丹麦男性罕见伊丽莎白按蚊脑膜炎病例。

JMM case reports Pub Date : 2018-08-09 eCollection Date: 2018-08-01 DOI:10.1099/jmmcr.0.005163
Hans Linde Nielsen, Irene Harder Tarpgaard, David Fuglsang-Damgaard, Philip Kjettinge Thomsen, Sylvain Brisse, Michael Dalager-Pedersen
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引用次数: 13

摘要

伊莉莎白杆菌(Elizabethkingia anophelis)是一种革兰氏阴性、需氧、非运动的杆菌,属于黄杆菌科。在过去5年中,它已作为一种机会性人类病原体出现,涉及新生儿脑膜炎和败血症以及院内暴发。它已从冈比亚按蚊的中肠中分离出来,但没有证据表明这种蚊子在人类感染中起作用,而且对传播给人类的途径所知甚少。最近主要来自东南亚的研究表明,该属的主要人类病原体是按蚊,而不是伊丽莎白脑膜炎杆菌。然而,由于现有的基质相关激光解吸电离飞行时间质谱(MALDI-TOF MS)系统在正确的物种识别方面的局限性,对物种水平的识别一直很困难。病例介绍:在此,我们报告一例罕见的按蚊脑膜炎病例,患者为丹麦男性,住院前7周曾到马来西亚旅行。从血液和脑脊液中分离出一种多重耐药的elizabeth ethkingia物种,并使用基因组测序来表征该分离物的系统发育位置,确定其与先前描述的亚谱系11相关。患者静脉注射莫西沙星和利福平治疗成功2周,无重大后遗症,但未发现传播源。结论:所有临床微生物学家都应该意识到MALDI-TOF MS系统在正确的物种鉴定方面的局限性,因此我们建议使用基因组测序在物种和亚谱系水平上进行正确的鉴定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Rare <i>Elizabethkingia anophelis</i> meningitis case in a Danish male.

Rare Elizabethkingia anophelis meningitis case in a Danish male.

Introduction: Elizabethkingia anophelis is a Gram-negative, aerobic, non-motile rod belonging to the family Flavobacteriaceae. Over the last 5 years, it has emerged as an opportunistic human pathogen involved in neonatal meningitis and sepsis, as well as nosocomial outbreaks. It has been isolated from the midgut of the Anopheles gambiae mosquito, but there is no evidence for a role of the mosquito in human infections, and very little is known regarding the routes of transmission to humans. Recent studies, primarily from South-East Asia, suggest that E. anophelis, and not Elizabethkingia meningoseptica, is the predominant human pathogen of this genus. However, identification to the species level has been difficult due to the limitations of the current MALDI-TOF MS (matrix-associated laser desorption ionization-time of flight MS) systems for correct species identification.

Case presentation: Here, we present a rare case of E. anophelis meningitis in a Danish male, who had a travel exposure to Malaysia 7 weeks before hospitalization. A multidrug-resistant Elizabethkingia species was isolated from blood and cerebrospinal fluid, and genomic sequencing was used to characterize the phylogenetic position of the isolate, which was determined as associated with previously described sublineage 11. The patient was successfully treated with intravenous moxifloxacin and rifampicin for 2 weeks with no major sequelae, but we did not find the source of transmission.

Conclusion: All clinical microbiologists should be aware of the present limitations of the MALDI-TOF MS systems for correct species identification, and therefore we recommend the use of genome sequencing for the correct identification at the species and sublineage level.

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