Chlorine dioxide disinfection of single and dual species biofilms, detached biofilm and planktonic cells

dc.contributor.authorBehnke, S.
dc.contributor.authorCamper, Anne K.
dc.date.accessioned2017-02-02T18:42:51Z
dc.date.available2017-02-02T18:42:51Z
dc.date.issued2012-07
dc.description.abstractDisinfection efficacy testing is usually done with planktonic cells or more recently, biofilms. While disinfectants are much less effective against biofilms compared to planktonic cells, questions regarding the disinfection tolerance of detached biofilm clusters remain largely unanswered. Burkholderia cepacia and Pseudomonas aeruginosa were grown in chemostats and biofilm tubing reactors, with the tubing reactor serving as a source of detached biofilm clusters. Chlorine dioxide susceptibility was assessed for B. cepacia and P. aeruginosa in these three sample types as monocultures and binary cultures. Similar doses of chlorine dioxide inactivated samples of chemostat and tubing reactor effluent and no statistically significant difference between the log10 reductions was found. This contrasts with chlorine, shown previously to be generally less effective against detached biofilm particles. Biofilms were more tolerant and required chlorine dioxide doses ten times higher than chemostat and tubing reactor effluent samples. A second species was advantageous in all sample types and resulted in lower log10 reductions when compared to the single species cultures, suggesting a beneficial interaction of the species.en_US
dc.identifier.citationBehnke S, Camper AK, "Chlorine dioxide disinfection of single and dual species biofilms, detached biofilm and planktonic cells," Biofouling: The Journal of Bioadhesion and Biofilm Research, July 2012 28(6):635–647en_US
dc.identifier.issn0892-7014
dc.identifier.urihttps://scholarworks.montana.edu/handle/1/12524
dc.titleChlorine dioxide disinfection of single and dual species biofilms, detached biofilm and planktonic cellsen_US
dc.typeArticleen_US
mus.citation.extentfirstpage635en_US
mus.citation.extentlastpage647en_US
mus.citation.issue6en_US
mus.citation.journaltitleBiofoulingen_US
mus.citation.volume28en_US
mus.data.thumbpage9en_US
mus.identifier.categoryChemical & Material Sciencesen_US
mus.identifier.categoryEngineering & Computer Scienceen_US
mus.identifier.categoryHealth & Medical Sciencesen_US
mus.identifier.categoryLife Sciences & Earth Sciencesen_US
mus.identifier.doi10.1080/08927014.2012.700705en_US
mus.relation.collegeCollege of Agricultureen_US
mus.relation.collegeCollege of Engineeringen_US
mus.relation.collegeCollege of Letters & Scienceen_US
mus.relation.departmentCell Biology & Neuroscience.en_US
mus.relation.departmentCenter for Biofilm Engineering.en_US
mus.relation.departmentChemical & Biological Engineering.en_US
mus.relation.departmentChemistry & Biochemistry.en_US
mus.relation.departmentHealth & Human Development.en_US
mus.relation.departmentMicrobiology & Immunology.en_US
mus.relation.researchgroupCenter for Biofilm Engineering.en_US
mus.relation.universityMontana State University - Bozemanen_US

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