Please wait a minute...
Journal of Integrative Agriculture  2012, Vol. 12 Issue (10): 1721-1728    DOI: 10.1016/S1671-2927(00)8706
ANIMAL SCIENCE · VETERINARY SCIENCE Advanced Online Publication | Current Issue | Archive | Adv Search |
Anti-Recombinant Gametocyte 56 Protein IgY Protected Chickens from Homologous Coccidian Infection
 DING Jun, LIU Qiao-rong, HAN Jin-peng, QIAN Wei-feng,  LIU Qun
1.Key Laboratory of Animal Epidemiology and Zoonosis, Ministry of Agriculture/College of Veterinary Medicine, China Agricultural University, Beijing 100193, P.R.China
Download:  PDF in ScienceDirect  
Export:  BibTeX | EndNote (RIS)      
摘要  Coccidiosis is caused by intra-cellular infection of Eimeria spp., which goes through a complex life cycle in the intestinal mucosa of infected hosts. Specific immunoglobulins (IgY) could be produced in egg yolk by immunizing hens with specific antigens. In the present study, we cloned the E. maxima gam56 gene, expressed the GST-GAM56 fusion protein and raised IgY to GST-GAM56 in hens. The anti-GST-GAM56 IgY antibody was isolated and used to treat chickens infected with E. maxima oocysts. Intramuscular injection of the antibodies provided minimal protection against parasite infection. However, oral dosing of the IgY 3 or 5 d after oocyst inoculation significantly improved body weight gain, reduced oocyst output and intestinal lesion score were reduced at 3 or 5 d after oocyst challenging, compared to the untreated control group. Our findings suggest that the IgY to gam56 could be an effective prophylactic or therapeutic agent against E. maxima infection in chickens and should have a practical application value.

Abstract  Coccidiosis is caused by intra-cellular infection of Eimeria spp., which goes through a complex life cycle in the intestinal mucosa of infected hosts. Specific immunoglobulins (IgY) could be produced in egg yolk by immunizing hens with specific antigens. In the present study, we cloned the E. maxima gam56 gene, expressed the GST-GAM56 fusion protein and raised IgY to GST-GAM56 in hens. The anti-GST-GAM56 IgY antibody was isolated and used to treat chickens infected with E. maxima oocysts. Intramuscular injection of the antibodies provided minimal protection against parasite infection. However, oral dosing of the IgY 3 or 5 d after oocyst inoculation significantly improved body weight gain, reduced oocyst output and intestinal lesion score were reduced at 3 or 5 d after oocyst challenging, compared to the untreated control group. Our findings suggest that the IgY to gam56 could be an effective prophylactic or therapeutic agent against E. maxima infection in chickens and should have a practical application value.
Keywords:  Eimeria maxima       recombinant GST-GAM56       IgY       therapeutic agent  
Received: 13 June 2011   Accepted:
Fund: 

This work was supported by the Program for Cheung Kong Scholars and Innovative Research Team in University of China (IRT0866).

Corresponding Authors:  Correspondence LIU Qun, Tel: +86-10-62734496, E-mail: qunliu@cau.edu.cn     E-mail:  qunliu@cau.edu.cn
About author:  DING Jun, E-mail: dingjun407@163.com

Cite this article: 

DING Jun, LIU Qiao-rong, HAN Jin-peng, QIAN Wei-feng, LIU Qun. 2012. Anti-Recombinant Gametocyte 56 Protein IgY Protected Chickens from Homologous Coccidian Infection. Journal of Integrative Agriculture, 12(10): 1721-1728.

[1]Belli S I, Witcombe D, Wallach M G, Smith N C. 2002.Functional genomics of gam56: characterisation of therole of a 56 kilodalton sexual stage antigen in oocystwall formation in Eimeria maxima. InternationalJournal for Parasitology, 32, 1727-1737.

[2]Cama V A, Sterling C R. 1991. Hyperimmune hens as anovel source of anti-Cryptosporidium antibodiessuitable for passive immune transfer. Journal ofProtozoology, 38, 42S-43S.

[3]Carlander D, Kollberg H, Wejaker P E, Larsson A. 2000.Peroral immunotherapy with yolk antibodies for theprevention and treatment of enteric infections.Immunologic Research, 21, 1-6.

[4]Chapman H D. 1997. Biochemical, genetic and appliedaspects of drug resistance in Eimeria parasites of thefowl. Avian Pathology, 26, 221-244.

[5]Crane M S, Murray P K, Gnozzio M J, MacDonald T T.1988. Passive protection of chickens against Eimeriatenella infection by monoclonal antibody. Infectionand Immunity, 56, 972-976.

[6]Devi CM, Bai MV, Lal AV, Umashankar P R, Krishnan L K.2002. An improved method for isolation of anti-vipervenom antibodies from chicken egg yolk. Journal ofBiochemical and Biophysical Methods, 51, 129-138.

[7]Ding J, Bao W, Liu Q, Yu Q, Abdille M H, Wei Z. 2008.Immunoprotection of chickens against Eimeriaacervulina by recombinant alpha-tubulin protein.Parasitology Reseacher, 103, 1133-1140.

[8]Erhard M H, Bergmann J, Renner M, Hofmann A, HeinritziK. 1996. Prophylactic effect of specific egg yolkantibodies in diarrhea caused by Escherichia coli K88(F4) in weaned piglets. Zentralbl Veterinarmed (A),43, 217-223.

[9]Jin L Z, Baidoo S K, Marquardt R R, Frohlich AA. 1998. Invitro inhibition of adhesion of enterotoxigenicEscherichia coli K88 to piglet intestinal mucus by eggyolkantibodies. FEMS Immunology Med Microbiology,21, 313-321.

[10]Johnson J R W. 1970. Anticoccidial drugs: lesion scoringtechniques in battery and floor-pen experiments withchickens. Experimental Parasitolology, 28, 30-36.

[11]Kuroki M, Ohta M, Ikemori Y, Icatlo Jr F C, Kobayashi C,Yokoyama H, Kodama Y. 1997. Field evaluation ofchicken egg yolk immunoglobulins specific for bovinerotavirus in neonatal calves. Archives of Virology, 142,843-851.

[12]Lillehoj H S, Lillehoj E P. 2000. Avian coccidiosis. a reviewof acquired intestinal immunity and vaccinationstrategies. Avian Diseases, 44, 408-425.

[13]Min W, Lillehoj H S, Burnside J, Weining K C, Staeheli P,Zhu J J. 2001. Adjuvant effects of IL-1beta, IL-2, IL-8,IL-15, IFN-alpha, IFN-gamma TGF-beta4 andlymphotactin on DNA vaccination against Eimeriaacervulina.

[14]Vaccine, 20, 267-274.

[15]Mine Y, Kovacs-Nolan J. 2002. Chicken egg yolk antibodiesas therapeutics in enteric infectious disease: a review.Journal of Medicinal Food, 5, 159-169.

[16]Polson A C T, Kruger J, von Maltzahn E, van der Merwe KJ. 1985. Improvements in the isolation of IgY from theyolks of eggs laid by immunized hens. Immunol Invest,14, 323-327.

[17]Rose M E. 1971. Immunity to coccidiosis: protective effectof transferred serum in Eimeria maxima infections.Parasitology, 62, 11-25.

[18]Rose M E, Long P L. 1971. Immunity to coccidiosis:protective effects of transferred serum and cellsinvestigated in chick embryos infected with Eimeria.Parasitology, 63, 299-313.

[19]Shin J H, Yang M, Nam S W, Kim J T, Myung N H, Bang WG, Roe I H. 2002. Use of egg yolk-derivedimmunoglobulin as an alternative to antibiotic treatmentfor control of Helicobacter pylori infection. ClinicalDiagnostic Laboratory Immunology, 9, 1061-1066.

[20]Sugita-Konishi Y, Ogawa M, Arai S, Kumagai S, Igimi S,Shimizu M. 2000. Blockade of Salmonella enteritidispassage across the basolateral barriers of humanintestinal epithelial cells by specific antibody.Microbiology and Immunology, 44, 473-479.

[21]Talebi AM G. 1995. Correlation between immune responsesand oocyst production in chickens monospecificallyinfected with Eimeria maxima. Avian Pathoogy, 24,485-495.

[22]Tini M, Jewell U R, Camenisch G, Chilov D, Gassmann M.2002. Generation and application of chicken egg-yolkantibodies. Comparative Biochemistry and Physiology(Part A: Molecular and Integrative Physiology), 131,569-574.

[23]Vermeulen A N. 1998. Progress in recombinant vaccinedevelopment against coccidiosis. a review andprospects into the next millennium. InternatinalJournal for Parasitology, 28, 1121-1130.

[24]Vermeulen A N, Schaap D C, Schetters T P. 2001. Control ofcoccidiosis in chickens by vaccination. VeterinaryParasitology, 100, 13-20.

[25]Wallach M, Halabi A, Pillemer G, Sar-Shalom O, MencherD, Gilad M, Bendheim U, Danforth H D, Augustine P C.1992. Maternal immunization with gametocyte antigensas a means of providing protective immunity againstEimeria maxima in chickens. Infection and Immunity,60, 2036-2039.

[26]Wallach M, Pillemer G, Yarus S, Halabi A, Pugatsch T,Mencher D. 1990. Passive immunization of chickensagainst Eimeria maxima infection with a monoclonalantibody developed against a gametocyte antigen.Infection and Immunity, 58, 557-562.

[27]Wallach M, Smith N C, Petracca M, Miller C M, Eckert J,Braun R. 1995. Eimeria maxima gametocyte antigens:potential use in a subunit maternal vaccine againstcoccidiosis in chickens. Vaccine, 13, 347-354.

[28]Warr G W, Magor K E, Higgins D A. 1995. IgY: clues to theorigins of modern antibodies. Immunology Today, 16,392-398.

[29]Williams R B. 1998. Epidemiological aspects of the use oflive anticoccidial vaccines for chickens. InternatinalJournal for Parasitology, 28, 1089-1098.

[30]Wu S Q, Wang M, Liu Q, Zhu Y J, Suo X, Jiang J S. 2004.Construction of DNA vaccines and their inducedprotective immunity against experimental Eimeriatenella infection. Parasitology Research, 94, 332-336.

[31]Yokoyama H, Peralta R C, Diaz R, Sendo S, Ikemori Y,Kodama Y. 1992. Passive protective effect of chickenegg yolk immunoglobulins against experimentalenterotoxigenic Escherichia coli infection in neonatalpiglets. Infection and Immunity, 60, 998-1007.

[32]Zhang X Y, Ding J, Liu Q. 2007. Cloning and expression ofthe gam56 gene of Eimeria maxima gametocytes.Chinese Journal of Veterinary Medicine, 43, 12-14. (inChinese)
No related articles found!
No Suggested Reading articles found!