Sequence and Phylogenetic Analysis of the First Complete Genome of Rice tungro spherical virus in Malaysia

被引:3
作者
Kannan, Maathavi [1 ]
Saad, Maisarah Mohamad [2 ]
Zainal, Zamri [1 ,3 ]
Kassim, Hakimi [1 ]
Ismail, Ismanizan [1 ,3 ]
Talip, Noraini [4 ]
Baharum, Syarul Nataqain [1 ]
Bunawan, Hamidun [1 ]
机构
[1] Univ Kebangsaan Malaysia, Inst Syst Biol, Bangi 43600, Malaysia
[2] MARDI Seberang Perai, Inst Rice Res Ctr, Jalan Paya Keladi Pinang Tunggal, Kepala Batas 13200, Penang, Malaysia
[3] Univ Kebangsaan Malaysia, Sch Biosci & Biotechnol, Bangi 43600, Selangor, Malaysia
[4] Univ Kebangsaan Malaysia, Sch Environm & Nat Resource Sci, Bangi 43600, Selangor, Malaysia
关键词
Genome; Malaysia; Phylogeny; Rice tungro spherical virus; NUCLEOTIDE-SEQUENCE; BACILLIFORM-VIRUS; COAT PROTEINS; DISEASE; BIOLOGY; EPIDEMIOLOGY; ACCUMULATION; REVEALS; ISOLATE;
D O I
10.30498/IJB.2020.2566
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Rice tungro disease (RID) is a viral disease mainly affecting rice in Asia. RID caused by Rice tungro bacilliform virus and Rice tungro spherical virus. To date, there are only 5 RTSV isolates have been reported. Objectives: In this study, we aimed to report the complete nucleotide sequence of Malaysian isolate of Rice tungro spherical virus Seberang Perai (RTSV-SP) for the first time. RTSV-SP was characterized and its evolutionary relationship with previously reported Indian and Philippines isolates were elucidated. Materials and Methods: RTSV-SP isolate was isolated from a recent outbreak in a paddy field in Seberang Perai zone of Malaysia. Its complete genome was amplified by RT-PCR, cloned and sequenced. Results: Sequence analysis indicated that the genome of RTSV-SP consisted of 12,173 nucleotides (nt). Comparative analysis of 6 complete genome sequences using Clustal Omega showed that Seberang Perai isolate shared the highest nucleotide identity (96.04%) with Philippine-A isolate, except that the sORF-2 of RTSV-SP is shorter than RTSV Philippine-A by 27 amino acid residues. RTSV-SP found to cluster in Southeast Asia (SEA) group based on the whole genome sequence phylogenetic analysis using MEGA X software. Conclusions: Phylogenetic classification of RTSV isolates based on the complete nucleotide sequences showed more distinctive clustering pattern with the addition of RTSV-SP whole genome to the available isolates. Present study described the isolation and molecular characterization of RTSV-SP.
引用
收藏
页码:9 / 17
页数:9
相关论文
共 45 条
[1]  
Ali Azgar Md., 2018, INT J CURR MICROBIOL, V7, P778, DOI [10.20546/ijcmas.2018.703.091., DOI 10.20546/IJCMAS.2018.703.091]
[2]  
Anjaneyulu A, 1995, RICE TUNGRO, P228
[3]   The biology, epidemiology, and management of rice tungro disease in Asia [J].
Azzam, O ;
Chancellor, TCB .
PLANT DISEASE, 2002, 86 (02) :88-100
[4]   Genetic composition and complexity of virus populations at tungro-endemic and outbreak rice sites [J].
Azzam, O ;
Arboleda, M ;
Umadhay, KML ;
de los Reyes, JB ;
Cruz, FS ;
Mackenzie, C ;
McNally, KL .
ARCHIVES OF VIROLOGY, 2000, 145 (12) :2643-2657
[5]   Dynamical roguing model for controlling the spread of tungro virus via Nephotettix Virescens in a rice field [J].
Blas, Nikki ;
David, Guido .
ASIAN MATHEMATICAL CONFERENCE 2016 (AMC 2016), 2017, 893
[6]  
Cabauatan P., 1985, PHILIPPINE PHYTOPATH, V21, P103, DOI DOI 10.3186/JJPHYT0PATH.49.545
[7]  
Chancellor TCB, 1999, P INT WORKSH TUNGR D, P166
[8]   Changes in level of virus accumulation and incidence of infection are critical in the characterization of Rice tungro bacilliform virus (RTBV) resistance in rice [J].
Cruz, FCS ;
Hull, R ;
Azzam, O .
ARCHIVES OF VIROLOGY, 2003, 148 (08) :1465-1483
[9]   Genetic engineering of rice to resist rice tungro disease [J].
Dai, Shunhong ;
Beachy, Roger N. .
IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-PLANT, 2009, 45 (05) :517-524
[10]   Immunological characterization of rice tungro spherical virus coat proteins and differentiation of isolates from the Philippines and India [J].
Druka, A ;
Burns, T ;
Zhang, SL ;
Hull, R .
JOURNAL OF GENERAL VIROLOGY, 1996, 77 :1975-1983