Biochemical properties, pathogenicity and genotyping of Paenibacillus larvae, a pathogen of the honey bee, Apis mellifera L.
Języki publikacji
PL
Abstrakty
EN
A characteristic of Paenibacillus larvae with a special reference to the current view on the systematics of this pathogen of the honey bee (Apis mellifrea L.) was presented. A great differentiation of the phenotypic and biochemical properties of the isolates often lead to errors in the diagnostics of AFB. The currently used methods of controlling AFB not only cannot eliminate the pathogen from AFB-affected colonies, but actually promote the selection of strains of higher pathogenicity to the honey bee larvae. The behavior of worker bees that quickly remove dead larvae from the sick colony may mask the symptoms of AFB. The genotyping of P. larvae should introduce PCR as a precise method for the diagnostics of AFB as soon as possible.
Uniwersytet Przyrodniczy w Lublinie, ul.Gleboka 30, 20-612 Lublin
Bibliografia
1. Aguilera M., Monteoliva-Sanchez M., Suarez A., Guerra V., Lizama C., Bennasar A., Ramos-Cormenzana A.: Paenibacillus jamilae sp. nov., an exopolysaccharide-producing bacterium able to grow in olive-mill wastewater. Int. J. Syst. Evol. Microbiol. 2001, 51, 1687-1692.
2. Alippi A. M.: Detection of Bacillus larvae spores in Argentinian honeys by using a semi-selective medium. Microbiologia 1995, 11, 343-350.
3. Alippi A. M., Aguilar M.: Characterization of isolates of Paenibacillus larvae subsp. larvae from diverse geographical origin by the polymerase chain reaction and BOX primers. J. Inveret. Path. 1998, 72, 21-27.
4. Alippi A. M., López A. C., Aguilar O. M.: A PCR-based method that permits specific detection of Paenibacillus larvae subsp. larvae, the cause of American Foulbrood of honey bees, at the subspecies level. Letters App. Microbiol. 2004, 39, 25-33.
5. Alippi A. M., López A. C., Aguilar O. M.: Differentiation of Paenibacillus larvae subsp. larvae, the cause of American Foulbrood of honeybees, by using PCR and restriction fragment analysis genes encoding 16S rRNA. Applied Environment. Microbiol. 2002, 68, 3655-3660.
6. Ash C., Priest F. G., Collins M. D.: Molecular identification of rRNA group 3 bacilli (Ash, Farrow, Wallbanks and Collins) using a PCR probe test. Proposal for the creation of a new genus Paenibacillus. Antonie Leeuwenhoek J. Microbiol. Serol. 1993, 64, 253-260.
7. Ashiralieva A., Genersch E.: Reclassification, genotypes and virulence of Paenibacillus larvae, the etiological agent of American foulbrood in honeybees - a review. Apidologie 2006, 37, 411-420.
8. Avaniss-Aghjani K., Jones K., Chapman D., Brunk C.: A molecular technique for identification of bacteria using small subunit rRNA sequences. BioTechniques 1994, 17, 253-260.
9. Berge O., Guinebretiere M. H., Achouak W., Normand P., Heulin T.: Paenibacillus graminis sp. nov. and Paenibacillus odorifer sp. nov., isolated from plant roots, soil and food. Int. J. Syst. Evol. Microbiol. 2002, 52, 607-616.
10. Bes M., Slim L. S., Becharina F., Meugnier H., Vandenesch F., Etienne J., Ferney J.: Population diversity of Staphylococcus intermedius isolates from various host species: Typing by 16S-23S intergenic ribosomal DNA spacer polimorphism analysis. J. Clin. Microbiol. 2002, 40, 2275-2277.
11. Brodsgaard C. J., Ritter W., Hanse H.: Response of in vitro reared honey bee larvae to various doses of Paenibacillus larvae spores. Apidologie 1998, 29, 569-578.
12. Carles-Nurit M. J., Christophle B., Broche S., Gouby A., Bouziges N., Ramuz M.: DNA polymorphism in methicillin-susceptible and methicillin-resistant strains of Staphylococcus aureus. J. Ciln. Microbiol. 1992, 30, 2092-2096.
13. Carpana E., Marocchi L., Gelmini L.: Evaluation of the API 50CHB system for the identification and biochemical characterization of Bacillus larvae. Apidologie 1995, 26, 11-16.
14. De Graaf D. C., De Vos P., Heyndrickx M., Van Trappen S., Peiren N., Jacobs F. J.: Identification of Paenibacillus larvae to the subspecies level: An obstacle for AFB diagnosis. J. Inert. Pathol. 2006, 91, 115-123.
15. Delaplane K. S.: American foulbrood. Am. Bee J. 1991, 131, 700-702.
16. Dobbelaere W., de Graaf D. C., Peters J. E., Jacobs F. J.: Comparison of two commercial kits for the biochemical characterization of Paenibacillus larvae subsp. larvae in the diagnosis of AFB. J. Apic. Res. 2001, 40, 37-40.
17. Drobniková V., Richter V., Häusler J., Pytelovà I.: Characterization of Bacillus larvae and related bacilli by chromatography of cell fatty acids. J. Apic. Res. 1994, 33, 69-74.
18. Evans J. D.: Diverse origins of tetracycline resistance in the honey bee bacterial pathogen Paenibacillus larvae. J. Invertebr. Pathol. 2003, 83, 46-50.
19. Fries I., Lindström A., Korpela S.: Vertical transmission of American foulbrood in honey bee (Apis mellifera). Vet. Mikrobiol. 2006, 114, 269-274.
20. Garbeva P., van Overbeek L. S., van Vuurde J. W. L., van Elsas J. D.: Analysis of endophytic bacterial communities of potato by planting and denaturing gradient gel electrophoresis (DGGE) of 16S rDNA based PCR fragments. Microb. Ecol. 2001, 41, 369-383.
21. Genersch E., Ashiralieva A., Fries I.: Strain- and genotype-specific differences in virulence of Paenibacillus larvae subsp. larvae, a bacterial pathogen causing american foulbrood disease in honeybees. Appl. Environ. Microbiol. 2005, 71, 7551-7555.
22. Genersch E., Forsgren E., Pentikainen J., Ashiralieva A., Rauch S., Kliwinski J., Freis L.: Reclassification of Paenibacillus larvae supsp. pulvifaciens and Paenibacillus larvae subsp. larvae as Paenibacillus larvae without subspecies differentiation. Int. J. Syst. Evol. Microbiol. 2006, 56, 501-511.
23. Genersch E., Otten C.: The use of repetitive element PCR fingerprinting (rep-PCR) for genetic subtyping of German field isolates of Paenibacillus larvae subsp. Larvae. Apidologie 2003, 34, 195-206.
24. Gowan V. A., Allsopp M. H., Davison S.: A PCR detection method for rapid identification of Paenibacillus larvae. App. and Envir. Microbiol. 1999, 65, 2243-2245.
25. Haseman L.: How long can spores of American foulbrood live? Amer. Bee. J. 1961, 101, 298-299.
26. Heyndrickx M., Vandemeulebroecke K., Hoste B., Janssen P., Kersters K., De Vos P., Logan N. A., Ali N., Berkeley R. C.: Reclassification of Paenibacillus (formerly Bacillus) pulvifaciens (Nakamura 1984) Ash et al. 1994, a later subjective synonym of Paenibacillus (formerly Bacillus) larvae (White 1906) Ash et al. 1994, as a subspecies of P. larvae, with emended descriptions of P. larvae as P. larvae subsp. larvae and P. larvae subsp. pulvifaciens. Int. J. Syst. Bacteriol. 1996, 46, 270-279.
27. Hornitzky M. A. Z., Nicholas P. J.: J-medim is superior to sheep blood agar and brain heart infusion agar for the isolation of Bacillus larvae from honey samples. J. Apic. Res. 1993, 32, 51-52.
28. Mansfeld-Giese K., Larsen J., Bødker L.: Bacterial populations associated with mycelium of arbuscular mycorrhizal fungus Glomus intraradices. FEMS Microbiol. Ecol. 2002, 41, 133-140.
29. Neundorf S., Hedtke K., Tangen G., Genersch E.: Biochemical characterization of different genotypes of Paenibacillus larvae subsp. larvae, a honey bee bacterial pathogen. Mcrobiology 2004, 150, 2381-2390.
30. Ordström S., Forsgren E., Fries I.: Comparative diagnosis of american foulbrood using samples of adult honey bees and honey. J. Api. Science 2002, 2, 5-12.
31. Peters M., Kilwinski J., Beringhoff A., Reckling D., Genersch E.: American foulbrood of the honey bee: Occurrence and distribution of different genotypes of Paenibacillus larvae in the administrative district of Arnsberg (North Rhine-Westphalia). J. Vet. Med. 2006, B53, 100-104.
32. Piuri M., Sanchez-Rivas C., Ruzal S. M.: A novel antimicrobial activity of a Paenibacillus polymyxa strain isolated from regional fermented sausages. Lett. Appl. Microbiol. 1998, 27, 9-13.
33. Plagemann O.: Eine einfache Kulturmethode zur bakteriologischen Identifizierung von Bacillus larvae mit Columbia-Blut-Schrägagar. Berl. Münch. Tierärztl. Wschr. 1985, 98, 61-62.
34. Quin X., Evans J. D., Aronstein K. A., Murray K. D., Weistock G. M.: Genome sequences of honey bee pathogens Paenibacillus larvae and Ascosphaera apis. Insect Mol. Biology 2006, 15, 715-718.
35. Reynaldi F. J., De Giusti M. R., Alippi A. M.: Inhibition of the growth of Ascosphaera apis by Bacillus and Paenibacillus strains isolated from honey. Rev. Argent. Microbiol. 2004, 36, 52-55.
36. Scheldeman P., Goossens K., Rodriguez-Diaz M., Pil A., Goris J., Herman L., De Vos P., Logan N. A., Heyndrickx M.: Paenibacillus lactis sp. nov., isolated from raw and heat-treated milk. Int. J. Syst. Evol. Microbiol. 2004, 54, 885-891.
37. Schuch D. M. T., Madden R. H., Sattler A.: An improved method for the detection and presumptive identification of Paenibacillus larvae subsp larvae spores in honey. J. Apic. Res. 2001, 40, 59-64.
38. Seldin L., Rosado A. S., Cruz D. W., Noberga A., van Elsas J. D., Paiża E.: Comparison of Paenibacillus azotofixans strain isolated from rhizoplane, rhizosphere and non-rhizosphere soil from maizeplanted in two different Brazylian soils. Appl. Environ. Microbiol. 1998, 64, 3860-3868.
39. Stahly D. P., Alippi A. M., Bakhiet N., Campana C. F., Novak C. C., Cox R.: PPL1c, a virulent mutant bacteriophage useful for identification of Paenibacillus larvae subespecies larvae. J. Invertebr. Pathol. 1999, 74, 295-296.
40. Tanner M. A., Everett Ch. L., Youvan D. C.: Molecular phylogenetic evidence for noninvasive zoonotic transmission of Staphylococcus intermedius from a canine pet to a human. J. Cin. Microbiol. 2000, 38, 1628-1631.
41. Velazquez E., de Miguel T., Poza M., Rivas R., Rossello-Mora R., Villa T. G.: Paenibacillus favisporus sp. nov., a xylanolytic bacterium isolated from cow faeces. Int. J. Syst. Evol. Microbiol. 2004, 54, 59-64.
42. Von der Weid I., Duarte G. F., van Elsas J. D., Seldin L.: Paenibacillus brasilensis sp. nov., a novel nitrogen-fixing species isolated from the maize rhizosphere in Brazil. Int. J. Syst. Evol. Microbiol. 2002, 52, 2147-2153.
43. Walker R., Powell A. A., Seddon B.: Bacillus isolates from the spermosphere of peas and dwarf french beans with antifungal activity against Botrytis cinerea and Pythium species. J. Appl. Microbiol. 1998, 84, 791-801.