Aktuální vědecké poznatky o imunitě a zdraví včel
Použitá literatura, na kteoru se odkazujeme v tištěné verzi článku.
1. Gallai, N., Salles, J.M., Settele, J., Vaissière, B. E. Economic valuation of the vulnerability of world agriculture confronted with pollinator decline. Ecol Econ 2009; 68(3): 810-821.
2. Goulson, D., Nicholls, E., Botías, C., Rotheray, E. L. Bee declines driven by combined stress from parasites, pesticides, and lack of flowers. Science 2015;347(6229):1255957.
3. Wilson-Rich, N., Spivak, M., Fefferman, N. H., Starks, P. T. Genetic, individual, and group facilitation of disease resistance in insect societies. Annu Rev Entomol 2009; 54:405-423.
4. Přidal, A. Stanovení počtu samiček kleštíka včelího (Varroa destructor) v zimní měli nemůže být spolehlivým podkladem pro včasnou diagnostiku varroózy. Veterinářství 2014; 64:373-375.
5. Panasiuk, B., Skowronek, W., Bienkowska, M., Gerula, D. Process of cleaning dead brood from cells in a honeybee colony. J Apic Sci 2010; 54(1): 5-11.
6. Büchler, R., Berg, S., Le Conte, Y. Breeding for resistance to Varroa destructor in Europe. Apidologie 2010; 41(3): 393-408.
7. Rosenkranz, P., Aumeier, P., Ziegelmann, B. Biology and control of Varroa destructor. J Invertebr Pathol 2010; 103 Suppl 1:S96-119.
8. Locke, B., Fries, I. Characteristics of honey bee colonies (Apis mellifera) in Sweden surviving Varroa destructor infestation. Apidologie 2011; 42(4): 533-542.
9. Le Conte, Y., De Vaublanc, G., Crauser, D., Jeanne, F., Rousselle, J. C., Becard, J. M. Honey bee colonies that have survived Varroa destructor. Apidologie 2007; 38(6): 566-572.
10. Danka, R. G., Harris, J. W., Villa, J. D. Expression of varroa sensitive hygiene (VSH) in commercial VSH honey bees (Hymenoptera: Apidae). J Econ Entomol 2011; 104(3): 745-749.
11. Simone, M., Evans, J. D., Spivak, M. Resin collection and social immunity in honey bees. Evolution 2009; 63(11): 3016-3022.
12. Bilikova, K., Popova, M., Trusheva, B.,Bankova, V. New anti-Paenibacillus larvae substances purified from propolis. Apidologie 2013; 44(3): 278-285.
13. Antúnez, K., Harriet, J., Gende, L., Maggi, M., Eguaras, M., Zunino, P. Efficacy of natural propolis extract in the control of American foulbrood. Vet Microbiol 2008; 131(3-4): 324-331.
14. Starks, P., Blackie, C., Seeley, T. Fever in honeybee colonies. Naturwissenschaften 2000; 87:229 - 231.
15. Lavine, M. D., Strand, M. R. Insect hemocytes and their role in immunity. Insect Biochem Molec 2002; 32(10): 1295-1309.
16. Evans, J. D., Aronstein, K., Chen, Y. P., Hetru, C., Imler, J. L., Jiang, H., Kanost, M., Thompson, G. J., Zou, Z., Hultmark, D. Immune pathways and defence mechanisms in honey bees Apis mellifera. Insect Mol Biol 2006; 15(5): 645-656.
17. Z. Gliński1, J. J. Infection and immunity in the honey bee Apis mellifera. Apiacta 2001; 36 (1):12 - 24.
18. Kanost, M. R., Gorman, M. J. Insect immunology. In: Phenoloxidases in insect immunity, San Diego, Academic Press, 1993:69-96.
19. Wilson-Rich, N., Dres, S. T.,Starks, P. T. The ontogeny of immunity: Development of innate immune strength in the honey bee (Apis mellifera). J Insect Physiol 2008; 54(10-11): 1392-1399.
20. Danihlík, J., Aronstein, K., Petřivalský, M. Antimicrobial peptides: A key component of honey bee innate immunity. J Apic Res in press.
21. Wimley, W. C., Hristova, K. Antimicrobial peptides: Successes, challenges and unanswered questions. J Membrane Biol 2011; 239(1-2): 27-34.
22. Li, Y., Xiang, Q., Zhang, Q., Huang, Y., Su, Z. Overview on the recent study of antimicrobial peptides: Origins, functions, relative mechanisms and application. Peptides 2012; 37(2): 207-215.
23. Cooper, E. L. Comparative immunology. Integrative zoology 2006; 1:32-43.
24. Hancock, R. E. W., Chapple, D. S. Peptide antibiotics. Antimicrob Agents Ch 1999; 43(6): 1317-1323.
25. Otvos, L., O, I., Rogers, M. E., Consolvo, P. J., Condie, B. A., Lovas, S., Bulet, P., Blaszczyk-Thurin, M. Interaction between heat shock proteins and antimicrobial peptides. Biochemistry 2000; 39(46): 14150-14159.
26. Brogden, K. A. Antimicrobial peptides: Pore formers or metabolic inhibitors in bacteria? Nat Rev Microbiol 2005; 3(3): 238-250.
27. Dainat, B., Evans, J. D., Chen, Y. P., Gauthier, L., Neumann, P. Predictive markers of honey bee colony collapse. Plos one 2012; 7(2): e32151.
28. Nazzi, F., Brown, S. P., Annoscia, D., Del Piccolo, F., Di Prisco, G., Varricchio, P., Della Vedova, G., Cattonaro, F., Caprio, E., Pennacchio, F. Synergistic parasite-pathogen interactions mediated by host immunity can drive the collapse of honeybee colonies. PLoS Pathog 2012; 8(6): e1002735.
29. Harpur, B. A., Chernyshova, A., Soltani, A., Tsvetkov, N., Mahjoorighasrodashti, M., Xu, Z., Zayed, A. No genetic tradeoffs between hygienic behaviour and individual innate immunity in the honey bee, Apis mellifera. Plos one 2014; 9(8): e104214.
30. Ingemar, F. Nosema ceranae in european honey bees (Apis mellifera). J Invertebr Pathol 2010; 103, Supplement: S73-S79.
31. Chen, Y. P., Siede, R. Honey bee viruses. Adv Virus Res 2007; 70: 33-80.
32. Kucharski, R., Maleszka, R. Transcriptional profiling reveals multifunctional roles for transferrin in the honeybee, Apis mellifera. J Insect Sci 2003; 3(27): 1-8.
33. Casteels, P., Ampe, C., Riviere, L., Van Damme, J., Elicone, C., Fleming, M., Jacobs, F., Tempst, P. Isolation and characterization of abaecin, a major antibacterial response peptide in the honeybee (Apis mellifera). Europ J Biochem 1990; 187(2): 381-386.
34. Evans, J. D. Transcriptional immune responses by honey bee larvae during invasion by the bacterial pathogen, Paenibacillus larvae. J Invertebr Pathol 2004; 85(2): 105-111.
35. Aronstein, K. A., Murray, K. D., Saldivar, E. Transcriptional responses in honey bee larvae infected with chalkbrood fungus. BMC Genomics 2010; 1:391.
36. Forsgren, E., Fries, I. Comparative virulence of Nosema ceranae and Nosema apis in individual european honey bees. Vet Parasitol 2010; 170(3–4): 212-217.
37. Chaimanee, V., Chantawannakul, P., Chen, Y., Evans, J. D., Pettis, J. S. Differential expression of immune genes of adult honey bee (Apis mellifera) after inoculated by Nosema ceranae. J Insect Physiol 2012; 58(8): 1090-1095.
38. Dussaubat, C., Brunet, J. L., Higes, M., Colbourne, J. K., Lopez, J., Choi, J. H., Martin-Hernandez, R., Botias, C., Cousin, M., McDonnell, C., Bonnet, M., Belzunces, L. P., Moritz, R. F., Le Conte, Y., Alaux, C. Gut pathology and responses to the microsporidium Nosema ceranae in the honey bee Apis mellifera. Plos one 2012; 7(5): e37017.
39. Mutinelli, F. in Eurbee 6 (Spain, 2014).
40. de Miranda, J. R., Genersch, E. Deformed wing virus. J Invertebr Pathol 2010; 103 Suppl 1(Supplement 1): S48-61.
41. Francis, R. M., Nielsen, S. L., Kryger, P. Varroa-virus interaction in collapsing honey bee colonies. Plos one 2013; 8(3): e57540.
42. Emsen, B., Hamiduzzaman, M. M., Goodwin, P. H., Guzman-Novoa, E. Lower virus infections in Varroa destructor-infested and uninfested brood and adult honey bees (Apis mellifera) of a low mite population growth colony compared to a high mite population growth colony. Plos one 2015; 10(2): e0118885.
43. Locke, B., Forsgren, E., de Miranda, J. R. Increased tolerance and resistance to virus infections: A possible factor in the survival of Varroa destructor-resistant honey bees (Apis mellifera). Plos one 2014; 9(6): e99998
44. Yang, X., Cox-Foster, D. Effects of parasitization by Varroa destructor on survivorship and physiological traits of Apis mellifera in correlation with viral incidence and microbial challenge. Parasitology 2007; 134(Pt 3): 405-412.
45. Yang, X., Cox-Foster, D. L. Impact of an ectoparasite on the immunity and pathology of an invertebrate: Evidence for host immunosuppression and viral amplification. Proc Natl Acad Sci USA 2005; 102(21): 7470-7475.
46. Navajas, M., Migeon, A., Alaux, C., Martin-Magniette, M., Robinson, G., Evans, J., Cros-Arteil, S., Crauser, D., Le Conte, Y. Differential gene expression of the honey bee Apis mellifera associated with Varroa destructor infection. BMC Genomics 2008; 9(1): 301.
47. Aronstein, K. A., Saldivar, E., Vega, R., Westmiller, S., Douglas, A. E. How varroa parasitism affects the immunological and nutritional status of the honey bee, Apis mellifera. Insects 2012; 3(3): 601-615.
48. Hubert, J., Nesvorna, M., Kamler, M., Kopecky, J., Tyl, J., Titera, D., Stara, J. Point mutations in the sodium channel gene conferring tau-fluvalinate resistance in Varroa destructor. Pest Manag Sci 2013; 70(6): 889-894.
49. Lodesani, M., Pellacani, A., Bergomi, S., Carpana, E., Rabitti, T., Lasagni, P. Residue determination for some products used against Varroa infestation in bees. Apidologie 1992; 23(3): 257-272.
50. Wu, J. Y., Anelli, C. M., Sheppard, W. S. Sub-lethal effects of pesticide residues in brood comb on worker honey bee (Apis mellifera) development and longevity. Plos one 2011; 6(2): e14720.
51. Bogdanov, S., Charriere, J. D., Imdorf, A., Kilchenmann, V., Fluri, P. Determination of residues in honey after treatments with formic and oxalic acid under field conditions. Apidologie 2002; 33(4): 399-409.
52. Wang, R. W., Liu, Z. Q., Dong, K., Elzen, P. J., Pettis, J., Huang, Z. Y. Association of novel mutations in a sodium channel gene with fluvalinate resistance in the mite, varroa destructor. J Apicult Res 2002; 41(1-2): 17-25.
53. Keyhani, J., Keyhani, E. Epr study of the effect of formate on cytochrome c oxidase. Biochem Biophys Res Commun 1980; 92(1): 327-333.
54. James, R. R., Xu, J. Mechanisms by which pesticides affect insect immunity. J Invertebr Pathol 2012; 109(0): 175-182.
55. Boncristiani, H., Underwood, R., Schwarz, R., Evans, J. D., Pettis, J., vanEngelsdorp, D. Direct effect of acaricides on pathogen loads and gene expression levels in honey bees Apis mellifera. J Insect Physiol 2012; 58(5): 613-620.
56. Garrido, P. M., Antunez, K., Martin, M., Porrini, M. P., Zunino, P., Eguaras, M. J. Immune-related gene expression in nurse honey bees (Apis mellifera) exposed to synthetic acaricides. J Insect Physiol 2013; 59(1): 113-119.
57. Locke, B., Forsgren, E., Fries, I., de Miranda, J. R. Acaricide treatment affects viral dynamics in Varroa destructor-infested honey bee colonies via both host physiology and mite control. Appl Environ Microb 2011; 78(1): 227-235.
58. Johnson, R. M., Pollock, H. S., Berenbaum, M. R. Synergistic interactions between in-hive miticides in Apis mellifera. Journal of Economic Entomology 2009; 102(2): 474-479.
59. Gruna, B. Potřebujeme povinné vyšetření zimní měli? Moderní včelař 20151): 18-20.
60. Hoage, T. R.,Rothenbu.Wc. Larval honey bee response to various doses of bacillus larvae spores. J Econ Entomol 1966; 59(1): 42-&.
61. Gende, L., Satta, A., Ligios, V., Ruiu, L., Buffa, F., Fernandez, N., Churio, S., Eguaras, M., Fiori, M., Floris, I. Searching for an American foulbrood early detection threshold by the determination of Paenibacillus larvae spore load in worker honey bees. B Insectol 2011; 64(2): 229-233.
62. Fries, I. Nosema ceranae in european honey bees (Apis mellifera). J Invertebr Pathol 2010; 103 Suppl 1(0): S73-79.
63. Jefferson, J. M., Dolstad, H. A., Sivalingam, M. D., Snow, J. W. Barrier immune effectors are maintained during transition from nurse to forager in the honey bee. Plos one 2013; 8(1): e54097.
64. Flenniken, M. L., Andino, R. Non-specific dsrna-mediated antiviral response in the honey bee. Plos one 2013; 8(10): e77263.
65. Tentcheva, D., Gauthier, L., Zappulla, N., Dainat, B., Cousserans, F., Colin, M. E., Bergoin, M. Prevalence and seasonal variations of six bee viruses in Apis mellifera L. and Varroa destructor mite populations in France. Appl Environ Microb 2004; 70(12): 7185-7191.
66. Johnson, R. M., Ellis, M. D., Mullin, C. A., Frazier, M. Pesticides and honey bee toxicity – USA. Apidologie 2010; 41(3): 312-331.
67. Chauzat, M. P., Faucon, J. P., Martel, A. C., Lachaize, J., Cougoule, N., Aubert, M. A survey of pesticide residues in pollen loads collected by honey bees in France. J Econ Entomol 2006; 99(2): 253-262.
68. Johnson, R. M. Honey bee toxicology. Ann Rev of Entomol 2015; 60:415-434.
69. Chan, Q., Melathopoulos, A., Pernal, S., Foster, L. The innate immune and systemic response in honey bees to a bacterial pathogen, Paenibacillus larvae. BMC Genomics 2009; 10(1): 387.
70. Gregorc, A., Pogacnik, A., Bowen, I. D. Cell death in honeybee (Apis mellifera) larvae treated with oxalic or formic acid. Apidologie 2004; 35(5): 453-460.
71. vanEngelsdorp, D., Evans, J. D., Saegerman, C., Mullin, C., Haubruge, E., Nguyen, B. K., Frazier, M., Frazier, J., Cox-Foster, D., Chen, Y. P., Underwood, R., Tarpy, D. R., Pettis, J. S. Colony collapse disorder: A descriptive study. Plos one 2009; 4(8): e6481.