Influence of milk, chicken residues and oxygen levels on biofilm formation on stainless steel, gene expression and small RNAs in Salmonella enterica

Food Control ◽  
2018 ◽  
Vol 90 ◽  
pp. 1-9 ◽  
Author(s):  
Alexandre Lamas ◽  
Patricia Regal ◽  
Beatriz Vázquez ◽  
José Manuel Miranda ◽  
Alberto Cepeda ◽  
...  
LWT ◽  
2018 ◽  
Vol 97 ◽  
pp. 1-8 ◽  
Author(s):  
Alexandre Lamas ◽  
Alba María Paz-Mendez ◽  
Patricia Regal ◽  
Beatriz Vazquez ◽  
José Manuel Miranda ◽  
...  

EcoSal Plus ◽  
2020 ◽  
Vol 9 (1) ◽  
Author(s):  
Jens Hör ◽  
Gianluca Matera ◽  
Jörg Vogel ◽  
Susan Gottesman ◽  
Gisela Storz

2014 ◽  
Vol 65 (1) ◽  
pp. 399-409 ◽  
Author(s):  
Rihab Lagha ◽  
Marie-Noëlle Bellon-Fontaine ◽  
Margareth Renault ◽  
Romain Briandet ◽  
Jean-Marie Herry ◽  
...  

2021 ◽  
Vol 9 (12) ◽  
pp. 2510
Author(s):  
Zhi Ma ◽  
Xia Tang ◽  
Kim Stanford ◽  
Xiaolong Chen ◽  
Tim A. McAllister ◽  
...  

Shiga toxin-producing Escherichia coli (STEC) and Salmonella enterica are important foodborne pathogens capable of forming both single- and multi-species biofilms. In this study, the mono- and dual-species biofilms were formed by STEC O113:H21 and Salmonella enterica serovar Choleraesuis 10708 on stainless steel in the presence of beef juice over 5 d at 22 °C. The dual-species biofilm mass was substantially (p < 0.05) greater than that produced by STEC O113:H21 or S. Choleraesuis 10708 alone. However, numbers (CFU/mL) of S. Choleraesuis 10708 or STEC O113:H21 cells in the dual-species biofilm were (p < 0.05) lower than their respective counts in single-species biofilms. In multi-species biofilms, the sensitivity of S. Choleraesuis 10708 to the antimicrobial peptide WK2 was reduced, but it was increased for STEC O113:H21. Visualization of the temporal and spatial development of dual-species biofilms using florescent protein labeling confirmed that WK2 reduced cell numbers within biofilms. Collectively, our results highlight the potential risk of cross-contamination by multi-species biofilms to food safety and suggest that WK2 may be developed as a novel antimicrobial or sanitizer for the control of biofilms on stainless steel.


2019 ◽  
Vol 7 (7) ◽  
pp. 196 ◽  
Author(s):  
Shi ◽  
Dittoe ◽  
Feye ◽  
Kogut ◽  
Ricke

Salmonella enterica is one of the most prevalent foodborne pathogens. The large quantity of serovar types results in the colonization of a large spectrum of hosts, with different environmental conditions and hazards. The aim of this study was to evaluate the differences in gene expression (bcsA and csgD) of Salmonella enterica serovars Heidelberg, Kentucky, and Enteritidis during biofilm formation using quantitative reverse-transcriptase polymerase chain reaction (qRT-PCR). Overall, there appeared to be differences in expression between the different serovars with high variation between strains. These data are important as they demonstrate considerable variability in gene expression between serovars and strains of poultry isolates of Salmonella enterica.


2019 ◽  
Vol 8 (2) ◽  
Author(s):  
Huhu Wang ◽  
Linlin Cai ◽  
Haijing Hu ◽  
Xinglian Xu ◽  
Guanghong Zhou

Here, we report the complete genome sequence of strain NMC 61 of Salmonella enterica serovar Enteritidis, which was previously isolated from conveyor belts during chicken slaughter and has the potential to form biofilms on several surfaces. The genome is predicted to contain 110 noncoding small RNAs on the chromosome.


2020 ◽  
Vol 86 (20) ◽  
Author(s):  
K. F. Griewisch ◽  
J. G. Pierce ◽  
J. R. Elfenbein

ABSTRACT Biofilms formed by Salmonella enterica are a frequent source of food supply contamination. Since biofilms are inherently resistant to disinfection, new agents capable of preventing biofilm formation are needed. Synthetic analogs of 4-oxazolidinone containing natural products have shown promise as antibiofilm compounds against Gram-positive bacteria. The purpose of our study was 2-fold: to establish the antibiofilm effects and mechanism of action of a synthetic 4-oxazolidinone analog (JJM-ox-3-70) and to establish mechanisms of resistance to this compound in Salmonella enterica serovar Typhimurium (S. Typhimurium). JJM-ox-3-70 inhibited biofilm formation but had no effect on cell growth. The antibiofilm effects were linked to disruption of curli fimbriae and flagellar gene expression and alteration in swimming motility, suggesting an effect on multiple cellular processes. Using a 2-step screening approach of defined multigene and single-gene deletion mutant libraries, we identified 3 mutants that produced less biofilm in the presence of JJM-ox-3-70 than the isogenic WT, with phenotypes reversed by complementation in trans. Genes responsible for S. Typhimurium resistance to the compound included acrB, a component of the major drug efflux pump AcrAB-TolC, and two genes of unknown function (STM0437 and STM1292). The results of this study suggest that JJM-ox-3-70 inhibits biofilm formation by indirect inhibition of extracellular matrix production that may be linked to disruption of flagellar motility. Further work is needed to establish the role of the newly characterized genes as potential mechanisms of biofilm intrinsic antimicrobial resistance. IMPORTANCE Biofilms are resistant to killing by disinfectants and antimicrobials. S. enterica biofilms facilitate long-term host colonization and persistence in food processing environments. Synthetic analogs of 4-oxazolidinone natural products show promise as antibiofilm agents. Here, we show that a synthetic 4-oxazolidinone analog inhibits Salmonella biofilm through effects on both motility and biofilm matrix gene expression. Furthermore, we identify three genes that promote Salmonella resistance to the antibiofilm effects of the compound. This work provides insight into the mechanism of antibiofilm effects of a synthetic 4-oxazolidinone analog in Gram-negative bacteria and demonstrates new mechanisms of intrinsic antimicrobial resistance in Salmonella biofilms.


2021 ◽  
pp. 101209
Author(s):  
Pantu Kumar Roy ◽  
Angela Ji-Won Ha ◽  
Md. Furkanur Rahaman Mizan ◽  
Md. Iqbal Hossain ◽  
Md. Ashrafudoulla ◽  
...  

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