Lin Baoquan, Zhong Dan, Qin Lu, Liu Qianqian, Wu Liya, Wang Bo, Wang Kuliang, Lu Xianfu, Deng Shan, Pan Liya
Department of Neurology, The Fourth Affiliated Hospital of Guangxi Medical University, Liuzhou, China.
Front Med (Lausanne). 2025 Aug 26;12:1639262. doi: 10.3389/fmed.2025.1639262. eCollection 2025.
Rabies is an acute zoonotic infectious disease caused by infection with a virus of the genus Lyssavirus. We report a case of paralytic rabies with a stroke-like onset, which was diagnosed using metagenomics next-generation sequencing (mNGS).
A 58-year-old man was admitted to the hospital with "numbness and weakness in the right upper extremity for 2 days, aggravated for 1 day." Twenty-five days before his admission, the patient was bitten on the back of right hand by an unvaccinated domestic dog, resulting in a penetrating injury, classified as grade III according to the rabies exposure classification method. Following admission, the patient exhibited rapidly progressive stroke symptoms, and on the second day, he suffered a sudden respiratory arrest accompanied by a weakened heartbeat and a decreased heart rate. He was treated with emergency tracheal intubation, cardiopulmonary resuscitation, and dehydration to lower cranial pressure.
The patient's condition deteriorated rapidly after admission. A lumbar puncture was conducted on the morning of the second day of admission, and cerebrospinal fluid (CSF) was sent to Weiyuan Genetic Laboratories (Guangzhou, China) for rabies virus identification. The patient died on the third day of admission. Pathogen capture macro-genomics was performed on CSF using an Illumina NextSeq second-generation sequencer, and nine rabies virus sequences, which shared more than 99% nucleotide homology with the genome sequence of the rabies virus Rabies lyssavirus (NCBI accession no. MN175989.1), were detected. The Q30 ratio of this test was 98.3%.
Compared to polymerase chain reaction (PCR) and direct fluorescent antibody (DFA) test, mNGS shortens the diagnostic window and improves sensitivity to low-virus or seronegative manifestations by simultaneously capturing and sequencing the entire pathogen genome. The mNGS technology can effectively aid in the diagnosis of paralytic rabies.
狂犬病是由狂犬病病毒属病毒感染引起的一种急性人畜共患传染病。我们报告一例以类似中风起病的麻痹型狂犬病病例,该病例通过宏基因组学下一代测序(mNGS)得以确诊。
一名58岁男性因“右上肢麻木无力2天,加重1天”入院。入院前25天,患者右手背被一只未接种疫苗的家犬咬伤,造成穿透伤,根据狂犬病暴露分级方法分类为III级。入院后,患者迅速出现进行性中风症状,第二天突然呼吸骤停,伴有心跳减弱和心率下降。对其进行了紧急气管插管、心肺复苏及脱水降颅压治疗。
患者入院后病情迅速恶化。入院第二天上午进行了腰椎穿刺,脑脊液(CSF)被送至广州微远基因实验室进行狂犬病病毒鉴定。患者于入院第三天死亡。使用Illumina NextSeq二代测序仪对脑脊液进行病原体捕获宏基因组学检测,检测到9条狂犬病病毒序列,这些序列与狂犬病病毒狂犬病病毒属(NCBI登录号:MN175989.1)的基因组序列核苷酸同源性超过99%。该检测的Q30比例为98.3%。
与聚合酶链反应(PCR)和直接荧光抗体(DFA)检测相比,mNGS通过同时捕获和测序整个病原体基因组,缩短了诊断窗口,提高了对低病毒或血清阴性表现的敏感性。mNGS技术可有效辅助麻痹型狂犬病的诊断。