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The Clinical Symptom and Anatomical Pathology of Tolaki Chicken which Infected Newcastle Disease Viral

Proceeding INTERNATIONAL SEMINAR IMPROVING TROPICAL ANIMAL PRODUCTION FOR FOOD SECURITY (2016)

Published
2016-07-13
Publisher
Proceeding INTERNATIONAL SEMINAR IMPROVING TROPICAL ANIMAL PRODUCTION FOR FOOD SECURITY
Language
eng

Abstract

This study aim was observatiion the clinical and anatomic pathology Tolaki chicken infected virus Newcastle Disease (ND) as an affirmation analysis of the cause of the viral disease. A total of 30Tolaki chickens divided into 3 groups based on the Mx (Myxovirus) gene genotype. Mx gene is a genethat is antiviral, producing three genotypes (AA, AG and GG), respectively 10 chicks kept in separatecages. Challenge test performed by infection with a virus gene ND VII eye drops at a dose of 104CLD50 /0.5 ml / head. The results showed that in the first week of chicken genotype AA, AG and GGgenerally show the same clinical symptoms such as ducking, breakaway, face swollen, snoring.Chicken looks decreased appetite and green diarrhea are found in the feces. The number of chickensthat died at the AA and AG there are three tails, while the GG Chicken found 6 tail. In the secondweek the AA genotype was not found green diarrhea, while the AG and GG discovered greendiarrhea. The number of chickens that died at the AA and AG there are two tails, while GG was founddead three tails. Total chickens that died at the AA and AG found as many as 5 tails, while the GG asmany as 9 tails. Generally the infected chicken ND virus causes swelling of the spleen,bleeding/redness of the intestine and trachea in all genotypes. Swelling of the spleen in the AAgenotype was found to be 20%, AG and GG 60% of 100%. Spleen were obtained blackish color on theGG genotype of 44.44%. Based on changes in anatomic pathology in this study was obtainedcharacteristics ND diseased chickens, so the chickens have been infected with the virus diagnosedND. Patognomosis changes in anatomical pathology characterized by hemorhagi enteritis in thegastrointestinal tract (gut) and respiratory tract (trachea). Based on the results of the ND viruschallenge test to prove the group challenged chickens have been infected with ND virus. ND virusinfection attacks the intestinal organs, trachea, and spleen affecting the decline of the immunesystem in all genotypes. AA and AG genotypes have better protective properties against ND virusinfection than genotype GG.Key Words: Clinical Symptom, Anatomy Pathology, Tolaki Chicken, and ND Viral

Collaboration network of the authors

11 authors · 18 co-authorship links

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  • IPB University
  • Gunadarma University
  • Affiliation unknown
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  • Same organisation
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Co-authorOrganisationJoint articles
Apri IriantoIPB University1
Asep GunawanIPB University1
Fitrianingsih FitrianingsihGunadarma University1
Surahmanto SurahmantoAffiliation unknown1
N. SandiahAffiliation unknown1
melfa andraini agathaAffiliation unknown1
Sofyan SjafAffiliation unknown1

Affiliations come from OpenAlex; journal OAI-PMH metadata carries none. Authors without an OpenAlex ID are matched by name, which can merge or split people.

Metadata source: OAI-PMH (metadata jurnal) https://ojs.uho.ac.id/index.php/P-ISITAPFFS/oai, first harvested 30 Okt 2026, last seen 1 Nov 2026.
Original metadata (oai_dc) 
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	<dc:title xml:lang="en-US">The Clinical Symptom and Anatomical Pathology of Tolaki Chicken  which Infected Newcastle Disease Viral</dc:title>
	<dc:creator>Pagala, M. A.</dc:creator>
	<dc:creator>Muladno, Muladno</dc:creator>
	<dc:creator>Sumatri, C.</dc:creator>
	<dc:creator>Murtini, S.</dc:creator>
	<dc:description xml:lang="en-US">This study aim was observatiion the clinical and anatomic pathology Tolaki chicken infected virus Newcastle Disease (ND) as an affirmation analysis of the cause of the viral disease. A total of 30Tolaki chickens divided into 3 groups based on the Mx (Myxovirus) gene genotype. Mx gene is a genethat is antiviral, producing three genotypes (AA, AG and GG), respectively 10 chicks kept in separatecages. Challenge test performed by infection with a virus gene ND VII eye drops at a dose of 104CLD50 /0.5 ml / head. The results showed that in the first week of chicken genotype AA, AG and GGgenerally show the same clinical symptoms such as ducking, breakaway, face swollen, snoring.Chicken looks decreased appetite and green diarrhea are found in the feces. The number of chickensthat died at the AA and AG there are three tails, while the GG Chicken found 6 tail. In the secondweek the AA genotype was not found green diarrhea, while the AG and GG discovered greendiarrhea. The number of chickens that died at the AA and AG there are two tails, while GG was founddead three tails. Total chickens that died at the AA and AG found as many as 5 tails, while the GG asmany as 9 tails. Generally the infected chicken ND virus causes swelling of the spleen,bleeding/redness of the intestine and trachea in all genotypes. Swelling of the spleen in the AAgenotype was found to be 20%, AG and GG 60% of 100%. Spleen were obtained blackish color on theGG genotype of 44.44%. Based on changes in anatomic pathology in this study was obtainedcharacteristics ND diseased chickens, so the chickens have been infected with the virus diagnosedND. Patognomosis changes in anatomical pathology characterized by hemorhagi enteritis in thegastrointestinal tract (gut) and respiratory tract (trachea). Based on the results of the ND viruschallenge test to prove the group challenged chickens have been infected with ND virus. ND virusinfection attacks the intestinal organs, trachea, and spleen affecting the decline of the immunesystem in all genotypes. AA and AG genotypes have better protective properties against ND virusinfection than genotype GG.Key Words: Clinical Symptom, Anatomy Pathology, Tolaki Chicken, and ND Viral</dc:description>
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	<dc:date>2016-07-13</dc:date>
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	<dc:identifier>https://ojs.uho.ac.id/index.php/P-ISITAPFFS/article/view/1133</dc:identifier>
	<dc:source xml:lang="en-US">Proceeding INTERNATIONAL SEMINAR IMPROVING TROPICAL ANIMAL PRODUCTION FOR FOOD SECURITY; PROCEEDING INTERNATIONAL SEMINAR</dc:source>
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