College of Veterinary Medicine, Federal University of Agriculture, P.M.B. 2240, Abeokuta, Ogun State, Nigeria; Department of Biomedical Sciences, Atlantic Veterinary College, University of Prince Edward Island, 550 University Avenue, Prince Edward Island, C1A 4P3, Canada.
College of Veterinary Medicine, Federal University of Agriculture, P.M.B. 2240, Abeokuta, Ogun State, Nigeria.
Acta Trop. 2019 Jul;195:15-22. doi: 10.1016/j.actatropica.2019.04.009. Epub 2019 Apr 11.
Giardiasis is a common gastrointestinal disease of humans and various animal species worldwide. In this study, 302 stool samples were collected from West African Dwarf and Sokoto Red breeds of goats in Ogun State, Nigeria, and screened for Giardia intestinalis coproantigens using enzyme-linked immunosorbent assay (ELISA). The genotypes of G. intestinalis in faecal samples collected from 152 goats raised on selected farms were identified by polymerase chain reaction (PCR) amplification and sequence analyses of the small subunit ribosomal RNA (ssu rRNA), glutamate dehydrogenase (gdh), triosephosphate isomerase (tpi) and β-giardin (bg) genes. Based on ELISA, an overall prevalence of 45.7% was recorded with the infection rates in pre-weaned (60.2%) and post-weaned goat kids (51.5%) being significantly (p < 0.05) higher than in adults (28.2%). Giardia intestinalis DNA was amplified in 31.6% and 29.6% of goat faeces at the ssu rRNA and gdh loci respectively. These were genotyped at the ssu rRNA locus as assemblages B (n = 13) and E (n = 36). Similar results were observed at the gdh locus except that eight isolates contained assemblage E mixed with either assemblage A or B. Additionally, sub-assemblages BI (n = 7) and BIII (n = 2) were identified with up to four single nucleotide polymorphisms (SNPs) occurring in these isolates. Multilocus genotypes (MLG) of all assemblage E isolates were identified using the ssu rRNA and gdh loci while MLG of all isolates containing assemblage B and mixed assemblages were determined after further typing at the tpi and bg loci. Forty-two MLG isolates were identified and these comprised 32, 8 and 2 (sub)-assemblage E, BI and BIII respectively. All isolates with mixed assemblages at the gdh locus were consequently designated as assemblage E by MLG. The assemblage E isolates from goats were genetically related to isolates from cattle, sheep and goats while the assemblage B isolates were related to isolates of human, pig and lemur origin. This suggests that G. intestinalis isolated from goats bred in Ogun State, Nigeria may be capable of cross-species transmission and may be of zoonotic importance.
贾第虫病是一种常见的人类和世界各地各种动物物种的胃肠道疾病。在这项研究中,从尼日利亚奥贡州的西非德瓦尔德和索科托红品种的山羊中采集了 302 份粪便样本,并使用酶联免疫吸附测定(ELISA)检测贾第虫肠道 coproantigens。从选定农场饲养的 152 只山羊的粪便样本中,通过聚合酶链反应(PCR)扩增和小亚基核糖体 RNA(ssu rRNA)、谷氨酸脱氢酶(gdh)、磷酸丙糖异构酶(tpi)和β-微管蛋白(bg)基因的序列分析鉴定了贾第虫的基因型。根据 ELISA,总体流行率为 45.7%,未断奶(60.2%)和断奶后山羊幼崽(51.5%)的感染率明显(p < 0.05)高于成年羊(28.2%)。在粪便中分别以 ssu rRNA 和 gdh 基因扩增了 31.6%和 29.6%的贾第虫 DNA。这些在 ssu rRNA 基因座上被分型为组合 B(n = 13)和 E(n = 36)。在 gdh 基因座上观察到类似的结果,只是 8 个分离物含有组合 E 与组合 A 或 B 混合。此外,还鉴定了亚组合 BI(n = 7)和 BIII(n = 2),这些分离物中发生了多达四个单核苷酸多态性(SNP)。使用 ssu rRNA 和 gdh 基因座鉴定了所有组合 E 分离物的多基因座基因型(MLG),而在 tpi 和 bg 基因座进一步分型后,确定了包含组合 B 和混合组合的所有分离物的 MLG。鉴定了 42 个 MLG 分离物,它们分别由 32、8 和 2(亚)组合 E、BI 和 BIII 组成。在 gdh 基因座上具有混合组合的所有分离物因此被 MLG 鉴定为组合 E。从尼日利亚奥贡州饲养的山羊中分离出的组合 E 分离物与牛、绵羊和山羊的分离物具有遗传关系,而组合 B 分离物与人类、猪和狐猴的分离物具有遗传关系。这表明从尼日利亚奥贡州饲养的山羊中分离出的贾第虫可能具有跨种传播的能力,并可能具有人畜共患的重要性。