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Micavibrio aeruginosavorus

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Micavibrio aeruginosavorus
Scientific classification
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M. aeruginosavorus
Binomial name
Micavibrio aeruginosavorus

Micavibrio aeruginosavorus is a species of epibiotic predatory bacteria. Unlike Bdellovibrio, Micavibrio do not invade the periplasmic space of their prey, but feed by attaching themselves to its surface.[1]

Micavibrio aeruginosavorus was initially discovered while searching for traces of the bacteria species Bdellovibrio in wastewater.[2] Similar to Bdellovibrio, M. aeruginosavorus was also found to have predatory tendencies against other bacteria, however the way that aeruginosavorus consumes its prey differs from Bdellovibrio in distinct ways. M. aeruginosavorus seek out their prey, primarily Pseudomonas aeruginosa, and attach to their cell wall using. Once attached, the predatory bacteria uses a specialized enzyme called Bdellovibrio-like protein (BLP) which allows it to break down the cell wall of P. Aeruginosa consumes the contents of the prey cell.[3] This essentially kills the prey cell while allowing the predator cell to grow and reproduce. During this process the predatory bacterium is free to move to a new host cell whenever it has expended the resources of the original cell. This differs from Bdellovibrio as those bacteria use pili to enter the space between the cell membrane and the cell wall of the host bacterium. Once inside the Bdellovibrio will replicate using the resources of the host cell until it is entirely broken down and a complete life cycle has passed, only then can the Bdellovibrio move on to a new host cell. While the medicinal use of predatory bacteria is still in an experimental phase, there have been some promising studies that show its usefulness as a tool against multidrug resistant infections. Predatory bacteria have been determined to attack bacteria of the genus Acinetobacter, Aeromonas, Bordetella, Burkholderia, Citrobacter, Enterobacter, Escherichia, Klebsiella, Listonella, Morganella, Proteus, Pseudomonas, Salmonella, Serratia, Shigella, Vibrio and Yersinia. A 2007 study found that Micavibrio aeruginosavorus was effective against reducing biofilm build up. This is an important development as biofilms that build up after surgical implants can be up to 1,000 more resistant to antibiotic medications, which could lead to devastating infections in these patients.[4] The safety of using predatory bacteria as medication is still being determined via in vivo and in vitro experimentation. A 2015 study found both the intravenous and respiratory administration of M. aeruginosavorus and B. bacteriovorus to rats to be relatively safe. While some reactions, including some inflammation and inflammatory cytokines, were detected they subsided within 24 hours and no lasting tissue damage was observed. Additionally, it was found that the predatory bacteria were safely and effectively eliminated from the body.[5]

References

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  1. ^ Wang, Z.; Kadouri, D. E.; Wu, M. (2011). "Genomic insights into an obligate epibiotic bacterial predator: Micavibrio aeruginosavorus ARL-13". BMC Genomics. 12: 453. doi:10.1186/1471-2164-12-453. PMC 3189940. PMID 21936919.
  2. ^ Lambina VA, Afinogenova AV, Romaĭ Penabad S, Konovalova SM, Pushkareva AP. Micavibrio admirandus gen. et sp. nov [Micavibrio admirandus gen. et sp. nov]. Mikrobiologiia. 1982 Jan-Feb;51(1):114-7. Russian. PMID 7070304.
  3. ^ Dashiff A, Junka RA, Libera M, Kadouri DE. Predation of human pathogens by the predatory bacteria Micavibrio aeruginosavorus and Bdellovibrio bacteriovorus. J Appl Microbiol. 2011 Feb;110(2):431-44. doi: 10.1111/j.1365-2672.2010.04900.x. Epub 2010 Nov 29. PMID 21114596.
  4. ^ Kadouri, Daniel, et al. “Vulnerability of Pathogenic Biofilms to Micavibrio Aeruginosavorus.” Applied and Environmental Microbiology, vol. 73, no. 2, 2007, pp. 605–614, https://doi.org/10.1128/aem.01893-06.
  5. ^ Shatzkes, K., Chae, R., Tang, C. et al. Examining the safety of respiratory and intravenous inoculation of Bdellovibrio bacteriovorus and Micavibrio aeruginosavorus in a mouse model. Sci Rep 5, 12899 (2015). https://doi.org/10.1038/srep12899