Anti-Salmonella Defence and Intestinal Homeostatic Maintenance In Vitro of a Consortium Containing Limosilactobacillus fermentum 3872 and Ligilactobacillus salivarius 7247 Strains in Human, Porcine, and Chicken Enterocytes

Author:

Abramov Vyacheslav M.12,Kosarev Igor V.12,Machulin Andrey V.3ORCID,Deryusheva Evgenia I.4,Priputnevich Tatiana V.2,Panin Alexander N.1,Chikileva Irina O.5ORCID,Abashina Tatiana N.3ORCID,Manoyan Ashot M.1ORCID,Akhmetzyanova Anna A.1ORCID,Blumenkrants Dmitriy A.1,Ivanova Olga E.1,Papazyan Tigran T.6,Nikonov Ilia N.7ORCID,Suzina Nataliya E.3ORCID,Melnikov Vyacheslav G.8ORCID,Khlebnikov Valentin S.9,Sakulin Vadim K.9,Samoilenko Vladimir A.3,Gordeev Alexey B.2,Sukhikh Gennady T.2,Uversky Vladimir N.10ORCID,Karlyshev Andrey V.11ORCID

Affiliation:

1. Federal Service for Veterinary and Phytosanitary Surveillance (Rosselkhoznadzor) Federal State Budgetary Institution “The Russian State Center for Animal Feed and Drug Standardization and Quality” (FGBU VGNKI), 123022 Moscow, Russia

2. Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health, 117997 Moscow, Russia

3. Skryabin Institute of Biochemistry and Physiology of Microorganisms, Federal Research Center “Pushchino Scientific Center for Biological Research of Russian Academy of Science”, Russian Academy of Science, 142290 Pushchino, Russia

4. Institute for Biological Instrumentation, Federal Research Center “Pushchino Scientific Center for Biological Research of Russian Academy of Science”, Russian Academy of Science, 142290 Pushchino, Russia

5. Blokhin National Research Center of Oncology, Ministry of Health RF, 115478 Moscow, Russia

6. Alltech Company Moscow, 105062 Moscow, Russia

7. Federal State Educational Institution of Higher Professional Education, Moscow State Academy of Veterinary Medicine and Biotechnology Named after K.I. Skryabin, 109472 Moscow, Russia

8. Gabrichevsky Research Institute for Epidemiology and Microbiology, 125212 Moscow, Russia

9. Institute of Immunological Engineering, 142380 Lyubuchany, Russia

10. Department of Molecular Medicine, Morsani College of Medicine, University of South Florida, Tampa, FL 33612, USA

11. Department of Biomolecular Sciences, School of Life Sciences, Chemistry and Pharmacy, Faculty of Health, Science, Social Care and Education, Kingston University London, Kingston upon Thames KT1 2EE, UK

Abstract

Limosilactobacillus fermentum strain 3872 (LF3872) was originally isolated from the breast milk of a healthy woman during lactation and the breastfeeding of a child. Ligilactobacillus salivarius strain 7247 (LS7247) was isolated at the same time from the intestines and reproductive system of a healthy woman. The genomes of these strains contain genes responsible for the production of peptidoglycan-degrading enzymes and factors that increase the permeability of the outer membrane of Gram-negative pathogens. In this work, the anti-Salmonella and intestinal homeostatic features of the LF3872 and LS7247 consortium were studied. A multi-drug resistant (MDR) strain of Salmonella enteritidis (SE) was used in the experiments. The consortium effectively inhibited the adhesion of SE to intact and activated human, porcine, and chicken enterocytes and reduced invasion. The consortium had a bactericidal effect on SE in 6 h of co-culturing. A gene expression analysis of SE showed that the cell-free supernatant (CFS) of the consortium inhibited the expression of virulence genes critical for the colonization of human and animal enterocytes. The CFS stimulated the production of an intestinal homeostatic factor—intestinal alkaline phosphatase (IAP)—in Caco-2 and HT-29 enterocytes. The consortium decreased the production of pro-inflammatory cytokines IL-8, TNF-α, and IL-1β, and TLR4 mRNA expression in human and animal enterocytes. It stimulated the expression of TLR9 in human and porcine enterocytes and stimulated the expression of TLR21 in chicken enterocytes. The consortium also protected the intestinal barrier functions through the increase of transepithelial electrical resistance (TEER) and the inhibition of paracellular permeability in the monolayers of human and animal enterocytes. The results obtained suggest that a LF3872 and LS7247 consortium can be used as an innovative feed additive to reduce the spread of MDR SE among the population and farm animals.

Funder

Government of the Russian Federation

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Microbiology (medical),General Pharmacology, Toxicology and Pharmaceutics,Biochemistry,Microbiology

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