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Differentiation, Distribution, and Elimination of Two Different Pineapple mealybug wilt-associated viruses Found in Pineapple

August 2001 , Volume 85 , Number  8
Pages  856 - 864

D. M. Sether , Department of Plant and Environmental Protection Sciences, University of Hawaii at Manoa, Honolulu 96822 ; A. V. Karasev , Department of Microbiology and Immunology, Thomas Jefferson University, Doylestown, PA 18901 ; C. Okumura , Department of Plant and Environmental Protection Sciences, University of Hawaii at Manoa ; C. Arakawa and F. Zee , National Clonal Germplasm Repository, P.O. Box 4487, Hilo, HI 96720 ; and M. M. Kislan , J. L. Busto , and J. S. Hu , Department of Plant and Environmental Protection Sciences, University of Hawaii at Manoa



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Accepted for publication 30 April 2001.
ABSTRACT

Surveys for Pineapple mealybug wilt-associated virus-1 (PMWaV-1) and PMWaV-2 were conducted on pineapple samples from Hawaii and around the world. Tissue blot immunoassays (TBIAs) with two different monoclonal antibodies (MAb) specific to either PMWaV-1 or PMWaV-2 indicated that both closteroviruses are widely distributed throughout the pineapple-growing areas of the world. In the worldwide survey, PMWaV-1 was found in 80% of the mea-lybug wilt of pineapple (MWP)-symptomatic and 78% of the asymptomatic pineapple plants tested. A subset of plants was tested for PMWaV-2; 100% of the symptomatic plants and 12% of the asymptomatic plants were positive for this virus. A reverse transcription-polymerase chain reaction (RT-PCR) assay was developed to differentiate between PMWaV-1 and PMWaV-2. Oligonucleotide primers were designed using distinct regions of the HSP 70 homolog genes of the two viruses. PMWaV-specific RT-PCR assays and TBIAs were used to screen the pineapple accessions maintained at the United States Department of Agriculture-Agricultural Research Service National Clonal Germplasm Repository for PMWaV infection; 73% of the accessions were found infected with at least one PMWaV. Pineapple accessions found PMWaV-free were challenged with viruliferous mealybugs to test for immunity to PMWaV-1. No immune germ plasm was identified. Potential alternative virus hosts were screened for infection with virus-specific RT-PCR assays and TBIAs and were also challenged with viruliferous mealybugs. No alternate hosts of PMWaV-1 or PMWaV-2 were identified. PMWaV-1 infection was eliminated through axillary and apical bud propagation from infected crowns. Strategies to manage MWP are discussed.


Additional keywords: closterovirus, Dysmicoccus spp., mealybug wilt of pineapple, MWP, PCV

© 2001 The American Phytopathological Society