Skip to main content
Top
Published in: Virology Journal 1/2023

Open Access 01-12-2023 | Pathology | Research

Marek’s disease in chicken farms from Northwest Ethiopia: gross pathology, virus isolation, and molecular characterization

Authors: Mastewal Birhan, Esayas Gelaye, Saddam Mohammed Ibrahim, Nega Berhane, Takele Abayneh, Belayneh Getachew, Aragaw Zemene, Kassahun Birie, Getaw Deresse, Kassaye Adamu, Bereket Dessalegn, Abebe Tesfaye Gessese, Mebrie Zemene Kinde, Molalegne Bitew

Published in: Virology Journal | Issue 1/2023

Login to get access

Abstract

Marek’s disease virus (MDV) is a highly contagious, immunosuppressive, and oncogenic chicken pathogen causing marek’s disease (MD). In this outbreak-based study, 70 dual-purpose chickens that originated from poultry farms in Northwest Ethiopia and suspected of MD were sampled for pathological and virological study from January 2020 to June 2020. Clinically, affected chickens showed inappetence, dyspnea, depression, shrunken combs, and paralysis of legs, wings, and neck, and death. Pathologically, single or multiple greyish white to yellow tumor-like nodular lesions of various size were appreciated in visceral organs. In addition, splenomegaly, hepatomegaly, renomegaly, and sciatic nerve enlargement were observed. Twenty-seven (27) pooled clinical samples i.e. 7 pooled spleen samples and 20 pooled feathers samples were aseptically collected. Confluent monolayer of Chicken Embryo Fibroblast cells was inoculated with a suspension of pathological samples. Of this, MDV-suggestive cytopathic effects were recorded in 5 (71.42%) and 17 (85%) pooled spleen and feather samples respectively. Molecular confirmation of pathogenic MDV was conducted using conventional PCR amplifying 318 bp of ICP4 gene of MDV-1, of which, 40.9% (9/22) tested positive. In addition, 5 PCR-positive samples from various farms were sequenced further confirming the identity of MDV. The ICP4 partial gene sequences were submitted to GenBank with the following accession numbers: OP485106, OP485107, OP485108, OP485109, and OP485110. Comparative phylogenetics showed, two of the isolates from the same site, Metema, seem to be clonal complexes forming distinct cluster. The other three isolates, two from Merawi and one from Debretabor, appear to represent distinct genotypes although the isolate from Debretabor is closer to the Metema clonal complex. On the other hand, the isolates from Merawi appeared genetically far related to the rest of the 3 isolates and clustered with Indian MDV strains included in the analysis. This study presented the first molecular evidence of MDV in chicken farms from Northwest Ethiopia. Biosecurity measures should strictly be implemented to hinder the spread of the virus. Nationwide studies on molecular characteristics of MDV isolates, their pathotypes, and estimation of the economic impact associated with the disease may help justify production and use of MD vaccines within the country.
Literature
1.
go back to reference Witter RL. Increased virulence of marek’s disease virus field isolates. Avian Dis. 1997;41(1):149.CrossRefPubMed Witter RL. Increased virulence of marek’s disease virus field isolates. Avian Dis. 1997;41(1):149.CrossRefPubMed
2.
go back to reference Atkins KE, Read AF, Savill NJ, Renz KG, Islam AF, Walkden-Brown SW, et al. Vaccination and reduced cohort duration can drive virulence evolution: marek’s disease virus and industrialized agriculture. Evolution (NY). 2013;67(3):851.CrossRef Atkins KE, Read AF, Savill NJ, Renz KG, Islam AF, Walkden-Brown SW, et al. Vaccination and reduced cohort duration can drive virulence evolution: marek’s disease virus and industrialized agriculture. Evolution (NY). 2013;67(3):851.CrossRef
3.
go back to reference Rozins C, Day T. The industrialization of farming may be driving virulence evolution. Evol Appl. 2017;10(2):189.CrossRefPubMed Rozins C, Day T. The industrialization of farming may be driving virulence evolution. Evol Appl. 2017;10(2):189.CrossRefPubMed
4.
go back to reference Schat KA, Skinner MA. Avian immunosuppressive diseases and immune evasion. In: avian immunology. 2021. Schat KA, Skinner MA. Avian immunosuppressive diseases and immune evasion. In: avian immunology. 2021.
5.
go back to reference Stamilla A, Messina A, Condorelli L, Licitra F, Antoci F, Lanza M, et al. Morphological and immunohistochemical examination of lymphoproliferative lesions caused by marek’s disease virus in breeder chickens. Animals. 2020;10(8):1280.CrossRefPubMedPubMedCentral Stamilla A, Messina A, Condorelli L, Licitra F, Antoci F, Lanza M, et al. Morphological and immunohistochemical examination of lymphoproliferative lesions caused by marek’s disease virus in breeder chickens. Animals. 2020;10(8):1280.CrossRefPubMedPubMedCentral
6.
go back to reference Read AF, Baigent SJ, Powers C, Kgosana LB, Blackwell L, Smith LP, et al. Imperfect vaccination can enhance the transmission of highly virulent pathogens. PLoS Biol. 2015;13(7):1002198.CrossRef Read AF, Baigent SJ, Powers C, Kgosana LB, Blackwell L, Smith LP, et al. Imperfect vaccination can enhance the transmission of highly virulent pathogens. PLoS Biol. 2015;13(7):1002198.CrossRef
7.
go back to reference Walker PJ, Siddell SG, Lefkowitz EJ, Mushegian AR, Dempsey DM, Dutilh BE, et al. Changes to virus taxonomy and the international code of virus classification and nomenclature ratified by the international committee on taxonomy of viruses (2019). Arch Virol. 2019;164(9):2417.CrossRefPubMed Walker PJ, Siddell SG, Lefkowitz EJ, Mushegian AR, Dempsey DM, Dutilh BE, et al. Changes to virus taxonomy and the international code of virus classification and nomenclature ratified by the international committee on taxonomy of viruses (2019). Arch Virol. 2019;164(9):2417.CrossRefPubMed
8.
go back to reference Witter RL. Characteristics of marek’s disease viruses isolated from vaccinated commercial chicken flocks: association of viral pathotype with lymphoma frequency. Avian Dis. 1983;27(1):113.CrossRefPubMed Witter RL. Characteristics of marek’s disease viruses isolated from vaccinated commercial chicken flocks: association of viral pathotype with lymphoma frequency. Avian Dis. 1983;27(1):113.CrossRefPubMed
9.
go back to reference Witter RL, Calnek BW, Buscaglia C, Gimeno IM, Schat KA. Classification of marek’s disease viruses according to pathotype: philosophy and methodology. Avian Pathol. 2005;34(2):75–90.CrossRefPubMed Witter RL, Calnek BW, Buscaglia C, Gimeno IM, Schat KA. Classification of marek’s disease viruses according to pathotype: philosophy and methodology. Avian Pathol. 2005;34(2):75–90.CrossRefPubMed
10.
go back to reference Reddy SM, Lupiani B, Gimeno IM, Silva RF, Lee LF, Witter RL. Rescue of a pathogenic marek’s disease virus with overlapping cosmid DNAs: use of a pp38 mutant to validate the technology for the study of gene function. Proc Natl Acad Sci USA. 2002;99(10):7054.CrossRefPubMedPubMedCentral Reddy SM, Lupiani B, Gimeno IM, Silva RF, Lee LF, Witter RL. Rescue of a pathogenic marek’s disease virus with overlapping cosmid DNAs: use of a pp38 mutant to validate the technology for the study of gene function. Proc Natl Acad Sci USA. 2002;99(10):7054.CrossRefPubMedPubMedCentral
11.
go back to reference Niikura M, Liu HC, Dodgson JB, Cheng HH. A comprehensive screen for chicken proteins that interact with proteins unique to virulent strains of marek’s disease virus. Poult Sci. 2004;83(7):1117.CrossRefPubMed Niikura M, Liu HC, Dodgson JB, Cheng HH. A comprehensive screen for chicken proteins that interact with proteins unique to virulent strains of marek’s disease virus. Poult Sci. 2004;83(7):1117.CrossRefPubMed
12.
go back to reference Tian F, Zhan F, VanderKraats ND, Hiken JF, Edwards JR, Zhang H, et al. DNMT gene expression and methylome in marek’s disease resistant and susceptible chickens prior to and following infection by MDV. Epigenetics. 2013;8(4):431.CrossRefPubMedPubMedCentral Tian F, Zhan F, VanderKraats ND, Hiken JF, Edwards JR, Zhang H, et al. DNMT gene expression and methylome in marek’s disease resistant and susceptible chickens prior to and following infection by MDV. Epigenetics. 2013;8(4):431.CrossRefPubMedPubMedCentral
13.
go back to reference Baigent SJ, Davison F. marek’s disease virus: biology and life cycle. In: marek’s disease. 2004. Baigent SJ, Davison F. marek’s disease virus: biology and life cycle. In: marek’s disease. 2004.
14.
go back to reference Das S, Das D, Panda SK, Sagarika S, Jena B. Clinico-pathological studies of marek’s disease in chickens. Int J Livest Res. 2018;8(1):207–17. Das S, Das D, Panda SK, Sagarika S, Jena B. Clinico-pathological studies of marek’s disease in chickens. Int J Livest Res. 2018;8(1):207–17.
15.
go back to reference Abreu DL da C, Santos FF, José DS, Tortelly R, Nascimento ER, Pereira VLA Pathological aspects of a subclinical marek’s disease case in free-range chickens. Rev Bras Cienc Avic. 2016;18(1): 197. Abreu DL da C, Santos FF, José DS, Tortelly R, Nascimento ER, Pereira VLA Pathological aspects of a subclinical marek’s disease case in free-range chickens. Rev Bras Cienc Avic. 2016;18(1): 197.
16.
go back to reference de Laney DB, Morrow CJ, Read KM, Tannock GA. The development and evaluation of two tissue culture-grown marek’s disease challenge viruses. Avian Pathol. 1998;27(5):472.CrossRefPubMed de Laney DB, Morrow CJ, Read KM, Tannock GA. The development and evaluation of two tissue culture-grown marek’s disease challenge viruses. Avian Pathol. 1998;27(5):472.CrossRefPubMed
17.
go back to reference Kalyani IH, Tajpara MM, Jhala MK, Bhanderi BB, Nayak JB, Purohit JH. Characterization of the ICP4 gene in pathogenic marek’s disease virus of poultry in Gujarat, India, using PCR and sequencing. Vet Arh. 2010;80(5):683. Kalyani IH, Tajpara MM, Jhala MK, Bhanderi BB, Nayak JB, Purohit JH. Characterization of the ICP4 gene in pathogenic marek’s disease virus of poultry in Gujarat, India, using PCR and sequencing. Vet Arh. 2010;80(5):683.
18.
go back to reference Angamuthu R, Baskaran S, Gopal DR, Devarajan J, Kathaperumal K. Rapid detection of the marek’s disease viral genome in chicken feathers by loop-mediated isothermal amplification. J Clin Microbiol. 2012;50(3):961.CrossRefPubMedPubMedCentral Angamuthu R, Baskaran S, Gopal DR, Devarajan J, Kathaperumal K. Rapid detection of the marek’s disease viral genome in chicken feathers by loop-mediated isothermal amplification. J Clin Microbiol. 2012;50(3):961.CrossRefPubMedPubMedCentral
19.
go back to reference Okazaki W, Purchase HG, Burmester BR. Protection against marek’s disease by vaccination with a herpesvirus of turkeys. Avian Dis. 1970;14(2):413.CrossRefPubMed Okazaki W, Purchase HG, Burmester BR. Protection against marek’s disease by vaccination with a herpesvirus of turkeys. Avian Dis. 1970;14(2):413.CrossRefPubMed
20.
go back to reference Schat KA, Calnek BW. Characterization of an apparently nononcogenic marek’s disease virus. J Natl Cancer Inst. 1978;60(5):1075.CrossRefPubMed Schat KA, Calnek BW. Characterization of an apparently nononcogenic marek’s disease virus. J Natl Cancer Inst. 1978;60(5):1075.CrossRefPubMed
21.
go back to reference Rispens BH, van Vloten H, Mastenbroek N, Maas HJ, Schat KA. Control of marek’s disease in the Netherlands. I. Isolation of an avirulent marek’s disease virus (strain CVI 988) and its use in laboratory vaccination trials. Avian Dis. 1972;16(1):108.CrossRefPubMed Rispens BH, van Vloten H, Mastenbroek N, Maas HJ, Schat KA. Control of marek’s disease in the Netherlands. I. Isolation of an avirulent marek’s disease virus (strain CVI 988) and its use in laboratory vaccination trials. Avian Dis. 1972;16(1):108.CrossRefPubMed
22.
go back to reference Puro K u, Bhattacharjee U, Baruah S, Sen A, Das S, Ghatak S, et al. Characterization of marek’s disease virus and phylogenetic analyses of meq gene from an outbreak in poultry in Meghalaya of Northeast India. Virusdisease. 2018;29(2): 167. Puro K u, Bhattacharjee U, Baruah S, Sen A, Das S, Ghatak S, et al. Characterization of marek’s disease virus and phylogenetic analyses of meq gene from an outbreak in poultry in Meghalaya of Northeast India. Virusdisease. 2018;29(2): 167.
23.
go back to reference Dunn JR, Gimeno IM. Current status of marek’s disease in the United States and worldwide based on a questionnaire survey. Avian Dis. 2013;57(2 SUPPL 1):483.CrossRefPubMed Dunn JR, Gimeno IM. Current status of marek’s disease in the United States and worldwide based on a questionnaire survey. Avian Dis. 2013;57(2 SUPPL 1):483.CrossRefPubMed
24.
go back to reference Morrow C, Fehler F. marek’s Disease: a worldwide problem. marek’s Disease. 2004; Morrow C, Fehler F. marek’s Disease: a worldwide problem. marek’s Disease. 2004;
25.
go back to reference Lobago F, Woldemeskel M. An outbreak of marek’s disease in chickens in central Ethiopia. Trop Anim Health Prod. 2004;36(4):397.CrossRefPubMed Lobago F, Woldemeskel M. An outbreak of marek’s disease in chickens in central Ethiopia. Trop Anim Health Prod. 2004;36(4):397.CrossRefPubMed
26.
go back to reference Duguma R, Yami A, Dana N, Hassen F, Esatu W. marek’s disease in local chicken strains of Ethiopia reared under confined management regime in central Ethiopia. Rev Med Vet (Toulouse). 2005;156(11):541. Duguma R, Yami A, Dana N, Hassen F, Esatu W. marek’s disease in local chicken strains of Ethiopia reared under confined management regime in central Ethiopia. Rev Med Vet (Toulouse). 2005;156(11):541.
27.
go back to reference Demeke B, Jenberie S, Tesfaye B, Ayelet G, Yami M, Lamien CE, et al. Investigation of marek’s disease virus from chickens in central Ethiopia. Trop Anim Health Prod. 2017;49(2):403.CrossRefPubMed Demeke B, Jenberie S, Tesfaye B, Ayelet G, Yami M, Lamien CE, et al. Investigation of marek’s disease virus from chickens in central Ethiopia. Trop Anim Health Prod. 2017;49(2):403.CrossRefPubMed
28.
go back to reference Bulbula A, Borena B, Tadesse B, Aliy A, Negessu D. Isolation and molecular detection of marek’s disease virus from outbreak cases in chicken in South Western Ethiopia. Veterinary Med: Res Reports. 2022;13:265–75. Bulbula A, Borena B, Tadesse B, Aliy A, Negessu D. Isolation and molecular detection of marek’s disease virus from outbreak cases in chicken in South Western Ethiopia. Veterinary Med: Res Reports. 2022;13:265–75.
29.
go back to reference OIE 2008. Manual of diagnostic tests and vaccines for terrestrial animals (mammals, birds and bees). Vol. 1, Parasitology. 2008. OIE 2008. Manual of diagnostic tests and vaccines for terrestrial animals (mammals, birds and bees). Vol. 1, Parasitology. 2008.
30.
go back to reference Woźniakowski G, Samorek-Salamonowicz E, Kozdruń W. Rapid detection of marek’s disease virus in feather follicles by loop-mediated amplification. Avian Dis. 2011;55(3):462.CrossRefPubMed Woźniakowski G, Samorek-Salamonowicz E, Kozdruń W. Rapid detection of marek’s disease virus in feather follicles by loop-mediated amplification. Avian Dis. 2011;55(3):462.CrossRefPubMed
33.
go back to reference Kimura M. Journal of molecular evolution a simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. J Mol Evol. 1980;16:117.CrossRef Kimura M. Journal of molecular evolution a simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. J Mol Evol. 1980;16:117.CrossRef
34.
go back to reference Felsenstein J. Confidence limits on phylogenies: an approach using bootstrap. Evolution (NY). 1985;39:783–91.CrossRef Felsenstein J. Confidence limits on phylogenies: an approach using bootstrap. Evolution (NY). 1985;39:783–91.CrossRef
35.
go back to reference Calnek BW, Hitchner SB. Localization of viral antigen in chickens infected with marek’s disease herpesvirus. J Natl Cancer Inst. 1969;43(4):935.PubMed Calnek BW, Hitchner SB. Localization of viral antigen in chickens infected with marek’s disease herpesvirus. J Natl Cancer Inst. 1969;43(4):935.PubMed
36.
go back to reference Witter RL, Nazerian K, Purchase HG, Burgoyne GH. Isolation from turkeys of a cell-associated herpesvirus antigenically related to marek’s disease virus. Am J Vet Res. 1970;31(3):525.PubMed Witter RL, Nazerian K, Purchase HG, Burgoyne GH. Isolation from turkeys of a cell-associated herpesvirus antigenically related to marek’s disease virus. Am J Vet Res. 1970;31(3):525.PubMed
37.
go back to reference Portz C, de Almeida LL, Bianco Júnior A, Reck H, Franco AC, Canal CW. Comparision of different cell cultures for replication of infectious laryngotracheitis virus from chickens. Acta Sci Vet. 2018;36(2):85. Portz C, de Almeida LL, Bianco Júnior A, Reck H, Franco AC, Canal CW. Comparision of different cell cultures for replication of infectious laryngotracheitis virus from chickens. Acta Sci Vet. 2018;36(2):85.
38.
go back to reference Lee LF, Armstrong RL, Nazerian K. Comparative studies of six avian herpesviruses. Avian Dis. 1972;16(4):799.CrossRefPubMed Lee LF, Armstrong RL, Nazerian K. Comparative studies of six avian herpesviruses. Avian Dis. 1972;16(4):799.CrossRefPubMed
40.
go back to reference El-Kenawy A, A E, El-Tholoth M. Isolation and identification of marek’s disease virus (MDV) from feather follicle epithelium and internal organs of diseased chickens in Dakahlia Governorate, Egypt. Mansoura Veterinary Med J 2019;20(2): 6-11. El-Kenawy A, A E, El-Tholoth M. Isolation and identification of marek’s disease virus (MDV) from feather follicle epithelium and internal organs of diseased chickens in Dakahlia Governorate, Egypt. Mansoura Veterinary Med J 2019;20(2): 6-11.
42.
go back to reference Cui ZZ, Lee LF, Liu JL, Kung HJ. Structural analysis and transcriptional mapping of the marek’s disease virus gene encoding pp38, an antigen associated with transformed cells. J Virol. 1991;65(12):6509.CrossRefPubMedPubMedCentral Cui ZZ, Lee LF, Liu JL, Kung HJ. Structural analysis and transcriptional mapping of the marek’s disease virus gene encoding pp38, an antigen associated with transformed cells. J Virol. 1991;65(12):6509.CrossRefPubMedPubMedCentral
Metadata
Title
Marek’s disease in chicken farms from Northwest Ethiopia: gross pathology, virus isolation, and molecular characterization
Authors
Mastewal Birhan
Esayas Gelaye
Saddam Mohammed Ibrahim
Nega Berhane
Takele Abayneh
Belayneh Getachew
Aragaw Zemene
Kassahun Birie
Getaw Deresse
Kassaye Adamu
Bereket Dessalegn
Abebe Tesfaye Gessese
Mebrie Zemene Kinde
Molalegne Bitew
Publication date
01-12-2023
Publisher
BioMed Central
Keyword
Pathology
Published in
Virology Journal / Issue 1/2023
Electronic ISSN: 1743-422X
DOI
https://doi.org/10.1186/s12985-023-02003-4

Other articles of this Issue 1/2023

Virology Journal 1/2023 Go to the issue
Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine

Highlights from the ACC 2024 Congress

Year in Review: Pediatric cardiology

Watch Dr. Anne Marie Valente present the last year's highlights in pediatric and congenital heart disease in the official ACC.24 Year in Review session.

Year in Review: Pulmonary vascular disease

The last year's highlights in pulmonary vascular disease are presented by Dr. Jane Leopold in this official video from ACC.24.

Year in Review: Valvular heart disease

Watch Prof. William Zoghbi present the last year's highlights in valvular heart disease from the official ACC.24 Year in Review session.

Year in Review: Heart failure and cardiomyopathies

Watch this official video from ACC.24. Dr. Biykem Bozkurt discusses last year's major advances in heart failure and cardiomyopathies.