeli Abdieli, Kang Yeseul, Bia Mohammed Mebarek, Eamudomkarn Chatanun, Mohanta Uday Kumar, Islam Kazi Mehetazul, Bhuiyan Jamal Uddin, Jeon Hyeong-Kyu, Eom Keeseon S
Department of Parasitology, Parasite Research Center and Parasite Resource Bank, School of Medicine, Chungbuk National University, Republic of Korea.
Department of Parasitology, Sylhet Agricultural University, Bangladesh.
J Parasitol Res. 2021 Feb 24;2021:8863283. doi: 10.1155/2021/8863283. eCollection 2021.
This study was aimed at describing two (2) intestinal nematodes from naturally infected native breed of goats () in Bangladesh, identified as (Curtice, 1890) Stossich 1899 and (Rudolphi, 1803) Cobb, 1898. The identification was made based on morphometric features and was confirmed by amplifying internal transcribed spacer (ITS) and cytochrome oxidase (1) gene. Well-developed lateral alae, distinct cervical papillae anteriorly to esophageal expansion, and male spicule length (0.73-0.79 mm, = 2) were characteristically observed in . At the same time, male spicule length (0.40-0.46 mm, = 2) and position of female vulvar flap (4.30-4.54 mm from posterior end, = 3) were observed in . DNA sequence homology of the ITS and 1 gene of both specimens revealed the same results, showing similarity to the GenBank sequences of (GenBank No. KC715827; JX188470) and (GenBank No. KJ724377; HQ389229). Phylogenetic analysis computed by maximum livelihood (ML) from the ITS nucleotide sequences revealed that the and isolates identified in this study were clustered in the same clade with isolates from China and Iran, respectively. This study, for the first time, illustrates the characteristics of and in Bangladesh, combining both morphological and molecular data. The universal primer-based polymerase chain reaction (PCR) protocol could be an economical and efficient option for researchers from poor resource settings for precise identification of nematodes. The information generated in this study may contribute to formulating effective control strategies against these nematodes.
本研究旨在描述来自孟加拉国自然感染本地品种山羊的两种肠道线虫,分别鉴定为1899年斯托西奇命名的(柯蒂斯,1890)和1898年科布命名的(鲁道夫,1803)。鉴定基于形态特征,并通过扩增内转录间隔区(ITS)和细胞色素氧化酶(1)基因进行确认。在中特征性地观察到发育良好的侧翼、食管扩张前方明显的颈乳突以及雄虫交合刺长度(0.73 - 0.79毫米,= 2)。同时,在中观察到雄虫交合刺长度(0.40 - 0.46毫米,= 2)和雌虫阴门瓣位置(距后端4.30 - 4.54毫米,= 3)。两个样本的ITS和1基因的DNA序列同源性显示相同结果,与(GenBank编号KC715827;JX188470)和(GenBank编号KJ724377;HQ389229)的GenBank序列相似。由ITS核苷酸序列通过最大似然法(ML)计算的系统发育分析表明,本研究中鉴定的和分离株分别与来自中国和伊朗的分离株聚集在同一进化枝中。本研究首次结合形态学和分子数据阐述了孟加拉国的和的特征。基于通用引物的聚合酶链反应(PCR)方案对于资源匮乏地区的研究人员精确鉴定线虫可能是一种经济有效的选择。本研究产生的信息可能有助于制定针对这些线虫的有效控制策略。