Antimicrobial, anti-adhesive and anti-biofilm potential of biosurfactants isolated from Pediococcus acidilactici and Lactobacillus plantarum against Staphylococcus aureus CMCC26003

Microbial Pathogenesis

Volumn 127, Issue , 2019, Pages 12-20

  Yan, Xin ^a,b   Gu, Shanshan ^a   Cui, Xingyang ^a   Shi, Yunjia ^a   Wen, Shanshan ^a   Chen, Hongyan ^b   Ge, Junwei ^a,c  

^a NORTHEAST AGRICULTURAL UNIVERSITY   (China)

^b INSTITUTE OF PLANT PROTECTION   (China)

^c Heilongjiang Key Laboratory for Animal Disease Control and Pharmaceutical Development   (China)

Author keywords

Anti adhesive activity; Anti Biofilm activity; Antimicrobial activity; Biosurfactant; Lactic acid bacteria; Staphylococcus aureus

Indexed keywords

AGRA PROTEIN; ANTIINFECTIVE AGENT; BACTERIAL PROTEIN; BIOSURFACTANT; CIDA PROTEIN; CRYSTAL VIOLET; DLTB PROTEIN; ICAA PROTEIN; OIL; SMAD ANCHOR FOR RECEPTOR ACTIVATION; SORTASEA PROTEIN; UNCLASSIFIED DRUG; BIOLOGICAL PRODUCT; SURFACTANT;

AGRA GENE; ANTI ADHESIVE ACTIVITY; ANTI BIOFILM ACTIVTIY; ANTIBACTERIAL ACTIVITY; ARTICLE; BACTERIAL GENE; BIOFILM; CIDA GENE; CONTROLLED STUDY; DLTB GENE; DRUG ACTIVITY; DRUG ISOLATION; ICAA GENE; IN VITRO STUDY; LACTOBACILLUS PLANTARUM; NONHUMAN; PEDIOCOCCUS ACIDILACTICI; PRIORITY JOURNAL; QUORUM SENSING; SARA GENE; SCANNING ELECTRON MICROSCOPY; SORTASEA GENE; STAPHYLOCOCCUS AUREUS; STAPHYLOCOCCUS AUREUS CMCC26003; SURFACE PROPERTY; BACTERIUM ADHERENCE; BIOSYNTHESIS; CHEMISTRY; DRUG EFFECT; GENE EXPRESSION PROFILING; GROWTH, DEVELOPMENT AND AGING; ISOLATION AND PURIFICATION; PHYSIOLOGY; STAINING;

ANTI-INFECTIVE AGENTS; BACTERIAL ADHESION; BACTERIAL PROTEINS; BIOFILMS; BIOLOGICAL PRODUCTS; GENE EXPRESSION PROFILING; GENTIAN VIOLET; LACTOBACILLUS PLANTARUM; MICROSCOPY, ELECTRON, SCANNING; PEDIOCOCCUS ACIDILACTICI; QUORUM SENSING; STAINING AND LABELING; STAPHYLOCOCCUS AUREUS; SURFACE-ACTIVE AGENTS;

EID: 85057486365     PISSN: 08824010     EISSN: 10961208     Source Type: Journal    
DOI: 10.1016/j.micpath.2018.11.039     Document Type: Article

References (42)

1. Diaz De Rienzo, M.A., Stevenson, P.S., Marchant, R., Banat, I.M., Effect of biosurfactants on Pseudomonas aeruginosa and Staphylococcus aureus biofilms in a BioFlux channel. Appl. Microbiol. Biotechnol. 100 (2016), 5773–5779.
2. Rivardo, F., Turner, R.J., Allegrone, G., Ceri, H., Martinotti, M.G., Anti-adhesion activity of two biosurfactants produced by Bacillus spp. prevents biofilm formation of human bacterial pathogens. Appl. Microbiol. Biotechnol. 83 (2009), 541–553.
3. Lee, J.H., Kim, Y.G., Yong Ryu, S., Lee, J., Calcium-chelating alizarin and other anthraquinones inhibit biofilm formation and the hemolytic activity of Staphylococcus aureus. Sci. Rep., 6, 2016, 19267.
4. Marino, A., Bellinghieri, V., Nostro, A., Miceli, N., Taviano, M.F., Guvenc, A., et al. In vitro effect of branch extracts of Juniperus species from Turkey on Staphylococcus aureus biofilm. FEMS Immunol. Med. Microbiol. 59 (2010), 470–476.
5. Shrestha, L., Kayama, S., Sasaki, M., Kato, F., Hisatsune, J., Tsuruda, K., et al. Inhibitory effects of antibiofilm compound 1 against Staphylococcus aureus biofilms. Microbiol. Immunol. 60 (2016), 148–159.
6. Luis, A., Silva, F., Sousa, S., Duarte, A.P., Domingues, F., Antistaphylococcal and biofilm inhibitory activities of gallic, caffeic, and chlorogenic acids. Biofouling 30 (2014), 69–79.
7. Lewis, K., Persister cells. Annu. Rev. Microbiol., 64, 2010, 357.
8. Merghni, A., Dallel, I., Noumi, E., Kadmi, Y., Hentati, H., Tobji, S., et al. Antioxidant and antiproliferative potential of biosurfactants isolated from Lactobacillus casei and their anti-biofilm effect in oral Staphylococcus aureus strains. Microb. Pathog. 104 (2017), 84–89.
9. Coronel-Leon, J., Marques, A.M., Bastida, J., Manresa, A., Optimizing the production of the biosurfactant lichenysin and its application in biofilm control. J. Appl. Microbiol. 120 (2016), 99–111.
10. Sharma, D., Saharan, B.S., Chauhan, N., Bansal, A., Procha, S., Production and structural characterization of Lactobacillus helveticus derived biosurfactant. TheScientificWorldJOURNAL, 2014, 2014, 493548.
11. Daverey, A., Pakshirajan, K., Kinetics of growth and enhanced sophorolipids production by Candida bombicola using a low-cost fermentative medium. Appl. Biochem. Biotechnol. 160 (2010), 2090–2101.
12. Benincasa, M., Abalos, A., Oliveira, I., Manresa, A., Chemical structure, surface properties and biological activities of the biosurfactant produced by Pseudomonas aeruginosa LBI from soapstock. Antonie Leeuwenhoek 85 (2004), 1–8.
13. Ahimou, F., Jacques, P., Deleu, M., Surfactin and iturin A effects on Bacillus subtilis surface hydrophobicity. Enzym. Microb. Technol., 27, 2000, 749.
14. Sharma, D., Saharan, B.S., Functional characterization of biomedical potential of biosurfactant produced by Lactobacillus helveticus. Biotechnol. Rep. 11 (2016), 27–35.
15. Madhu, A.N., Prapulla, S.G., Evaluation and functional characterization of a biosurfactant produced by Lactobacillus plantarum CFR 2194. Appl. Biochem. Biotechnol. 172 (2014), 1777–1789.
16. Rodrigues, L.R., Teixeira, J.A., van der Mei, H.C., Oliveira, R., Isolation and partial characterization of a biosurfactant produced by Streptococcus thermophilus A. Colloids Surfaces B Biointerfaces 53 (2006), 105–112.
17. Rodrigues, L., van der Mei, H., Teixeira, J.A., Oliveira, R., Biosurfactant from Lactococcus lactis 53 inhibits microbial adhesion on silicone rubber. Appl. Microbiol. Biotechnol. 66 (2004), 306–311.
18. Gudina, E.J., Rocha, V., Teixeira, J.A., Rodrigues, L.R., Antimicrobial and antiadhesive properties of a biosurfactant isolated from Lactobacillus paracasei ssp. paracasei A20. Lett. Appl. Microbiol. 50 (2010), 419–424.
19. Diaz De Rienzo, M.A., Stevenson, P., Marchant, R., Banat, I.M., Antibacterial properties of biosurfactants against selected Gram-positive and -negative bacteria. FEMS Microbiol. Lett., 363, 2016, fnv224.
20. Karthik Sambanthamoorthy, X.F., Patel, Ruchi, Patel, Sneha, Paranavitana, Chrysanthi, Antimicrobial and antibiofilm potential of biosurfactants isolated from lactobacilli against multi-drug-resistant pathogens. BMC Microbiol. 14 (2014), 3–9.
21. Masaaki Morikawa, Y.H., Imanaka, Tadayuki, A study on the structure-function relationship of lipopeptide biosurfactants. Biochim. Biophys. Acta 1488 (2000), 211–218.
22. Wiegand, I., Hilpert, K., Hancock, R.E., Agar and broth dilution methods to determine the minimal inhibitory concentration (MIC) of antimicrobial substances. Nat. Protoc. 3 (2008), 163–175.
23. Graziano, T.S., Cuzzullin, M.C., Franco, G.C., Schwartz-Filho, H.O., de Andrade, E.D., Groppo, F.C., et al. Statins and antimicrobial effects: simvastatin as a potential drug against Staphylococcus aureus biofilm. PLoS One, 10, 2015, e0128098.
24. Yadav, M.K., Chae, S.W., Im, G.J., Chung, J.W., Song, J.J., Eugenol: a phyto-compound effective against methicillin-resistant and methicillin-sensitive Staphylococcus aureus clinical strain biofilms. PLoS One, 10, 2015, e0119564.
25. Zhang, H.M., Z, W., Zhang, W.Y., Yang, A.L., Liu, Y.L., Jiang, Y., Huang, S.S., Su, J.Y., Inhibitory effects of citral, cinnamaldehyde, and tea polyphenols on mixed biofilm formation by foodborne Staphylococcus aureus and Salmonella enteritidis. J. Food Protect. 77 (2014), 927–933.
26. -ΔΔCt calculation as an alternate method of data analysis for quantitative PCR of BCR-ABL P210 transcripts. Diagn. Mol. Pathol. 1 (2006), 56–61.
27. Satpute, S.K., B, B.D., Dhakephalkar, P.K., Chopade, B.A., Assessment of different screening methods for selecting biosurfactant producing marine bacteria. Indian J. Mar. Sci. 37 (2008), 243–250.
28. Xue, T., Zhao, L., Sun, B., LuxS/AI-2 system is involved in antibiotic susceptibility and autolysis in Staphylococcus aureus NCTC 8325. Int. J. Antimicrob. Agents 41 (2013), 85–89.
29. Dan Yu, L.Z., Xue, Ting, Sun, Baolin, Staphylococcus aureus autoinducer-2 quorum sensing decreases biofilm formation in an icaRdependent manner. BMC Microbiol. 12 (2012), 2–12.
30. Chen, Y., Liu, T., Wang, K., Hou, C., Cai, S., Huang, Y., et al. Baicalein inhibits Staphylococcus aureus biofilm formation and the quorum sensing system in vitro. PLoS One, 11, 2016, e0153468.
31. Guo, N., Zhao, X., Li, W., Shi, C., Meng, R., Liu, Z., et al. The synergy of berberine chloride and totarol against Staphylococcus aureus grown in planktonic and biofilm cultures. J. Med. Microbiol. 64 (2015), 891–900.
32. Huang, Q., Fei, J., Yu, H.J., Gou, Y.B., Huang, X.K., Effects of human beta-defensin-3 on biofilm formation regulating genes dltB and icaA in Staphylococcus aureus. Mol. Med. Rep. 10 (2014), 825–831.
33. Yan, X., Gu, S., Shi, Y., Cui, X., Wen, S., Ge, J., The effect of emodin on Staphylococcus aureus strains in planktonic form and biofilm formation in vitro. Arch. Microbiol. 199 (2017), 1267–1275.
34. Chopra, I., Hesse, L., O'Neill, A.J., Exploiting current understanding of antibiotic action for discovery of new drugs. J. Appl. Microbiol., 92, 2002, 4S.
35. Ciandrini, E., Campana, R., Casettari, L., Perinelli, D.R., Fagioli, L., Manti, A., et al. Characterization of biosurfactants produced by Lactobacillus spp. and their activity against oral streptococci biofilm. Appl. Microbiol. Biotechnol. 100 (2016), 6767–6777.
36. Walencka, E., R, S., Sadowska, B., Rozalska, B., The influence of Lactobacillus acidophilus-derived surfactants on staphylococcal adhesion and biofilm formation. Folia Microbiol. 53 (2008), 61–66.
37. Peschel, A., Otto, M., Jack, R.W., Inactivation of the dlt operon in Staphylococcus aureus confers sensitivity to defensins, protegrins, and other antimicrobial peptides. J. Biol. Chem. 274 (1999), 8405–8410.
38. Das, T., Sharma, P.K., Busscher, H.J., van der Mei, H.C., Krom, B.P., Role of extracellular DNA in initial bacterial adhesion and surface aggregation. Appl. Environ. Microbiol. 76 (2010), 3405–3408.
39. Castillo-Juarez, I., Maeda, T., Mandujano-Tinoco, E.A., Tomas, M., Perez-Eretza, B., Garcia-Contreras, S.J., et al. Role of quorum sensing in bacterial infections. World J. Clin. Cases 3 (2015), 575–598.
40. Truchado, P., Giménezbastida, J.A., Larrosa, M., Castroibáñez, I., Espín, J.C., Tomásbarberán, F.A., et al. Inhibition of quorum sensing (QS) in Yersinia enterocolitica by an orange extract rich in glycosylated flavanones. J. Agric. Food Chem. 60 (2012), 8885–8894.
41. Kleerebezem, M., Quadri, L.E.N., Kuipers, O.P., Quorum sensing by peptide pheromones and two-component signal-transduction systems in Gram-positive bacteria. Mol. Microbiol. 24 (1997), 895–904.
42. Weiss, E.C., Zielinska, A., Beenken, K.E., Spencer, H.J., Daily, S.J., Smeltzer, M.S., Impact of sarA on daptomycin susceptibility of Staphylococcus aureus biofilms in vivo. Antimicrob. Agents Chemother. 53 (2009), 4096–4102.