Characterization of Potential Virulence, Resistance to Antibiotics and Heavy Metals, and Biofilm-forming Capabilities of Soil Lignocellulolytic BacteriaShow others and affiliations
2023 (English)In: Microbial Physiology, ISSN 2673-1665, Vol. 33, no 1, p. 36-48Article in journal (Refereed) Published
Abstract [en]
Soil bacteria participate in self-immobilization processes for survival, persistence and producing virulence factors in some niches or hosts through their capacities of autoaggregation, cell surface hydrophobicity, biofilm formation, and antibiotic and heavy metal resistance. This study investigated potential virulence, antibiotics and heavy metals resistance, solvent adhesion, and biofilm-forming capabilities of six cellulolytic bacteria isolated from soil samples: Paenarthrobacter sp. MKAL1, Hymenobacter sp. MKAL2, Mycobacterium sp. MKAL3, Stenotrophomonas sp. MKAL4, Chryseobacterium sp. MKAL5 and Bacillus sp. MKAL6. Strains were subjected to phenotypic methods, including heavy metal and antibiotic susceptibility and virulence factors (protease, lipase, capsule production, autoaggregation, hydrophobicity and biofilm formation). The effect of ciprofloxacin was also investigated on bacterial susceptibility over time, cell membrane and biofilm formation. Strains MKAL2, MKAL5 and MKAL6 exhibited protease and lipase activities, while only MKAL6 produced capsules. All strains were capable of aggregating, forming biofilm and adhering to solvents. Strains tolerated high amounts of chromium, lead, zinc, nickel and manganese and were resistant to lincomycin. Ciprofloxacin exhibited bactericidal activity against these strains. Although the phenotypic evaluation of virulence factors of bacteria can indicate their pathogenic nature, an in-depth genetic study of virulence, antibiotic and heavy metal resistance genes is required.
Place, publisher, year, edition, pages
S. Karger, 2023. Vol. 33, no 1, p. 36-48
National Category
Medical Biotechnology (with a focus on Cell Biology (including Stem Cell Biology), Molecular Biology, Microbiology, Biochemistry or Biopharmacy)
Identifiers
URN: urn:nbn:se:oru:diva-117551DOI: 10.1159/000530228ISI: 000954781700001PubMedID: 36944321Scopus ID: 2-s2.0-85171345032OAI: oai:DiVA.org:oru-117551DiVA, id: diva2:1917800
Note
This project was supported by the Natural Science and Engineering Research Council of Canada (NSERC) Discovery Grant (RGPIN-2017-05366) to W.Q.
2024-12-032024-12-032024-12-03Bibliographically approved