Newcastle disease virus surveillance in Argentina: Use of reverse transcription-polymerase chain reaction and sequencing for molecular typification

被引:6
作者
Berinstein, A
Seal, BS
Zanetti, F
Kaloghlian, A
Segade, G
Carrillo, E
机构
[1] Inst Nacl Tecnol Agropecuaria, Ctr Invest Ciencias Vet, Inst Biotecnol, RA-1708 Buenos Aires, DF, Argentina
[2] USDA ARS, SE Poultry Res Lab, Athens, GA 30605 USA
[3] SENASA, DILAB, Dept Virol Aviar, RA-1640 Buenos Aires, DF, Argentina
关键词
avian paramyxovirus; avian diseases; sequence analysis; reverse transcription-polymerase chain reaction;
D O I
10.2307/1592751
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Newcastle disease virus (NDV) remains a major pathogen of poultry where highly virulent strains require reporting to the Office of International Epizootes. NDV is a paramyxovirus existing as different strains classified on the basis of severity of the disease they cause. The present study was conducted in Argentina to determine the prevalence of highly virulent velogenic NDV strains in commercial poultry farms. Tracheal and cloacal swabs from 693 flocks, representing 14% of the broiler production, were collected and pooled. A pool amplified twice in embryonated eggs presented a limited hemagglutination titer. We performed reverse transcription coupled to polymerase chain reaction to amplify fusion and matrix protein gene sequences of the isolate and the strain Trenque Lauquen, isolated in Argentina during an outbreak in 1970-71 and previously characterized as velogenic viscerotropic by biological methods. The amino acid sequences were deduced From nucleotide sequences of the amplification products and the pathotype predicted according to the sequences obtained. From the samples analyzed, we found only one type of NDV, being the isolate identified as lentogenic NDV. This strain is probably the one used in vaccination of flocks where that sample was obtained. These data have allowed us to consider a velogenic NDV-free status in Argentina's commercia poultry
引用
收藏
页码:792 / 797
页数:6
相关论文
共 22 条
[1]  
Alexander D.J., 1997, Diseases of poultry, V10th, P541
[2]  
Alexander D.J., 1989, LAB MANUAL ISOLATION, V3rd, P114
[3]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[4]   DEDUCED AMINO-ACID-SEQUENCES AT THE FUSION PROTEIN CLEAVAGE SITE OF NEWCASTLE-DISEASE VIRUSES SHOWING VARIATION IN ANTIGENICITY AND PATHOGENICITY [J].
COLLINS, MS ;
BASHIRUDDIN, JB ;
ALEXANDER, DJ .
ARCHIVES OF VIROLOGY, 1993, 128 (3-4) :363-370
[5]   QUANTITATIVE BASIC RESIDUE REQUIREMENTS IN THE CLEAVAGE-ACTIVATION SITE OF THE FUSION GLYCOPROTEIN AS A DETERMINANT OF VIRULENCE FOR NEWCASTLE-DISEASE VIRUS [J].
GLICKMAN, RL ;
SYDDALL, RJ ;
IORIO, RM ;
SHEEHAN, JP ;
BRATT, MA .
JOURNAL OF VIROLOGY, 1988, 62 (01) :354-356
[6]   MAMMALIAN SUBTILISIN-RELATED PROTEINASES IN CLEAVAGE ACTIVATION OF THE PARAMYXOVIRUS FUSION GLYCOPROTEIN - SUPERIORITY OF FURIN PACE TO PC2 OR PC1/PC3 [J].
GOTOH, B ;
OHNISHI, Y ;
INOCENCIO, NM ;
ESAKI, E ;
NAKAYAMA, K ;
BARR, PJ ;
THOMAS, G ;
NAGAI, Y .
JOURNAL OF VIROLOGY, 1992, 66 (11) :6391-6397
[7]  
HEDGES SB, 1992, MOL BIOL EVOL, V9, P366
[8]  
Kaleta E. F., 1988, Newcastle disease., P197
[9]   ISOLATION OF CLONED MOLONEY MURINE LEUKEMIA-VIRUS REVERSE-TRANSCRIPTASE LACKING RIBONUCLEASE - H ACTIVITY [J].
KOTEWICZ, ML ;
SAMPSON, CM ;
DALESSIO, JM ;
GERARD, GF .
NUCLEIC ACIDS RESEARCH, 1988, 16 (01) :265-277
[10]  
Le L, 1988, Virus Genes, V1, P333