Department of Laboratory Medicine, Taoyuan, Taiwan; Department of Medical Biotechnology and Laboratory Science, Taoyuan, Taiwan; Graduate Institute of Biomedical Sciences, Taoyuan, Taiwan.
Department of Internal Medicine, Division of Infectious Diseases, Taoyuan, Taiwan.
Clin Microbiol Infect. 2018 Nov;24(11):1195-1199. doi: 10.1016/j.cmi.2018.02.015. Epub 2018 Feb 17.
Clostridium innocuum can cause extraintestinal infection in patients with underlying diseases. The role of C. innocuum in antibiotic-associated diarrhoea (AAD) remains unknown.
Clinical information of 103 patients from whom C. innocuum was isolated was reviewed. We carried out cellular and animal experiments to examine the pathogenic potential of C. innocuum in AAD.
Eighty-eight per cent (91/103) of the 103 patients received antibiotics within 2 weeks of diarrhoea onset. Patients were further classified into two groups, severe colitis and diarrhoea, according to clinical severity level. The mortality rate was 13.6% (14/103) among the patients from whom C. innocuum was isolated. The lowest concentrations at which 90% of the isolates were inhibited for metronidazole and vancomycin were 0.5 and 16 mg/L, respectively. All isolates tested were susceptible to metronidazole but resistant to vancomycin. Nineteen randomly selected isolates (ten from severe colitis group, nine from diarrhoea group) were subjected to further in vitro cellular examinations. The level of cytotoxicity to Vero cells was significantly higher in isolates from the severe colitis group at both 24 and 48 hours after inoculation (24 and 48 hours, p 0.042 and 0.033, respectively). We observed apoptotic changes that subsequently led to cell death in C. innocuum-infected Vero cells. Tissue damages, necrotic changes and oedema were observed in the mouse ileal loop infected by C. innocuum.
Vancomycin-resistant C. innocuum may play a potential role as a causative agent of AAD. The clinical manifestations of AAD caused by C. innocuum were diarrhoea or severe colitis, including pseudomembranous colitis.
无害梭菌可引起基础疾病患者的肠道外感染。无害梭菌在抗生素相关性腹泻(AAD)中的作用尚不清楚。
回顾了 103 例从患者中分离出无害梭菌的临床资料。我们进行了细胞和动物实验,以研究无害梭菌在 AAD 中的致病潜力。
88%(91/103)的 103 例患者在腹泻发作后 2 周内接受了抗生素治疗。根据临床严重程度,将患者进一步分为严重结肠炎和腹泻两组。从分离出无害梭菌的患者中,死亡率为 13.6%(14/103)。甲硝唑和万古霉素对 90%分离株的最低抑制浓度分别为 0.5 和 16mg/L。所有分离株均对甲硝唑敏感,但对万古霉素耐药。对 19 株随机选择的分离株(严重结肠炎组 10 株,腹泻组 9 株)进行了进一步的体外细胞检测。接种后 24 小时和 48 小时,严重结肠炎组分离株对 Vero 细胞的细胞毒性明显更高(24 小时和 48 小时,p 0.042 和 0.033)。我们观察到感染无害梭菌的 Vero 细胞发生凋亡变化,随后导致细胞死亡。在感染无害梭菌的小鼠回肠袢中观察到组织损伤、坏死变化和水肿。
万古霉素耐药的无害梭菌可能在 AAD 的发病机制中起潜在作用。无害梭菌引起的 AAD 的临床表现为腹泻或严重结肠炎,包括伪膜性结肠炎。