Zheng Guochao, Alsarakibi Muhamd, Liu Yuanjia, Hu Wei, Luo Qin, Tan Liping, Li Guoqing
College of Veterinary Medicine, South China Agricultural University, Guangzhou, Guangdong Province, 510642, People's Republic of China.
Korean J Parasitol. 2014 Jun;52(3):299-304. doi: 10.3347/kjp.2014.52.3.299. Epub 2014 Jun 26.
This study aimed to identify the assemblages (or subassemblages) of Giardia duodenalis by using normal or nested PCR based on 4 genetic loci: glutamate dehydrogenase (gdh), triose phosphate isomerase (tpi), β-giardin (bg), and small subunit ribosomal DNA (18S rRNA) genes. For this work, a total of 216 dogs' fecal samples were collected in Guangdong, China. The phylogenetic trees were constructed with MEGA5.2 by using the neighbor-joining method. Results showed that 9.7% (21/216) samples were found to be positive; moreover, 10 samples were single infection (7 isolates assemblage A, 2 isolates assemblage C, and 1 isolate assemblage D) and 11 samples were mixed infections where assemblage A was predominant, which was potentially zoonotic. These findings showed that most of the dogs in Guangdong were infected or mixed-infected with assemblage A, and multi-locus sequence typing could be the best selection for the genotype analysis of dog-derived Giardia isolates.
本研究旨在通过基于4个基因位点(谷氨酸脱氢酶(gdh)、磷酸丙糖异构酶(tpi)、β-贾第虫蛋白(bg)和小亚基核糖体DNA(18S rRNA)基因)的常规或巢式PCR来鉴定十二指肠贾第虫的组合(或亚组合)。为此,在中国广东共收集了216份犬粪便样本。使用邻接法通过MEGA5.2构建系统发育树。结果显示,9.7%(21/216)的样本呈阳性;此外,10份样本为单一感染(7株为A组合,2株为C组合,1株为D组合),11份样本为混合感染,其中A组合占主导,具有潜在人兽共患病性。这些发现表明,广东的大多数犬感染或混合感染了A组合,多位点序列分型可能是犬源贾第虫分离株基因型分析的最佳选择。