Heat-resistant and biofilm-forming Escherichia coli in pasteurized milk from Brazil

• Published in: Brazilian journal of microbiology 2023-06, Vol.54 (2), p.1035-1046
• Main Authors: Machado, Maxsueli Aparecida Moura, Castro, Vinicius Silva, da Cunha-Neto, Adelino, Vallim, Deyse Christina, Pereira, Rodrigo de Castro Lisbôa, dos Reis, Jaqueline Oliveira, de Almeida, Patrícia Veiga, Galvan, Diego, Conte-Junior, Carlos Adam, Figueiredo, Eduardo Eustáquio de Souza
• Format: Article
• Language: English
• Subjects: Animals; Anti-Bacterial Agents - pharmacology; Antibiotics; Antiinfectives and antibacterials; Antimicrobial agents; Biofilms; Biomedical and Life Sciences; Brazil; Coliforms; E coli; Electrophoresis; Enterobacteriaceae; Escherichia coli; Escherichia coli - genetics; Food contamination; Food Microbiology; Food Microbiology - Research Paper; Gene expression; Genotypes; Heat resistance; Hot Temperature; Legislation; Life Sciences; Medical Microbiology; Microbial Ecology; Microbial Genetics and Genomics; Microbiology; Milk; Milk - microbiology; Mycology; Pasteurization; Pasteurized milk; Phenotypes; Pulsed-field gel electrophoresis; Thermal resistance; Water baths
• ISSN: 1517-8382; 1678-4405
• DOI: 10.1007/s42770-023-00920-8

Escherichia coli harboring a transmissible locus of stress tolerance (tLST) and the ability to form biofilms represent a serious risk in dairy production. Thus, we aimed to evaluate the microbiological quality of pasteurized milk from two dairy producers in Mato Grosso, Brazil, with a focus on determining the possible presence of E. coli with heat resistance (60 °C/6 min), biofilm-forming potential phenotypes and genotypes, and antimicrobial susceptibility. For this, fifty pasteurized milk samples from producers named A and B were obtained for 5 weeks to investigate the presence of Enterobacteriaceae members , coliforms, and E. coli . For heat resistance, E. coli isolates were exposed to a water bath at 60 °C for 0 and 6 min. In antibiogram analysis, eight antibiotics belonging to six antimicrobial classes were analyzed. The potential to form biofilms was quantified at 570 nm, and curli expression by Congo Red was analyzed. To determine the genotypic profile, we performed PCR for the tLST and rpoS genes, and pulsed-field gel electrophoresis (PFGE) was used to investigate the clonal profile of the isolates. Thus, producer A presented unsatisfactory microbiological conditions regarding Enterobacteriaceae and coliforms for weeks 4 and 5, while all samples analyzed for producer B were contaminated at above-the-limit levels established by national and international legislation. These unsatisfactory conditions enabled us to isolate 31 E. coli from both producers (7 isolates from producer A and 24 isolates from producer B). In this way, 6 E. coli isolates (5 from producer A and 1 from producer B) were highly heat resistant. However, although only 6 E. coli showed a highly heat-resistant profile, 97% (30/31) of all E. coli were tLST-positive. In contrast, all isolates were sensitive to all antimicrobials tested. In addition, moderate or weak biofilm potential was verified in 51.6% (16/31), and the expression of curli and presence of rpoS was not always related to this biofilm potential. Therefore, the results emphasize the spreading of heat-resistant E. coli with tLST in both producers and indicate the biofilm as a possible source of contamination during milk pasteurization. However, the possibility of E. coli producing biofilm and surviving pasteurization temperatures cannot be ruled out, and this should be investigated.