Properties of different lactic acid bacteria isolated from Apis mellifera L. bee-gut

Microbiological Research

Volumn 166, Issue 1, 2011, Pages 1-13

  Carina Audisio, M ^a,b,c   Torres, María J ^a,b   Sabaté, Daniela C ^a,b   Ibarguren, Carolina ^a,b   Apella, María C ^b,d  

^a Instituto de Investigaciones para la Industria Quimica Salta   (Argentina)

^b Consejo Nacional de Investigaciones Científicas y Técnicas ^*  (Argentina)

^c UNIVERSIDAD NACIONAL DE SALTA   (Argentina)

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

Author keywords

Apis mellifera L.; Bee gut microbiota; Lactic acid bacteria; Lactobacillus johnsonii

Indexed keywords

16S RRNA; AMERICAN FOULBROOD; APIS MELLIFERA; BACTERIOCINS; CHEMICAL NATURE; E. FAECIUM STRAIN; ENTEROCOCCUS FAECIUM; ENTEROCOCCUS SPP; FOOD-BORNE PATHOGENS; FUNCTIONAL PROPERTIES; IN-VITRO; LACTIC ACID BACTERIA; LACTOBACILLUS JOHNSONII; LACTOBACILLUS SPP; MICROBIOTAS; PAENIBACILLUS LARVAE; PCR REACTIONS; SDS-PAGE; STRUCTURAL GENE;

BACTERIA; BACTERIOLOGY; BODY FLUIDS; ESSENTIAL OILS; RNA; SURFACE PROPERTIES;

LACTIC ACID;

ANTIINFECTIVE AGENT; BACTERIAL DNA; BACTERIOCIN; LACTIC ACID; RNA 16S;

BACTERIUM; GENE; HONEYBEE; LARVA; METABOLITE; PATHOGEN; POLYMERASE CHAIN REACTION;

ANIMAL; ANTIBIOSIS; ARTICLE; BEE; BIODIVERSITY; BIOSYNTHESIS; CHEMISTRY; CLASSIFICATION; DRUG EFFECT; ENTEROCOCCUS; ENTEROCOCCUS FAECIUM; GENETICS; GENOTYPE; INTESTINE; ISOLATION AND PURIFICATION; LACTOBACILLUS; LISTERIA; MICROBIOLOGICAL EXAMINATION; MICROBIOLOGY; PAENIBACILLUS; PHENOTYPE; PHYLOGENY; PHYSIOLOGY; SURFACE PROPERTY;

ANIMALS; ANTI-BACTERIAL AGENTS; ANTIBIOSIS; BACTERIOCINS; BEES; BIODIVERSITY; DNA, BACTERIAL; ENTEROCOCCUS; ENTEROCOCCUS FAECIUM; GENOTYPE; INTESTINES; LACTIC ACID; LACTOBACILLUS; LISTERIA; MICROBIAL SENSITIVITY TESTS; PAENIBACILLUS; PHENOTYPE; PHYLOGENY; RNA, RIBOSOMAL, 16S; SURFACE PROPERTIES;

APIS MELLIFERA; APOIDEA; BACTERIA (MICROORGANISMS); ENTEROCOCCUS; ENTEROCOCCUS FAECIUM; LACTOBACILLUS; LACTOBACILLUS JOHNSONII; LISTERIA; PAENIBACILLUS; PAENIBACILLUS LARVAE;

EID: 78449269822     PISSN: 09445013     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.micres.2010.01.003     Document Type: Article

References (42)

1. Alippi A.M., Reynaldi F.J. Inhibition of the growth of Paenibacillus larvae the causal agent of American Foulbrood of honey bees by selected strains of aerobic spore forming bacteria isolated from apiarian sources. J Invertebr Pathol 2006, 91:141-146.
2. Audisio M.C., Terzolo H.R., Apella M.C. Bacteriocin from honeybee beebread Enterococcus avium, active against Listeria monocytogenes. Appl Environ Microbiol 2005, 71:3373-3375.
3. Berger B.R., Pridmore D., Barretto C., Delmas-Julien F., Schreiber K., Arigoni F., et al. Similarity and differences in the Lactobacillus acidophilus group identified by polyphasic analysis and comparative genomics. J Bacteriol 2007, 189:1311-1321.
4. Boekhorst J., Siezen R.J., Zwahlen M.C., Vilanova D., Pridmore R.D., Mercenier A., et al. The complete genomes of Lactobacillus plantarum and Lactobacillus johnsonii reveal extensive differences in chromosome organization and gene content. Microbiol 2004, 150:3601-3611.
5. Cole J.R., Wang Q., Cardenas E., Fish J., Chai B., Farris R.J., et al. The ribosomal database project: improved alignments and new tools for rRNA analysis. Nucl Acids Res 2009, 37:D141-D145.
6. Daffonchio D., Borin S., Frova G., Manachini P., Sorlini C. PCR fingerprinting of whole genomes: the spacers between the 16S and 23S rRNA genes and of intergenic tRNA gene regions reveals a different intraespecific genomic variability of Bacillus cereus and Bacillus licheniformis. Int J Syst Bacteriol 1998, 48:107-116.
7. Devriese L.A., Collins M.D., Wirth R. The genus Enterococcus. The Prokaryotes 1992, vol. II:1465-1481. Springer-Verlag, New York.
8. Dingman D.W., Stahly D.P. Medium promoting sporulation of Bacillus larvae and metabolism of medium components. Appl Environ Microbiol 1983, 46:860-869.
9. du Toit M., Franz C.M., Dicks L.M., Holzapfel W.H. Preliminary characterization of bacteriocins produced by Enterococcus faecium and Enterococcus faecalis isolated from pig faeces. J Appl Microbiol 2000, 88:482-494.
10. Evans J.D. Diverse origins of tetracycline resistance in the honey bee bacterial pathogen Paenibacillus larvae. J Invertebr Pathol 2003, 83:46-50.
11. Evans J.D., Armstrong T.M. Inhibition of the American foulbrood bacterium, Paenibacillus larvae larvae, by bacteria isolated from honey bees. J Apicult Res 2005, 44:168-171.
12. Foulquié-Moreno M.R., Sarantinopoulos P., Tsakalidou E., De Vuyst L. The role and application of enterococci in food and health. Int J Food Microbiol 2006, 1:1-24.
13. Gilliam M., Morton H.L. Bacteria belonging to the genus Bacillus isolated from honey bees, Apis mellifera, fed 2,4-D and antibiotics. Apidologie 1978, 9:213-222.
14. Gilliam M., Prest D.B. Microbiology of feces of the larval honey bee, Apis mellifera. J Invert Pathol 1987, 49:70-75.
15. Gilliam M. Identification and roles of non-pathogenic microflora associated with honey bees. FEMS Microbiol Lett 1997, 155:1-10.
16. Glinski Z., Jarosz J. Mechanical and biochemical defences of honey bees. Bee World 1995, 76:110-118.
17. Hammes W.P., Weiss N., Holzapfel W. The genera Lactobacillus and Carnobacterium. The Prokaryotes 1992, vol. II:1535-1594. Springer-Verlag, New York.
18. Handley P.S., Harty D.W.S., Wyatt J.E., Brown C.R., Doran J.P., Gibbs A.C.C. A comparison of the adhesion, coaggregation and cell-surface hydrophobicity properties of fibrilar and fimbriate strains of Streptococcus salivarius. J Gen Microbiol 1987, 133:3207-3217.
19. Jack R., Tagg H., Ray B. Bacteriocins of Gram-positive bacteria. Microbiol Rev 1995, 59:171-200.
20. Johnson J.L., Phelps C.F., Cummins C.S., London J., Gasser F. Taxonomy of Lactobacillus acidophilus group. Int J Syst Bacteriol 1980, 30:53-68.
21. Kačániova M., Chlebo R., Kopernichý M., Trakocvická A. Microflora of the honeybee gastrointestinal tract. Folia Microbiol 2004, 49:169-171.
22. Kos B., Suskovic J., Vukovic S., Simpraga M., Frece J., Matosic S. Adhesion and aggregation ability of probiotic strain Lactobacillus acidophilus M92. J Appl Microbiol 2003, 94:981-987.
23. Lyapunov Y., Kuzyaev R.Z., Khismatullin R.G., Bezgodova O.A. Intestinal enterobacteria of the hibernating Apis mellifera mellifera L. bees. Microbiology 2008, 77:373-379.
24. Máchová M., Rada V., Huk J., Smékal Fr Development of probiotics for bees. Apiacta 1997, 4:99-111.
25. Mohr K.I., Tebbe C. Diversity and phylotype consistency of bacteria in the guts of three bee species (Apoidea) at an oilseed rape field. Environ Microbiol 2006, 8:258-272.
26. Mrázek J., Štrosová L., Fliegerova K., Kott T., Kopečný J. Diversity of insect intestinal microflora. Folia Microbiol 2008, 53:229-233.
27. Naidu A.S., Bidlack W.R., Clemens R.A. Probiotic spectra of lactic acid bacteria (LAB). Crit Rev Food Sci Nutr 1999, 39:13-126.
28. Ogawa M., Shimizu K., Nomoto K., Tanaka R., Hamabata T., Yamasaki S., et al. Inhibition of in vitro growth of Shiga toxin-producing Escherichia coli O157:H7 by probiotic Lactobacillus strains due to production of lactic acid. Int J Food Microbiol 2001, 68:135-140.
29. Olofsson T.C., Vásquez A. Detection and identification of a novel lactic acid bacterial flora within the honey stomach of the honeybee Apis mellifera. Curr Microbiol 2008, 57:356-363.
30. Poeta P., Costa D., Rojo-Bezares B., Zarazaga M., Klibi N., Rodrigues C., et al. Detection of antimicrobial activities and bacteriocin structural genes in faecal enterococci of wild animals. Microbiol Res 2007, 162:257-263.
31. Pospiech A., Neumann B. A versatile quick-prep of genomic DNA from Gram-positive bacteria. Trends Genet 1995, 11:217-218.
32. Pot B., Hertel C., Ludwig W., Descheemaeker P., Kersters K., Schleifer K.H. Identification and classification of Lactobacillus acidophilus, L. gasseri and L. johnsonii strains by SDS-PAGE and rRNA-targeted oligonucleotide probe hybridization. J Gen Microbiol 1993, 139:513-517.
33. Rada V., Máchová M., Huk J., Marounek M., Duskova B. Microflora in the honeybee digestive tract: count, characteristics and sensitivity to veterinary drugs. Apidologie 1997, 28:357-365.
34. Rousseau M., Tysset C., Durand C. Presence of streptococci of the Lancefield D group in healthy working bees (Alpis mellifica L.). Interpretation of their presence in alimentary bacteriology. Bull Acad Vet Fr 1969, 42:173-186.
35. Sabaté D.C., Carrillo L., Audisio M.C. Inhibition of Paenibacillus larvae and Ascosphaera apis by Bacillus subtilis isolated from honeybee gut and honey samples. Res Microbiol 2009, 160:193-199.
36. Schäger H. Tricine-SDS-PAGE. Nature protocols 2006, 1:16-22.
37. Snowdon J.A., Cliver D.O. Microorganisms in honey. Int J Food Microbiol 1996, 31:1-26.
38. Ventura M., Jankovic I., Walker D.C., Pridmore R.C., Zink R. Identification and characterization of novel surface proteins in Lactobacillus johnsonii and Lactobacillus gasseri. Appl Environ Microbiol 2002, 68:6172-6181.
39. Ying C., Lei W., Jiazhong L., Zhantao S., Liguo A. Identification and purification of a novel adhesion-associated protein in a new strain of Lactobacillus, L15, from flounder (Paralichthys olivaceus). Vet Microbiol 2007, 122:116-122.
40. Williams D.L. Review. A veterinary approach to the European honey bee (Apis mellifera). Vet J 2000, 160:61-73.
41. Wilson A.R., Sigee D., Epton H.A. Anti-bacterial activity of Lactobacillus plantarum strain SK1 against Listeria monocytogenes is due to lactic acid production. J Appl Microbiol 2005, 99:1516-1522.
42. Zhao X.Q., Bai F.W. Yeast flocculation: new story in fuel ethanol production. Biotechnol Adv 2009, 27:849-856.