Intra-species diversity of Clostridium perfringens: A diverse genetic repertoire reveals its pathogenic potential

被引:18
作者
Camargo, Anny [1 ,2 ]
Guerrero-Araya, Enzo [3 ]
Castaneda, Sergio [1 ]
Vega, Laura [1 ]
Cardenas-Alvarez, Maria X. [1 ,4 ]
Rodriguez, Cesar [5 ]
Paredes-Sabja, Daniel [3 ,6 ]
David Ramirez, Juan [1 ,7 ]
Munoz, Marina [1 ,3 ]
机构
[1] Univ Rosario, Fac Ciencias Nat, Ctr Invest Microbiol & Biotecnol UR CIMBIUR, Bogota, Colombia
[2] Univ Boyaca, Fac Hlth Sci, Tunja, Colombia
[3] ANID, Millennium Sci Initiat Program, Millennium Nucleus Biol Intestinal Microbiota, Santiago, Chile
[4] Univ N Carolina, Dept Pharmacol, Chapel Hill, NC 27515 USA
[5] Univ Costa Rica, Fac Microbiol, Ctr Invest Enfermedades Trop, Lab Invest Bacteriol Anaerobia, San Jose, Costa Rica
[6] Texas A&M Univ, Dept Biol, College Stn, TX 77843 USA
[7] Icahn Sch Med Mt Sinai, Dept Pathol Mol & Cell Based Med, Mol Microbiol Lab, New York, NY 10029 USA
关键词
Clostridium perfringens; intra-species diversity; multilocus sequence typing; genomic epidemiology; toxinotypes; EPSILON-TOXIN; ANTIMICROBIAL RESISTANCE; ANTIBIOTIC-RESISTANCE; ALPHA-TOXIN; SEQUENCE; VIRULENCE; GENOMICS; SHEEP; PREVALENCE; ENTERITIS;
D O I
10.3389/fmicb.2022.952081
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Clostridium perfringens is the causative agent of many enterotoxic diseases in humans and animals, and it is present in diverse environments (soil, food, sewage, and water). Multilocus Sequence Typing (MLST) and Whole Genome Sequencing (WGS) have provided a general approach about genetic diversity of C. perfringens; however, those studies are limited to specific locations and often include a reduced number of genomes. In this study, 372 C. perfringens genomes from multiple locations and sources were used to assess the genetic diversity and phylogenetic relatedness of this pathogen. In silico MLST was used for typing the isolates, and the resulting sequence types (ST) were assigned to clonal complexes (CC) based on allelic profiles that differ from its founder by up to double-locus variants. A pangenome analysis was conducted, and a core genome-based phylogenetic tree was created to define phylogenetic groups. Additionally, key virulence factors, toxinotypes, and antibiotic resistance genes were identified using ABRicate against Virulence Factor Database (VFDB), TOXiper, and Resfinder, respectively. The majority of the C. perfringens genomes found in publicly available databases were derived from food (n = 85) and bird (n = 85) isolates. A total of 195 STs, some of them shared between sources such as food and human, horses and dogs, and environment and birds, were grouped in 25 CC and distributed along five phylogenetic groups. Fifty-three percent of the genomes were allocated to toxinotype A, followed by F (32%) and G (7%). The most frequently found virulence factors based on > 70% coverage and 99.95% identity were plc (100%), nanH (99%), ccp (99%), and colA (98%), which encode an alpha-toxin, a sialidase, an alpha-clostripain, and a collagenase, respectively, while tetA (39.5%) and tetB (36.2%), which mediate tetracycline resistance determinants, were the most common antibiotic resistance genes detected. The analyses conducted here showed a better view of the presence of this pathogen across several host species. They also confirm that the genetic diversity of C. perfringens is based on a large number of virulence factors that vary among phylogroups, and antibiotic resistance markers, especially to tetracyclines, aminoglycosides, and macrolides. Those characteristics highlight the importance of C. perfringens as a one of the most common causes of foodborne illness.
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