Laboratory Diagnosis and Molecular Epidemiological Characterization of the First Imported Case of Lassa Fever in China.

Yu Liang Feng, Wei Li, Ming Feng Jiang, Hong Rong Zhong, Wei Wu, Lyu Bo Tian, Guo Chen, Zhen Hua Chen, Can Luo, Rong Mei Yuan, Xing Yu Zhou, Jian Dong Li, Xiao Rong Yang, Ming Pan
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Abstract

Objective: This study reports the first imported case of Lassa fever (LF) in China. Laboratory detection and molecular epidemiological analysis of the Lassa virus (LASV) from this case offer valuable insights for the prevention and control of LF.

Methods: Samples of cerebrospinal fluid (CSF), blood, urine, saliva, and environmental materials were collected from the patient and their close contacts for LASV nucleotide detection. Whole-genome sequencing was performed on positive samples to analyze the genetic characteristics of the virus.

Results: LASV was detected in the patient's CSF, blood, and urine, while all samples from close contacts and the environment tested negative. The virus belongs to the lineage IV strain and shares the highest homology with strains from Sierra Leone. The variability in the glycoprotein complex (GPC) among different strains ranged from 3.9% to 15.1%, higher than previously reported for the seven known lineages. Amino acid mutation analysis revealed multiple mutations within the GPC immunogenic epitopes, increasing strain diversity and potentially impacting immune response.

Conclusion: The case was confirmed through nucleotide detection, with no evidence of secondary transmission or viral spread. The LASV strain identified belongs to lineage IV, with broader GPC variability than previously reported. Mutations in the immune-related sites of GPC may affect immune responses, necessitating heightened vigilance regarding the virus.

中国首例输入性拉沙热的实验室诊断和分子流行病学特征
目的:报告中国首例输入性拉沙热病例。本病例拉沙病毒的实验室检测和分子流行病学分析为预防和控制LF提供了有价值的见解。方法:采集患者及其密切接触者脑脊液、血液、尿液、唾液及环境资料进行LASV核苷酸检测。对阳性样本进行全基因组测序,分析病毒的遗传特征。结果:在患者脑脊液、血液和尿液中检测到LASV,密切接触者和环境样本均为阴性。该病毒属于谱系IV株,与来自塞拉利昂的毒株具有最高的同源性。糖蛋白复合物(GPC)在不同菌株之间的变异范围为3.9%至15.1%,高于先前报道的7个已知谱系。氨基酸突变分析显示,GPC免疫原性表位存在多个突变,增加了菌株多样性并可能影响免疫反应。结论:该病例经核酸检测证实,无二次传播和病毒传播证据。所鉴定的LASV毒株属于谱系IV,其GPC变异性比先前报道的更广泛。GPC免疫相关位点的突变可能影响免疫反应,因此需要提高对该病毒的警惕。
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