Lactic acid bacteria isolated from bovine mammary microbiota: Potential allies against bovine mastitis

PLoS ONE

Volumn 10, Issue 12, 2015, Pages

  Bouchard, Damien S ^a,b,h   Seridan, Bianca ^a,b,c   Saraoui, Taous ^a,b,i   Rault, Lucie ^a,b   Germon, Pierre ^d   Gonzalez Moreno, Candelaria ^e   Nader Macias, Fatima M E ^e   Baud, Damien ^f   François, Patrice ^f   Chuat, Victoria ^a,b   Chain, Florian ^g   Langella, Philippe ^g   Nicoli, Jacques ^c   Le Loir, Yves ^a,b   Even, Sergine ^a,b  

^a UMR1253   (France)

^b AGROCAMPUS OUEST   (France)

^c FEDERAL UNIVERSITY OF MINAS GERAIS   (Brazil)

^d UR1282   (France)

^e CENTRO DE REFERENCIA PARA LACTOBACILOS CERELA CONICET   (Argentina)

^f GENEVA UNIVERSITY HOSPITALS   (Switzerland)

^g CEMAGREF   (France)

^h ANSES ANMV   (France)

ⁱ LUNAM UNIVERSITÉ   (France)

Author keywords

[No Author keywords available]

Indexed keywords

INTERLEUKIN 8; BACTERIAL RNA; RNA 16S;

ANIMAL CELL; ANTIBACTERIAL ACTIVITY; ANTIBIOTIC RESISTANCE; ANTIINFLAMMATORY ACTIVITY; ARTICLE; BACTERIAL COLONIZATION; BACTERIAL GENE; BACTERIUM ISOLATION; BOVINE MASTITIS; BREAST; BREAST EPITHELIUM CELL; BREAST MICROFLORA; CELL AGGREGATION; CONTROLLED STUDY; CYTOKINE RELEASE; ESCHERICHIA COLI; GENE SEQUENCE; GENETIC MARKER; HYDROPHOBICITY; IMMUNOMODULATION; LACTIC ACID BACTERIUM; LACTOBACILLUS; LACTOBACILLUS BREVIS; LACTOBACILLUS PLANTARUM; LACTOCOCCUS; MICROFLORA; NIPPLE; NONHUMAN; STAPHYLOCOCCUS AUREUS; STREPTOCOCCUS UBERIS; SURFACE PROPERTY; ANIMAL; BACTERIAL GENOME; BACTERIAL INFECTION; BACTERIUM ADHERENCE; BOVINE; DNA SEQUENCE; FEMALE; GENETICS; HT-29 CELL LINE; HUMAN; ISOLATION AND PURIFICATION; MICROBIOLOGY; MILK; MOLECULAR GENETICS; MOLECULAR TYPING; UDDER; VETERINARY;

ANIMALS; BACTERIAL ADHESION; BACTERIAL INFECTIONS; CATTLE; FEMALE; GENOME, BACTERIAL; HT29 CELLS; HUMANS; LACTOBACILLUS; LACTOCOCCUS; MAMMARY GLANDS, ANIMAL; MASTITIS, BOVINE; MICROBIOTA; MILK; MOLECULAR SEQUENCE DATA; MOLECULAR TYPING; RNA, BACTERIAL; RNA, RIBOSOMAL, 16S; SEQUENCE ANALYSIS, DNA;

EID: 84958025711     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0144831     Document Type: Article

References (42)

1. Contreras GA, Rodriguez JM. Mastitis: Comparative etiology and epidemiology. J Mammary Gland Biol Neoplasia. 2011; 16: 339-356. doi: 10.1007/s10911-011-9234-0 PMID: 21947764
2. Le Marechal C, Thiery R, Vautor E, Le Loir Y. Mastitis impact on technological properties of milk and quality of milk products-A review. Dairy Sci Technol. 2011; 91: 247-282.
3. Behnsen J, Deriu E, Sassone-Corsi M, Raffatellu M. Probiotics: Properties, Examples, and Specific Applications. Cold Spring Harb Perspect Med. 2013; 3: A010074. doi: 10.1101/cshperspect.a010074 PMID: 23457295
4. Reid G, Kim SO, Kohler GA. Selecting, testing and understanding probiotic microorganisms. FEMS Immunol Med Microbiol. 2006; 46: 149-157. doi: 10.1111/j.1574-695X.2005.00026.x PMID: 16487295
5. Even S, Bouchard D, Le Loir Y. Lactic acid bacteria to modulate virulence expression in pathogenic bacteria: An alternative to killing? Interactive probiotics. CRC Press. Boca Raton, USA: Pessione E. (Eds.); 2014. pp. 52-80.
6. Sengupta R, Altermann E, Anderson RC, McNabb WC, Moughan PJ, Roy NC. The role of cell surface architecture of lactobacilli in host-microbe interactions in the gastrointestinal tract. Mediators Inflamm. 2013; 2013: 237921. doi: 10.1155/2013/237921 PMID: 23576850
7. Arroyo R, Martin V, Maldonado A, Jimenez E, Fernandez L, Rodriguez JM. Treatment of infectious mastitis during lactation: Antibiotics versus oral administration of Lactobacilli isolated from breast milk. Clin Infect Dis. 2010; 50: 1551-1558. doi: 10.1086/652763 PMID: 20455694
8. Espeche MC, Pellegrino M, Frola I, Larriestra A, Bogni C, Nader-Macias ME. Lactic acid bacteria from raw milk as potentially beneficial strains to prevent bovine mastitis. Anaerobe. 2012; 18: 103-109. doi: 10.1016/j.anaerobe.2012.01.002 PMID: 22261519
9. Klostermann K, Crispie F, Flynn J, Ross RP, Hill C, Meaney W. Intramammary infusion of a live culture of Lactococcus lactis for treatment of bovine mastitis: Comparison with antibiotic treatment in field trials. J Dairy Res. 2008; 75: 365-373. doi: 10.1017/S0022029908003373 PMID: 18680622
10. Frola ID, Pellegrino MS, Espeche MC, Giraudo JA, Nader-Macias ME, Bogni CI. Effects of intramammary inoculation of Lactobacillus perolens CRL1724 in lactating cows' udders. J Dairy Res. 2012; 79: 84-92. doi: 10.1017/S0022029911000835 PMID: 22077995
11. Frola ID, Pellegrino MS, Magnano G, Giraudo JA, Espeche MC, Nader-Macias ME, et al. Histological examination of non-lactating bovine udders inoculated with Lactobacillus perolens CRL 1724. J Dairy Res. 2013; 80: 28-35. doi: 10.1017/S0022029912000581 PMID: 23199568
12. Bouchard DS, Rault L, Berkova N, Le Loir Y, Even S. Inhibition of Staphylococcus aureus invasion into bovine mammary epithelial cells by contact with live Lactobacillus casei. Appl Environ Microbiol. 2013; 79: 877-885. doi: 10.1128/AEM.03323-12 PMID: 23183972
13. Charlier C, Cretenet M, Even S, Le Loir Y. Interactions between Staphylococcus aureus and lactic acid bacteria: An old story with new perspectives. Int J Food Microbiol. 2009; 131: 30-39. doi: 10.1016/j. ijfoodmicro.2008.06.032 PMID: 18687499
14. Vandevoorde L, Christiaens H, Verstraete W. Prevalence of coaggregation reactions among chicken lactobacilli. J Appl Bacteriol. 1992; 72: 214-219. PMID: 1568947
15. Riollet C, Rainard P, Poutrel B. Differential induction of complement fragment C5a and inflammatory cytokines during intramammary infections with Escherichia coli and Staphylococcus aureus. Clin Diagn Lab Immunol. 2000; 7: 161-167. PMID: 10702487
16. Godon JJ, Zumstein E, Dabert P, Habouzit F, Moletta R. Molecular microbial diversity of an anaerobic digestor as determined by small-subunit rDNA sequence analysis. Appl Environ Microbiol. 1997; 63: 2802-2813. PMID: 9212428
17. Smith CL, Cantor CR. Purification, specific fragmentation, and separation of large DNA molecules. Methods Enzymol. 1987; 155: 449-467. PMID: 3431468
18. Lortal S, Rouault A, Guezenec S, Gautier M. Lactobacillus helveticus: Strain typing and genome size estimation by pulsed field gel electrophoresis. Curr Microbiol. 1997; 34: 180-185. PMID: 9009072
19. Juarez Tomas MS, Ocana VS, Wiese B, Nader-Macias ME. Growth and lactic acid production by vaginal Lactobacillus acidophilus CRL 1259, and inhibition of uropathogenic Escherichia coli. J Med Microbiol. 2003; 52: 1117-1124. PMID: 14614071
20. Bouchard D, Peton V, Almeida S, Le Maréchal C, Miyoshi A, Azevedo V, et al. Genome sequence of Staphylococcus aureus Newbould 305, a strain associated with mild bovine mastitis. J Bacteriol. 2012; 194: 6292-6293. doi: 10.1128/JB.01188-12 PMID: 23105046
21. Herron-Olson L, Fitzgerald JR, Musser JM, Kapur V. Molecular correlates of host specialization in Staphylococcus aureus. PloS One. 2007; 2: E1120. doi: 10.1371/journal.pone.0001120 PMID: 17971880
22. Roussel P, Cunha P, Porcherie A, Petzl W, Gilbert FB, Riollet C, et al. Investigating the contribution of IL-17A and IL-17F to the host response during Escherichia coli mastitis. Vet Res. 2015.
23. Kechaou N, Chain F, Gratadoux JJ, Blugeon S, Bertho N, Chevalier C, et al. Identification of one novel candidate probiotic Lactobacillus plantarum strain active against influenza virus infection in mice by a large-scale screening. Appl Environ Microbiol. 2013; 79: 1491-1499. doi: 10.1128/AEM.03075-12 PMID: 23263960
24. Delcher AL, Bratke KA, Powers EC, Salzberg SL. Identifying bacterial genes and endosymbiont DNA with Glimmer. Bioinforma Oxf Engl. 2007; 23: 673-679. doi: 10.1093/bioinformatics/btm009
25. Barinov A, Loux V, Hammani A, Nicolas P, Langella P, Ehrlich D, et al. Prediction of surface exposed proteins in Streptococcus pyogenes, with a potential application to other Gram-positive bacteria. Proteomics. 2009; 9: 61-73. doi: 10.1002/pmic.200800195 PMID: 19053137
26. Marchler-Bauer A, Derbyshire MK, Gonzales NR, Lu S, Chitsaz F, Geer LY, et al. CDD: NCBI's conserved domain database. Nucleic Acids Res. 2014; doi: 10.1093/nar/gku1221
27. R development Core Team. R: A Language and Environment for Statistical computing. Vienna, Austria: R Foundation for Statistical Computing; 2013. Available: Http://www.R-project.org
28. Mazé A, Boël G, Zúñiga M, Bourand A, Loux V, Yebra MJ, et al. Complete genome sequence of the probiotic Lactobacillus casei strain BL23. J Bacteriol. 2010; 192: 2647-2648. doi: 10.1128/JB.00076-10 PMID: 20348264
29. Zuily S, Mami Z, Meune C. Lactococcus garvieae endocarditis. Arch Cardiovasc Dis. 2011; 104: 138-139. doi: 10.1016/j.acvd.2010.05.005 PMID: 21402350
30. Suojala L, Kaartinen L, Pyörälä S. Treatment for bovine Escherichia coli mastitis-an evidence-based approach. J Vet Pharmacol Ther. 2013; 36: 521-531. doi: 10.1111/jvp.12057 PMID: 23679229
31. Suojala L, Simojoki H, Mustonen K, Kaartinen L, Pyörälä S. Efficacy of enrofloxacin in the treatment of naturally occurring acute clinical Escherichia coli mastitis. J Dairy Sci. 2010; 93: 1960-1969. doi: 10.3168/jds.2009-2462 PMID: 20412909
32. ANSES. Assessment of the risks of emergence of antimicrobial resistance associated with modes of antibiotic use in the field of animal health. 2014.
33. Espeche MC, Otero MC, Sesma F, Nader-Macias ME. Screening of surface properties and antagonistic substances production by lactic acid bacteria isolated from the mammary gland of healthy and mastitic cows. Vet Microbiol. 2009; 135: 346-357. doi: 10.1016/j.vetmic.2008.09.078 PMID: 19041199
34. Otero MC, Morelli L, Nader-Macias ME. Probiotic properties of vaginal lactic acid bacteria to prevent metritis in cattle. Lett Appl Microbiol. 2006; 43: 91-97. PMID: 16834727
35. Nader-Macias ME, Otero MC, Espeche MC, Maldonado NC. Advances in the design of probiotic products for the prevention of major diseases in dairy cattle. J Ind Microbiol Biotechnol. 2008; 35: 1387-1395. doi: 10.1007/s10295-008-0438-2 PMID: 18758837
36. Younes JA, van der Mei HC, van den Heuvel E, Busscher HJ, Reid G. Adhesion forces and coaggregation between vaginal staphylococci and lactobacilli. PLoSOne. 2012; 7: E36917. doi: 10.1371/journal. pone.0036917
37. Lebeer S, Vanderleyden J, De Keersmaecker SCJ. Host interactions of probiotic bacterial surface molecules: Comparison with commensals and pathogens. Nat Rev Microbiol. 2010; 8: 171-184. doi: 10.1038/nrmicro2297 PMID: 20157338
38. Turpin W, Humblot C, Noordine M-L, Thomas M, Guyot J-P. Lactobacillaceae and cell adhesion: Genomic and functional screening. PloS One. 2012; 7: E38034. doi: 10.1371/journal.pone.0038034 PMID: 22675431
39. Innocentin S, Guimaraes V, Miyoshi A, Azevedo V, Langella P, Chatel JM, et al. Lactococcus lactis expressing either Staphylococcus aureus fibronectin-binding protein A or Listeria monocytogenes internalin A can efficiently internalize and deliver DNA in human epithelial cells. Appl Environ Microbiol. 2009; 75: 4870-4878. doi: 10.1128/AEM.00825-09 PMID: 19482952
40. Bierne H, Sabet C, Personnic N, Cossart P. Internalins: A complex family of leucine-rich repeat-containing proteins in Listeria monocytogenes. Microbes Infect Inst Pasteur. 2007; 9: 1156-1166. doi: 10.1016/j.micinf.2007.05.003
41. Dogan B, Klaessig S, Rishniw M, Almeida RA, Oliver SP, Simpson K, et al. Adherent and invasive Escherichia coli are associated with persistent bovine mastitis. Vet Microbiol. 2006; 116: 270-282. doi: 10.1016/j.vetmic.2006.04.023 PMID: 16787715
42. Deplanche M, Filho RAE-A, Alekseeva L, Ladier E, Jardin J, Henry G, et al. Phenol-soluble modulin a induces G2/M phase transition delay in eukaryotic HeLa cells. FASEB J Off Publ Fed Am Soc Exp Biol. 2015; 29: 1950-1959. doi: 10.1096/fj.14-260513