» Articles » PMID: 28798736

O157:H7 Acid Sensitivity Correlates with Flocculation Phenotype During Nutrient Limitation

Overview
Journal Front Microbiol
Specialty Microbiology
Date 2017 Aug 12
PMID 28798736
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Shiga toxin producing (STEC) strains vary in acid resistance; however, little is known about the underlying mechanisms that result in strain specific differences. Among 25 STEC O157:H7 strains tested, 7 strains flocculated when grown statically for 18 h in minimal salts medium at 37°C, while 18 strains did not. Interestingly, the flocculation phenotype (cells came out of suspension) was found to correlate with degree of acid sensitivity in an assay with 400 mM acetic acid solution at pH 3.3 targeting acidified foods. Strains exhibiting flocculation were more acid sensitive and were designated FAS, for flocculation acid sensitive, while the acid resistant strain designated PAR for planktonic acid resistant. Flocculation was not observed for any strains during growth in complex medium (Luria Bertani broth). STEC strains B201 and B241 were chosen as representative FAS (2.4 log reduction) and PAR (0.15 log reduction) strains, respectively, due to differences in acid resistance and flocculation phenotype. Results from electron microscopy showed evidence of fimbriae production in B201, whereas fimbriae were not observed in B241.Curli fimbriae production was identified through plating on Congo red differential medium, and all FAS strains showed curli fimbriae production. Surprisingly, 5 PAR strains also had evidence of curli production. Transcriptomic and targeted gene expression data for B201 and B241indicated that and (curli and acid induced chaperone genes, respectively) expression positively correlated with the phenotypic differences observed for these strains. These data suggest that FAS strains grown in minimal medium express curli, resulting in a flocculation phenotype. This may be regulated by GcvB, which positively regulates curli fimbriae production and represses acid chaperone proteins. RpoS and other regulatory mechanisms may impact curli fimbriae production, as well. These findings may help elucidate mechanisms underlying differences among STEC strains in relating acid resistance and biofilm formation.

Citing Articles

Phenotypic and genomic comparison of three human outbreak and one cattle-associated Shiga toxin-producing O157:H7.

Peroutka-Bigus N, Nielsen D, Trachsel J, Mou K, Sharma V, Kudva I Microbiol Spectr. 2024; 12(10):e0414023.

PMID: 39254337 PMC: 11451603. DOI: 10.1128/spectrum.04140-23.


Expression and Functional Characterization of Various Chaperon-Usher Fimbriae, Curli Fimbriae, and Type 4 Pili of Enterohemorrhagic O157:H7 Sakai.

Elpers L, Hensel M Front Microbiol. 2020; 11:378.

PMID: 32265855 PMC: 7098969. DOI: 10.3389/fmicb.2020.00378.

References
1.
Uhlich G, Chen C, Cottrell B, Hofmann C, Dudley E, Strobaugh T . Phage insertion in mlrA and variations in rpoS limit curli expression and biofilm formation in Escherichia coli serotype O157: H7. Microbiology (Reading). 2013; 159(Pt 8):1586-1596. DOI: 10.1099/mic.0.066118-0. View

2.
Ogasawara H, Hasegawa A, Kanda E, Miki T, Yamamoto K, Ishihama A . Genomic SELEX search for target promoters under the control of the PhoQP-RstBA signal relay cascade. J Bacteriol. 2007; 189(13):4791-9. PMC: 1913430. DOI: 10.1128/JB.00319-07. View

3.
Oh D, Pan Y, Berry E, Cooley M, Mandrell R, Breidt Jr F . Escherichia coli O157:H7 strains isolated from environmental sources differ significantly in acetic acid resistance compared with human outbreak strains. J Food Prot. 2009; 72(3):503-9. DOI: 10.4315/0362-028x-72.3.503. View

4.
Iyer R, Williams C, Miller C . Arginine-agmatine antiporter in extreme acid resistance in Escherichia coli. J Bacteriol. 2003; 185(22):6556-61. PMC: 262112. DOI: 10.1128/JB.185.22.6556-6561.2003. View

5.
Jorgensen M, Nielsen J, Boysen A, Franch T, Moller-Jensen J, Valentin-Hansen P . Small regulatory RNAs control the multi-cellular adhesive lifestyle of Escherichia coli. Mol Microbiol. 2012; 84(1):36-50. DOI: 10.1111/j.1365-2958.2012.07976.x. View