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Adherence of Bacteria to Plant Surfaces Measured in the Laboratory
Published on: June 19, 2018
[Study of antibiotic influence on adherence capacity of gram positive and gram negative bacteria to the cellular
Carmen Balotescu1, Anca-Michaela Israil, Veronica Lazăr
1I.N.C.D.M.I. Cantacuzino, Bucureşti.
Abstract:
Bacterial adherence to the cellular substrate (skin and mucosa) represents a precondition of infectious pathology. It was demonstrated that bacteria which adhere and form biofilms on catheters and other inert materials used in medicine are resistant to the therapeutic antibiotic concentrations being protected by the biofilm mathrix and generating severe and hard to treat infections. There are only few studies on the influence of antibiotics on the bacterial adhesins synthesis and bacterial adherence to the cellular substrate. The purpose of this study was to investigate the influence of subinhibitory concentrations of antibiotics on adherence capacity of Listeria monocytogenes, Vibrio cholerae and Aeromonas hydrophyla to the cellular substrate represented by HEp-2 cells. Suspensions (approximately 10(10) cells/ml) of bacterial cultures developed on solid media were incubated for 30 minutes in the presence of subinhibitory concentrations of penicillin, ampicillin, amoxicilin with clavulanic acid, ceftazidim, norfloxacin, kanamycin, chloramphenicole and vancomycin. Study of bacterial adherence to the cellular substrate was done by Cravioto's modified method. The quantitative evaluation of adherence/invasion capacity of bacterial suspensions pretreated with antibiotics was done by comparing the adherence/invasion index with controls without antibiotics. Penicillin, amoxicillin with clavulanic acid and vancomycin have significantly stimulated the adherence of Listeria monocytogenes strain and inhibited the adherence of Vibrio cholerae and Aeromonas hydrophyla strains. Ampicillin and chloramphenicole exhibited no significant effect on bacterial adherence capacity. The influence of kanamycin, ceftazidim and norfloxacin could not be interpreted due to the occurrence of a severe cytotoxic effect manifested by cell monolayer detaching, probably due to the action of antibiotic suspensions or to the increase of bacterial virulence under the selective pressure of the antibiotic.
Insights
Subinhibitory antibiotic concentrations can alter bacterial adherence. Penicillin, amoxicillin-clavulanic acid, and vancomycin stimulated Listeria monocytogenes adherence while inhibiting Vibrio cholerae and Aeromonas hydrophyla. Other antibiotics showed cytotoxic effects.
Area of Science:
- Microbiology
- Infectious Diseases
- Pharmacology
Context:
- Bacterial adherence to host cells is crucial for infection development.
- Biofilm formation on medical devices confers antibiotic resistance, complicating treatment.
- Limited research exists on how antibiotics affect bacterial adhesin synthesis and cellular adherence.
Purpose:
- To investigate the impact of subinhibitory antibiotic concentrations on the adherence of Listeria monocytogenes, Vibrio cholerae, and Aeromonas hydrophyla to HEp-2 cells.
- To quantify changes in bacterial adherence and invasion following antibiotic pretreatment.
Summary:
- Bacteria were incubated with subinhibitory concentrations of various antibiotics (penicillin, ampicillin, amoxicillin/clavulanic acid, ceftazidime, norfloxacin, kanamycin, chloramphenicol, vancomycin).
- Penicillin, amoxicillin/clavulanic acid, and vancomycin significantly enhanced Listeria monocytogenes adherence but reduced adherence of Vibrio cholerae and Aeromonas hydrophyla.
- Ampicillin and chloramphenicol had no significant effect; kanamycin, ceftazidime, and norfloxacin induced cytotoxicity, preventing interpretation.
Impact:
- Reveals differential effects of specific antibiotics on bacterial adherence, potentially influencing infection dynamics.
- Highlights the need to consider sub-lethal antibiotic effects on bacterial virulence factors.
- Suggests that some antibiotics may inadvertently promote adherence of certain pathogens or cause cytotoxic effects complicating in vitro studies.
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