August
2001
, Volume
85
, Number
8
Pages
856
-
864
Authors
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
Affiliations
Go to article:
RelatedArticle
Accepted for publication 30 April 2001.
Abstract
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.
JnArticleKeywords
Additional keywords:
closterovirus,
Dysmicoccus spp.,
mealybug wilt of pineapple,
MWP,
PCV
Page Content
ArticleCopyright
© 2001 The American Phytopathological Society