Difference between revisions of "PMID:12039754"
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+ | {| id="O4f6a58808d969" class=" tableEdit PMID_info_table" | ||
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+ | !align=left |Citation | ||
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+ | '''Djordjevic, D, Wiedmann, M and McLandsborough, LA''' (2002) Microtiter plate assay for assessment of Listeria monocytogenes biofilm formation.''Appl. Environ. Microbiol.'' '''68''':2950-8 | ||
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+ | !align=left |Abstract | ||
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+ | Listeria monocytogenes has the ability to form biofilms on food-processing surfaces, potentially leading to food product contamination. The objective of this research was to standardize a polyvinyl chloride (PVC) microtiter plate assay to compare the ability of L. monocytogenes strains to form biofilms. A total of 31 coded L. monocytogenes strains were grown in defined medium (modified Welshimer's broth) at 32 degrees C for 20 and 40 h in PVC microtiter plate wells. Biofilm formation was indirectly assessed by staining with 1% crystal violet and measuring crystal violet absorbance, using destaining solution. Cellular growth rates and final cell densities did not correlate with biofilm formation, indicating that differences in biofilm formation under the same environmental conditions were not due to growth rate differences. The mean biofilm production of lineage I strains was significantly greater than that observed for lineage II and lineage III strains. The results from the standardized microtiter plate biofilm assay were also compared to biofilm formation on PVC and stainless steel as assayed by quantitative epifluorescence microscopy. Results showed similar trends for the microscopic and microtiter plate assays, indicating that the PVC microtiter plate assay can be used as a rapid, simple method to screen for differences in biofilm production between strains or growth conditions prior to performing labor-intensive microscopic analyses. | ||
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+ | !align=left |Links | ||
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+ | [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=12039754 PubMed] | ||
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+ | !align=left |Keywords | ||
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+ | Bacterial Adhesion; Biofilms; Listeria monocytogenes; Polyvinyl Chloride; Stainless Steel | ||
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+ | <!--box uid=d41d8cd98f00b204e9800998ecf8427e.2884.O4f6a58808d969--> | ||
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+ | ==Main Points of the Paper == | ||
+ | {{LitSignificance}} | ||
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+ | == Materials and Methods Used == | ||
+ | {{LitMaterials}} | ||
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+ | ==Phenotype Annotations== | ||
+ | {{AnnotationTableHelp}} | ||
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+ | {| id="J4f6a5880a1d8c" class=" tableEdit Phenotype_Table_2" | ||
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+ | !|Phenotype of!!Taxon Information!!Genotype Information (if known)!!Condition Information!!OMP ID!!OMP Term Name!!ECO ID!!ECO Term Name!!Notes!!Status | ||
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+ | ==Notes== | ||
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+ | ==References== | ||
+ | {{RefHelp}} | ||
+ | <references/> | ||
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+ | |||
+ | [[Category:Publication]] |
Revision as of 17:38, 21 March 2012
Citation |
Djordjevic, D, Wiedmann, M and McLandsborough, LA (2002) Microtiter plate assay for assessment of Listeria monocytogenes biofilm formation.Appl. Environ. Microbiol. 68:2950-8 |
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Abstract |
Listeria monocytogenes has the ability to form biofilms on food-processing surfaces, potentially leading to food product contamination. The objective of this research was to standardize a polyvinyl chloride (PVC) microtiter plate assay to compare the ability of L. monocytogenes strains to form biofilms. A total of 31 coded L. monocytogenes strains were grown in defined medium (modified Welshimer's broth) at 32 degrees C for 20 and 40 h in PVC microtiter plate wells. Biofilm formation was indirectly assessed by staining with 1% crystal violet and measuring crystal violet absorbance, using destaining solution. Cellular growth rates and final cell densities did not correlate with biofilm formation, indicating that differences in biofilm formation under the same environmental conditions were not due to growth rate differences. The mean biofilm production of lineage I strains was significantly greater than that observed for lineage II and lineage III strains. The results from the standardized microtiter plate biofilm assay were also compared to biofilm formation on PVC and stainless steel as assayed by quantitative epifluorescence microscopy. Results showed similar trends for the microscopic and microtiter plate assays, indicating that the PVC microtiter plate assay can be used as a rapid, simple method to screen for differences in biofilm production between strains or growth conditions prior to performing labor-intensive microscopic analyses. |
Links | |
Keywords |
Bacterial Adhesion; Biofilms; Listeria monocytogenes; Polyvinyl Chloride; Stainless Steel |
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Main Points of the Paper
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Materials and Methods Used
Please list the materials and methods used in this paper (strains, plasmids, antibodies, etc).
Phenotype Annotations
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Phenotype of | Taxon Information | Genotype Information (if known) | Condition Information | OMP ID | OMP Term Name | ECO ID | ECO Term Name | Notes | Status |
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Notes
References
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