MLST analysis reveals a highly conserved core genome among poultry isolates of Clostridium septicum

• Published in: Anaerobe Vol. 15; no. 3; pp. 99 - 106
• Main Authors: Neumann, Anthony P., Rehberger, Thomas G.
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.06.2009
• Subjects: Animals; Bacterial Typing Techniques; Chickens - microbiology; Clostridium difficile; Clostridium Infections - microbiology; Clostridium Infections - veterinary; Clostridium perfringens; Clostridium septicum; Clostridium septicum - classification; Clostridium septicum - genetics; Clostridium septicum - isolation & purification; Cluster Analysis; DNA Fingerprinting; DNA, Bacterial - chemistry; DNA, Bacterial - genetics; Gangrenous dermatitis; Genotype; Malignant edema; MLST; Molecular Epidemiology; Phylogeny; Poultry; Poultry Diseases - microbiology; Sequence Analysis, DNA; Sequence Homology; Turkeys - microbiology; United States; United States; Malignant edema; Clostridium septicum; Gangrenous dermatitis; MLST; Poultry
• ISSN: 1075-9964; 1095-8274
• DOI: 10.1016/j.anaerobe.2009.01.005

Clostridium septicum is a highly virulent, anaerobic bacterium capable of establishing necrotizing tissue infections and forming heat resistant endospores. Disease is primarily facilitated by secretion of numerous toxic products including a lethal pore-forming cytolysin. Spontaneously occurring clostridial myonecrosis involving C. septicum has recently reemerged as a concern for many poultry producers. However, despite its increasing prevalence, the epidemiology of infection and population structure of C. septicum remains largely unknown. In this study a multilocus sequence typing (MLST) approach was utilized to examine evolutionary relationships within a diverse collection of C. septicum isolates recovered from poultry flocks experiencing episodes of gangrenous dermatitis. The 109 isolates examined represented 42 turkey flocks and 24 different flocks of broiler chickens as well as C. septicum type strain, ATCC 12464. Isolates were recovered predominantly from gangrenous lesions although isolates from livers, gastrointestinal tracts, spleens and blood were included. The loci analyzed were csa, the major lethal toxin produced by C. septicum, and the housekeeping genes gyrA, groEL, dnaK, recA, tpi, ddl, colA and glpK. These loci were included in part because of their previous use in MLST analysis of Clostridium perfringens and Clostridium difficile. Results indicated a high level of conservation present within these housekeeping gene fragments when compared to what has been previously reported for the aforementioned clostridia. Of the 5352 bp of sequence data examined for each isolate, 99.7% (5335/5352) was absolutely conserved among the 109 isolates. Only one of the ten unique sequence types, or allelic profiles, identified among the isolates was recovered from both turkeys and broiler chickens suggesting some host species preference. Phylogenetic analyses identified two unique clusters, or clonal complexes, among these poultry isolates which may have important epidemiological implications for poultry producers in the United States. This work indicates a predominantly clonal population structure for C. septicum although some evidence of recombination was also observed.