中国存在康氏立克次体感染病灶

Infectious Medicine Pub Date : 2023-12-01 Epub Date: 2023-09-17 DOI:10.1016/j.imj.2023.09.002
Nannan Xu , Hui Liu , Chunmei Qu , Sai Wen , Wenlu Zou , Caiyun Chang , Gang Wang
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引用次数: 0

摘要

中国并不是立克次体的流行区,因此没有常规的临床诊断方法。本研究旨在确定在华东地区被蜱虫叮咬的两名发热患者是否真的感染了康氏立克次体。研究人员使用通用立克次体引物,通过实时荧光定量PCR技术扩增了患者血样中的柠檬酸合成酶基因(gltA)。对阳性样本采用巢式 PCR 扩增外膜蛋白 A 基因(ombA)。通过核酸测序对 PCR 产物进行进一步鉴定和分析。两名患者的 gltA 和 ompA 基因均扩增阳性。两名患者的 ompA 基因核苷酸序列(303 bp)与 GenBank 中的 R. conorii 印度蜱斑疹伤寒菌株具有高度同源性(99%)。针对R. conorii的IgG增加了4倍多,为SFG立克次体感染提供了支持性证据。多西环素治疗后的迅速恢复也支持了立克次氏体感染的病因。华东地区的医生应警惕人类感染立克次体。基于PCR的诊断方法为立克次体病的诊断提供了一种快速、精确的途径,可提高患者的识别和管理水平。
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The presence of foci of Rickettsia conorii infection in China

China is not considered as an endemic area of Rickettsia conorii, so there is no routine clinical way to diagnose this infection. This study aims to determine whether 2 febrile patients who had a tick bite in East China were indeed infected with R. conorii. The citrate synthase gene (gltA) was amplified with universal rickettsial primers by real-time fluorescent PCR from the patients’ blood samples. Nested PCR was used to amplify the outer membrane protein A gene (ompA) for positive specimens. PCR products were further identified and analyzed through nucleic acid sequencing. Positive amplification of the gltA and ompA genes was found in both patients. The nucleotide sequences (303 bp) of the ompA gene of the 2 patients had high homology (99%) with the R. conorii Indian tick typhus strain in GenBank. A more than 4-fold increase in IgG against R. conorii provided supportive evidence of SFG Rickettsia infection. And the rapid recovery after doxycycline treatment also supported a rickettsial cause for the disease. Physicians in East China should be aware of human infections with R. conorii. PCR-based diagnostic methods offer a rapid and precise way to diagnose rickettsiosis, improving patient identification and management.

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