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      Data on quantitation of Bacillus cereus sensu lato biofilms by microtiter plate biofilm formation assay

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          Abstract

          The microtiter plate biofilm formation assay is a method for the study of early biofilm formation on abiotic surfaces. It is a colorimetric technique that uses dyes, such as crystal violet, to stain attached biofilms and to quantify by using an absorbance microtiter plate reader. In this data, we evaluated the ability of 12 Bacillus cereus sensu lato isolated from soil and milk powder samples for their production of biofilms after a total of 48 hr incubation period in the 96-well microtiter plate. The biofilm production was induced by initially exposing them in diluted tryptic soy broth at its first 24 hr and then replacing with freshly prepared double strength broth for the next incubation period at 30 °C. The optical densities of the bacterial growth in the wells were read at the absorbance wavelength of 630 nm while the stained biofilms that solubilized in absolute ethanol were read at 570 nm. The biofilm measurements were calculated and the degree of biofilm production of each isolate was classified according to biofilm formation categories adapted from previous researchers. Therefore, the assay concluded the negative impact of B. cereus group by ability to form biofilms on abiotic surfaces, such as food contact surfaces in food production industries and the wide application of the current methods in research and industrial fields.

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          Biofilm formation as a novel phenotypic feature of adherent-invasive Escherichia coli (AIEC)

          Background Crohn's disease (CD) is a high morbidity chronic inflammatory disorder of unknown aetiology. Adherent-invasive Escherichia coli (AIEC) has been recently implicated in the origin and perpetuation of CD. Because bacterial biofilms in the gut mucosa are suspected to play a role in CD and biofilm formation is a feature of certain pathogenic E. coli strains, we compared the biofilm formation capacity of 27 AIEC and 38 non-AIEC strains isolated from the intestinal mucosa. Biofilm formation capacity was then contrasted with the AIEC phenotype, the serotype, the phylotype, and the presence of virulence genes. Results Specific biofilm formation (SBF) indices were higher amongst AIEC than non-AIEC strains (P = 0.012). In addition, 65.4% of moderate to strong biofilms producers were AIEC, whereas 74.4% of weak biofilm producers were non-AIEC (P = 0.002). These data indicate that AIEC strains were more efficient biofilm producers than non-AIEC strains. Moreover, adhesion (P = 0.009) and invasion (P = 0.003) indices correlated positively with higher SBF indices. Additionally, motility (100%, P < 0.001), H1 type flagellin (53.8%, P < 0.001), serogroups O83 (19.2%, P = 0.008) and O22 (26.9%, P = 0.001), the presence of virulence genes such as sfa/focDE (38.5%, P = 0.003) and ibeA (26.9%, P = 0.017), and B2 phylotype (80.8%, P < 0.001) were frequent characteristics amongst biofilm producers. Conclusion The principal contribution of the present work is the finding that biofilm formation capacity is a novel, complementary pathogenic feature of the recently described AIEC pathovar. Characterization of AIEC specific genetic determinants, and the regulatory pathways, involved in biofilm formation will likely bring new insights into AIEC pathogenesis.
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            Author and article information

            Contributors
            Journal
            Data Brief
            Data Brief
            Data in Brief
            Elsevier
            2352-3409
            05 December 2019
            February 2020
            05 December 2019
            : 28
            : 104951
            Affiliations
            [a ]The Graduate School, University of Santo Tomas, España, Manila 1008, Philippines
            [b ]Department of Biological Sciences, College of Science, University of Santo Tomas, España, Manila 1008, Philippines
            [c ]Research Center for the Natural and Applied Sciences, Thomas Aquinas Research Complex, University of Santo Tomas, España, Manila 1008, Philippines
            Author notes
            []Corresponding author. The Graduate School, University of Santo Tomas, España, Manila 1008, Philippines. rener.sdejesus@ 123456gmail.com
            Article
            S2352-3409(19)31306-X 104951
            10.1016/j.dib.2019.104951
            6926131
            31890796
            a5ee42be-128d-48b1-87cf-8f4e8e27d73e
            © 2019 The Author(s)

            This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

            History
            : 2 September 2019
            : 25 November 2019
            : 28 November 2019
            Categories
            Immunology and Microbiology

            microbiology,1% crystal violet solution,96-well microtiter plate,absorbance microtiter plate reader

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