Cutillas C, Oliveros R, de Rojas M, Guevara D C
Department of Microbiology and Parasitology, Faculty of Pharmacy, Sevilla University, Profesor García González s/n, 41012 Sevilla, Spain,
Parasitol Res. 2002 Jun;88(6):574-82. doi: 10.1007/s00436-002-0596-5. Epub 2002 Mar 22.
Trichuris muris has been isolated from murid hosts ( Apodemus sylvaticus and Mus musculus) and Trichuris arvicolae from arvicolid rodents in Barcelona, Spain. Genomic DNA was isolated and the ITS1-5.8S-ITS2 segment from the ribosomal DNA (rDNA) was amplified and sequenced using polymerase chain reaction techniques. The ITS2 of both populations isolated from Apodemus and Mus was 382 nucleotides in length and had a GC content of about 60.73%, while the ITS2 of T. arvicolae was 442 nucleotides in length and had a GC content of about 59.8%. Furthermore, the ITS1 of Trichuris from murids was 448 nucleotides in length and had a GC content of about 56.47%, while T. arvicolae was 446 nucleotides in length and had 57.62% of GC content. A total of 161 and 173 nucleotides were observed along the 5.8S gene of T. murisand T. arvicolae, respectively; This difference in nucleotides was due to the insertion of a DNA segment (transposon) in the 5.8S sequence of the latter species. Slight intraindividual and intraspecific variations were detected in the rDNA of both species. The presence of microsatellites was observed in all of the individuals assayed. Sequence analysis of the internal transcribed spacers and the 5.8S gene demonstrated no sequence differences between T. muris isolated from both of its murid hosts. Nevertheless, clear differences were detected between the ITS2, ITS1 and 5.8S gene of T. muris and T. arvicolae. This corroborates the existence of two separate Trichuris species in murid and arvicolid hosts. Furthermore, a phylogenetic analysis was carried out and endonucleases restriction maps were elaborated for both species.
在西班牙巴塞罗那,已从鼠科宿主(林姬鼠和小家鼠)中分离出鼠鞭虫,从田鼠科啮齿动物中分离出田鼠鞭虫。分离出基因组DNA,并使用聚合酶链反应技术扩增和测序核糖体DNA(rDNA)的ITS1-5.8S-ITS2片段。从林姬鼠和小家鼠中分离出的两个群体的ITS2长度均为382个核苷酸,GC含量约为60.73%,而田鼠鞭虫的ITS2长度为442个核苷酸,GC含量约为59.8%。此外,鼠科动物的鞭虫ITS1长度为448个核苷酸,GC含量约为56.47%,而田鼠鞭虫ITS1长度为446个核苷酸,GC含量为57.62%。在鼠鞭虫和田鼠鞭虫的5.8S基因中分别观察到总共161和173个核苷酸;这种核苷酸差异是由于后一种物种的5.8S序列中插入了一个DNA片段(转座子)。在两个物种的rDNA中均检测到轻微的个体内和种内变异。在所有检测的个体中均观察到微卫星的存在。内部转录间隔区和5.8S基因的序列分析表明,从其两个鼠科宿主中分离出的鼠鞭虫之间没有序列差异。然而,在鼠鞭虫和田鼠鞭虫的ITS2、ITS1和5.8S基因之间检测到明显差异。这证实了在鼠科和田鼠科宿主中存在两个独立的鞭虫物种。此外,还进行了系统发育分析,并为这两个物种绘制了内切酶限制图谱。