Molecular diagnostic development for begomovirus-betasatellite complexes undergoing diversification: A case study

被引:12
作者
Brown, Judith K. [1 ]
Ur-Rehman, Muhammad Zia [2 ]
Avelar, Sofia [1 ]
Chingandu, N. [1 ]
Hameed, Usman [2 ]
Haider, Saleem [2 ]
Ilyas, Muhammad [1 ]
机构
[1] Univ Arizona, Sch Plant Sci, Tucson, AZ 85721 USA
[2] Univ Punjab, Inst Agr Sci, Lahore, Pakistan
关键词
Emergent plant viruses; Geminiviridae; Genomic surveillance; Next-generation sequencing; Polymerase chain reaction; LEAF CURL DISEASE; PCR-MEDIATED AMPLIFICATION; DNA-BETA SATELLITE; UNIVERSAL PRIMERS; GEZIRA-VIRUS; COTTON; IDENTIFICATION; COMPONENTS; GENETICS;
D O I
10.1016/j.virusres.2017.04.014
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
At least five begomoviral species that cause leaf curl disease of cotton have emerged recently in Asia and Africa, reducing fiber quality and yield. The potential for the spread of these viruses to other cotton-vegetable growing regions throughout the world is extensive, owing to routine, global transport of alternative hosts of the leaf curl viruses, especially ornamentals. The research reported here describes the design and validation of polymerase chain reaction (PCR) primers undertaken to facilitate molecular detection of the two most-prevalent leaf curl associated begomovirus-betasatellite complexes in the Indian Subcontinent and Africa, the Cotton leaf curl Kokhran virus-Burewala strain and Cotton leaf curl Gezira virus, endemic to Asia and Africa, respectively. Ongoing genomic diversification of these begomoviral-satellite complexes was evident based on nucleotide sequence alignments, and analysis of single nucleotide polymorphisms, both factors that created new challenges for primer design. The additional requirement for species and strain-specific, and betasatellite-specific primer design, imposes further constraints on primer design and validation due to the large number of related species and strains extant in 'core leaf curl virus complex', now with expanded distribution in south Asia, the Pacific region, and Africa-Arabian Peninsula that have relatively highly conserved coding and non-coding regions, which precludes much of the genome-betasatellite sequence when selecting primer 'targets'. Here, PCR primers were successfully designed and validated for detection of cloned viral genomes and betasatellites for representative 'core leaf curl' strains and species, distant relatives, and total DNA isolated from selected plant species. The application of molecular diagnostics to screen plant imports prior to export or release from ports of entry is expected to greatly reduce the likelihood of exotic leaf curl virus introductions that could dramatically affect the production of cotton as well as vegetable and ornamental crop hosts.
引用
收藏
页码:29 / 41
页数:13
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