Bacterial Community Assessed by Utilization of Single Carbon Sources in Broiler Ground Meat after Treatment with an Antioxidant, Carnosine, and Cold Plasma

Author:

YEH HUNG-YUEH1,LINE JOHN E.1,HINTON ARTHUR1,GAO YUE234,ZHUANG HONG2

Affiliation:

1. U.S. Department of Agriculture, Agricultural Research Service, U.S. National Poultry Research Center, Poultry Microbiological Safety and Processing Research Unit, 950 College Station Road, Athens, Georgia 30605-2720, USA (ORCID: https://orcid.org/0000-0003-0806-2428 [H.Y.Y.])

2. U.S. Department of Agriculture, Agricultural Research Service, U.S. National Poultry Research Center, Quality and Safety Assessment Research Unit, 950 College Station Road, Athens, Georgia 30605-2720, USA

3. National Center of Meat Quality and Safety Control, Nanjing Agricultural University, Nanjing 210095, People's Republic of China

4. Suzhou Polytechnic Institute of Agriculture, Suzhou 215008, People's Republic of China

Abstract

ABSTRACT Contaminated poultry meat is a major source of human foodborne illnesses. Many interventions have been developed to reduce and/or eliminate human foodborne pathogens in poultry products; however, treatments with cold plasma or carnosine or their combination have not been extensively investigated. In this study, the bacterial microflora of poultry meat samples after treatments with cold plasma and carnosine were characterized with EcoPlates in the OmniLog system. The plates were incubated at 25°C for 7 days in the OmniLog chamber, and bacterial growth was monitored by recording formazan production every 30 min at an optical density of 590 nm. The kinetics of lag, log, and stationary phases of bacterial growth followed the Gompertz sigmoidal model but with different inflection times and asymptotes at the log phase and the stationary phase, respectively. Results indicated that treatment of poultry meat samples with cold plasma technology and carnosine could inhibit growth of the bacteria in the treated meat samples. Of 31 chemicals tested, phenylethylamine, α-d-lactose, d,l-α-glycerol phosphate, 2-hydroxybenzoic acid, γ-hydroxybutyric acid, α-ketobutyric acid, and d-malic acid could not be metabolized by bacteria in the meat samples. Future research is required to determine whether these seven chemicals that inhibited growth of bacteria in these meat samples can be used as food preservatives for extending the shelf life of these products. Whether the bacterial flora can be an indicator of effectiveness for meat samples treated with cold plasma, carnosine, or both needs further study. HIGHLIGHTS

Publisher

International Association for Food Protection

Subject

Microbiology,Food Science

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