Godbole Ravi, Gaur Avantika, Nayar Priyanka, Kiruthiga Kala, D'Costa Pradeep, Manchanda Rumma, Khilari Ajinkya, Shanmugam Dhanasekaran, Muglikar Kalpana D, Kundu Krishnendu
Department of Pathology, King Edward Memorial Hospital, Pune, India.
Biochemical Sciences Division, National Chemical Laboratory, Pune, India.
Am J Trop Med Hyg. 2022 Feb 21;106(5):1421-5. doi: 10.4269/ajtmh.20-1118.
Human babesiosis is a rare disease, caused by Babesia species and commonly transmitted by tick bite. Although human babesiosis is known to be asymptomatic in immunocompetent hosts, clinical cases of severe babesiosis have been reported from splenectomized or immunocompromised individuals. To our knowledge, only one case of human babesiosis in India has been previously reported. Here, we report a case of severe babesiosis with high parasitemia (∼70%) in a 30-year-old asplenic farmer. The patient presented with fever, yellowish discoloration of skin, oliguria, and anemia; he eventually developed multiorgan failure syndrome and died. Peripheral blood films were prepared and used to confirm the presence of piroplasms by microscopy. Total DNA isolated from blood was used for 18S ribosomal RNA gene fragment amplification by polymerase chain reaction, which was subject to Sanger sequencing. Although 18S sequence indicated that the Babesia species infecting the patient was similar to that of other Babesia species originating from wild mammals, species identification could not be done. Phylogenetic analysis revealed that the patient-derived pathogen is distinct because it forms a separate clade in the cladogram.
人巴贝斯虫病是一种罕见疾病,由巴贝斯虫属物种引起,通常通过蜱叮咬传播。虽然已知人巴贝斯虫病在免疫功能正常的宿主中无症状,但已报道过脾切除或免疫功能低下个体出现严重巴贝斯虫病的临床病例。据我们所知,此前印度仅报道过一例人巴贝斯虫病病例。在此,我们报告一例30岁无脾农民发生的严重巴贝斯虫病伴高寄生虫血症(约70%)的病例。该患者出现发热、皮肤黄染、少尿和贫血;最终发展为多器官功能衰竭综合征并死亡。制备外周血涂片并通过显微镜检查确认梨形虫的存在。从血液中分离的总DNA用于通过聚合酶链反应扩增18S核糖体RNA基因片段,并进行桑格测序。虽然18S序列表明感染该患者的巴贝斯虫物种与源自野生哺乳动物的其他巴贝斯虫物种相似,但无法进行物种鉴定。系统发育分析显示,源自该患者的病原体是独特的,因为它在系统发育树中形成了一个单独的分支。