Assessment of food microbiological indicators applied on poultry carcasses by culture combined MALDI-TOF MS identification and 16S rRNA amplicon sequencing.

Food Microbiol

Department of Veterinary Public Health and Food Safety, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820, Merelbeke, Belgium. Electronic address:

Published: September 2019

AI Article Synopsis

  • Standard culture methods are still the main way to examine bacterial contamination in food, but culture-independent methods may be more reliable.
  • The study assessed the effects of different incubation temperatures on bacterial diversity in chicken carcasses and found no significant differences in bacterial levels.
  • Advanced techniques like 16S rRNA amplicon sequencing showed more bacterial diversity, highlighting the importance of DNA extraction methods and the presence of non-viable bacteria in results interpretation.

Article Abstract

Examination of the bacterial contamination on food products is still largely performed by standardized culture methods, though culture-independent methods are suggested as a more reliable approach. Knowledge of the diversity of bacteria isolated from food as well as the impact of the plate incubation conditions applied are still understudied. The impact of incubation at 7 °C and 30 °C on total aerobic bacterial count and diversity, and the performance of ISO methods generally applied in microbiological quality examination were assessed by culture combined MALDI-TOF MS identification and 16S rRNA amplicon sequencing. Examining breast skin of 16 chicken carcasses, no significant impact of the incubation temperature on the total aerobic bacteria level and diversity was detected, limiting the usefulness of additional psychrophilic examination. Bacteria phenotypically similar to Pseudomonas, were identified on selective CFC plates, and on MRS agar plates for lactic acid bacteria, Escherichia coli and Staphylococcus were commonly present. Application of 16S rRNA amplicon sequencing revealed a higher bacterial diversity, but the impact of the DNA extraction kit applied, and the detection of non-viable bacteria should be taken into account to interpret the final outcome.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.fm.2019.01.018DOI Listing

Publication Analysis

Top Keywords

16s rrna
12
rrna amplicon
12
amplicon sequencing
12
culture combined
8
combined maldi-tof
8
maldi-tof identification
8
identification 16s
8
impact incubation
8
total aerobic
8
bacteria
5

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!