TY - JOUR
T1 - Molecular diagnostic development for begomovirus-betasatellite complexes undergoing diversification
T2 - A case study
AU - Brown, Judith K.
AU - Ur-Rehman, Muhammad Zia
AU - Avelar, Sofia
AU - Chingandu, N.
AU - Hameed, Usman
AU - Haider, Saleem
AU - Ilyas, Muhammad
N1 - Funding Information: Funding supporting this study was received from a USDA-ARS Non-Assistance Cooperative Agreement 58-6402-2-763, Cotton Incorporated-Core Program Funds Project 06-829, and the USDA-FAS Borlaug Fellowship Program. The authors would like to thank the co-PI's, Drs. Brian Scheffler and Jodi Scheffler (USDA-ARS Cotton Genetics and Genomics Laboratory, Stoneville, MI), and J.K. Brown (University of Arizona, Tucson, AZ) for project coordination, and the Management Entity, ICARDA, for management and coordination of the activities carried out in Pakistan. Funding Information: Funding supporting this study was received from a USDA-ARS Non-Assistance Cooperative Agreement 58-6402-2-763 , Cotton Incorporated-Core Program Funds Project 06-829 , and the USDA-FAS Borlaug Fellowship Program . The authors would like to thank the co-PI’s, Drs. Brian Scheffler and Jodi Scheffler (USDA-ARS Cotton Genetics and Genomics Laboratory, Stoneville, MI), and J.K. Brown (University of Arizona, Tucson, AZ) for project coordination, and the Management Entity, ICARDA, for management and coordination of the activities carried out in Pakistan. Publisher Copyright: © 2017 Elsevier B.V.
PY - 2017/9/15
Y1 - 2017/9/15
N2 - 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.
AB - 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.
KW - Emergent plant viruses
KW - Geminiviridae
KW - Genomic surveillance
KW - Next-generation sequencing
KW - Polymerase chain reaction
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U2 - 10.1016/j.virusres.2017.04.014
DO - 10.1016/j.virusres.2017.04.014
M3 - Article
C2 - 28438632
SN - 0168-1702
VL - 241
SP - 29
EP - 41
JO - Virus research
JF - Virus research
ER -