Transcriptomic and proteomic analysis of the virulence inducing effect of ciprofloxacin on enterohemorrhagic Escherichia coli.
Anne Cecilie Riihonen KijewskiIngun Lund WitsøArvind Y M SundaramOla Brønstad BrynildsrudKristin PettersenEirik Byrkjeflot AnonsenJan Haug AnonsenMarina Elisabeth AspholmPublished in: PloS one (2024)
Enterohemorrhagic E. coli (EHEC) is considered to be the most dangerous pathotype of E. coli, as it causes severe conditions such as hemorrhagic colitis (HC) and hemolytic uremic syndrome (HUS). Antibiotic treatment of EHEC infections is generally not recommended since it may promote the production of the Shiga toxin (Stx) and lead to worsened symptoms. This study explores how exposure to the fluoroquinolone ciprofloxacin reorganizes the transcriptome and proteome of EHEC O157:H7 strain EDL933, with special emphasis on virulence-associated factors. As expected, exposure to ciprofloxacin caused an extensive upregulation of SOS-response- and Stx-phage proteins, including Stx. A range of other virulence-associated factors were also upregulated, including many genes encoded by the LEE-pathogenicity island, the enterohemolysin gene (ehxA), as well as several genes and proteins involved in LPS production. However, a large proportion of the genes and proteins (17 and 8%, respectively) whose expression was upregulated upon ciprofloxacin exposure (17 and 8%, respectively) are not functionally assigned. This indicates a knowledge gap in our understanding of mechanisms involved in EHECs response to antibiotic-induced stress. Altogether, the results contribute to better understanding of how exposure to ciprofloxacin influences the virulome of EHEC and generates a knowledge base for further studies on how EHEC responds to antibiotic-induced stress. A deeper understanding on how EHEC responds to antibiotics will facilitate development of novel and safer treatments for EHEC infections.
Keyphrases
- escherichia coli
- pseudomonas aeruginosa
- biofilm formation
- genome wide
- cystic fibrosis
- genome wide identification
- poor prognosis
- high glucose
- klebsiella pneumoniae
- dna methylation
- diabetic rats
- staphylococcus aureus
- drug induced
- cell proliferation
- gene expression
- inflammatory response
- genome wide analysis
- oxidative stress
- binding protein
- combination therapy