Lee Seung-Ok, Na Dong-Kyeun, Kim Chul-Min, Li Ying-Hua, Cho Yoon-Hee, Park Jin-Ho, Lee John-Hwa, Eo Seong-Kug, Klein Terry A, Chae Joon-Seok
Bio-Safety Research Institute and College of Veterinary Medicine, Chonbuk National University, Jeonju, Korea.
J Vet Sci. 2005 Jun;6(2):151-5.
Genomic DNAs extracted from 1,288 Haemaphysalis longicornis ticks collected from grass vegetation and various animals from nine provinces of Korea were subjected to screening by genus-specific (Ehrlichia spp. or Anaplasma spp.) real-time TaqMan PCR and speciesspecific (E. chaffeensis) nested-PCR based on amplification of 16S rRNA gene fragments. In all, 611 (47.4%) ticks tested positive for genus-specific amplification of 116 bp fragment of 16S rRNA of Ehrlichia spp. or Anaplasma spp. Subsequently, 396 bp E. chaffeensis-specific fragment of 16S rRNA was amplified from 4.2% (26/611) tick samples. The comparison of the nucleotide sequence of 16S rRNA gene from one tick (EC-PGHL, GeneBank accession number AY35042) with the sequences of 20 E. chaffeensis strains available in the database showed that EC-PGHL was 100% identical or similar to the Arkansas (AF416764), the Sapulpa (U60476) and the 91HE17 (U23503) strains. The phylogenetic analysis also revealed that the E. chaffeensis EC-PGHL formed a single cluster with the above strains. This is the first study to report molecular detection and phylogenetic analysis of E. chaffeensis from H. longicornis ticks in Korea. The implicit significance of E. chaffeensis infection in H. longicornis ticks in Korea is discussed.
从韩国九个省份的草地植被和各种动物身上采集的1288只长角血蜱中提取基因组DNA,通过基于16S rRNA基因片段扩增的属特异性(埃立克体属或无形体属)实时TaqMan PCR和种特异性(查菲埃立克体)巢式PCR进行筛选。总共有611只(47.4%)蜱对埃立克体属或无形体属16S rRNA的116 bp片段进行属特异性扩增检测呈阳性。随后,从4.2%(26/611)的蜱样本中扩增出了16S rRNA的396 bp查菲埃立克体特异性片段。将一只蜱(EC-PGHL,基因库登录号AY35042)的16S rRNA基因核苷酸序列与数据库中现有的20株查菲埃立克体菌株序列进行比较,结果显示EC-PGHL与阿肯色州菌株(AF416764)、萨普尔帕菌株(U60476)和91HE17菌株(U23503)的序列100%相同或相似。系统发育分析还表明,查菲埃立克体EC-PGHL与上述菌株形成了一个单独的聚类。这是首次报道在韩国长角血蜱中对查菲埃立克体进行分子检测和系统发育分析的研究。文中还讨论了韩国长角血蜱感染查菲埃立克体的潜在意义。