Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA; Northwestern University, Feinberg School of Medicine, Chicago, IL, USA.
Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.
Anaerobe. 2022 Jun;75:102555. doi: 10.1016/j.anaerobe.2022.102555. Epub 2022 Mar 31.
Previously considered solely an opportunistic pathogen, Clostridium innocuum (CI) was recently reported in Taiwan to be an emerging cause of antibiotic-associated diarrhea and clinically indistinguishable from Clostridioides difficile (CD) infection. We previously identified CI culture supernatant being cross-reactive with commercial CD toxin enzyme immunoassays. We aimed to identify and characterize the cross-reacting protein and determine whether it functioned as a human toxin.
We performed western blots using CI culture supernatants and CD anti-toxin antibodies and identified interacting bands. We identified protein(s) using tandem mass spectrometry and evaluated them by cytotoxicity assays.
CI, but not CD, was isolated from stool of 12 children and adults with diarrhea. Culture supernatant from 6/12 CI isolates, and an ATCC reference strain, tested positive for CD toxins (total 7/13 isolates) by commercial EIA. Using two of these isolates, we identified two ∼40 kDa hypothetical proteins, CI_01447 and CI_01448, and confirmed cross-reactivity with CD anti-toxin antibodies by enzyme immunoassay and Western blot. Whole-genome sequencing confirmed all 13 isolates contained both genes, which were highly conserved. We observed no cytopathic or cytotoxic effects to HeLa cells when treated with these proteins. We identified amino acid sequence similarity to the NlpC/P60 family of proteins.
Our findings do not suggest CI proteins CI_01448 and CI_01447, which cross-react with antibodies against CD toxins A and B, are toxic to HeLa cells. Further studies are needed to determine the function of these cross-reacting proteins and the potential virulence factors that could be responsible for CI diarrheal disease.
先前被认为仅是一种机会性病原体的无丙二酸柠檬酸杆菌(CI)最近在台湾被报道为一种与抗生素相关腹泻的新兴病因,且与艰难梭菌(CD)感染在临床上无法区分。我们先前发现 CI 培养上清液与商业 CD 毒素酶免疫测定法发生交叉反应。我们旨在鉴定和表征发生交叉反应的蛋白,并确定其是否具有作为人类毒素的功能。
我们使用 CI 培养上清液和 CD 抗毒素抗体进行 Western blot 实验,并鉴定相互作用的条带。我们使用串联质谱法鉴定蛋白,并通过细胞毒性测定评估它们。
CI 而非 CD 从 12 例腹泻儿童和成人的粪便中分离出来。来自 6/12 CI 分离株和 ATCC 参考株的培养上清液通过商业 EIA 检测出对 CD 毒素呈阳性(总共 13 个分离株中有 7 个)。使用其中的两个分离株,我们鉴定出两个约 40 kDa 的假设蛋白 CI_01447 和 CI_01448,并通过酶免疫测定和 Western blot 证实与 CD 抗毒素抗体发生交叉反应。全基因组测序证实所有 13 个分离株均含有这两个基因,它们高度保守。当用这些蛋白处理时,我们未观察到对 HeLa 细胞产生细胞病变或细胞毒性作用。我们鉴定出与 NlpC/P60 家族蛋白的氨基酸序列相似性。
我们的研究结果表明,与 CD 毒素 A 和 B 的抗体发生交叉反应的 CI 蛋白 CI_01448 和 CI_01447 对 HeLa 细胞没有毒性。需要进一步的研究来确定这些发生交叉反应的蛋白的功能以及可能导致 CI 腹泻病的潜在毒力因子。