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首页> 外文期刊>BMC Infectious Diseases >Case report: whole genome sequencing based investigation of maternal-neonatal listeriosis in Sichuan, China
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Case report: whole genome sequencing based investigation of maternal-neonatal listeriosis in Sichuan, China

机译:病例报告:基于全基因组测序的中国四川母婴李斯特菌病调查

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Neonatal listeriosis is a rare but severe disease manifesting as septicemia and central nervous system (CNS) infections with a high fatality rate of around 20 to 30%. Whole genome sequencing (WGS) is a promising technique for pathogen identification and infection source tracing with its high resolution. A case of neonatal sepsis with listeriosis was reported with positive blood culture for Listeria monocytogenes. The case was investigated to confirm the vertical transmission of the infection and identify the potential food source of the maternal L. monocytogenes infection using WGS. L. monocytogenes was isolated from the neonate’s blood sample the day after caesarean delivery and from the mother’s genital and pudenda swab samples 5?days and 13?days after caesarean delivery. WGS showed that the isolate from the neonate was identical to the genome type of the isolates from the mother, with only one of the 4 isolates from the mother differing by one single nucleotide polymorphism (SNP). By WGS, one L. monocytogenes isolate from a ready-to-eat (RTE) meat sample in the patients’ community market shared the same sequence type but was ruled out as the cause of infection, with 57 SNP differences to the strain causing the maternal-neonatal infection. The food isolate also carried a novel plasmid pLM1686 that harbored heavy metal resistance genes. After caesarean section, the mother was treated with a third generation cephalosporin which L. monocytogenes is naturally resistant to, which may explain why genital and pudenda swabs were still culture-positive for L. monocytogenes 13?days after delivery. Genital swab culture for L. monocytogenes had been informative in the diagnosis of maternal listeriosis in this case. The high resolution of WGS confirmed the maternal-neonatal transmission of L. monocytogenes infection and ruled out the L. monocytogenes contaminated RTE meat from the local market as the direct source of the mother’s infection.
机译:新生儿李斯特菌病是一种罕见但严重的疾病,表现为败血病和中枢神经系统(CNS)感染,死亡率很高,约为20%至30%。全基因组测序(WGS)具有高分辨率,是一种有前途的病原体鉴定和感染源追踪技术。报道了一例新生儿李斯特氏菌败血症,血液培养中出现单核细胞增生性李斯特菌。对该病例进行了调查,以确认感染的垂直传播,并使用WGS来确定产妇单核细胞增生李斯特菌感染的潜在食物来源。剖腹产后第二天从新生儿的血液样本中分离出单核细胞增生李斯特氏菌,剖腹产后5天和13天从母亲的生殖器和pudenda拭子样本中分离出单核细胞增生李斯特菌。 WGS显示,来自新生儿的分离株与来自母亲的分离株的基因组类型相同,来自母亲的4个分离株中只有一个具有一个单核苷酸多态性(SNP)。通过WGS,在患者社区市场上从即食(RTE)肉样品中分离出的一种单核细胞增生李斯特菌具有相同的序列类型,但被排除为感染的原因,与导致该病的菌株的SNP差异为57产妇-新生儿感染。该食品分离株还携带了带有重金属抗性基因的新型质粒pLM1686。剖腹产后,母亲接受了单核细胞增生李斯特菌天然抗性的第三代头孢菌素治疗,这可能解释了为什么生殖器和普登达拭子在分娩后13天仍对单核细胞增生李斯特菌培养阳性。在这种情况下,针对单核细胞增生李斯特菌的拭子培养对诊断母亲李斯特菌病具有重要意义。 WGS的高分辨率证实了单核细胞增生李斯特氏菌感染的母婴传播,并排除了当地市场上被单核细胞增生李斯特氏菌污染的RTE肉作为母亲感染的直接来源。

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