Evaluation of Some Organic Acids as Potential Decontaminants of Vibrio parahaemolyticus in Fresh Shrimp
World Journal of Dairy & Food Sciences • 2012
Publication Information
Authors
A.M. Salem; R.A. Amin
Keywords
Shrimp; V. parahemolyticus; Citric Acid; Acetic Acid
Journal
World Journal of Dairy & Food Sciences
Publisher
IDOSI
Volume
7
Issue
1
Pages
41-48
publication.type
International
Paper Link
Not Available
Supplementary Materials
Not Available
Abstract
Citric acid and acetic acid were evaluated for their effects on the growth and survival of
Vibrio parahaemolyticus artificially inoculated into fresh shrimp. Fresh shrimp samples were dipped in Tryptic
Soy Broth (TSB) containing (~10 Colony Forming Units (CFU)/ml) (7 log CFU/g) of Vibrio parahaemolyticus
7
and left for 30 min. at room temperature (25°C) to allow attachment. Initial counts of Vibrio parahaemolyticus
inshrimp samples immediately after dipping in TSB broth were 10.91 log CFU/g. Inoculated shrimp samples
(25°C) were dipped in citric acid 5% and 10% and acetic acid 4% and 8% for 5, 15, 30, 60 minutes and 24 hours.
Initial counts of Vibrio parahaemolyticus in shrimp samples decreased following treatment with citric acid 5%
and 10% for 5 min. by 5.68 log CFU/g (52.06%) and 7.91 log CFU/g (72.5%), respectively and following treatment
withacetic acid 4% for 5 min. by 6.61 log CFU/g (60.59%). Growth of Vibrio parahaemolyticus in shrimp
samples was completely inhibited after being dippedin acetic acid 8% for 5 min., acetic acid 4% for 15 min and
citric acid 10% for 30 min.When compared to several other mild preservation procedures, treatment with citric
andacetic acids is inexpensive and uncomplicated method. Results of the present study are envisaged to be
useful for commercial applications for effective decontamination of shrimp.
Vibrio parahaemolyticus artificially inoculated into fresh shrimp. Fresh shrimp samples were dipped in Tryptic
Soy Broth (TSB) containing (~10 Colony Forming Units (CFU)/ml) (7 log CFU/g) of Vibrio parahaemolyticus
7
and left for 30 min. at room temperature (25°C) to allow attachment. Initial counts of Vibrio parahaemolyticus
inshrimp samples immediately after dipping in TSB broth were 10.91 log CFU/g. Inoculated shrimp samples
(25°C) were dipped in citric acid 5% and 10% and acetic acid 4% and 8% for 5, 15, 30, 60 minutes and 24 hours.
Initial counts of Vibrio parahaemolyticus in shrimp samples decreased following treatment with citric acid 5%
and 10% for 5 min. by 5.68 log CFU/g (52.06%) and 7.91 log CFU/g (72.5%), respectively and following treatment
withacetic acid 4% for 5 min. by 6.61 log CFU/g (60.59%). Growth of Vibrio parahaemolyticus in shrimp
samples was completely inhibited after being dippedin acetic acid 8% for 5 min., acetic acid 4% for 15 min and
citric acid 10% for 30 min.When compared to several other mild preservation procedures, treatment with citric
andacetic acids is inexpensive and uncomplicated method. Results of the present study are envisaged to be
useful for commercial applications for effective decontamination of shrimp.
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