Intraspecific Diversity and Pathogenicity of <i>Bacillus thuringiensis</i> Isolates from an Emetic Illness

This study describes an emetic food-borne intoxication associated with a <i>Bacillus cereus</i> 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 il...

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Main Authors: Jintana Pheepakpraw, Thida Kaewkod, Maytiya Konkit, Sasiprapa Krongdang, Kanyaluck Jantakee, Rueankaew Praphruet, Sakunnee Bovonsombut, Aussara Panya, Yingmanee Tragoolpua, Niall A. Logan, Thararat Chitov
Format: Article
Language:English
Published: MDPI AG 2023-01-01
Series:Toxins
Subjects:
Online Access:https://www.mdpi.com/2072-6651/15/2/89
Description
Summary:This study describes an emetic food-borne intoxication associated with a <i>Bacillus cereus</i> 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 <i>Bacillus thuringiensis</i>. According to multilocus sequence typing (MLST) analysis, intraspecific diversity was found within the <i>B. thuringiensis</i> 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 <i>cereulide synthetase</i> (<i>ces</i>) gene cluster. The heat-treated culture supernatants of three emetic <i>B. thuringiensis</i> isolates, FC2, FC7, and FC8, caused vacuolation and exhibited toxicity to Caco-2 cells, with CC<sub>50</sub> 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.
ISSN:2072-6651