Organic Acid Production and Food Pathogen Suppression by Probiotic and .

Front Microbiol

Key Laboratory of Dairy Science, Ministry of Education, College of Food Sciences, Northeast Agricultural University, Harbin, China.

Published: April 2019

Foodborne pathogens are a major source of morbidity and mortality worldwide. For this cause, exploring various effective ways of suppressing their spread is at the forefront of many research projects. The current study aims to investigate the organic acid production of KLDS 3.1003 and KLDS 1.0207 strains, their suppression of and immuno-modulatory effects against ATCC 25922 and ATCC 25923 pathogens. First, lactic and acetic acid production using three carbon sources - 1% glucose (control), 1% sucrose, and 1% fructo-oligosaccharides (FOS) - was determined by HPLC. For the section, a total of 40 BALB/c mice were purchased and divided into 10 treatment groups (control and nine treatments). Animals were given 1 week to acclimatize and then fed treatment diets for 14 days. Afterward, hematological (RBC, WBC, HB, PLT, Neutrophils, Eosinophils, Lymphocytes, and Monocytes) and histopathological analyses were carried out. All analyses were done in triplicate. Results show that lactic and acetic acid productions for both strains increased with supplementation and were highest after 1% FOS addition. Regardless of carbon source, KLDS 1.0207 produced higher ( < 0.05) amounts of lactic and acetic acids than KLDS 3.1003. Also, generally better hematological parameters in probiotic groups than the control ( < 0.05) were observed. In some instances, mice in probiotic treatment groups had better immunity levels (lymphocytes, monocytes, neutrophils, eosinophils) than those in the control and pathogen groups. Histopathological studies showed that no anomalies were associated with KLDS 3.1003 and KLDS 1.0207 administration. In conclusion, KLDS 3.1003 and KLDS 1.0207 strains are not only probiotic candidates but can have therapeutic applications.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6479190PMC
http://dx.doi.org/10.3389/fmicb.2019.00782DOI Listing

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