Makouloutou Patrice, Rana Hari Bahadur, Adhikari Bishunu, Devkota Bhuminand, Dhakal Ishwari Prasad, Sato Hiroshi
Laboratory of Parasitology, Joint Faculty of Veterinary Medicine, Yamaguchi University, Yoshida, Yamaguchi, Japan.
J Parasitol. 2013 Aug;99(4):669-76. doi: 10.1645/12-143.1. Epub 2013 Feb 19.
Whole-length esophagi of 111 Murrah cross water buffaloes (Bubalus bubalis) were collected in the Kathmandu and Chitwan districts of Nepal from December 2009 to February 2010. Gullet worms showing a typical epithelium-dwelling character were detected in 13 of 53 (24.5%) buffaloes in Kathmandu and in 5 of 58 (8.6%) buffaloes in Chitwan. The worms' morphology and measurements were identical to those of Gongylonema pulchrum Molin, 1857, except for the length of the left spicules relative to the body length. Scanning electron microscopy did not detect any further morphological differences regarding the collected specimen from Nepal compared with G. pulchrum . The ribosomal RNA gene (rDNA), including internal transcribed spacer (ITS) 1 and 2, and a partial region of the cytochrome c oxidase subunit I (COI) of mitochondrial DNA of the worms were characterized and compared with those of G. pulchrum collected from cattle, deer, wild boars, and monkeys in Japan and from cattle in Iran. The 18S, 5.8S, and 28S rDNA nucleotide sequences of the buffalo-collected worms had 99.8% (1,779/1,782), 100% (158/158), and 98.3-98.8% (3,494-3,507/3,551) identities, respectively, with those of G. pulchrum from the other host mammals. The ITS regions exhibited higher variations between the buffalo-collected worms and G. pulchrum from the other host mammals (85-88% identity for ITS1 and 56-80% identity for ITS2). The COI also showed lower identities (89.2-90.2%), although only a single amino acid substitution was noted compared with the majority of G. pulchrum samples collected in Japan. Based on these molecular genetic characters in the rDNA and COI mitochondrial DNA, together with a shorter left spicule length relative to body length, the gullet worms isolated from buffaloes in Nepal might belong to a distinct local or buffalo-preferring population of G. pulchrum, although its geographical distribution on the continent and host specificity remain to be clarified.
2009年12月至2010年2月期间,在尼泊尔加德满都和奇旺地区收集了111头穆拉杂交水牛(Bubalus bubalis)的全长食管。在加德满都的53头水牛中,有13头(24.5%)检测到具有典型上皮内寄生特征的食管线虫;在奇旺的58头水牛中,有5头(8.6%)检测到此类线虫。除左交合刺长度与体长的比例外,这些线虫的形态和测量数据与1857年的美丽筒线虫(Gongylonema pulchrum Molin)相同。扫描电子显微镜检查未发现尼泊尔采集的标本与美丽筒线虫在形态上有任何进一步差异。对这些线虫的核糖体RNA基因(rDNA),包括内部转录间隔区(ITS)1和2,以及线粒体DNA细胞色素c氧化酶亚基I(COI)的部分区域进行了特征分析,并与从日本的牛、鹿、野猪和猴子以及伊朗的牛身上采集的美丽筒线虫进行了比较。从水牛身上采集的线虫的18S、5.8S和28S rDNA核苷酸序列与其他宿主哺乳动物的美丽筒线虫的序列分别具有99.8%(1779/1782)、100%(158/158)和98.3 - 98.8%(3494 - 3507/3551)的同源性。ITS区域在从水牛身上采集的线虫与其他宿主哺乳动物的美丽筒线虫之间表现出更高的差异(ITS1的同源性为85 - 88%,ITS2的同源性为56 - 80%)。COI也显示出较低的同源性(89.2 - 90.2%),尽管与在日本采集的大多数美丽筒线虫样本相比,仅发现一个氨基酸替换。基于rDNA和COI线粒体DNA中的这些分子遗传特征,以及相对于体长较短的左交合刺长度,从尼泊尔水牛身上分离出的食管线虫可能属于美丽筒线虫的一个独特的本地种群或偏好水牛的种群,尽管其在该大陆的地理分布和宿主特异性仍有待阐明。