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Efficacy of Organic Acid Treatments for the Reduction of Listeria monocytogenes on Hard Boiled Eggs.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Efficacy of Organic Acid Treatments for the Reduction of Listeria monocytogenes on Hard Boiled Eggs./
作者:
Khouja, Bashayer.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2022,
面頁冊數:
57 p.
附註:
Source: Masters Abstracts International, Volume: 83-12.
Contained By:
Masters Abstracts International83-12.
標題:
Food science. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=29164161
ISBN:
9798438784494
Efficacy of Organic Acid Treatments for the Reduction of Listeria monocytogenes on Hard Boiled Eggs.
Khouja, Bashayer.
Efficacy of Organic Acid Treatments for the Reduction of Listeria monocytogenes on Hard Boiled Eggs.
- Ann Arbor : ProQuest Dissertations & Theses, 2022 - 57 p.
Source: Masters Abstracts International, Volume: 83-12.
Thesis (M.S.)--Illinois Institute of Technology, 2022.
This item must not be sold to any third party vendors.
Ready-to-eat hard-boiled eggs (HBEs) are a popular and convenient choice for consumers and food servicers. Recent recalls of hard-boiled eggs have highlighted the susceptibility of contamination with Listeria monocytogenes. HBEs are generally treated with antibacterials to ensure the safety and quality of the product. While citric acid is often used, research has determined it is not effective in some situations; therefore, the assessment of additional organic acids is necessary. This study examined the efficacy of acetic, lactic, and malic acid on the reduction of L. monocytogenes on HBEs after a 24- hour treatment trials and 28 days storage trials. Fresh eggs were cooked in boiling water, peeled, and stored at 4 °C for 24h before use. For treatment trials, HBEs were dip- inoculated with a 4-strain cocktail of rifampicin-resistant L. monocytogenes, resulting in 8 log CFU/egg. Following air drying, hard-boiled eggs were treated at 5 or 25 °C with 2% acetic, lactic, or malic acid. L monocytogenes populations were enumerated in intervals up to 24h by homogenization of HBEs with BLEB and cultivation on BHIrif. For pre- treatment storage trials, HBEs were first dip-inoculated with a rifampicin- resistant 4- strain L. monocytogenes cocktail for 20 min, resulting in 1 log CFU/egg, airdried for 10 min, followed by treatment with 2% acetic, lactic, or malic acid for 24 h at either 5 or 25 °C. For post-treatment inoculation trials, HBEs were first soaked in 2% acetic, lactic, or malic acid for 24 h at either 5 or 25 °C, airdried for 10 min, spot-inoculated at 1 log CFU/egg, and then dried for 20 min. All HBEs were individually stored in bags at 5 °C for up to 28 days. The presence of L. monocytogenes was determined at intervals during storage by enrichment with BLEB on BHIrif and Brilliance Listeria Agar. Triplicate eggs were assessed for each timepoint, and three independent trials were conducted. Data were analyzed by Student's t-test, ANOVA, and Fisher's exact test, p ≤ 0.05. The initial inoculation level of L. monocytogenes on HBEs was 8.27±0.37 log CFU/egg. After 24 h treatment, all L. monocytogenes populations were significantly reduced on HBEs. At 5 °C, populations were reduced by 3.15±0.70,3.46±0.02, and 4.78±0.23 log CFU/egg. Compared to 5 °C, a significantly higher population reduction occurred with acetic and lactic acid when treatment occurred at 25 °C. The inactivation of L. monocytogenes on HBEs for the storage trials was associated with the order of the contamination: pre-or post-the acid treatment. Prior storage, L. monocytogenes was detected on 100% of the HBEs. Malic acid pre-treatment was significantly effective in eliminating L. monocytogenes on HBEs at 5 and 25 °C, while acetic acid was effective only at 5 °C. All acids did not eliminate L. monocytogenes in the case of post-treatment contamination at any tested temperature. The results of this study aid in understanding the efficacy of organic acid treatments against L. monocytogenes on HBEs. Results are useful in the development of preventive controls and guidelines to ensure the safety of HBEs.
ISBN: 9798438784494Subjects--Topical Terms:
3173303
Food science.
Subjects--Index Terms:
Food microbiology
Efficacy of Organic Acid Treatments for the Reduction of Listeria monocytogenes on Hard Boiled Eggs.
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Ready-to-eat hard-boiled eggs (HBEs) are a popular and convenient choice for consumers and food servicers. Recent recalls of hard-boiled eggs have highlighted the susceptibility of contamination with Listeria monocytogenes. HBEs are generally treated with antibacterials to ensure the safety and quality of the product. While citric acid is often used, research has determined it is not effective in some situations; therefore, the assessment of additional organic acids is necessary. This study examined the efficacy of acetic, lactic, and malic acid on the reduction of L. monocytogenes on HBEs after a 24- hour treatment trials and 28 days storage trials. Fresh eggs were cooked in boiling water, peeled, and stored at 4 °C for 24h before use. For treatment trials, HBEs were dip- inoculated with a 4-strain cocktail of rifampicin-resistant L. monocytogenes, resulting in 8 log CFU/egg. Following air drying, hard-boiled eggs were treated at 5 or 25 °C with 2% acetic, lactic, or malic acid. L monocytogenes populations were enumerated in intervals up to 24h by homogenization of HBEs with BLEB and cultivation on BHIrif. For pre- treatment storage trials, HBEs were first dip-inoculated with a rifampicin- resistant 4- strain L. monocytogenes cocktail for 20 min, resulting in 1 log CFU/egg, airdried for 10 min, followed by treatment with 2% acetic, lactic, or malic acid for 24 h at either 5 or 25 °C. For post-treatment inoculation trials, HBEs were first soaked in 2% acetic, lactic, or malic acid for 24 h at either 5 or 25 °C, airdried for 10 min, spot-inoculated at 1 log CFU/egg, and then dried for 20 min. All HBEs were individually stored in bags at 5 °C for up to 28 days. The presence of L. monocytogenes was determined at intervals during storage by enrichment with BLEB on BHIrif and Brilliance Listeria Agar. Triplicate eggs were assessed for each timepoint, and three independent trials were conducted. Data were analyzed by Student's t-test, ANOVA, and Fisher's exact test, p ≤ 0.05. The initial inoculation level of L. monocytogenes on HBEs was 8.27±0.37 log CFU/egg. After 24 h treatment, all L. monocytogenes populations were significantly reduced on HBEs. At 5 °C, populations were reduced by 3.15±0.70,3.46±0.02, and 4.78±0.23 log CFU/egg. Compared to 5 °C, a significantly higher population reduction occurred with acetic and lactic acid when treatment occurred at 25 °C. The inactivation of L. monocytogenes on HBEs for the storage trials was associated with the order of the contamination: pre-or post-the acid treatment. Prior storage, L. monocytogenes was detected on 100% of the HBEs. Malic acid pre-treatment was significantly effective in eliminating L. monocytogenes on HBEs at 5 and 25 °C, while acetic acid was effective only at 5 °C. All acids did not eliminate L. monocytogenes in the case of post-treatment contamination at any tested temperature. The results of this study aid in understanding the efficacy of organic acid treatments against L. monocytogenes on HBEs. Results are useful in the development of preventive controls and guidelines to ensure the safety of HBEs.
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