Classification of Fowl Adenovirus Serotypes by Use of High-Resolution Melting-Curve Analysis of the Hexon Gene Region

被引:123
作者
Steer, Penelope A. [1 ]
Kirkpatrick, Naomi C. [1 ]
O'Rourke, Denise [1 ]
Noormohammadi, Amir H. [1 ]
机构
[1] Univ Melbourne, Fac Vet Sci, Werribee, Vic 3030, Australia
关键词
POLYMERASE-CHAIN-REACTION; INCLUSION-BODY HEPATITIS; RESTRICTION ENZYME ANALYSIS; REAL-TIME PCR; HYDROPERICARDIUM SYNDROME; GIZZARD EROSION; AVIAN ADENOVIRUSES; VERTICAL TRANSMISSION; PHYLOGENETIC ANALYSIS; RAPID DETECTION;
D O I
10.1128/JCM.01567-08
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Identification of fowl adenovirus (FAdV) serotypes is of importance in epidemiological studies of disease outbreaks and the adoption of vaccination strategies. In this study, real-time PCR and subsequent high-resolution melting (HRM)-curve analysis of three regions of the hexon gene were developed and assessed for their potential in differentiating 12 FAdV reference serotypes. The results were compared to previously described PCR and restriction enzyme analyses of the hexon gene. Both HRM-curve analysis of a 191-bp region of the hexon gene and restriction enzyme analysis failed to distinguish a number of serotypes used in this study. In addition, PCR of the region spanning nucleotides (nt) 144 to 1040 failed to amplify FAdV-5 in sufficient quantities for further analysis. However, HRM-curve analysis of the region spanning nt 301 to 890 proved a sensitive and specific method of differentiating all 12 serotypes. All melt curves were highly reproducible, and replicates of each serotype were correctly genotyped with a mean confidence value of more than 99% using normalized HRM curves. Sequencing analysis revealed that each profile was related to a unique sequence, with some sequences sharing greater than 94% identity. Melting-curve profiles were found to be related mainly to GC composition and distribution throughout the amplicons, regardless of sequence identity. The results presented in this study show that the closed-tube method of PCR and HRM-curve analysis provides an accurate, rapid, and robust genotyping technique for the identification of FAdV serotypes and can be used as a model for developing genotyping techniques for other pathogens.
引用
收藏
页码:311 / 321
页数:11
相关论文
共 63 条
[1]   Sequence of the avian adenovirus FAV 1 (CELO) DNA encoding the hexon-associated protein pVI and hexon [J].
Akopian, TA ;
Doronin, KK ;
Karpov, VA ;
Naroditsky, BS .
ARCHIVES OF VIROLOGY, 1996, 141 (09) :1759-1765
[2]  
Alvarado IR, 2007, AVIAN DIS, V51, P27, DOI 10.1637/0005-2086(2007)051[0027:GCPAPS]2.0.CO
[3]  
2
[4]   The hydropericardium syndrome in poultry - A current scenario [J].
Balamurugan, V ;
Kataria, JM .
VETERINARY RESEARCH COMMUNICATIONS, 2004, 28 (02) :127-148
[5]  
Benson DA, 2017, NUCLEIC ACIDS RES, V45, pD37, DOI [10.1093/nar/gkp1024, 10.1093/nar/gkw1070, 10.1093/nar/gkq1079, 10.1093/nar/gkl986, 10.1093/nar/gkr1202, 10.1093/nar/gkx1094, 10.1093/nar/gks1195, 10.1093/nar/gkn723, 10.1093/nar/gkg057]
[6]  
Buchen-Osmond C., 2006, ICTVDB THE UNIVERSAL
[7]   Rapid detection and identification of clinically important bacteria by high-resolution melting analysis after broad-range ribosomal RNA real-time PCR [J].
Cheng, Ju-Chien ;
Huang, Chien-Ling ;
Lin, Chung-Ching ;
Chen, Chi-Ching ;
Chang, Yi-Chih ;
Chang, Shy-Shin ;
Tseng, Ching-Ping .
CLINICAL CHEMISTRY, 2006, 52 (11) :1997-2004
[8]   A comparison of high-resolution melting analysis with denaturing high-performance liquid chromatography for mutation scanning - Cystic fibrosis transmembrane conductance regulator gene as a model [J].
Chou, LS ;
Lyon, E ;
Wittwer, CT .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2005, 124 (03) :330-338
[9]  
Dahiya S, 2002, AVIAN DIS, V46, P230, DOI 10.1637/0005-2086(2002)046[0230:FASAWO]2.0.CO
[10]  
2