Phenotypic characterisation of Clostridium difficile PCR ribotype 251, an emerging multi-locus sequence type clade 2 strain in Australia

Anaerobe ◽  
2019 ◽  
Vol 60 ◽  
pp. 102066 ◽  
Author(s):  
Stacey Hong ◽  
Daniel R. Knight ◽  
Barbara Chang ◽  
Robert J. Carman ◽  
Thomas V. Riley
2010 ◽  
Vol 59 (5) ◽  
pp. 556-562 ◽  
Author(s):  
Haru Kato ◽  
Hideaki Kato ◽  
Yoichiro Ito ◽  
Takayuki Akahane ◽  
Sayuri Izumida ◽  
...  

A typing system for Clostridium difficile using sequencing of the surface-layer protein A encoding gene (slpA) was evaluated and used to analyse clinical isolates in Japan. A total of 160 stool specimens from symptomatic patients in Japan was examined and 87 C. difficile isolates were recovered. slpA sequence typing was found to have reliable typability and discriminatory power in comparison with PCR ribotyping, and the typing results were highly reproducible and comparable. slpA sequence typing was used to type C. difficile in DNA extracted directly from stool specimens. Among the 90 stool specimens in which direct typing results were obtained, 77 specimens were positive for C. difficile culture, and typing results from isolated strains agreed with those from direct typing in all 77 specimens. The slpA sequence type smz was dominant at all four hospitals examined, and this endemic type was detected by culture and/or direct typing in 61 (62 %) of 99 stool specimens positive for toxic culture and/or direct slpA sequence typing. Comparison of epidemic strains reported throughout the world revealed one isolate identified as slpA sequence type gc8, which was found to correspond to PCR ribotype 027 (BI/NAP1/027), whereas no isolates were found with the slpA gene identical to that of PCR ribotype 078 strain. slpA sequence typing is valuable for comparison of C. difficile strains epidemic in diverse areas because the typing results are reproducible and can easily be shared. In addition, slpA sequence typing could be applied to direct typing without culture.


mBio ◽  
2019 ◽  
Vol 10 (2) ◽  
Author(s):  
Daniel R. Knight ◽  
Brian Kullin ◽  
Grace O. Androga ◽  
Frederic Barbut ◽  
Catherine Eckert ◽  
...  

ABSTRACTClostridioides difficile(Clostridium difficile) sequence type 11 (ST11) is well established in production animal populations worldwide and contributes considerably to the global burden ofC. difficileinfection (CDI) in humans. Increasing evidence of shared ancestry and genetic overlap of PCR ribotype 078 (RT078), the most common ST11 sublineage, between human and animal populations suggests that CDI may be a zoonosis. We performed whole-genome sequencing (WGS) on a collection of 207 ST11 and closely related ST258 isolates of human and veterinary/environmental origin, comprising 16 RTs collected from Australia, Asia, Europe, and North America. Core genome single nucleotide variant (SNV) analysis identified multiple intraspecies and interspecies clonal groups (isolates separated by ≤2 core genome SNVs) in all the major RT sublineages: 078, 126, 127, 033, and 288. Clonal groups comprised isolates spread across different states, countries, and continents, indicative of reciprocal long-range dissemination and possible zoonotic/anthroponotic transmission. Antimicrobial resistance genotypes and phenotypes varied across host species, geographic regions, and RTs and included macrolide/lincosamide resistance (Tn6194[ermB]), tetracycline resistance (Tn6190[tetM] and Tn6164[tet44]), and fluoroquinolone resistance (gyrA/Bmutations), as well as numerous aminoglycoside resistance cassettes. The population was defined by a large “open” pan-genome (10,378 genes), a remarkably small core genome of 2,058 genes (only 19.8% of the gene pool), and an accessory genome containing a large and diverse collection of important prophages of theSiphoviridaeandMyoviridae. This study provides novel insights into strain relatedness and genetic variability ofC. difficileST11, a lineage of global One Health importance.IMPORTANCEHistorically,Clostridioides difficile(Clostridium difficile) has been associated with life-threatening diarrhea in hospitalized patients. Increasing rates ofC. difficileinfection (CDI) in the community suggest exposure toC. difficilereservoirs outside the hospital, including animals, the environment, or food.C. difficilesequence type 11 (ST11) is known to infect/colonize livestock worldwide and comprises multiple ribotypes, many of which cause disease in humans, suggesting CDI may be a zoonosis. Using high-resolution genomics, we investigated the evolution and zoonotic potential of ST11 and a new closely related ST258 lineage sourced from diverse origins. We found multiple intra- and interspecies clonal transmission events in all ribotype sublineages. Clones were spread across multiple continents, often without any health care association, indicative of zoonotic/anthroponotic long-range dissemination in the community. ST11 possesses a massive pan-genome and numerous clinically important antimicrobial resistance elements and prophages, which likely contribute to the success of this globally disseminated lineage of One Health importance.


2019 ◽  
Vol 309 (5) ◽  
pp. 270-273 ◽  
Author(s):  
Huiluo Cao ◽  
Sally Cheuk-Ying Wong ◽  
Wing-Cheong Yam ◽  
Melissa Chun-Jiao Liu ◽  
Kin-Hung Chow ◽  
...  

2016 ◽  
Vol 37 (6) ◽  
pp. 680-684
Author(s):  
Geraldine Moloney ◽  
Micheál Mac Aogáin ◽  
Maureen Kelleghan ◽  
Brian O’Connell ◽  
Caroline Hurley ◽  
...  

OBJECTIVETo use next-generation sequencing (NGS) analysis to enhance epidemiological information to identify and resolve a Clostridium difficile outbreak and to evaluate its effectiveness beyond the capacity of current standard PCR ribotyping.METHODSNGS analysis was performed as part of prospective surveillance of all detected C. difficile isolates at a university hospital. An outbreak of a novel C. difficile sequence type (ST)-295 was identified in a hospital and a community hostel for homeless adults. Phylogenetic analysis was performed of all ST-295 and closest ST-2 isolates. Epidemiological details were obtained from hospital records and the public health review of the community hostel.RESULTSWe identified 7 patients with C. difficile ST-295 infections between June 2013 and April 2015. Of these patients, 3 had nosocomial exposure to this infection and 3 had possible hostel exposure. Current Society for Healthcare Epidemiology of America (SHEA)— Infectious Diseases Society of America (IDSA) surveillance definitions (2010) were considered in light of our NGS findings. The initial transmission was not detectable using current criteria, because of 16 weeks between ST-295 exposure and symptoms. We included 3 patients with hostel exposure who met surveillance criteria of hospital-acquired infection due to their hospital admissions.CONCLUSIONNGS analysis enhanced epidemiological information and helped identify and resolve an outbreak beyond the capacity of standard PCR ribotyping. In this cluster of cases, NGS was used to identify a hostel as the likely source of community-based C. difficile transmission.Infect Control Hosp Epidemiol 2016;37:680–684


2016 ◽  
Vol 4 (5) ◽  
Author(s):  
E. Riccobono ◽  
V. Di Pilato ◽  
N. Della Malva ◽  
S. Meini ◽  
F. Ciraolo ◽  
...  

Clostridium difficile , belonging to ribotype 018 (RT018), is one of the most prevalent genotypes circulating in hospital settings in Italy. Here, we report the draft genome of C. difficile CD8-15 belonging to RT018, isolated from a patient with fatal C. difficile -associated infection.


2010 ◽  
Vol 44 (4) ◽  
pp. 13
Author(s):  
SHARON WORCESTER

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