Persistence of Listeria innocua on Fresh Apples during Long-Term Controlled Atmosphere Cold Storage with Postharvest Fungal Decay

Author:

HAMILTON ALEXIS1ORCID,RUIZ-LLACSAHUANGA BLANCA1,MENDOZA MANOELLA2,MATTHEIS JAMES3,HANRAHAN INES2,CRITZER FAITH J.1

Affiliation:

1. School of Food Science, Irrigated Agriculture Research and Extension Center, Washington State University, Prosser, Washington 99350

2. Washington Tree Fruit Research Commission, 1719 Springwater Avenue, Wenatchee, Washington 98801

3. U.S. Department of Agriculture, Agricultural Research Service, Physiology and Pathology of Tree Fruits Research Unit, 1104 North Western Avenue, Wenatchee, Washington 98801, USA

Abstract

ABSTRACT Recent apple-related recall and outbreak events have exposed a need for better food safety controls along the supply chain. Following harvest, apples can be stored under a controlled atmosphere for up to 1 year after harvest before packing and distribution, making the crop susceptible to many opportunities for contamination that increase the quantity of postharvest losses. Botrytis cinerea and Penicillium expansum cause significant rot-associated losses to the apple industry. These fungi can colonize and destroy apple tissue as storage duration increases, which may also impact the growth of saprophytic foodborne pathogens like Listeria monocytogenes. Thus, the objective of this study was to observe population changes of Listeria innocua as a surrogate for L. monocytogenes on apples inoculated with B. cinerea or P. expansum under long-term controlled atmosphere cold storage conditions to identify the effect of postharvest mold growth on growth patterns of a microorganism relevant to food safety. ‘Gala' and ‘WA 38’ apples (n = 1,080) were harvested, treated with pyrimethanil, and inoculated with L. innocua only or with L. innocua and one of the mold species on wounded and unwounded portions of the apple equator. Apples were treated with 1-methylcyclopropene and stored at a controlled atmosphere (2 kPa O2, 1 kPa CO2, 1°C) for 1 week and 1, 3, 6, 9, and 11 months before enumeration. After 3 months, L. innocua consistently fell below the limit of detection (2.35 Log CFU/g), and samples were enriched following a modified Bacteriological Analytical Manual method with PCR confirmation. Listeria persistence was dependent on the storage duration and type of fungal contamination (P ≤ 0.05). Surface wounding may impact these trends, depending on the apple variety. Prevalence of L. innocua was greater in Gala apples. Future studies should more closely examine the interactions on the fruit surface that occur during the seemingly critical time frame of 3 to 6 months in storage. HIGHLIGHTS

Publisher

International Association for Food Protection

Subject

Microbiology,Food Science

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