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2005 Caribbean Division
Meeting Abstracts
June 27-July 1, 2005 - San José, Costa Rica
Posted online April 18, 2006
Confirmation of the presence of Xylella fastidiosa in plants of
grapevine in Costa Rica. E. AGUILAR (1), W. Villalobos (1), L. Garita
(1), and C. Rivera (1,2). (1) Centro de Investigación en Biología Celular y
Molecular (CIBCM), Universidad de Costa Rica (UCR), San José-Costa Rica; (2)
Facultad de Microbiología, UCR.
Pierce’s Disease was reported for the first time in Costa Rica in 1979;
the causal agent was isolated in 1980. The pathogen was known as Pierce’s
Disease bacteria and was identified as Xylella fastidiosa. The
presence of X. fastidiosa was confirmed in grapevine in three zones
of Costa Rica. In each zone leaves with similar symptoms to Pierce Disease
were collected. The samples were positive by DAS-ELISA using specific
antibodies for X. fastidiosa (Agdia Inc. Elkhart Indiana).
Rod-shaped, Gram negative, catalase positive, oxidase negative bacteria were
isolated from petioles using PW medium. Bacterial colonies were visible 6 to
7 days. Colonies were smooth, opalescent, with entire margins and a diameter
of 2 to 3 mm. DNA was extracted from purified isolates and PCR was performed
using 272-1-int, 272-2-int and RST31, RST33. Bands of 500bp and a 733pb were
amplified respectively. Electron micrographs showed bacteria 1–4 µm long
with a cell wall with ridges and furrows identical to the morphology
reported for X. fastidiosa.
Morphological, pathogenic, and molecular characterization of Phoma spp.
isolated from onion (Allium cepa L.) fields. I. E. BADILLO-VARGAS
(1), J. Calle-Bellido (2), and L. I. Rivera Vargas (1). (1) Departments of Crop
Protection and (2) Agronomy and Soil, University of Puerto Rico - Mayaguez
Campus, P.R. 00681-9030.
Onion (Allium cepa L.) is fourth in economic importance among
horticultural crops in Puerto Rico. Bulbs and roots are attacked by various
pathogens and affect production. The objective was to characterize eighteen
Phoma soil isolates based on morphology, pathogenicity, and molecular
characteristics. Isolates were on potato dextrose, oatmeal, and malt agar.
Semi-permanent slides were done to observe hyphae, conidia, pycnidia,
chlamydospores, and swollen cells. Pathogenicity tests were run in the
laboratory and field using ‘Mercedes’ and ‘Excalibur’. Observed symptomatic
plants were used for isolations. Phoma putaminum Speg. and possibly P.
macrostoma var. incolorata were identified and are first reports in
Puerto Rico and the Caribbean. Pathogenicity tests in vitro showed severe
necrosis in young bulbs and roots with P. putaminum and pink root rot
with P. macrostoma var. incolorata. Field tests are in progress.
Genomic DNA was extracted to amplify the ITS region of the rDNA using PCR.
Restriction enzyme Hind III created a polymorphic pattern from the amplified
rDNA separating both species. Sequencing the rDNA and phylogenic analysis is
planned.
Foliar bacteria associated to onions in Puerto Rico. J. CALLE-BELLIDO
(1), M. Alameda (1), and L. I. Rivera-Vargas (2). (1) Departments Agronomy and
Soils and (2) Crop Protection, University of Puerto Rico-Mayaguez Campus,
Mayaguez, P.R. 00681. E-mail: jcalleb@yahoo.com.
Little is known on the importance of bacterial diseases occurring in onions
in Puerto Rico. Foliage from several fields was sampled during a full growing
season. Fifty foliar isolates were identified using the Biolog®
method, 19 of which may have phytopathogenic potential. We determined that six of
eight isolates were pathogenic, as verified using field and laboratory tests. The
pathogenic bacteria were the following genera: Pseudomonas,
Xanthomonas, Acidovorax, Burkholderia, and Pantoea.
Morphological and molecular characterization of soil borne phytopathogenic
fungi associated to onions. J. CALLE-BELLIDO (1) and L. I. Rivera-Vargas
(2). Departments of (1) Agronomy and Soils, and (2) Crop Protection, University
of Puerto Rico, Mayaguez Campus, Mayaguez, P.R. 00681. E-mail:
jcalleb@yahoo.com, cuchysg@yahoo.com.
Onion is an important crop in Puerto Rico, where its production is limited by
pathogenic fungi. Sampling from commercial fields yielded isolates of
Fusarium (140), Alternaria (18), and Phoma (18). Among these,
the most prevalent were: Fusarium solani and F. equiseti;
Alternaria tennuisima and several isolates of Alternaria
“semiarborescent” group; Phoma putaminun and Phoma macrostoma
var. incolorata. For molecular characterization of these isolates, we
amplified rDNA’s ITS region and performed restriction fragment length
polymorphisms (RFLP) analyses. Patterns of restriction were converted into a
binary matrix to construct dendograms under multivariate analysis using
Jaccard’s distance. Phylogenetic trees based on ITS sequences were used for
comparisons among Fusarium isolates.
Isolation, description, and identification of bacteria associated with
diseased coffee and avocado from Costa Rica. C. CHACON (1), M.
Montero-Astúa (1), J. S. Hartung (2), W. B. Li (2), L. Garita (1), and C.
Rivera (1,3). (1) Centro de Investigación en Biología Celular y Molecular,
Universidad de Costa Rica, San Pedro 2060; (2) USDA-ARS Fruit Laboratory,
Beltsville, MD 20705; (3) Facultad de Microbiología.
The interaction of endophytic bacteria with citrus and citrus variegated
chlorosis (CVC) was previously analyzed. X. fastidiosa is the cause
of crespera of coffee and is associated with CVC-like symptoms in avocado.
Bacteria were obtained during attempts to isolate X. fastidiosa from
symptomatic coffee and avocado. Coffee strains and some avocado strains were
characterized by colony morphology, Gram stain, biochemical assays, and
electron microscopy. M. mesophilicum was isolated from symptomatic
avocados and 10 trees were PCR positive. Pseudomonas syringae-glycinea,
Pantoea agglomerans, C. flaccumfaciens-betae/oortii, Moraxella
nonliquefaciens, and Enterobacter intermedius were isolated and
identified by fatty-acid methyl ester analysis. Plans are to confirm them as
endophytes, determine their identity/frequency, and determine an interaction
with X. fastidiosa in crespera in the two diseases.
Incidence and morphological characterization of Alternaria spp.
occurring in onions in southern Puerto Rico. J. FERNANDEZ, L. I. Rivera, and
I. Cabrera. P.O. Box 9030, Department of Crop Protection, University of Puerto
Rico-Mayaguez Campus, Mayaguez, P.R. 00681.
Alternaria late blight of onions, causes losses in Puerto Rico. The
disease was studied by determining the incidence of Alternaria spp. at
the different stages of growth associated with foliage damage. Every 14 days,
leaf samples of ‘Mercedes’ and ‘Excalibur’ were taken in experimental and
commercial fields. A systematic experimental design in a zigzag pattern was
used. Leaves segments were cut, disinfected, transferred to PDA with
streptomycin and incubated at 27°C. After 7 days, the presence of Alternaria
was determined. An incidence of 52% and 48% was obtained in 60- to 100-day-old
plants of ‘Mercedes’ and ‘Excalibur’, respectively, in commercial fields. The
incidence in experimental fields was lower, up to 33% and 25% on ‘Mercedes’ and
‘Excalibur’, respectively. Initial lesions were observed in 60–70 day old
plants. A total of 280 isolates were obtained. Of these, 32 selected ones
were identified as A. destruens, A. tenuissima, A. palandui,
and A. porn (A. alli). About 59% of selected isolates were
placed within “semi-arborescent”, a group not described taxonomically.
Leafhoppers (Hemiptera: Cicadellidae) as potential vectors of Xylella
fastidiosa in Costa Rica. J. GARITA-CAMBRONERO (1), C. Godoy (2),
W. Villalobos (1), and C. Rivera (1,3). (1) Centro de Investigacion en
Biologia Celular y Molecular (CIBCM), Universidad de Costa Rica, San Pedro
de Montes de Oca, Apartado postal 2060, San Jose, Costa Rica; (2) Instituto
Nacional de Biodiversidad (INBio), Santo Domingo de Heredia, Costa Rica; (3)
Facultad de Microbiologia.
The presence of Xylella fastidiosa was studied in 11 species of
cicadellids of the cicadelleni tribe by DAS/ELISA test, using specific
antibodies (Agdia Inc. Elkhart, IN). Collections were made in 2003–04 at
nine coffee production zones of Costa Rica using vacuum directly over the
crop. Specimens were counted, identified by species.
They were placed in groups of two in 1.5-ml
microfuge tubes and ground with a sterile toothpick in 200 µl of extraction
buffer. All species contained bacteria in the foregut but only the species
Kapateira nsp., Graphocephala bivittata, G. permagna,
Fusigonalia lativittata, and Isogonalia adunca carried Xylella
fastidiosa in more than 35% of the tested insects. Smaller samples of
Dilobopterus instratus, D. hyalinatulus, Erythrogonia lecta,
E. sonora, and Hortensia similis were analyzed and more need
testing and confirmation by PCR.
Population dynamics and ecological relationships of ten leafhopper
species (Hemiptera: Cicadellidae), potential vectors of Xylella
fastidiosa in Costa Rica. J. GARITA-CAMBRONERO (1), C. Godoy (2), W.
Villalobos (1), and C. Rivera (1,3). (1) Centro de Investigacion en Biologia
Celular y Molecular, Universidad de Costa Rica, San Pedro de Montes de Oca,
Apartado postal 2060, San Jose; (2) Instituto Nacional de Biodiversidad,
Santo Domingo de Heredia, Costa Rica; (3) Facultad de Microbiologia.
A study was done in three coffee producing zones in 2002–2004. The zones
were coffee monoculture (CM), coffee-citrus (CC), and coffee-avocado (CA). In
each zone 4 plots of 40 plants were selected. In each plot 2 yellow sticky
traps were used and changed weekly for 2 years. Trapped cicadellids were
counted and identified. Similar population patterns of different species
were seen in CA and CC but differences were found in the CM.
Graphocephala bivittata (85%) and Erhytrogonia sonora (0.02%)
were the most and less frequent species in the CM. Graphocephala permagna
(34%) and E. sonora (0.11%) in the CC, and G. permagna
(73.76%) and Macugonalia testudinaria (0.44%) in CA were found. In CC
a greater variability and more equitable distribution of individuals
(67.63%) was found. CM had the highest number of expected individuals. No
similarity between the number of trapped individuals and the theoretical
number in any zone was seen, which lead to an unbalanced population state.
Citrus leprosis disease is associated with a bipartite positive-sense RNA
virus. A. S. GUERRA-MORENO (1), K. L. Manjunath (1), R. F. Lee (2), and
R. H. Brlansky (1). (1) University of Florida, CREC, 700 Experiment Station
Road, Lake Alfred 33850; and (2) USDA, ARS, NCGRCD, Riverside, CA 92507.
Citrus leprosis, a damaging disease of citrus in South America, has
recently moved northward into Central America and threatens citrus in
Central and North America. Cytoplasmic and nuclear rhabdovirus-like
particles have been associated with leprosis. Screening of a cDNA library,
made from cytoplasmic leprosis infected tissue led to the identification of
viral sequences. Northern hybridizations and RT-PCR assays showed an
association only with cytoplasmic-leprosis. Northern blot analysis, using
DIG-labeled DNA and RNA probes specific to Citrus leprosis virus
sequences showed two banding patterns. Probes of clones from RNA1 hybridized
with two RNAs of approximately 9–10 kb and 1.0–1.5 kb, while probes of RNA 2
clones hybridized with four RNAs of 4.7, 2.5, 1.6, and 1.0 kb. The
genome-walking method for sequencing led to the entire sequence of RNA 1.
RNA1 has two ORF’s. ORF1 codes for a large protein (276 kDa), with
similarity to viral replicase polyprotein. The ORF2 codes for a small
protein, with no similarity to known viral proteins.
The world according to Xylella fastidiosa. J. HARTUNG.
USDA-ARS Fruit Lab. PGQO 10300 Baltimore Ave., Building 010 A, Room 238
BARC-West Beltsville, MD 20705.
The ‘Anaheim Disease’ of grapevines was described in the 1880’s and
represented a crisis for California viticulture. As time passed and the
industry adjusted the disease, now known as Pierce’s disease, became a
sporadic nuisance rather than a crisis. Recently the disease has regained
crisis status in California and the pathogen, Xylella fastidiosa, has
emerged over the past decade from an obscure plant pathogen to one of the
most feared ones. This followed the emergence of a serious disease of sweet
orange in Brazil caused by a ‘new strain’ of the pathogen. This talk will
discuss the history of the pathogen and how it emerged to threaten diverse
horticultural industries. What factors have facilitated its spread, and what
factors may facilitate its control? Will the available full-genome sequence
lead to practical disease control? Or will the study of the ecology and
environmental interactions of the pathogen provide avenues to control of the
diseases caused by X. fastidiosa? These questions will be discussed
and future research will be proposed with the goal of returning
X. fastidiosa to a status of a sporadic nuisance rather than a crisis.
A method for the quantification of sweet orange and grapefruit stem
pitting caused by Citrus tristeza virus. D. S. HOWD and R.
H. Brlansky. University of Florida, Citrus Research and Education Center,
700 Experiment Station Rd., Lake Alfred, FL 33850.
Citrus tristeza virus (CTV) isolates may cause a variety of host
symptoms. One of the most severe is stem-pitting, which may reduce tree
vigor, fruit yield, and size. Stem pitting is a consequence of the disruption
of the cambium and abnormal growth of the phloem into the xylem. The
determination of the amount of stem pitting usually involves a visual rating
system where the results may vary. A more precise system is needed to
determine the total area involved in pitting so as to correlate the effects
of pitting on tree vigor and yield. In this study, we show the use of ASSESS
image analysis software (L. Lamari, APS Press) for the quantification of
percent area pitted in sweet orange and grapefruit affected by CTV isolates.
Analysis of the population diversity in selected Florida isolates of
Citrus tristeza virus. A. S. Kahlon, K. L. Munjunath, and R. H.
BRLANSKY. University of Florida, CREC, Lake Alfred, FL 33850.
Citrus tristeza virus (CTV) affects citrus worldwide and symptoms
vary from none to decline and death of trees on sour orange rootstock and/or
stem pitting. Studies were done to molecularly characterize selected Florida
CTV isolates to determine the effect of graft and aphid transmission (AT) on
the population diversity. The diversity of three biologically different
isolates was analyzed using multiple molecular markers (MMM) and the
heteroduplex mobility assay (HMA). MMM is based on the RT-PCR amplification
of genotype specific PCR products using primers sets derived from the
analogous sites within the genomes of four different genotypic isolates.
Amplified products give a profile for an isolate. Each of the three isolates
studied was a mixture of isolates. A 403 bp region of the genome (nt
1082-1484) in the leader protease domain of the ORF 1 a was amplified and
cloned using a pair of universal primers. HMA was done to detect genotypes
using clones from the amplified PCR product of each isolate. Different CTV
genotypes were present in each of the isolates, but only one was dominant.
The isolates were graft and single AT and the populations were studied. The
populations usually did not change upon graft transmission, but often
changed after AT.
Serological detection of the cytoplasmic Citrus leprosis virus
from infected citrus. K. L. Manjunath (1), E. Rangel (2), A. S.
GUERRA-MORENO (1), R. H. Brlansky (1), and R. F. Lee (3). (1) University of
Florida, Dept. Plant Path and CREC, Lake Alfred, FL 33850; (2) CENIAP, Plant
Virus Laboratory, Maracay, Venezuela; (3) USDA ARS, NCGRCD, Riverside, CA
92507.
Citrus leprosis, a serious disease of citrus in South America, has
recently spread into Central America. Serological detection is needed for
disease management. Disease identification is based on visual symptoms and
electron microscopy. We have demonstrated the presence of two distinct
viruses, cytoplasmic and nuclear associated with the disease by nucleic acid
hybridizations. With sequence information from the cytoplasmic type of
Citrus leprosis virus (CiLV), a highly expressed gene was cloned into
the bacterial expression vector, pET 27b. The leprosis protein with a
carboxy-terminal fusion of HSV and 6x histidine tags was expressed in the
expression host, E. coli, strain BL21. The expressed protein was
purified using a Ni-NTA agarose column. Polyclonal antibodies were developed
against the purified and insoluable proteins. A protein in cytoplasmic
CiLV-infected plants but not in healthy plants was detected using Western
blots.
Combate biologico de la pudricion acuosa blanda causada por
Sclerotinia sclerotiorum (Lib) de Bary, en lechuga mediante el uso de
Trichoderma viride Pers ex SF Gray. X. MATA and M. Obregon. Inst.
Nac. Aprendizaje, San Jose, Costa Rica.
La pudricion acuosa blanda es una de las enfermedades de mayor
importancia en la produccion de lechuga y ocasiona hasta un 75% de perdidas
en rendimiento. Su combate se realiza mediante aplicaciones de funguicidas
que tienen poco efecto, ya que este patogeno produce micelio y esclerocios.
Se evaluo en campo el combate ejercido por T. viride. Se
utilizaron 6 tratamientos T(1) = 3 × 10(^6) conidios/ml, T(2) = 4 × 10(^6),
T(3) = 5 × 10(^6), T(4) = 4 × 10(^6), T(5) = testigo y T(6) = benomyl y 6
repeticiones. Habia diferencias significativas de los tratamientos T(1),
T(2), T(3) y T(4) con respecto a los tratamientos T(5) y T(6). En los
ultimos se observo una reduccion en los rendimientos de 87 y 91%,
respectivamente. Esto obedece, a que los funguicidas recomendados afectan
unicamente la germinacion de esporas, crecimiento del tubo germinativo,
micelio, y formación de apresorios, pero no ejercen un efecto sobre los
esclerocios, los cuales son el inoculo primario; mientras que T. viride
tiene la capacidad de micoparasitar esas estructuras de sobrevivencia.
Applications of Trichoderma formulations in horticulture.
E. MONTE (1), I. Grondona (2), M. Gomez (2), A. Azpilicueta (2), A.
Rodriguez (2), M. Rey (2), and A. Liobell (3). (1) Centro Hispano-Luso de
Investigaciones Agrarias, University of Salamanca, Plaza Doctores de la
Reina s/n, 37007 Salamanca, Spain; (2) NewBioTechnic, S.A. (NBT), Paseo de
Bollullos de la Mitacion 6. Parque Industrial A-49 (PIBO) 41110 Bollullos de
la Mitacion, Seville, Spain; (3) IBVF Isla de la Cartuja, CSIC/University of
Seville, Spain.
Trichoderma is an effective biocontrol for plant pathogenic fungi and
viral vectors. Strain choice is important for effective and safe control.
Trichoderma has many strategies for fungal antagonism and indirect
effects on plants such as growth promotion, systemic resistance induction,
and improved fertility. Some strains produce antibiotics and their
suitability for control must be assessed. Other strains produce no
antibiotics and may be useful in production systems since no adverse effects
occur. We assessed natural strains and developed TUSAL®, a mixture of T.
harzianum and T. viride, that effects pathogens. In the field it
had effects on root development and production increased in trials. The
impact of TUSAL® on beneficial organisms was assessed, and molecular
methods developed to monitor strains and performance. Protein extracts were
tested as biofungicides defining the concentration as fungicide effects.
Protein production genes were introduced into organisms for lab production.
Protein effect was studied separately, with conidia and with minimal
fungicide doses. Both Trichoderma and proteins are patented and the
formulation is being registered by NBT.
Trichoderma as an alternative to methyl bromide in strawberries.
E. MONTE (1), M. Rey (2), M. Lorito (3), A. Liobell (4), and I. Grondona
(2). (1) Centro Hispano-Luso de Investigaciones Agrarias, University of
Salamanca, Avda. Campo Charro s/n, 37007 Salamanca, Spain; (2)
NewBioTechnic, S.A. (NBT), Paseo Bollullos Mitacion 6 Parque Industrial PIBO
41110 Bollullos de la Mitacion, Seville, Spain; (3) University Federico II,
Naples, Italy; (4) IBVF Isla de la Cartuja, CSIC/University of Seville,
Spain.
Methyl bromide (MeBr) soil fumigation is the main method for preplant
disinfestation in strawberries. Pathogens and weeds are controlled and
yields are good. MeBr environmental effects are unacceptable and
alternatives are needed. IPM has been a IV FP EU-funded project to identify
alternatives via biological, physical and low-chemical approaches to
protection based on natural Trichoderma strains active against
the fungal pathogens Collelotrichum, Phytophthora, and
Botrytis, and to find strains of Trichoderma active with
solarization. Combined approaches effectively control pests and diseases and
minimize environmental damage. Other approaches are certification of plant
material, solarization and chemicals, Trichoderma cell formulations,
Trichoderma proteins, induction of systemic resistance, and soil-less
systems.
Molecular comparison of Xylella fastidiosa isolates from Costa
Rica, North and South America. M. MONTERO-ASTUA (1), J. S. Hartung (2),
E. Aguilar (1), C. Chacon (1), and C. Rivera (1,3). (1) Centro de
Investigacion en Biologia Celular y Molecular, Universidad de Costa Rica
(UCR), San Pedro 2060; (2) USDA-ARS Fruit Laboratory, Beltsville, MD; (3)
Facultad de Microbiologia.
Diseases caused by Xylella fastidiosa have been described as
emerging problems and threats to grape production in North America and sweet
orange production in Brazil. X. fastidiosa has been detected and
isolated from grapes, coffee, and citrus in Costa Rica. Genetic analyses of
local X. fastidiosa have been done using techniques such as RAPDs and
repetitive element PCR. No Costa Rican isolates have been included and
problems with reproducibility of RAPDs have been recognized. X.
fastidiosa isolates from Costa Rica, Brazil, and the US were analyzed by
variable number tandem repeats-PCR (VNTRs). Nine primer pairs for specific
short sequence repeat (SSR) loci were used. Three primer pairs failed to
render a product or amplification was inconsistent. Amplification of
specific SSR loci was useful to distinguish strains from different
geographic origins and hosts. Variability was found within North, Central
and South American populations. The relationship of Costa Rican strains with
those from South and North America will be determined.
Variability in colony morphology of Xylella fastidiosa isolates
from Costa Rica and North America. M. MONTERO-ASTUA (1), J. S. Hartung
(2), W. B. Li (2), E. Aguilar (1), C. Chacon (1), and C. Rivera (1,3). (1)
Centro de Investigacion en Biología Celular y Molecular, Universidad de
Costa Rica, San Pedro 2060; (2) USDA-ARS Fruit Laboratory, Beltsville, MD;
(3) Facultad de Microbiologia.
Xylella fastidiosa causes the diseases Pierce’s disease of grapes,
citrus variegated chlorosis (CVC), and coffee leaf scorch (CLS). Different
growth rates and colonies have been described. Isolates from different hosts
in the US and Costa Rica had various morphologies on PW. Colony morphology
was not associated with an isolate and colonies with two morphologies grew
on the same plate. Subcultures of a specific morphology often produced
colonies with different morphologies. Colonies showed similar growth rates,
becoming visible 7–9 days. Single colonies tested with primers for X.
fastidiosa (272-1-int/272-2-int) produced the expected product. Some
were tested with universal primers (FD1/RP1) for bacterial 16S rDNA subunit
and the products were digested with restriction enzymes (HinfI,
TaqI, Sau3AI, HaeIII, AluI). The 16S rDNA
products had the same digestion patterns. Cultures of X. fastidiosa
can present variable colony morphologies. Conversion among morphologies was
observed.
Plasmodiophoromycetes as virus vectors, a complex pathosystem threatening
economically important world wide crops. M. MONTERO-ASTUA (1) and C.
Rivera (1,2). (1) Centro de Investigacion en Biologia Celular y Molecular
(CIBCM), Universidad de Costa Rica, (UCR), San Pedro 2060; (2) Facultad de
Microbiología, UCR.
Three plasmodiophorid species, Polymyxa betae, P. graminis,
and Spongospora subterranean are recognized vectors of economically
important plant viruses. Some of these viral diseases were reported more
than 50 years ago and latter their relationship to a plasmodiophorid vector
was suggested. Some of these viruses are found worldwide and are now
considered as crop threats. S. subterranean f. sp. subterranean,
the cause of potato powdery scab and vector of Potato mop top virus,
is special because both fungus and virus are considered as serious threats
to potato production and are emerging diseases in the Americas. Chemical
control of plasmodiophorids is erratic and resistance to certain viruses is
under study. The molecular basis of transmission has been studied and viral
genomes analyzed; however the virus-vector interaction, epidemiology and
ecology are poorly understood. Development of molecular techniques for
detection and quantification of these diseases promises to solve many
questions.
Spongospora subterranean as a vector of Potato mop-top pomovirus
in Costa Rica. M. MONTERO-ASTUA (1), V. Vasquez (1), W. Turechek (2),
and C. Rivera (1,3). (1) Centro de Investigacion en Biologia Celular y
Molecular, Universidad de Costa Rica, San Pedro 2060; (2) USDA-ARS Fruit
Laboratory, Beltsville, MD 20705; (3) Facultad de Microbiologia.
Spongospora subterranean f. sp. subterranean is the cause of
potato powdery scab and vector of Potato mop-top pomovirus (PMTV).
The vector and virus cause tuber blemishes and affect growth and yield. They
are production threats in northern Europe and Australia and as emerging
diseases in the Americas. S. subterranean and PMTV are soil-borne but
their field association is not understood. In 2001–2004 a survey was done to
assess occurrence and association in potato plantations. Paired tuber and
leaf samples from 39 plantations were analyzed by ELISA using specific
antibodies to S. subterranean and PMTV. The Jaccard index of
association was 0.245 indicating a significant association (alpha = 0.05)
according to a randomization test. PMTV soil transmission to bait plants was
determined by bioassay, ELISA and PCR for PMTV and S. subterranean.
Transmission to plants suggests soil contamination by PMTV bearing S.
subterranean sporeballs or vector transmission. S. subterranean
is an important factor of PMTV in Costa Rica.
Geographical distribution and incidence of Sugarcane yellow leaf virus
in Costa Rica. L. MOREIRA (1,2), E. Chavarria Soto (3), W. Villalobos
(1), and C. Rivera (1,4). (1) Centro de Investigacion en Biologia Celular y
Molecular (CIBCM), Universidad de Costa Rica (UCR); (2) Facultad de Ciencias
Agroalimentarias, UCR; (3) Direccion de Investigacion y Extension de la Cana
de Azucar (DIECA), Liga Agricola Industrial de la Cana de Azucar (LAICA),
Costa Rica; (4) Facultad de Microbiologia.
Sugarcane yellow leaf was found in Costa Rica in 1994. Six years later,
Sugarcane yellow leaf polerovirus (ScYLV) was confirmed in sugarcane
by tissue printing, indirect ELISA, and
immunosorbent electron microscopy. A
geographical survey for ScYLV was done in 2000–2003 in 6 commercial
plantation regions. Random sampling was done in
2000 one-hectare plots identified using GPS. Ten thousand 5–10 month old
stalks were collected in plant and/or ratoon crops. DAS-ELISA was used to
detect ScYLV. The average incidence of ScYLV was 43.0%. The Central Valley
showed the major incidence (61.6%) while the South and Central Pacific
regions had the lowest (27.6 and 27.8%, respectively). Incidences in
Guanacaste, North- and Atlantic-region were 47.3%, 38.7%, and 43.8%,
respectively. Incidence and distribution of ScYLV were developed using GPS.
Alternaria brown spot of citrus: Worldwide distribution and economic
impact. N. A. PERES (1) and L. W. Timmer (2). (1) University of Florida,
GCREC, Wimauma, FL; (2) CREC, Lake Alfred, FL.
Alternaria brown spot (ABS), caused by Alternaria alternate,
produces necrotic spots on young leaves, fruits, and twigs, and corky lesions
on fruit of tangerines and their hybrids. ABS was first reported in
Australia in 1903 and subsequently in Florida in 1974, Israel in 1989, and
South Africa and Cuba in 1992. New outbreaks have been reported in Turkey,
Spain, Italy, Colombia, Brazil, Argentina, and Peru, and in Iran. Hybrids
with Dancy mandarin as a parent, such as Orlando, Minneola, Fortune, Nova
and Page, as well as Murcott tangor, are susceptible to ABS. Conidia of
A. alternate are air-borne and their release is triggered by rainfall
and/or sudden changes in humidity. The number of fungicide applications for
disease control varies according to the variety and disease history. The
Alter-rater model for timing fungicide sprays was developed in Florida and
evaluated in Brazil. Ten or more fungicide applications per year may be
necessary for good disease control and, thus, production of susceptible
varieties may be limited to varieties that have sufficient value to justify
control costs.
Trichoderma transcriptomics and its usefulness in plant protection.
M. B. Rubio (1), M. R. Hermosa (1), R. E. Cardoza (1,2), S. Gutierrez (2),
M. Rey (3), A. Liobell (4), and ENRIQUE MONTE (1). (1) Centro Hispano-Luso
de lnvestigaciones Agrarias, University of Salamanca, Plaza Doctores de la
Reina s/n, 37007 Salamanca, Spain, emv@usal.es; (2) Area of Microbiology,
University of Leon, Ponferrada Campus, Ponferrada, Leon, Spain; (3)
NewBioTechnic, S.A. (NBT), Paseo de Bollullos de la Mitacion 6. Parque
Industrial A-49 (PIBO) 41110 Bollullos de la Mitacion, Seville, Spain; (4)
IBVF Isla de la Cartuja, CSIC/University of Seville, Seville, Spain.
Trichoderma is of biotechnological value, but its genome is poorly
surveyed compared to other model microorganisms. Some strains are
used in industrial enzyme production, agriculture and bioremediation. It is
less developed as a model to study and understand microbial interactions
with plants and pests. Due to its ubiquity and rapid substrate colonization
species have been used as biocontrol organisms for agriculture and their
enzymes are used in industry. There is interest beyond its phenotype to
exploit its genetic systems using functional genomics. TRICHOEST is a
project, funded by the EU (FP5, QLRT-2001-02032), to analyze the
transcriptome of selected strains with biocontrol potential, in regards to
antagonism, nutrient stress and plant interactions. Selected clone sequences
were done and cloned in appropriate vectors. Expression studies were
performed. To determine the biological relevance of selected genes,
strains lacking a functional copy of a given gene were obtained. Expression
studies with DNA-arrays, containing PCR products from unigenes identified in
T. harzianum 2413, were done using RNA probes from the wild type
strain and transformants grown under simulated mycoparasitism.
Identification of a new phytoplasma associated with whiteness diseased
Sechium edule (Cucurbitaceae), in Costa Rica. G. SABORIO-R (1), W.
Villalobos (1), F. Albertazzi (1,2), and C. Rivera (1,3). (1) Centro de
Investigación en Biologia Celular y Molecular, Universidad de Costa Rica
(UCR), San Pedro de Montes de Oca, San Jose, Costa Rica; (2) Escuela de
Biología, UCR; (3) Facultad de Microbiología.
Chayote (Sechium edule (Jacq.) Sw), a vegetable crop in Central
America, is cultivated for local consumption and exportation. Since 2000, a
new disease has been seen in plants in the Ujarras Valley, Cartago Province.
The disease has affected 20% of the fields and caused 100% fruit loss
because of induced fruit oxidation during post-harvest.
Infected plants show white petioles and whiteness of fruits and stems,
symptoms associated with phytoplasma diseases. Symptomatic plants were
collected and tested by nested PCR and RLFP-PCR using universal primers,
P1\P7 and R16R2\R16F2n, to amplify phytoplasma 16S rDNA sequences. Results
suggest that a phytoplasma belonging to the 16SrI subgroup aster yellow is
associated with the charyote whiteness disease which is different than the
witches-broom disease of chayote reported previously. Partial sequence of
the16S rDNA was deposited in GenBank (AY928382).
Identification of viruses in blackberries in Costa Rica. V. Vásquez
(1), L. MOREIRA (1,2), and Carmen Rivera (1,3). (1) Centro de Investigacion
en Biologia Celular y Molecular (CIBCM), Universidad de Costa Rica (UCR);
(2) Facultad de Ciencias Agroalimentarias, UCR; (3) Facultad de
Microbiología, UCR.
During 2004 a preliminary survey of 14 viruses was conducted in
blackberry (Rubus spp.) plantations in Los Santos, Costa Rica. Only
three viruses Tomato ringspot virus (ToRSV), Raspberry bushy dwarf
virus (RBDV), and Tobacco streak virus (TSV) were detected by
DAS-ELISA using specific antibodies and the procedures of Agdia Inc.,
Elkhart, Indiana. Afterwards, a symptomatic sampling in 15 plantations was
done. A total of 236 samples were analyzed by DAS-ELISA against TSV, ToRSV,
and RBDV. The majority of the plants (63%) were infected with RBDV. TSV and
ToRSV were found in the 42% and 23% of the plants, respectively. The 37% of
the plants presented single infection and the 43% presented mixed infections
of two or the three viruses. Most common combination was RBDV and TSV. No
plantation was virus-free; all had at least one of the three analyzed
viruses.
Geographical distribution and incidence of Xylella fastidiosa in
coffee plantations in Costa Rica. W. VILLALOBOS (1), Carlos Mario
Rodriguez (2), and C. Rivera (1,3). (1) Centro de Investigacion en Biologia
Celular y Molecular (CIBCM), Universidad de Costa Rica; (2) Instituto del
Café (ICAFE); (3) Facultad de Microbiología.
In early 1990s a new disease in coffee in Desamparados and Los Santos
(South region of San José) was found. Growers called it “crespera disease,”
since foliar symptoms show malformation with curly narrows. The symptom was
associated with zinc deficiency. Later Xylella fastidiosa was
detected in symptomatic plants by DAS-ELISA and electron microscopy. The
bacteria was cultured and detected by PCR. A survey was done in 2000 to
determine the geographical distribution of the disease. 980 samples were
collected and analyzed by DAS-ELISA. The bacteria were detected in most
plantations. Simultaneously, the incidence of X. fastidiosa was
evaluated in the fields. A survey was carried out to find coffee fields with
the lowest incidence in the central region. In a plantation with 6%
incidence four plots of 40 plants each were selected. Each plant in the
plots was mapped and evaluated by ELISA every six months. After three years
the incidence at the plots reach 100%, but only a few plants showed
characteristic symptoms.
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