Do Thom, Ngasaman Ruttayaporn, Saechan Vannarat, Pitaksakulrat Opal, Liu Mingming, Xuan Xuenan, Inpankaew Tawin
Department of Parasitology, Faculty of Veterinary Medicine, Kasetsart University, Bangkok 10900, Thailand.
Faculty of Veterinary Science, Prince of Songkla University, Songkhla 90110, Thailand.
Pathogens. 2021 May 22;10(6):639. doi: 10.3390/pathogens10060639.
In southern Thailand, the increasingly growing population of stray dogs is a concern to public health and environmental safety because of the lack of medical attention and control. More importantly, these animals are considered reservoirs for many zoonotic pathogens. The objective of this study was to molecularly detect canine vector-borne pathogens, and to perform genetic characterization of present in stray dogs from southern Thailand. Blood samples were collected from 174 stray dogs in two provinces (Songkhla and Narathiwat) in southern Thailand. PCR analyses were executed using specific primers based on the spp. 18S rRNA gene, Internal transcribed spacer 1 (ITS1) region, citrate synthase (gltA) gene, spp. 18S rRNA gene and heat shock protein (groEL) gene. The most common canine vector-borne pathogen found infecting stray dogs in this study was (24.7%) followed by (14.9%), (8.0%), (6.3%), and (1.72%). Concurrent infection with more than one pathogen occurred in 72 cases. Phylogenetic analysis based on the ITS1 region and 18S rRNA gene revealed that the isolates from this study shared a large proportion of their identities with each other and with other reported genotypes from Asia. This study highlights the molecular detection of in dogs in Thailand for the first time and presents the genetic characterization by sequencing the ITS1 region and 18S rRNA gene of from Thailand. Follow-up studies are needed to elucidate the origin, distribution, and vectors of parasites circulating in dogs in Thailand, as well as to determine to what extent dogs are important reservoir hosts for zoonotic canine vector-borne disease infection in the studied area.
在泰国南部,由于缺乏医疗护理和管控,流浪狗数量的不断增加对公共卫生和环境安全构成了威胁。更重要的是,这些动物被认为是许多人畜共患病原体的宿主。本研究的目的是从分子水平上检测犬类媒介传播的病原体,并对泰国南部流浪狗体内存在的病原体进行基因特征分析。从泰国南部两个省份(宋卡和北大年)的174只流浪狗身上采集了血样。使用基于特定物种的18S rRNA基因、内部转录间隔区1(ITS1)区域、柠檬酸合酶(gltA)基因、特定物种的18S rRNA基因和热休克蛋白(groEL)基因的特异性引物进行PCR分析。在本研究中,感染流浪狗的最常见的犬类媒介传播病原体是[具体病原体名称1](24.7%),其次是[具体病原体名称2](14.9%)、[具体病原体名称3](8.0%)、[具体病原体名称4](6.3%)和[具体病原体名称5](1.72%)。72例出现了一种以上病原体的合并感染。基于ITS1区域和18S rRNA基因的系统发育分析表明,本研究中的[具体病原体名称]分离株彼此之间以及与亚洲其他报道的[具体病原体名称]基因型具有很大比例的相同特征。本研究首次突出了在泰国狗身上对[具体病原体名称]的分子检测,并通过对泰国[具体病原体名称]的ITS1区域和18S rRNA基因进行测序展示了其基因特征。需要开展后续研究以阐明泰国狗体内循环的[具体病原体名称]寄生虫的起源、分布和传播媒介,以及确定在所研究地区狗作为人畜共患犬类媒介传播疾病感染的重要储存宿主的程度。