» Articles » PMID: 17098913

Vulnerability of Pathogenic Biofilms to Micavibrio Aeruginosavorus

Overview
Date 2006 Nov 14
PMID 17098913
Citations 42
Authors
Affiliations
Soon will be listed here.
Abstract

The host specificity of the gram-negative exoparasitic predatory bacterium Micavibrio aeruginosavorus was examined. M. aeruginosavorus preyed on Pseudomonas aeruginosa, as previously reported, as well as Burkholderia cepacia, Klebsiella pneumoniae, and numerous clinical isolates of these species. In a static assay, a reduction in biofilm biomass was observed as early as 3 hours after exposure to M. aeruginosavorus, and an approximately 100-fold reduction in biofilm cell viability was detected following a 24-h exposure to the predator. We observed that an initial titer of Micavibrio as low as 10 PFU/well or a time of exposure to the predator as short as 30 min was sufficient to reduce a P. aeruginosa biofilm. The ability of Micavibrio to reduce an existing biofilm was confirmed by scanning electron microscopy. In static and flow cell experiments, M. aeruginosavorus was able to modify the overall P. aeruginosa biofilm structure and markedly decreased the viability of P. aeruginosa. The altered biofilm structure was likely caused by an increase in cell-cell interactions brought about by the presence of the predator or active predation. We also conducted a screen to identify genes important for P. aeruginosa-Micavibrio interaction, but no candidates were isolated among the approximately 10,000 mutants tested.

Citing Articles

Predatory potentials of novel isolates against multidrug-resistant and extremely drug-resistant bacterial pathogens of animals and plants.

Selvaraj S, Gayathri S, Varalakshmi P, Nagarajan N, Palaniswami R, Ashokkumar B 3 Biotech. 2025; 15(3):69.

PMID: 40026678 PMC: 11868474. DOI: 10.1007/s13205-025-04230-8.


Predatory Bacteria in the Treatment of Infectious Diseases and Beyond.

Alexakis K, Baliou S, Ioannou P Infect Dis Rep. 2024; 16(4):684-698.

PMID: 39195003 PMC: 11354112. DOI: 10.3390/idr16040052.


Flagellar stator genes control a trophic shift from obligate to facultative predation and biofilm formation in a bacterial predator.

Mookherjee A, Mitra M, Sason G, Jose P, Martinenko M, Pietrokovski S mBio. 2024; 15(8):e0071524.

PMID: 39037271 PMC: 11323537. DOI: 10.1128/mbio.00715-24.


Assessing Antibiotic-Resistant Genes in University Dormitory Washing Machines.

Chen W, Zhang Y, Mi J Microorganisms. 2024; 12(6).

PMID: 38930496 PMC: 11205806. DOI: 10.3390/microorganisms12061112.


Predatory bacteria as potential biofilm control and eradication agents in the food industry.

Mun W, Choi S, Upatissa S, Mitchell R Food Sci Biotechnol. 2023; 32(12):1729-1743.

PMID: 37780591 PMC: 10533476. DOI: 10.1007/s10068-023-01310-4.


References
1.
Brooun A, Liu S, Lewis K . A dose-response study of antibiotic resistance in Pseudomonas aeruginosa biofilms. Antimicrob Agents Chemother. 2000; 44(3):640-6. PMC: 89739. DOI: 10.1128/AAC.44.3.640-646.2000. View

2.
Singh P, Schaefer A, Parsek M, Moninger T, Welsh M, Greenberg E . Quorum-sensing signals indicate that cystic fibrosis lungs are infected with bacterial biofilms. Nature. 2000; 407(6805):762-4. DOI: 10.1038/35037627. View

3.
Davey M, OToole G . Microbial biofilms: from ecology to molecular genetics. Microbiol Mol Biol Rev. 2000; 64(4):847-67. PMC: 99016. DOI: 10.1128/MMBR.64.4.847-867.2000. View

4.
Mattison R, Harayama S . The predatory soil flagellate Heteromita globosa stimulates toluene biodegradation by a Pseudomonas sp. FEMS Microbiol Lett. 2001; 194(1):39-45. DOI: 10.1111/j.1574-6968.2001.tb09443.x. View

5.
Mah T, OToole G . Mechanisms of biofilm resistance to antimicrobial agents. Trends Microbiol. 2001; 9(1):34-9. DOI: 10.1016/s0966-842x(00)01913-2. View