Intraspecific Diversity and Pathogenicity of Bacillus thuringiensis Isolates from an Emetic Illness.
Jintana PheepakprawThida KaewkodMaytiya KonkitSasiprapa KrongdangKanyaluck JantakeeRueankaew PraphruetSakunnee BovonsombutAussara PanyaYingmanee TragoolpuaNiall A LoganThararat ChitovPublished in: Toxins (2023)
This study describes an emetic food-borne intoxication associated with a Bacillus cereus group species and the characterization of the bacterial isolates from the incident in aspects of molecular tying, genetic factors, cytotoxicity, and pathogenic mechanisms relating to emetic illness. Through the polyphasic identification approach, all seven isolates obtained from food and clinical samples were identified as Bacillus thuringiensis . According to multilocus sequence typing (MLST) analysis, intraspecific diversity was found within the B. thuringiensis isolates. Four allelic profiles were found, including two previously known STs (ST8 and ST15) and two new STs (ST2804 and ST2805). All isolates harbored gene fragments located in the cereulide synthetase ( ces ) gene cluster. The heat-treated culture supernatants of three emetic B. thuringiensis isolates, FC2, FC7, and FC8, caused vacuolation and exhibited toxicity to Caco-2 cells, with CC 50 values of 56.57, 72.17, and 79.94 µg/mL, respectively. The flow cytometry with the Annexin V/PI assay revealed both apoptosis and necrosis mechanisms, but necrosis was the prominent mechanism that caused Caco-2 cell destruction by FC2, the most toxic isolate.
Keyphrases
- genetic diversity
- flow cytometry
- cell cycle arrest
- genome wide
- copy number
- induced apoptosis
- oxidative stress
- single cell
- bacillus subtilis
- endoplasmic reticulum stress
- cardiovascular disease
- cell death
- human health
- stem cells
- high throughput
- genome wide identification
- gene expression
- mesenchymal stem cells
- signaling pathway
- cystic fibrosis
- risk assessment
- climate change
- cell proliferation
- biofilm formation