Survival of Listeria Strains and Shelf Life Determination of Fresh Blueberries (Vaccinium corymbosum) Treated with Cold Atmospheric Plasma

Author:

Concha-Meyer Anibal A.12ORCID,González-Esparza Alexandra1,Cullen Patrick J.3,Veloso Felipe45ORCID,Favre Mario4,Valenzuela Julio C.4,Toloza Lorena6ORCID,Niemira Brendan A.7ORCID

Affiliation:

1. Instituto de Ciencia y Tecnología de los Alimentos, Facultad de Ciencias Agrarias y Alimentarias, Universidad Austral de Chile, Campus Isla Teja s/n, Valdivia 5090000, Chile

2. Centro de Estudios en Alimentos Procesados (CEAP), CONICYT-Regional, Gore Maule, R09I2001, Casilla 1007, Talca 3460000, Chile

3. School of Chemical and Biomolecular Engineering, University of Sydney, Sydney 2006, Australia

4. Instituto de Física, Pontificia Universidad Católica de Chile, Casilla 306, Santiago 7820436, Chile

5. Centro de Investigación en Nanotecnología y Materiales Avanzados CIEN-UC, Pontificia Universidad Católica de Chile, Santiago 7820436, Chile

6. Department of Experimental and Health Sciences, Pompeu Fabra University, 08002 Barcelona, Spain

7. USDA–ARS, Eastern Regional Research Center, Characterization and Interventions for Foodborne Pathogens Unit, Wyndmoor, PA 19038, USA

Abstract

Fresh blueberries are delicate, hand-picked, packaged, and refrigerated fruits vulnerable to spoilage and contamination. Cold atmospheric plasma (CAP) is a promising antimicrobial technology; therefore, this study evaluated the CAP treatment effect on acid-tolerant Listeria innocua and Listeria monocytogenes and evaluated changes in the quality of the treated fruit. Samples were spot-inoculated with pH 5.5 and 6.0 acid-adapted Listeria species. Samples were treated with gliding arc CAP for 15, 30, 45, and 60 s and evaluated after 0, 1, 4, 7, and 11 days of storage at 4 °C and 90% humidity for the following quality parameters: total aerobic counts, yeast and molds, texture, color, soluble solids, pH, and titratable acidity. CAP treatments of 30 s and over demonstrated significant reductions in pathogens under both the resistant strain and pH conditions. Sixty-second CAP achieved a 0.54 Log CFU g−1 reduction in L. monocytogenes (pH 5.5) and 0.28 Log CFU g−1 for L. monocytogenes (pH 6.0). Yeast and mold counts on day 0 showed statistically significant reductions after 30, 45, and 60 s CAP with an average 2.34 Log CFU g−1 reduction when compared to non-CAP treated samples. Quality parameters did not show major significant differences among CAP treatments during shelf life. CAP is an effective antimicrobial treatment that does not significantly affect fruit quality.

Funder

Agencia Nacional de Investigación y Desarrollo Chile/FONDECYT de Iniciación

Agencia Nacional de Investigación y Desarrollo Chile/IDeA I+D

Agencia Nacional de Investigación y Desarrollo Chile/Gore Maule/CEAP

Publisher

MDPI AG

Reference49 articles.

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