آمار

تعداد نشریات281
تعداد نشریات سازمان80
تعداد شماره‌ها2,370
تعداد مقالات27,508
تعداد مشاهده مقاله15,239,115
تعداد دریافت فایل اصل مقاله12,086,061
Moharrami, M, Mojgani, N, Bagheri, M, Toutiaee, S. (1401). Role of Honey Bee Gut Microbiota in the Control of American Foulbrood and European Foulbrood Diseases. سامانه مدیریت نشریات علمی, 77(4), 1331-1339. doi: 10.22092/ari.2022.358073.2146
M Moharrami; N Mojgani; M Bagheri; S Toutiaee. "Role of Honey Bee Gut Microbiota in the Control of American Foulbrood and European Foulbrood Diseases". سامانه مدیریت نشریات علمی, 77, 4, 1401, 1331-1339. doi: 10.22092/ari.2022.358073.2146
Moharrami, M, Mojgani, N, Bagheri, M, Toutiaee, S. (1401). 'Role of Honey Bee Gut Microbiota in the Control of American Foulbrood and European Foulbrood Diseases', سامانه مدیریت نشریات علمی, 77(4), pp. 1331-1339. doi: 10.22092/ari.2022.358073.2146
Moharrami, M, Mojgani, N, Bagheri, M, Toutiaee, S. Role of Honey Bee Gut Microbiota in the Control of American Foulbrood and European Foulbrood Diseases. سامانه مدیریت نشریات علمی, 1401; 77(4): 1331-1339. doi: 10.22092/ari.2022.358073.2146

Role of Honey Bee Gut Microbiota in the Control of American Foulbrood and European Foulbrood Diseases

Archives of Razi Institute
مقاله 3، دوره 77، شماره 4، مهر و آبان 2022، صفحه 1331-1339  XML اصل مقاله (531.94 K)
نوع مقاله: Review Article
شناسه دیجیتال (DOI): 10.22092/ari.2022.358073.2146
نویسندگان
M Moharrami1؛ N Mojgani email orcid 1؛ M Bagheriorcid 1؛ S Toutiaee1، 2
1Razi Vaccine and Serum Research Institute, Agricultural Research, Education and Extension Organization (AREEO) Karaj, 31976-19751, Iran
2Department of Microbiology, Islamic Azad University, Karaj, Iran
چکیده
American foulbrood (AFB) and European foulbrood (EFB) are the two most important honey bee brood diseases which impose heavy economic losses to the apiculture industry worldwide by reducing bee population and honey production. Treatment with antibiotics has led to the emergence of antibiotic-resistant strains, calling for alternative safe treatment procedures that could control these diseases. Honey bee gut microbiota is known to affect the overall health of honey bees by enhancing their resistance to a number of diseases via modulation of the immune response and production of different antimicrobial metabolites. The majority of these gut resident bacteria are identified as probiotic bacteria and secure the health of these tiny insects. In the present review, we highlighted the significance of the honey bee gut microbial community and their probiotic potency for the prevention of AFB and EFB diseases in honey bees.
کلیدواژه‌ها
American foulbrood disease؛ European foulbrood disease؛ probiotics؛ honeybee microbiota
عنوان مقاله [English]
میکروبیوم روده زنبور عسل و نقش آن در کنترل بیماری های لوک آمریکایی و اروپایی
چکیده [English]
بیماری‌های لوک آمریکایی (AFB) ولوک اروپایی (EFB) دو بیماری مهم زنبور عسل هستند که با ایجاد کاهش جمعیت زنبور عسل و تولید عسل، خسارت‌های اقتصادی جدی به صنعت زنبورداری در سطح جهان وارد می‌کنند. درمان با آنتی‌بیوتیک‌ها منجر به پیدایش سویه‌های مقاوم به آنتی‌بیوتیک شده است که نیازمند روش‌های درمانی ایمن جایگزین است تا بتواند این بیماری‌ها را کنترل کند. میکروبیوم روده زنبور عسل با افزایش مقاومت آنها در برابر تعدادی از بیماری ها از طریق تعدیل پاسخ ایمنی و تولید متابولیت های ضد میکروبی مختلف، بر سلامت کلی زنبورهای عسل تأثیر می گذارد. اکثر این باکتری های ساکن روده به عنوان باکتری های پروبیوتیک شناخته می شوند که مانند سایر حیوانات سلامت این حشرات کوچک را تضمین می کنند. ما درمقاله مروری حاضر،اهمیت جامعه میکروبی روده زنبور عسل و قدرت پروبیوتیکی آنها را برای پیشگیری از بیماری AFB و EFB در زنبورهای عسل برجسته می‌کنیم.
کلیدواژه‌ها [English]
بیماری لوک آمریکایی, بیماری لوک اروپایی, پروبیوتیک, میکروبیوم زنبور عسل
مراجع
  1. Zheng H, Steele MI, Leonard SP, Motta EVS, Moran NA. Honey bees as models for gut microbiota research. Lab Anim (NY). 2018;47(11):317-25.
  2. Daisley BA, Pitek AP, Chmiel JA, Gibbons S, Chernyshova AM, Al KF, et al. Lactobacillus spp. attenuate antibiotic-induced immune and microbiota dysregulation in honey bees. Commun Biol. 2020;3(1):534.
  3. Hamdi C, Balloi A, Essanaa J, Crotti E, Gonella E, Raddadi N, et al. Gut microbiome dysbiosis and honeybee health. J Appl Entomol. 2011;135(7):524-33.
  4. Naug D. Nutritional stress due to habitat loss may explain recent honeybee colony collapses. Biol Conserv. 2009;142(10):2369-72.
  5. Neov B, Georgieva A, Shumkova R, Radoslavov G, Hristov P. Biotic and Abiotic Factors Associated with Colonies Mortalities of Managed Honey Bee (Apis mellifera). Diversity. 2019;11(12):237.
  6. Forsgren E, Locke B, Sircoulomb F, Schäfer MO. Bacterial Diseases in Honeybees. Curr Clin Microbiol Rep. 2018;5(1):18-25.
  7. Milbrath MO, Fowler PD, Abban SK, Lopez D, Evans JD. Validation of Diagnostic Methods for European Foulbrood on Commercial Honey Bee Colonies in the United States. J Insect Sci. 2021;21(6).
  8. Biová J, Bzdil J, Dostálková S, Petřivalský M, Brus J, Carra E, et al. American Foulbrood in the Czech Republic: ERIC II Genotype of Paenibacillus Larvae Is Prevalent. Front Vet Sci. 2021;8.
  9. Stephan JG, de Miranda JR, Forsgren E. American foulbrood in a honeybee colony: spore-symptom relationship and feedbacks. BMC Ecol. 2020;20(1):15.
  10. Teo AY, Tan HM. Inhibition of Clostridium perfringens by a novel strain of Bacillus subtilis isolated from the gastrointestinal tracts of healthy chickens. Appl Environ Microbiol. 2005;71(8):4185-90.
  1. Tootiaie S, Moharrami M, Mojgani N. Honeybee Gut: Reservoir of Probiotic Bacteria. In: Mojgani N, Dadar M, editors. Probiotic Bacteria and Postbiotic Metabolites: Role in Animal and Human Health. Singapore: Springer Singapore; 2021. p. 221-36.
  2. Khalkhali S, Mojgani N. Enterococcus faecium; a Suitable Probiotic Candidate for Modulation of Immune Responses Against Pathogens. Int J Basic Sci Med. 2017;2(2):77-82.
  3. Mojgani N, Hussaini F, Vaseji N. Characterization of indigenous lactobacillus strains for probiotic properties. Jundishapur J Microbiol. 2015;8(2):e17523.
  4. Evans JD, Armstrong TN. Antagonistic interactions between honey bee bacterial symbionts and implications for disease. BMC Ecol. 2006;6:4.
  5. Cai J, Collins MD. Evidence for a close phylogenetic relationship between Melissococcus pluton, the causative agent of European foulbrood disease, and the genus Enterococcus. Int J Syst Bacteriol. 1994;44(2):365-7.
  6. Thompson HM, Brown MA. Is contact colony treatment with antibiotics an effective control for European foulbrood? Bee World. 2001;82(3):130-8.
  7. Martel AC, Zeggane S, Drajnudel P, Faucon JP, Aubert M. Tetracycline residues in honey after hive treatment. Food Addit Contam. 2006;23(3):265-73.
  8. Thompson HM, Levine SL, Doering J, Norman S, Manson P, Sutton P, et al. Evaluating exposure and potential effects on honeybee brood (Apis mellifera) development using glyphosate as an example. Integr Environ Assess Manag. 2014;10(3):463-70.
  9. Baffoni L, Alberoni D, Gaggìa F, Braglia C, Stanton C, Ross PR, et al. Honeybees exposure to veterinary drugs: how the gut microbiota is affected. Microbiol Spectr. 2021;9(1):176-21.
  10. Miyagi T, Peng CY, Chuang RY, Mussen EC, Spivak MS, Doi RH. Verification of oxytetracycline-resistant American foulbrood pathogen Paenibacillus larvae in the United States. J Invertebr Pathol. 2000;75(1):95-6.
  11. Cariveau DP, Elijah Powell J, Koch H, Winfree R, Moran NA. Variation in gut microbial communities and its association with pathogen infection in wild bumble bees (Bombus). ISME J. 2014;8(12):2369-79.
  12. Wu M, Sugimura Y, Iwata K, Takaya N, Takamatsu D, Kobayashi M, et al. Inhibitory effect of gut bacteria from the Japanese honey bee, Apis cerana japonica, against Melissococcus plutonius, the causal agent of European foulbrood disease. J Insect Sci. 2014;14(1).
  1. Pachla A, Ptaszyńska AA, Wicha M, Oleńska E, Małek W. Fascinating fructophilic lactic acid bacteria associated with various fructose-rich niches. Ann Univ Mariae Curie Sklodowska Med. 2019;72(2):41-50.
  2. Kesnerova L, Mars RAT, Ellegaard KM, Troilo M, Sauer U, Engel P. Disentangling metabolic functions of bacteria in the honey bee gut. PLoS Biol. 2017;15(12):2003467.
  3. Ellegaard KM, Engel P. Genomic diversity landscape of the honey bee gut microbiota. Nat Commun. 2019;10(1):446.
  4. Kwong WK, Mancenido AL, Moran NA. Immune system stimulation by the native gut microbiota of honey bees. R Soc Open Sci. 2017;4(2):170003.
  5. Kesnerova L, Emery O, Troilo M, Liberti J, Erkosar B, Engel P. Gut microbiota structure differs between honeybees in winter and summer. ISME J. 2020;14(3):801-14.
  6. Endo A, Salminen S. Honeybees and beehives are rich sources for fructophilic lactic acid bacteria. Syst Appl Microbiol. 2013;36(6):444-8.
  7. Lamei S, Stephan JG, Nilson B, Sieuwerts S, Riesbeck K, de Miranda JR, et al. Feeding Honeybee Colonies with Honeybee-Specific Lactic Acid Bacteria (Hbs-LAB) Does Not Affect Colony-Level Hbs-LAB Composition or Paenibacillus larvae Spore Levels, Although American Foulbrood Affected Colonies Harbor a More Diverse Hbs-LAB Community. Microb Ecol. 2020;79(3):743-55.
  8. Lazzeri AM, Mangia NP, Mura ME, Floris I, Satta A, Ruiu L. Potential of novel food-borne Lactobacillus isolates against the honeybee pathogen Paenibacillus larvae. Biocontrol Sci Technol. 2020;30(9):897-908.
  9. Vásquez A, Olofsson TC. The lactic acid bacteria involved in the production of bee pollen and bee bread. J Apic Res. 2009;48(3):189-95.
  10. Ramos OY, Basualdo M, Libonatti C, Vega MF. Current status and application of lactic acid bacteria in animal production systems with a focus on bacteria from honey bee colonies. J Appl Microbiol. 2020;128(5):1248-60.
  11. Crotti E, Rizzi A, Chouaia B, Ricci I, Favia G, Alma A, et al. Acetic acid bacteria, newly emerging symbionts of insects. Appl Environ Microbiol. 2010;76(21):6963-70.
  12. Kazimierczak-Baryczko M, Szymaś B. Improvement of the composition of pollen substitute for honey bee (Apis mellifera L.), through implementation of probiotic preparations. J Apic Sci. 2006;50(1):15-23.
  13. Pachla A, Ptaszynska AA, Wicha M, Kunat M, Wydrych J, Olenska E, et al. Insight into probiotic properties of lactic acid bacterial endosymbionts of Apis mellifera L. derived from the Polish apiary. Saudi J Biol Sci. 2021;28(3):1890-9.
  14. Honey Chandran C, Keerthi T. Probiotic potency of Lactobacillus plantarum KX519413 and KX519414 isolated from honey bee gut. FEMS Microbiol Lett. 2018;365(4).
  15. Toutiaee S, Mojgani N, Harzandi N, Moharrami M, Mokhberosafa L. In‐vitro probiotic and safety attributes of Bacillus spp isolated from beebread, honey samples and digestive tract of honeybees Apis mellifera. Lett Appl Microbiol. 2022;74.
  16. GILLIAM M. Microbiology of pollen and bee bread : The genus bacillus. Apidologie. 1979;10(3):269-74.
  17. Sabate DC, Carrillo L, Audisio MC. Inhibition of Paenibacillus larvae and Ascosphaera apis by Bacillus subtilis isolated from honeybee gut and honey samples. Res Microbiol. 2009;160(3):193-9.
  18. Duc le H, Hong HA, Barbosa TM, Henriques AO, Cutting SM. Characterization of Bacillus probiotics available for human use. Appl Environ Microbiol. 2004;70(4):2161-71.
  19. Leonard SP, Powell JE, Perutka J, Geng P, Heckmann LC, Horak RD, et al. Engineered symbionts activate honey bee immunity and limit pathogens. Science. 2020;367(6477):573-6.
  20. Carina Audisio M, Torres MJ, Sabate DC, Ibarguren C, Apella MC. Properties of different lactic acid bacteria isolated from Apis mellifera L. bee-gut. Microbiol Res. 2011;166(1):1-13.
  21. Arredondo D, Castelli L, Porrini MP, Garrido PM, Eguaras MJ, Zunino P, et al. Lactobacillus kunkeei strains decreased the infection by honey bee pathogens Paenibacillus larvae and Nosema ceranae. Benef Microbes. 2018;9(2):279-90.
  22. Yoshiyama M, Wu M, Sugimura Y, Takaya N, Kimoto-Nira H, Suzuki C. Inhibition of Paenibacillus larvae by lactic acid bacteria isolated from fermented materials. J Invertebr Pathol. 2013;112(1):62-7.
  23. Killer J, Dubna S, Sedlacek I, Svec P. Lactobacillus apis sp. nov., from the stomach of honeybees (Apis mellifera), having an in vitro inhibitory effect on the causative agents of American and European foulbrood. Int J Syst Evol Microbiol. 2014;64(Pt 1):152-7.
  24. Moran NA. Genomics of the honey bee microbiome. Curr Opin Insect Sci. 2015;10:22-8.
  25. Kwong WK, Moran NA. Gut microbial communities of social bees. Nat Rev Microbiol. 2016;14(6):374-84.
  26. Yoshiyama M, Kimura K. Bacteria in the gut of Japanese honeybee, Apis cerana japonica, and their antagonistic effect against Paenibacillus larvae, the causal agent of American foulbrood. J Invertebr Pathol. 2009;102(2):91-6.
  1. Alippi AM, Reynaldi FJ. Inhibition of the growth of Paenibacillus larvae, the causal agent of American foulbrood of honeybees, by selected strains of aerobic spore-forming bacteria isolated from apiarian sources. J Invertebr Pathol. 2006;91(3):141-6.
  2. Mojgani N, Razmgah N, Karimi torshizi MA, Sanjabi M. Effects of three Bacillus specious on hatchability, growth performance and serum biochemistry in Japanese quails fed diet contaminated with Aflatoxin B1. Acta Sci Anim Sci. 2020;42.
آمار
تعداد مشاهده مقاله: 99
تعداد دریافت فایل اصل مقاله: 62


Contact Us | Help & Support | Site Map
counter

Journal Management System. Designed by sinaweb.