Literature DB >> 22194351

Haemolysin E- and enterohaemolysin-derived haemolytic activity of O55/O157 strains and other Escherichia coli lineages.

Kazunori Murase1, Tadasuke Ooka, Atsushi Iguchi, Yoshitoshi Ogura, Keisuke Nakayama, Md Asadulghani, Md Rakibul Islam, Hirotaka Hiyoshi, Toshio Kodama, Lothar Beutin, Tetsuya Hayashi.   

Abstract

Among three haemolysins identified thus far in Escherichia coli, alpha-haemolysin (HlyA) is encoded on the pathogenicity islands of extraintestinal pathogenic strains, while enterohaemolysin (EhxA) is encoded on the virulence plasmids of enterohaemorrhagic E. coli (EHEC) strains. In contrast, the gene for haemolysin E (HlyE) is located on the E. coli chromosome backbone and is therefore widely distributed among E. coli strains. However, because hlyE gene expression is repressed by the H-NS protein and because the gene has been disrupted in many strains, its haemolytic activity cannot be detected in wild-type strains by routine screening on blood agar plates. In this study, we found that the HlyE-derived haemolytic activity of enteropathogenic E. coli (EPEC) O55 : H7 can be detected after anaerobic cultivation on a washed blood agar plate (EHX plate) that is used to detect the production of EhxA. We also found that the haemolytic activity of EHEC O157 : H7 observed on EHX plates under aerobic and anaerobic growth conditions is derived from EhxA and HlyE, respectively; this differential expression of the two haemolysins occurs at the transcriptional level. Our analysis of 60 E. coli strains of various pathotypes and phylogenies for their repertoires of haemolysin genes, haemolytic phenotypes and hlyE gene sequences revealed that HlyE activity can generally be detected on EHX plates under anaerobic growth conditions if the gene is intact. Furthermore, our results indicate that hlyE gene inactivation occurred in three of the five E. coli lineages (phylogroups A, B1 and B2), which demonstrates phylogroup-specific gene disruption patterns.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 22194351     DOI: 10.1099/mic.0.054775-0

Source DB:  PubMed          Journal:  Microbiology        ISSN: 1350-0872            Impact factor:   2.777


  7 in total

1.  Dual role of CsrA in regulating the hemolytic activity of Escherichia coli O157:H7.

Authors:  Zhibin Sun; Ning Zhou; Wenting Zhang; Yan Xu; Yu-Feng Yao
Journal:  Virulence       Date:  2022-12       Impact factor: 5.428

2.  An Environmental Shiga Toxin-Producing Escherichia coli O145 Clonal Population Exhibits High-Level Phenotypic Variation That Includes Virulence Traits.

Authors:  Michelle Qiu Carter; Beatriz Quinones; Xiaohua He; Wayne Zhong; Jacqueline W Louie; Bertram G Lee; Jaszemyn C Yambao; Robert E Mandrell; Michael B Cooley
Journal:  Appl Environ Microbiol       Date:  2015-12-04       Impact factor: 4.792

3.  Prevalence of hemolysin genes and comparison of ehxA subtype patterns in Shiga toxin-producing Escherichia coli (STEC) and non-STEC strains from clinical, food, and animal sources.

Authors:  Sandra C Lorenz; Insook Son; Anna Maounounen-Laasri; Andrew Lin; Markus Fischer; Julie A Kase
Journal:  Appl Environ Microbiol       Date:  2013-08-09       Impact factor: 4.792

Review 4.  Transcriptional regulation of bacterial virulence gene expression by molecular oxygen and nitric oxide.

Authors:  Jeffrey Green; Matthew D Rolfe; Laura J Smith
Journal:  Virulence       Date:  2014-10-31       Impact factor: 5.882

5.  A sensitive method for the recovery of Escherichia coli serogroup O55 including Shiga toxin-producing variants for potential use in outbreaks.

Authors:  M Kirchner; E Sayers; S Cawthraw; N Duggett; R Gosling; C Jenkins; T J Dallman; D Mueller-Doblies; M F Anjum
Journal:  J Appl Microbiol       Date:  2019-07-07       Impact factor: 3.772

Review 6.  Cytolysin A (ClyA): A Bacterial Virulence Factor with Potential Applications in Nanopore Technology, Vaccine Development, and Tumor Therapy.

Authors:  Kazunori Murase
Journal:  Toxins (Basel)       Date:  2022-01-21       Impact factor: 4.546

7.  Elevated recombinant clyA gene expression in the uropathogenic Escherichia coli strain 536, a clue to explain pathoadaptive mutations in a subset of extraintestinal E. coli strains.

Authors:  Constance Oben Ayuk Enow; Jan Oscarsson; Nikola Zlatkov; Marie Westermark; Marylise Duperthuy; Sun Nyunt Wai; Bernt Eric Uhlin
Journal:  BMC Microbiol       Date:  2014-09-02       Impact factor: 3.605

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.