Parasitic and Honeybee Disease Laboratory, Bacterial and Parasitic Disease Division, Department of Animal & Plant Health Research, Animal and Plant Quarantine Agency, Gimcheon, 39660, Republic of Korea.
Faculty of Biotechnology, Thai Nguyen University of Sciences, Thai Nguyen, Vietnam.
BMC Vet Res. 2022 May 27;18(1):199. doi: 10.1186/s12917-022-03311-7.
Rickettsia spp. are important tick-borne pathogens that cause various human and animal diseases worldwide. A tool for rapid and accurate detection of the pathogens from its vectors is necessary for prevention of Rickettsioses propagation in humans and animals, which are infested by ticks. Therefore, this study was conducted to evaluate a molecular tool, ultra-rapid real-time PCR (UR-qPCR), for rapid and accurate detection of Rickettsia spp. from 5644 ticks in 408 pools collected from livestock and their surrounding environments in Gangwon and Jeju province in South Korea.
The UR-qPCR of Rickettsia DNA showed a limit of detection of 2.72 × 10 copies of Rickettsia DNA and no cross reaction with other tick-borne pathogens, namely Anaplasma phagocytophilum, Ehrlichia chaffeensis, E. canis, Toxoplasma gondii, and Borrelia burgdorferi. In addition, the PCR assay also showed possibility of various Rickettsia species detection including R. monacensis, "Candidatus R. longicornii", R. japonica, R. roultii, and R. tamurae. The collected ticks were identified with major species belonged to Haemaphysalis longicornis (81.62%), followed by H. flava (15.19%), and Ixodes nipponensis (3.19%). Rickettsia detection from tick samples using the UR-qPCR showed that the minimum infection rate (MIR) of Rickettsia in collected ticks was 1.24‰ and that all positive pools contained H. longicornis, equal to the MIR of 1.39‰ of this species. Additionally, MIR of Rickettsia spp. detected in ticks collected in Gangwon and Jeju was 1.53‰ and 0.84‰, respectively. Furthermore, the sequencing results of the 17 kDa protein antigen gene and ompA gene showed that Rickettsia spp. sequences from all pools were related to "Candidatus R. longicornii" and "Candidatus R. jingxinensis".
The UR-qPCR system was demonstrated to be useful tool for accurate and rapid detection of Rickettsia from its vector, ixodid ticks, within 20 min. The data on Rickettsia spp. in ticks detected in this study provide useful information on the distribution of Rickettsia in previously unstudied Korean provinces, which are important for the prevention and control of the spread of rickettsioses in both animals and humans in the country.
立克次体是重要的蜱传病原体,可导致全球人类和动物的各种疾病。因此,需要一种工具来快速准确地从其载体中检测病原体,以预防在被蜱虫寄生的人类和动物中传播立克次体病。因此,本研究旨在评估一种分子工具,即超快速实时 PCR(UR-qPCR),用于快速准确地从韩国江原道和济州道的牲畜及其周围环境中采集的 5644 只蜱虫的 408 个池中检测立克次体 spp。
Rickettsia DNA 的 UR-qPCR 检测限为 2.72×10 拷贝的 Rickettsia DNA,与其他蜱传病原体(即嗜吞噬细胞无形体、查菲埃氏埃立克体、犬埃立克体、刚地弓形虫和伯氏疏螺旋体)无交叉反应。此外,PCR 检测还显示了检测各种立克次体物种的可能性,包括 R. monacensis、“长角立克次体候选种”、R. japonica、R. roultii 和 R. tamurae。从采集的蜱虫中鉴定出主要物种为长角血蜱(81.62%),其次是黄胸血蜱(15.19%)和日本革蜱(3.19%)。使用 UR-qPCR 从蜱虫样本中检测立克次体显示,采集的蜱虫中立克次体的最低感染率(MIR)为 1.24‰,所有阳性池均含有长角血蜱,相当于该物种 1.39‰的 MIR。此外,在江原道和济州道采集的蜱虫中,立克次体 spp 的 MIR 分别为 1.53‰和 0.84‰。此外,17kDa 蛋白抗原基因和 ompA 基因的测序结果表明,所有池中的立克次体 spp 序列均与“长角立克次体候选种”和“荆新立克次体候选种”有关。
该 UR-qPCR 系统被证明是一种有用的工具,可在 20 分钟内准确快速地从其载体,即硬蜱中检测立克次体。本研究中检测到的蜱虫中立克次体 spp 的数据提供了有关在韩国以前未研究的省份中分布的有用信息,这对于预防和控制该国动物和人类中立克次体病的传播非常重要。