Nallan Krishnamoorthy, Rajan Gopinathan, Sivathanu Lallitha, Devaraju Panneer, Thiruppathi Balaji, Kumar Ashwani, Rajaiah Paramasivan
ICMR-Vector Control Research Centre, Field Unit, Madurai 625 002, India.
Department of Microbiology, Government Medical College and Hospital, Theni 625 512, India.
Trop Med Infect Dis. 2023 Mar 16;8(3):174. doi: 10.3390/tropicalmed8030174.
Scrub typhus (St) is a re-emerging mite-transmitted public health problem in Southeast Asia with escalating case incidences in the endemic areas. Though, more than 40 genotypes of the causative agent () have been documented, the information on the circulating genotypes in India is scanty. A hospital-based retrospective screening was undertaken to map the circulating molecular subtypes of the etiological agent in serologically confirmed scrub typhus (St) human cases, by targeting the GroEL gene of using the nested polymerase chain reaction method. Nine out of 34 samples (26%) yielded positive results and DNA sequencing analysis of six positive samples out of nine revealed that the sequences were related to three major genotypes, such as Karp (HSB1, FAR1), Kato (Wuj/2014, UT76), and Kawasaki (Kuroki, Boryong, Gilliam, and Hwasung). Additionally, the St-positive samples exhibited 100% and 99.45%; 97.53% and 97.81%; 96.99% nucleotide identity with the closely related Karp, Kato, and Kawasaki-related sequences, respectively. Overall, 94% of the nucleotides were conserved, and the variable site was 20/365 (5.5%). The prevalence of multiple genotypes among human cases further stresses the need to conduct in-depth studies to map the genotypes and their clinical relevance, and the contributing risk factors for the emergence of St cases in this area.
恙虫病是东南亚地区再度出现的由螨虫传播的公共卫生问题,流行地区的病例发病率不断上升。尽管已记录了40多种病原体( )的基因型,但印度关于流行基因型的信息却很少。通过使用巢式聚合酶链反应方法靶向 的GroEL基因,对血清学确诊的恙虫病(St)人类病例进行了一项基于医院的回顾性筛查,以绘制病原体的流行分子亚型。34个样本中有9个(26%)检测结果呈阳性,对9个阳性样本中的6个进行DNA测序分析后发现,这些序列与三种主要基因型有关,如Karp(HSB1、FAR1)、Kato(Wuj/2014、UT76)和Kawasaki(Kuroki、Boryong、Gilliam和Hwasung)。此外,St阳性样本与密切相关的Karp、Kato和Kawasaki相关序列的核苷酸同一性分别为100%和99.45%;97.53%和97.81%;96.99%。总体而言,94%的核苷酸是保守的,可变位点为20/365(5.5%)。人类病例中多种基因型的流行进一步凸显了开展深入研究以绘制基因型及其临床相关性以及该地区St病例出现的相关危险因素的必要性。