Literature DB >> 34143328

Antibiotic-mediated expression analysis of Shiga toxin 1 and 2 in multi-drug-resistant Shiga toxigenic Escherichia coli.

Aniqa Rehman1, Saadia Andleeb1, Sidra Rahmat Ullah1, Zeeshan Mustafa1, Danish Gul1, Khalid Mehmood2,3.   

Abstract

Shiga toxin-producing Escherichia coli (STEC) is an important foodborne pathogens, known to cause enteric infections especially diarrhea, mainly attributed to Shiga toxins (Stxs). The use of certain antibiotics for treating this infection is controversial, owing to an increased risk for producing Stxs (Stx 1 and Stx 2). Increased antibiotic resistance is also thought to be involved in the pathogenesis of STEC diseases. The purpose of this study was to analyze the effects of antibiotics on induction of Stx 1 and Stx 2 in clinical STEC isolates and to investigate the relationships between increased resistance and Stx production. Fifteen clinical isolates were treated with sub minimum inhibitory concentrations (Sub MIC) of clinically used antibiotics (ciprofloxacin, fosfomycin, tigecycline, and meropenem), and the changes in expression levels of stx1 and stx2 genes were estimated using qRT-PCR. The expressions of Shiga toxins were found to be increased up to 6.5- and eightfold under ciprofloxacin and tigecycline Sub MIC, respectively. Fosfomycin had weak induction effect of up to twofold, whereas meropenem had the weakest influence on such expression. Resistant isolates were found to be more prone to increased expression of toxins.

Entities:  

Year:  2021        PMID: 34143328     DOI: 10.1007/s12223-021-00882-0

Source DB:  PubMed          Journal:  Folia Microbiol (Praha)        ISSN: 0015-5632            Impact factor:   2.099


  2 in total

1.  Antimicrobials effective for inhibition of enterohaemorrhagic Escherichia coli strains O26, O111, and O157 and their effects on Shiga toxin releases.

Authors:  John Hwa Lee; Barry D Stein
Journal:  J Microbiol Biotechnol       Date:  2009-10       Impact factor: 2.351

Review 2.  Advances in pathogenesis and therapy of hemolytic uremic syndrome caused by Shiga toxin-2.

Authors:  Cristina Ibarra; María Marta Amaral; Marina S Palermo
Journal:  IUBMB Life       Date:  2013-09-06       Impact factor: 3.885

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.