A series of three cases of severe Clostridium difficile infection in Australia associated with a binary toxin producing clade 2 ribotype 251 strain. (February 2019)

• Record Type: Journal Article
• Authors: Wehrhahn, Michael C.; Keighley, Caitlin; Kurtovic, Jelica; Knight, Daniel R.; Hong, Stacey; Hutton, Melanie L.; Lyras, Dena; Wang, Qinning; Leong, Rupert; Borody, Tom; Edye, Michael; Riley, Thomas V.
• Is Part Of: Anaerobe. Volume 55(2019)
• Page Start: 117
• Page End: 123
• Publication Date: 2019-02
• Subjects: Clostridium difficile -- Ribotype 251 -- Severe infection -- Fatal infection; Anaerobic infections -- Periodicals; Anaerobic bacteria -- Periodicals; Bacterial diseases -- Periodicals; Computer network resources; Anaerobic protozoa -- Periodicals; 579.3
• DOI: 10.1016/j.anaerobe.2018.11.009
• Languages: English
• ISSNs: 1075-9964

Abstract

Abstract: Three patients with severe Clostridium difficile infection (CDI) caused by an unusual strain of C. difficile, PCR ribotype (RT) 251, were identified in New South Wales, Australia. All cases presented with severe diarrhoea, two had multiple recurrences and one died following a colectomy. C. difficile RT251 strains were isolated by toxigenic culture. Genetic characterisation was performed using techniques including toxin gene profiling, PCR ribotyping, whole genome sequencing (WGS), in-silico multi-locus-sequence-typing (MLST) and core-genome single nucleotide variant (SNV) analyses. Antimicrobial susceptibility was determined using an agar incorporation method. In vitro toxin production was confirmed by Vero cell cytotoxicity assay and pathogenicity was assessed in a murine model of CDI. All RT251 isolates contained toxin A ( tcdA ), toxin B ( tcdB ) and binary toxin ( cdtA and cdtB ) genes. Core-genome analyses revealed the RT251 strains were clonal, with 0–5 SNVs between isolates. WGS and MLST clustered RT251 in the same evolutionary clade (clade 2) as RT027. Despite comparatively lower levels of in vitro toxin production, in the murine model RT251 infection resembled RT027 infection. Mice showed marked weight loss, severe disease within 48 h post-infection and death. All isolates were susceptible to metronidazole and vancomycin. Our observations suggest C. difficile RT251 causes severe disease and emphasise the importance of ongoing surveillance for new and emerging strains of C. difficile with enhanced virulence. Highlights: Three cases of severe Clostridium difficile infection caused by Ribotype 251. Mouse model confirms RT251 causes a rapidly fatal disease comparable to RT027. RT251 belongs to the same evolutionary clade as RT027. Arrival of RT251 in Australia possibly through imported food products.