Fukumoto Tatsuya, Matsuo Junji, Okubo Torahiko, Nakamura Shinji, Miyamoto Kentaro, Oka Kentaro, Takahashi Motomichi, Akizawa Kouji, Shibuya Hitoshi, Shimizu Chikara, Yamaguchi Hiroyuki
Hokkaido University Hospital, Nishi-5 Kita-14 Jo, Kita-ku, Sapporo, Hokkaido, 060-8648, Japan.
Department of Medical Laboratory Science, Faculty of Health Sciences, Hokkaido University Graduate School of Health Sciences, Nishi-5 Kita-12 Jo, Kita-ku, Sapporo, Hokkaido, 060-0812, Japan.
BMC Microbiol. 2016 Dec 15;16(1):292. doi: 10.1186/s12866-016-0906-1.
Environmental chlamydiae belonging to the Parachlamydiaceae are obligate intracellular bacteria that infect Acanthamoeba, a free-living amoeba, and are a risk for hospital-acquired pneumonia. However, whether amoebae harboring environmental chlamydiae actually survive in hospital environments is unknown. We therefore isolated living amoebae with symbiotic chlamydiae from hospital environments.
One hundred smear samples were collected from Hokkaido University Hospital, Sapporo, Japan; 50 in winter (February to March, 2012) and 50 in summer (August, 2012), and used for the study. Acanthamoebae were isolated from the smear samples, and endosymbiotic chlamydial traits were assessed by infectivity, cytokine induction, and draft genomic analysis. From these, 23 amoebae were enriched on agar plates spread with heat-killed Escherichia coli. Amoeba prevalence was greater in the summer-collected samples (15/30, 50%) than those of the winter season (8/30, 26.7%), possibly indicating a seasonal variation (p = 0.096). Morphological assessment of cysts revealed 21 amoebae (21/23, 91%) to be Acanthamoeba, and cultures in PYG medium were established for 11 of these amoebae. Three amoebae contained environmental chlamydiae; however, only one amoeba (Acanthamoeba T4) with an environmental chlamydia (Protochlamydia W-9) was shown the infectious ability to Acanthamoeba C3 (reference amoebae). While Protochlamydia W-9 could infect C3 amoeba, it failed to replicate in immortal human epithelial, although exposure of HEp-2 cells to living bacteria induced the proinflammatory cytokine, IL-8. Comparative genome analysis with KEGG revealed similar genomic features compared with other Protochlamydia genomes (UWE25 and R18), except for a lack of genes encoding the type IV secretion system. Interestingly, resistance genes associated with several antibiotics and toxic compounds were identified.
These findings are the first demonstration of the distribution in a hospital of a living Acanthamoeba carrying an endosymbiotic chlamydial pathogen.
属于副衣原体科的环境衣原体是专性细胞内细菌,可感染自由生活的阿米巴原虫棘阿米巴,是医院获得性肺炎的一个危险因素。然而,携带环境衣原体的阿米巴原虫是否真的能在医院环境中存活尚不清楚。因此,我们从医院环境中分离出了带有共生衣原体的活阿米巴原虫。
从日本北海道大学医院收集了100份涂片样本;冬季(2012年2月至3月)50份,夏季(2012年8月)50份,并用于该研究。从涂片样本中分离出棘阿米巴原虫,并通过感染性、细胞因子诱导和基因组草图分析评估内共生衣原体特征。其中,23株阿米巴原虫在涂布有热灭活大肠杆菌的琼脂平板上富集。夏季采集样本中的阿米巴原虫患病率(15/30,50%)高于冬季(8/30,26.7%),这可能表明存在季节性差异(p = 0.096)。对囊肿的形态学评估显示,21株阿米巴原虫(21/23,91%)为棘阿米巴原虫,并为其中11株在PYG培养基中建立了培养物。3株阿米巴原虫含有环境衣原体;然而,只有1株带有环境衣原体(原衣原体W-9)的阿米巴原虫(棘阿米巴原虫T4)对棘阿米巴原虫C3(参照阿米巴原虫)显示出感染能力。虽然原衣原体W-9可感染C3阿米巴原虫,但它在永生的人上皮细胞中无法复制,尽管将HEp-2细胞暴露于活细菌可诱导促炎细胞因子IL-8。与KEGG的比较基因组分析显示,与其他原衣原体基因组(UWE25和R18)相比,其基因组特征相似,但缺乏编码IV型分泌系统的基因。有趣的是,鉴定出了与几种抗生素和有毒化合物相关的抗性基因。
这些发现首次证明了携带内共生衣原体病原体的活棘阿米巴原虫在医院中的分布情况。