一种新的类芽孢杆菌香港类芽孢杆菌引起的嗜中性粒细胞减少热患者的假菌血症。

J L L Teng, P C Y Woo, K W Leung, S K P Lau, M K M Wong, K Y Yuen
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引用次数: 44

摘要

目的:从一名患有中性粒细胞减少热和假菌血症的9岁中国男孩的血培养中分离出一株革兰氏阴性需氧直或微弯杆状菌(HKU3)。方法:采用常规生化试验、扫描电镜和透射电镜等标准生化方法对分离物进行表型研究。采用聚合酶链反应(PCR)扩增该细菌的16S rRNA基因并测序。将PCR产物序列与Genbank中已知的16S rRNA基因序列进行多序列比对。采用热变性法测定G + C含量。采用PileUp方法构建了系统发育树。结果:该菌株的细胞呈好氧、产孢、革兰氏阴性的直棒状或微弯棒状。在37℃环境空气中培养24小时后,细菌在马血琼脂上生长为直径1毫米的非溶血性灰色菌落。在5% CO(2)中未见生长增强。孵育72小时后,它在50℃下生长为针尖菌落,但在65℃或麦康基琼脂上不能生长。它是静止的。它产生过氧化氢酶(弱阳性)和细胞色素氧化酶。它还原硝酸盐,产生-半乳糖苷酶,水解胰蛋白酶,利用乙酸钠。这种细菌的扫描电子显微照片显示出笔直或略微弯曲的杆状物。细菌细胞壁的透射电子显微照片显示有多个电子致密层,包括外膜、中间层和内细胞质膜,与其革兰氏涂片外观相符。16S rRNA基因测序结果显示,该菌的16S rRNA基因序列与macerans Paenibacillus、borealis Paenibacillus、ehimensis Bacillus和Paenibacillus olymyticus分别有7.7%、8.0%、8.2%和8.6%的差异。细菌中G + C的平均(SD)含量为47.6 (2.1)mol%。在系统发育上,它属于芽孢杆菌属(以前称为3群芽孢杆菌)。结论:一种表现出表型和基因型特征的细菌与密切相关的芽孢杆菌成员非常不同,是中性粒细胞减少热患者假菌血症的原因。提出了一个新种——香港芽孢杆菌,其类型菌株为HKU3。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pseudobacteraemia in a patient with neutropenic fever caused by a novel paenibacillus species: Paenibacillus hongkongensis sp. nov.

Aims: To characterise a strain of Gram negative aerobic straight or slightly curved rods (HKU3) isolated from the blood culture of a 9 year old Chinese boy with neutropenic fever and pseudobacteraemia.

Methods: The isolate was phenotypically investigated by standard biochemical methods using conventional biochemical tests, scanning electron microscopy, and transmission electron microscopy. Genotypically, the 16S rRNA gene of the bacterium was amplified by the polymerase chain reaction (PCR) and sequenced. The sequence of the PCR product was compared with known 16S rRNA gene sequences in the Genbank by multiple sequence alignment. The G + C content was determined by thermal denaturation. A phylogenetic tree was constructed by the PileUp method.

Results: The cells of the bacterial strain were aerobic, sporulating, Gram negative straight or slight curved rods. The bacterium grew on horse blood agar as non-haemolytic, grey colonies of 1 mm in diameter after 24 hours of incubation at 37 degrees C in ambient air. No enhancement of growth was seen in 5% CO(2). It grew at 50 degrees C as pinpoint colonies after 72 hours of incubation, but did not grow at 65 degrees C or on MacConkey agar. It was non-motile. It produced catalase (weakly positive) and cytochrome oxidase. It reduced nitrate, produced beta galactosidase, hydrolysed esculin, and utilised sodium acetate. A scanning electron micrograph of the bacterium showed straight or slightly curved rods. A transmission electron micrograph of the cell wall of the bacterium revealed multiple electron dense layers, including the outer membrane, middle murein layer, and inner cytoplasmic membrane, compatible with its Gram smear appearance. 16S rRNA gene sequencing showed that there were 7.7%, 8.0%, 8.2%, and 8.6% differences between the 16S rRNA gene sequence of the bacterium and those of Paenibacillus macerans, Paenibacillus borealis, Bacillus ehimensis, and Paenibacillus amylolyticus, respectively. The mean (SD) G + C content of the bacterium was 47.6 (2.1) mol%. Phylogenetically, it belongs to the genus paenibacillus (previously called group 3 bacillus).

Conclusions: A bacterium that exhibited phenotypic and genotypic characteristics that are very different from closely related members of paenibacillus was the cause of pseudobacteraemia in a patient with neutropenic fever. A new species, Paenibacillus hongkongensis sp. nov. is proposed, for which HKU3 is the type strain.

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