Ability of Lactobacillus plantarum lipoteichoic acid to inhibit Vibrio anguillarum-induced inflammation and apoptosis in silvery pomfret (Pampus argenteus) intestinal epithelial cells

Fish and Shellfish Immunology

Volumn 54, Issue , 2016, Pages 573-579

  Gao, Quanxin ^a   Gao, Qian ^b   Min, Minghua ^a   Zhang, Chenjie ^a   Peng, Shiming ^a   Shi, Zhaohong ^a  

^a SOUTH CHINA SEA FISHERIES RESEARCH INSTITUTE   (China)

^b Shibo High Tech Hospital   (China)

Author keywords

Apoptosis; Inflammation; Lactobacillus plantarum; Lipoteichoic acid; Vibrio anguillarum

Indexed keywords

LIPOPOLYSACCHARIDE; LIPOTEICHOIC ACID; PROBIOTIC AGENT; TEICHOIC ACID;

ANIMAL; APOPTOSIS; BIOASSAY; CHEMISTRY; DRUG EFFECTS; EPITHELIUM CELL; FISH DISEASES; IN VITRO STUDY; INFLAMMATION; INTESTINE; LACTOBACILLUS PLANTARUM; MICROBIOLOGY; PERCIFORMES; PHYSIOLOGY; VIBRIO; VIBRIO INFECTIONS;

ANIMALS; APOPTOSIS; BIOLOGICAL ASSAY; EPITHELIAL CELLS; FISH DISEASES; IN VITRO TECHNIQUES; INFLAMMATION; INTESTINES; LACTOBACILLUS PLANTARUM; LIPOPOLYSACCHARIDES; PERCIFORMES; PROBIOTICS; TEICHOIC ACIDS; VIBRIO; VIBRIO INFECTIONS;

EID: 84989863448     PISSN: 10504648     EISSN: 10959947     Source Type: Journal    
DOI: 10.1016/j.fsi.2016.05.013     Document Type: Article

References (28)

1. [1] Nayak, S.K., Probiotics and immunity: a fish perspective. Fish. Shellfish Immun. 29 (2010), 2–14.
2. [2] Dash, G., Raman, R.P., Prasad, K.P., Makesh, M., Pradeep, M.A., Sen, S., Evaluation of Lactobacillus plantarum as feed supplement on host associated microflora, growth, feed efficiency, carcass biochemical composition and immune response of giant freshwater prawn, Macrobrachium rosenbergii (de Man, 1879). Aquaculture 432 (2014), 225–236.
3. [3] Talpur, A.D., Ikhwanuddin, M., Abdullah, M.D.D., Bolong, A.M.A., Indigenous Lactobacillus plantarum as probiotic for larviculture of blue swimming crab, Portunus pelagicus (Linnaeus, 1758): effects on survival, digestive enzyme activities and water quality. Aquaculture 416 (2013), 173–178.
4. [4] Touraki, M., Karamanlidou, G., Karavida, P., Chrysi, K., Evaluation of the probiotics Bacillus subtilis and Lactobacillus plantarum bioencapsulated in Artemia nauplii against vibriosis in European sea bass larvae (Dicentrarchus labrax, L.). World J. Microb. Biot. 28 (2012), 2425–2433.
5. [5] Baik, J.E., Jang, Y.O., Kang, S.S., Cho, K., Yun, C.H., Han, S.H., Differential profiles of gastrointestinal proteins interacting with peptidoglycans from Lactobacillus plantarum and Staphylococcus aureus. Mol. Immunol. 65 (2015), 77–85.
6. [6] Ramiah, K., van Reenen, C.A., Dicks, L.M.T., Surface-bound proteins of Lactobacillus plantarum 423 that contribute to adhesion of Caco-2 cells and displacement of Clostridium sporogenes and Enterococcus faecalis. Res. Microbiol. 159 (2008), 470–475.
7. [7] Yadav, A.K., Tyagi, A., Kaushik, J.K., Saklani, A.C., Grover, S., Batish, V.K., Role of surface layer collagen binding protein from indigenous Lactobacillus plantarum 91 in adhesion and its anti-adhesion potential against gut pathogen. Microbiol. Res. 168 (2013), 639–645.
8. [8] Kim, H.G., Lee, S.Y., Kim, N.R., Lee, H.Y., Ko, M.Y., Jung, B.J., Kim, C.M., Lee, J.M., Park, J.H., Han, S.H., Chung, D.K., Lactobacillus plantarum lipoteichoic acid down-regulated Shigella flexneri peptidoglycan-induced inflammation. Mol. Immunol. 48 (2011), 382–391.
9. [9] Kaji, R., Kiyoshima-Shibata, J., Nagaoka, M., Nanno, M., Shida, K., Bacterial teichoic acids reverse predominant IL-12 production induced by certain Lactobacillus strains into predominant IL-10 production via TLR2-dependent ERK activation in macrophages. J. Immunol. 184 (2010), 3505–3513.
10. [10] Kim, H.G., Kim, N.R., Gim, M.G., Lee, J.M., Lee, S.Y., Ko, M.Y., Kim, J.Y., Han, S.H., Chung, D.K., Lipoteichoic acid isolated from Lactobacillus plantarum inhibits lipopolysaccharide-induced TNF-α production in THP-1 cells and endotoxin shock in mice. J. Immunol. 180 (2008), 2553–2561.
11. [11] Noh, S.Y., Kang, S.S., Yun, C.H., Han, S.H., Lipoteichoic acid from Lactobacillus plantarum inhibits Pam2CSK4-induced IL-8 production in human intestinal epithelial cells. Mol. Immunol. 64 (2014), 183–189.
12. [12] Wei, W., Xu, H.Y., Wang, Q.Y., Zhang, X., Chang, K.M., Wu, C.W., Zhang, Y.X., Identification of differentially expressed genes in large yellow croaker (Pseudosciaena crocea) induced by attenuated live Vibrio anguillarum. Aquaculture 291 (2009), 124–129.
13. [13] Kang, S.S., Ryu, Y.H., Baik, J.E., Yun, C.H., Lee, K., Chung, D.K., Han, S.H., Lipoteichoic acid from Lactobacillus plantarum induces nitric oxide production in the presence of interferon-γ in murine macrophages. Mol. Immunol. 48 (2011), 2170–2177.
14. [14] Gao, Q.X., Xiao, Y.P., Sun, P., Peng, S.M., Yin, F., Ma, X.M., Shi, Z.H., In vitro protective efficacy of Clostridium butyricum against fish pathogen infections. Indian J. Microbiol. 53 (2013), 453–459.
15. [15] Gao, Q.X., Qi, L.L., Wu, T.X., Wang, J.B., Ability of Clostridium butyricum to inhibit Escherichia coli-induced apoptosis in chicken embryo intestinal cells. Vet. Microbiol. 160 (2012), 395–401.
16. [16] Gao, Q.X., Qi, L.L., Wu, T.X., Wang, J.B., Clostridium butyricum activates TLR2-mediated MyD88-independent signaling pathway in HT-29 cells. Mol. Cell. Biochem. 361 (2011), 31–37.
17. [17] Gao, Q.X., Wu, T.X., Wang, J.B., Zhuang, Q.C., Inhibition of bacterial adhesion to HT-29 cells by lipoteichoic acid extracted from Clostridium butyricum. Afr. J. Biotechnol. 10 (2011), 7633–7639.
18. [18] Valenzuela-Muñoz, V., Gallardo-Escárate, C., Molecular cloning and expression of IRAK-4, IL-17 and I-κB genes in Haliotis rufescens challenged with Vibrio anguillarum. Fish. Shellfish Immun. 36 (2014), 503–509.
19. [19] Cao, J.L., Chen, J.J., Wang, J.D., Jia, R.H., Xue, W.J., Luo, Y.J., Gan, X., Effects of fluoride on liver apoptosis and Bcl-2, Bax protein expression in freshwater teleost, Cyprinus carpio. Chemosphere 91 (2013), 1203–1212.
20. [20] Zídek, Z., Farghali, H., Komíčková, E., Intrinsic nitric oxide-stimulatory activity of lipoteichoic acids from different gram-positive bacteria. Nitric Oxide 23 (2010), 300–310.
21. [21] Eom, J.S., Song, J., Choi, H.S., Protective effects of a novel probiotic strain of Lactobacillus plantarum JSA22 from traditional fermented soybean food against infection by Salmonella enterica serovar typhimurium. J. Microbiol. Biotechnol. 25 (2015), 479–491.
22. [22] Kim, H.G., Gim, M.G., Kim, J.Y., Hwang, H.J., Ham, M.S., Lee, J.M., Hartung, T., Rark, J.W., Han, S.H., Chung, D.K., Lipoteichoic acid from Lactobacillus plantarum elicits both the production of Interleukin-23p19 and suppression of pathogen-mediated interleukin-10 in THP-1 cells. FEMS Immunol. Med. Mic. 49 (2007), 205–214.
23. [23] Denkin, S.M., Nelson, D.R., Induction of protease activity in Vibrio anguillarum by gastrointestinal mucus. Appl. Environ. Microb. 65 (1999), 3555–3560.
24. [24] Kim, H.G., Lee, S.Y., Kim, N.R., Ko, M.Y., Lee, J.M., Yi, T.H., Chung, S.K., Chung, D.K., Inhibitory effects of Lactobacillus plantarum lipoteichoic acid (LTA) on Staphylococcus aureus LTA-induced tumor necrosis factor-alpha production. J. Microbiol. Biotechnol. 18 (2008), 1191–1196.
25. [25] Kim, H., Jung, B.J., Jeong, J., Chun, H., Chung, D.K., Lipoteichoic acid from Lactobacillus plantarum inhibits the expression of platelet-activating factor receptor induced by Staphylococcus aureus lipoteichoic acid or Escherichia coli lipopolysaccharide in human monocyte-like cells. J. Microbiol. Biotechnol. 24 (2014), 1051–1058.
26. [26] Kim, H., Kim, H.S., Park, W.J., Chung, D.K., Inhibitory Effect of Lactobacillus plantarum extracts on HT-29 colon cancer cell apoptosis induced by Staphylococcus aureus and its alpha-toxin. J. Microbiol. Biotechnol. 25 (2015), 1849–1855.
27. [27] Kim, J.Y., Kim, H., Jung, B.J., Kim, N., Park, J.E., Chung, D.K., Lipoteichoic acid isolated from Lactobacillus plantarum suppresses LPS-mediated atherosclerotic plaque inflammation. Mol. Cells 35 (2013), 115–124.
28. [28] Li, R.J., Zhang, R., Zhang, L., Zou, J.J., Xing, Q., Dou, H.Q., Hu, X.L., Zhang, L.L., Wang, R.J., Bao, Z.M., Characterizations and expression analyses of NF-κB and Rel genes in the Yesso scallop (Patinopecten yessoensis) suggest specific response patterns against Gram-negative infection in bivalves. Fish. Shellfish Immun. 44 (2015), 611–621.