Activity of Bacteriophage and Complex Tannins against Biofilm-Forming Shiga Toxin-Producing <i>Escherichia coli</i> from Canada and South Africa

Bacteriophages, natural killers of bacteria, and plant secondary metabolites, such as condensed tannins, are potential agents for the control of foodborne pathogens. The first objective of this study evaluated the efficacy of a bacteriophage SA21RB in reducing pre-formed biofilms on stainless-steel...

Full description

Bibliographic Details
Main Authors: Emmanuel W. Bumunang, Collins N. Ateba, Kim Stanford, Yan D. Niu, Y. Wang, Tim A. McAllister
Format: Article
Language:English
Published: MDPI AG 2020-05-01
Series:Antibiotics
Subjects:
Online Access:https://www.mdpi.com/2079-6382/9/5/257
Description
Summary:Bacteriophages, natural killers of bacteria, and plant secondary metabolites, such as condensed tannins, are potential agents for the control of foodborne pathogens. The first objective of this study evaluated the efficacy of a bacteriophage SA21RB in reducing pre-formed biofilms on stainless-steel produced by two Shiga toxin-producing <i>Escherichia coli</i> (STEC) strains, one from South Africa and the other from Canada. The second objective examined the anti-bacterial and anti-biofilm activity of condensed tannin (CT) from purple prairie clover and phlorotannins (PT) from brown seaweed against these strains. For 24-h-old biofilms, (O113:H21; 6.2 log<sub>10</sub> colony-forming units per square centimeter (CFU/cm<sup>2</sup>) and O154:H10; 5.4 log<sub>10</sub> CFU/cm<sup>2</sup>), 3 h of exposure to phage (10<sup>13</sup> plaque-forming units per milliliter (PFU/mL)) reduced (<i>p</i> ≤ 0.05) the number of viable cells attached to stainless-steel coupons by 2.5 and 2.1 log<sub>10</sub> CFU/cm<sup>2</sup> for O113:H21 and O154:H10, respectively. However, as biofilms matured, the ability of phage to control biofilm formation declined. In biofilms formed for 72 h (O113:H21; 5.4 log<sub>10</sub> CFU/cm<sup>2</sup> and O154:H10; 7 log<sub>10</sub> CFU/cm<sup>2</sup>), reductions after the same duration of phage treatment were only 0.9 and 1.3 log<sub>10</sub> CFU/cm<sup>2</sup> for O113:H21 and O154:H10, respectively. Initial screening of CT and PT for anti-bacterial activity by a microplate assay indicated that both STEC strains were less sensitive (<i>p</i> ≤ 0.05) to CT than PT over a concentration range of 25–400 µg/mL. Based on the lower activity of CT (25–400 µg/mL), they were not further examined. Accordingly, PT (50 µg/mL) inhibited (<i>p</i> ≤ 0.05) biofilm formation for up to 24 h of incubation at 22 °C, but this inhibition progressively declined over 72 h for both O154:H10 and O113:H21. Scanning electron microscopy revealed that both SA21RB and PT eliminated 24 h biofilms, but that both strains were able to adhere and form biofilms on stainless-steel coupons at longer incubation times. These findings revealed that phage SA21RB is more effective at disrupting 24 than 72 h biofilms and that PT were able to inhibit biofilm formation of both <i>E. coli</i> O154:H10 and O113:H21 for up to 24 h.
ISSN:2079-6382