School of Biotechnology and Biomolecular Sciences, The University of New South Wales, Sydney, New South Wales, Australia.
PLoS One. 2011;6(12):e29045. doi: 10.1371/journal.pone.0029045. Epub 2011 Dec 14.
Campylobacter concisus has garnered increasing attention due to its association with intestinal disease, thus, the pathogenic potential of strains isolated from different intestinal diseases was investigated. A method to isolate C. concisus was developed and the ability of eight strains from chronic and acute intestinal diseases to adhere to and invade intestinal epithelial cells was determined. Features associated with bacterial invasion were investigated using comparative genomic analyses and the effect of C. concisus on host protein expression was examined using proteomics. Our isolation method from intestinal biopsies resulted in the isolation of three C. concisus strains from children with Crohn's disease or chronic gastroenteritis. Four C. concisus strains from patients with chronic intestinal diseases can attach to and invade host cells using mechanisms such as chemoattraction to mucin, aggregation, flagellum-mediated attachment, "membrane ruffling", cell penetration and damage. C. concisus strains isolated from patients with chronic intestinal diseases have significantly higher invasive potential than those from acute intestinal diseases. Investigation of the cause of this increased pathogenic potential revealed a plasmid to be responsible. 78 and 47 proteins were upregulated and downregulated in cells infected with C. concisus, respectively. Functional analysis of these proteins showed that C. concisus infection regulated processes related to interleukin-12 production, proteasome activation and NF-κB activation. Infection with all eight C. concisus strains resulted in host cells producing high levels of interleukin-12, however, only strains capable of invading host cells resulted in interferon-γ production as confirmed by ELISA. These findings considerably support the emergence of C. concisus as an intestinal pathogen, but more significantly, provide novel insights into the host immune response and an explanation for the heterogeneity observed in the outcome of C. concisus infection. Moreover, response to infection with invasive strains has substantial similarities to that observed in the inflamed mucosa of Crohn's disease patients.
由于与肠道疾病的关联,弯曲菌属(Campylobacter concisus)日益受到关注,因此,研究了从不同肠道疾病中分离的菌株的致病潜力。开发了一种分离 C. concisus 的方法,并确定了来自慢性和急性肠道疾病的 8 株菌对肠上皮细胞的粘附和侵袭能力。使用比较基因组分析研究了与细菌侵袭相关的特征,并使用蛋白质组学研究了 C. concisus 对宿主蛋白表达的影响。我们从肠道活检中分离 C. concisus 的方法导致从克罗恩病或慢性胃肠炎患儿中分离出 3 株 C. concisus。来自慢性肠道疾病患者的 4 株 C. concisus 菌株可以通过化学吸引粘蛋白、聚集、鞭毛介导的附着、“膜皱襞”、细胞穿透和损伤等机制附着和侵入宿主细胞。从慢性肠道疾病患者中分离的 C. concisus 菌株比急性肠道疾病患者的侵袭潜力明显更高。对这种增加的致病潜力的原因进行调查发现,这是由质粒引起的。感染 C. concisus 的细胞中分别有 78 种和 47 种蛋白上调和下调。这些蛋白的功能分析表明,C. concisus 感染调节了与白细胞介素-12 产生、蛋白酶体激活和 NF-κB 激活相关的过程。感染 8 株 C. concisus 菌株均可导致宿主细胞产生高水平的白细胞介素-12,但只有能侵入宿主细胞的菌株才能通过 ELISA 证实产生干扰素-γ。这些发现极大地支持了 C. concisus 作为肠道病原体的出现,但更重要的是,为宿主免疫反应提供了新的见解,并解释了 C. concisus 感染结果的异质性。此外,对侵袭性菌株感染的反应与在克罗恩病患者的炎症黏膜中观察到的反应有很大的相似性。