Diagnosing Interveinal Chlorosis in Soybeans — it’s not just SDS

Arsenic has been considered the most poisonous inorganic soil pollutant to living creatures. For this reason, the interest in phytoremediation species has been increasing in the last years. Particularly for the State of Minas Gerais, where areas of former mining activities are prone to the occurrence of acid drainage, the demand is great for suitable species to be used in the revegetation and "cleaning" of As-polluted areas. This study was carried out to evaluate the potential of seedlings of Eucalyptus grandis (Hill) Maiden and E. cloeziana F. Muell, for phytoremediation of As-polluted soils. Soil samples were incubated for a period of 15 days with different As (Na2HAsO4) doses (0, 50, 100, 200, and 400 mg dm-3). After 30 days of exposure the basal leaves of E. cloeziana plants exhibited purple spots with interveinal chlorosis, followed by necrosis and death of the apical bud at the 400 mg dm-3 dose. Increasing As doses in the soil reduced root and shoot dry matter, plant height and diameter in both species, although the reduction was more pronounced in E. cloeziana plants. In both species, As concentrations were highest in the root system; the highest root concentration was found in E. cloeziana plants (305.7 mg kg-1) resulting from a dose of 400 mg dm-3. The highest As accumulation was observed in E. grandis plants, which was confirmed as a species with potential for As phytoextraction, tending to accumulate As in the root system and stem.

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Widespread Outbreak of Cucurbit yellow stunting disorder virus in Melon, Squash, and Watermelon Crops in the Sonoran Desert of Arizona and Sonora, Mexico

Plant Disease ◽

10.1094/pdis-91-6-0773a ◽

2007 ◽

Vol 91 (6) ◽

pp. 773-773 ◽

Cited By ~ 24

Author(s):

J. K. Brown ◽

J. C. Guerrero ◽

M. Matheron ◽

M. Olsen ◽

A. M. Idris

Keyword(s):

Sonoran Desert ◽

Citrullus Lanatus ◽

Middle Eastern ◽

Analysis Data ◽

Universal Primers ◽

Interveinal Chlorosis ◽

Eastern Hemisphere ◽

Experimental Laboratory ◽

Honeydew Melon ◽

First Time

Bright yellow, interveinal chlorosis was observed for the first time on leaves of the older and mid-growth of cucurbit plants in southern Arizona and Sonora (Mexico) during September and October of 2006. Some cultivars exhibited substantial yield losses of 30 to 80%. In Arizona, symptoms were in Cucumis melo (muskmelon and honeydew melon) fields in the Yuma Valley and Hyder. In Sonora, honeydew and muskmelon, Cucurbita pepo (acorn, spaghetti, and summer [yellow and zucchini] squash), and Citrullus lanatus (watermelon) were symptomatic in Hermosillo, whereas, in Caborca, honeydew and cantaloupe developed similar symptoms. Interveinal chlorosis was observed in 60 to 100% of the plants in each field. Crops planted mid-to-late season were 100% infected, whereas, the early-season fields experienced approximately 60 to 80% incidence. All symptomatic fields in the Sonoran Desert and vicinity were infested by the whitefly Bemisia tabaci (Genn.), which was identified as the ‘B biotype’ on the basis of mitochondria COI sequence analysis (data not shown). Whitefly population levels were variable and ranged from 5 to 200 per plant. Total RNA was isolated from leaf samples collected from symptomatic plants using Tri Reagent (Molecular Research Center, Cincinnati, OH). Purified RNA was used in reverse transcriptase-PCR with primers specific to the Cucurbit yellow stunting disorder virus (CYSDV) coat protein (CP) gene (RNA2-deoxyribonucleotide coordinates 4927-4950 and 5657-5679) for the suspected whitefly-transmitted bipartite CYSDV (4). PCR yielded the CYSDV CP fragment, at 753 bp (GenBank Accession Nos. EF21058 and EF21059), which was cloned into pGEM T-Easy and sequenced in both directions using universal primers. The CYSDV CP nucleotide sequences (n = 16) obtained from acorn squash, honeydew melon, muskmelon, yellow squash, and watermelon had 99 to 100% identity. The Arizona (AZ) and Sonora (SON) CYSDV CP sequences shared 99 to 100% identity with previously described CYSDV isolates from the Eastern Hemisphere (GenBank Accession Nos. DQ903105 and DQ903108) and also with two isolates of CYSDV collected during 2004 from Zacapa Valley, Guatemala (GenBank Accession Nos. EF21060 and EF21061) (J. K. Brown, unpublished data). CYSDV is a member of the genus Crinivirus, family Closteroviridae. CYSDV was first identified in cucumber and melon crops in the Middle East approximately 15 years ago and 10 years ago in Spain (1). Most recently, this virus was introduced into Texas (2), Guatemala (J. K. Brown, unpublished data), and Arizona and California (3). CYSDV has therefore emerged as an important and potentially worldwide threat to the production of cultivated cucurbits (3). The threat appears to be significant in light of the introduction or establishment of the exotic B. tabaci biotypes B and Q vectors, which also originated in the Middle Eastern-North African-Mediterranean region. To our knowledge, this is the first report of CYSDV infecting field-grown C. pepo (four types) and watermelon, reported previously only as experimental laboratory hosts, and of CYSDV in two types of melon (C. melo) in Mexico. References: (1) A. Celix et al. Phytopathology 86:1370, 1996. (2) J. Kao et al. Plant Dis. 84:101, 2000. (3) Y.-W. Kuo et al. Plant Dis. 91:330, 2007. (4) L. Rubio et al. J. Gen. Virol. 82:929, 2001.

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First Report of Tomato chlorosis virus Infecting Tomato in Georgia

Plant Disease ◽

10.1094/pdis-02-11-0122 ◽

2011 ◽

Vol 95 (7) ◽

pp. 881-881 ◽

Cited By ~ 1

Author(s):

S. Sundaraj ◽

R. Srinivasan ◽

C. G. Webster ◽

S. Adkins ◽

K. Perry ◽

...

Keyword(s):

Nucleic Acid Hybridization ◽

N Gene ◽

Natural Occurrence ◽

Rt Pcr ◽

Specific Primers ◽

Tomato Production ◽

First Report ◽

Interveinal Chlorosis ◽

Cp Gene ◽

Tomato Chlorosis Virus

Tomato yellow leaf curl virus (TYLCV) and Tomato spotted wilt virus (TSWV) are prevalent in field-grown tomato (Solanum lycopersicum) production in Georgia. Typical TYLCV symptoms were observed during varietal trials in fall 2009 and 2010 to screen genotypes against TYLCV at the Coastal Plain Experiment Station, Tifton, GA. However, foliar symptoms atypical of TYLCV including interveinal chlorosis, purpling, brittleness, and mottling on upper and middle leaves and bronzing and intense interveinal chlorosis on lower leaves were also observed. Heavy whitefly (Bemisia tabaci (Gennadius), B biotype) infestation was also observed on all tomato genotypes. Preliminary tests (PCR and nucleic acid hybridization) in fall 2009 indicated the presence of TYLCV, TSWV, Cucumber mosaic virus, and Tomato chlorosis virus (ToCV); all with the exception of ToCV have been reported in Georgia. Sixteen additional symptomatic leaf samples were randomly collected in fall 2010 and the preliminary results from 2009 were used to guide testing. DNA and RNA were individually extracted using commercially available kits and used for PCR testing for ToCV, TYLCV, and TSWV. Reverse transcription (RT)-PCR with ToCV CP gene specific primers (4) produced approximately 750-bp amplicons from nine of the 16 leaf samples. Four of the nine CP gene amplicons were purified and directly sequenced in both directions. The sequences were 99.4 to 100.0% identical with each other (GenBank Accession Nos. HQ879840 to HQ879843). They were 99.3 to 99.5%, 97.2 to 97.5%, and 98.6 to 98.9% identical to ToCV CP sequences from Florida (Accession No. AY903448), Spain (Accession No. DQ136146), and Greece (Accession No. EU284744), respectively. The presence of ToCV was confirmed by amplifying a portion of the HSP70h gene using the primers HSP-1F and HSP-1R (1). RT-PCR produced approximately 900-bp amplicons in the same nine samples. Four HSP70h gene amplicons were purified and directly sequenced in both directions. The sequences were 99.4 to 99.7% identical to each other (Accession Nos. HQ879844 to HQ879847). They were 99.2 to 99.5%, 98.0 to 98.4%, and 98.9 to 99.3% identical to HSP70h sequences from Florida (Accession No. AY903448), Spain (Accession No. DQ136146), and Greece (Accession No. EU284744), respectively. TYLCV was also detected in all 16 samples by PCR using degenerate begomovirus primers PAL1v 1978 and PARIc 496 (3) followed by sequencing. TSWV was also detected in two of the ToCVinfected samples by RT-PCR with TSWV N gene specific primers (2) followed by sequencing. To our knowledge, this is the first report of the natural occurrence of ToCV in Georgia. Further studies are required to quantify the yield losses from ToCV alone and synergistic interactions between ToCV in combination with TSWV and/or TYLCV in tomato production in Georgia. References: (1) T. Hirota et al. J. Gen. Plant Pathol. 76:168, 2010. (2) R. K. Jain et al. Plant Dis. 82:900, 1998. (3) M. R. Rojas et al. Plant Dis. 77:340, 1993. (4) L. Segev et al. Plant Dis. 88:1160, 2004.

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OBSERVATIONS OF INTERVEINAL CHLOROSIS ON MALUS SARGENTII

HortScience ◽

10.21273/hortsci.25.8.848c ◽

1990 ◽

Vol 25 (8) ◽

pp. 848c-848

Author(s):

T. Scott Starr ◽

L. F. Thompson

Keyword(s):

Soil Analysis ◽

Nutrient Deficiencies ◽

Mg Deficiency ◽

Interveinal Chlorosis ◽

Foliar N

Interveinal chlorosis has been observed on the oldest leaves of several varieties of flowering crabapple (Malus sargentii Rehl). Our objective was to identify the cause of this disorder. Foliage and soil from 20 Sargent crabapple trees growing on 12 different sites were analyzed for possible nutrient deficiencies or excesses. Analyses showed N to be slightly low, Ca high, and Mg low in all leaf samples. Soil analysis showed Ca to be abnormally high at all sites. We concluded that the leaf discoloration was caused by a Mg deficiency due to Ca suppression of the Mg and that the low foliar N might be a contributing factor in the interveinal chlorosis.

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Potted Gerbera Production in a Subirrigation System Using Low-concentration Nutrient Solutions

HortScience ◽

10.21273/hortsci.39.6.1283 ◽

2004 ◽

Vol 39 (6) ◽

pp. 1283-1286 ◽

Cited By ~ 24

Author(s):

Youbin Zheng ◽

Thomas Graham ◽

Stefan Richard ◽

Mike Dixon

Keyword(s):

Nutrient Solution ◽

Final Stage ◽

Crop Production ◽

Dry Weight ◽

Interveinal Chlorosis ◽

Nutrient Levels ◽

Stage 4 ◽

Total Dry Weight ◽

Substrate Ph ◽

Nutrient Solutions

To determine whether currently used commercial nutrient solution concentrations can be reduced during the final stage (last 4 to 5 weeks) of production of potted gerbera (Gerbera jamesonii `Shogun') under recirculating subirrigation conditions, plants were grown under one of four nutrient levels (10%, 25%, 50%, and 100% of full strength). Nutrient concentration levels did not affect leaf area, flower number and appearance, and plant total dry weight. There were no significant differences in the greenness (as measured by SPAD meter) of leaves from plants that received the 50% and 100% strength nutrient solutions. However, leaves from plants that received the 10% and 25% strength solution showed significantly less greenness than that of the plants that received 50% and 100% strength nutrient solutions. There were interveinal chlorosis symptoms on the younger leaves of some plants in the 10% and 25% strength nutrient treatments. It is suspected that this interveinal chlorosis was due to iron (Fe) deficiency caused by the increased substrate pH. It is concluded that the nutrient solution concentrations typically used for potted gerbera production in commercial greenhouses at the final stage (4 to 5 weeks) under recirculating subirrigation conditions, can be safely reduced by at least 50% without adversely affecting crop production. Nutrient salts accumulated in the top section of the growth substrate under all treatments levels; however, no phytotoxic effects were observed. No differences in water use (141 mL per plant per day) were observed amid the various nutrient levels. Fertilizer inputs were reduced in the 50%, 25%, and 10% treatments by 54%, 75%, and 90% respectively, relative to the 100% treatment. After 4 weeks under recirculating conditions, the qualities of the nutrient solutions were still within acceptable limits.

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Dry Edible Bean (Phaseolus vulgaris) Response to Imazethapyr

Weed Technology ◽

10.1017/s0890037x00033194 ◽

1991 ◽

Vol 5 (1) ◽

pp. 22-26 ◽

Cited By ~ 55

Author(s):

Robert G. Wilson ◽

Stephen D. Miller

Keyword(s):

Phaseolus Vulgaris ◽

Untreated Control ◽

Bean Seed ◽

Interveinal Chlorosis ◽

Bean Cultivar ◽

Dry Edible Bean ◽

Seed Yields

Imazethapyr at 0.07 and 0.10 kg ai ha-1applied preplant incorporated (PPI), preemergence (PRE), and postemergence (POST) was evaluated at two locations in 1988 and 1989 for safety to dry edible beans. Bean stunting, leaf crinkling, and interveinal chlorosis were evident from imazethapyr and varied from 1 to 57%. Imazethapyr significantly reduced bean height and delayed maturity. PPI and POST applications of imazethapyr at 0.07 and 0.10 kg ha-1did not reduce bean seed yields compared to yields of the untreated control. Bean cultivar by herbicide interactions were significant for bean injury but varied with year and location.

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Chino del tomate virus:Relationships to Other Begomoviruses and Identification of A-Component Variants that Affect Symptom Expression

Phytopathology ◽

10.1094/phyto.2000.90.5.546 ◽

2000 ◽

Vol 90 (5) ◽

pp. 546-552 ◽

Cited By ~ 18

Author(s):

J. K. Brown ◽

Kristin M. Ostrow ◽

Ali M. Idris ◽

Drake C. Stenger

Keyword(s):

Amino Acid ◽

Genotypic Variation ◽

Symptom Expression ◽

Wild Type ◽

Disease Symptoms ◽

Phenotypic Differences ◽

Interveinal Chlorosis ◽

Leaf Curling ◽

Symptom Phenotype ◽

Severe Leaf

Phylogenetic and distance analyses place Chino del tomate virus (CdTV) in the New World clade of begomoviruses and indicate that CdTV and Tomato leaf crumple virus (TLCrV) are closely related strains of the same virus. One cloned CdTV A component (pCdTV-H6), when inoculated to tomato with the B component (pCdTV-B52), produced mild symptoms and low DNA titers. Another cloned CdTV A component (pCdTV-H8), when coinoculated to tomato with the B component, produced moderate leaf curling and veinal chlorosis similar to that of TLCrV. Coinoculation of both CdTV A components and the B component to tomato produced wild-type chino del tomate (CdT) disease symptoms consisting of severe leaf curling, veinal and interveinal chlorosis, and stunting. The two CdTV A components were nearly identical, except at nucleotide positions 1,722 and 2,324. The polymorphism at nucleotide 1,722 resulted in a change at Rep amino acid 261. The second polymorphism at nucleotide 2,324 resulted in changes at Rep amino acid 60 and AC4 amino acid 10. Two chimeric A components constructed by reciprocal exchange of a fragment bearing the polymorphic site at nucleotide 1,722 were evaluated for symptom phenotype. One chimeric A component (pCdTV-H86) produced wild-type CdT symptoms when coinoculated to tomato with the B component. The reciprocal chimeric A component (pCdTV-H68), when coin-oculated to tomato with the B component, also produced severe leaf curling, veinal chlorosis, and stunting. However, pCdTV-H68 induced less obvious interveinal chlorosis than wild-type or pCdTV-H86. Examination of A component genotypes recovered from tomato coinoculated with pCdTV-H6 and pCdTV-H8 indicated that recombination occurred to produce a genotype identical to pCdTV-H86. These results indicate that subtle genotypic variation has significant effects on symptom expression and may explain phenotypic differences observed among isolates and cloned DNAs of CdTV and TLCrV.

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First Report of Tomato chlorosis virus in Potato in Brazil

Plant Disease ◽

10.1094/pdis-12-11-1068-pdn ◽

2012 ◽

Vol 96 (4) ◽

pp. 593-593 ◽

Cited By ~ 18

Author(s):

D. M. S. Freitas ◽

I. Nardin ◽

N. Shimoyama ◽

J. A. C. Souza-Dias ◽

J. A. M. Rezende

Keyword(s):

Leaf Roll ◽

Rt Pcr ◽

Specific Primers ◽

Total Rna ◽

First Report ◽

Interveinal Chlorosis ◽

Potato Plants ◽

The World ◽

Tomato Chlorosis Virus ◽

Biotype B

Potato plants (Solanum tuberosum cv. Ágata) exhibiting symptoms of leaf roll and interveinal chlorosis, especially on older leaves, were found in a commercial crop in the County of Cristalina, State of Goiás, Brazil in June 2011. The crop was severely infested by whitefly Bemisia tabaci biotype B. Four potato tubers from symptomatic plants were indexed for the presence of the following viruses: Tomato chlorosis virus (ToCV), Potato leaf roll virus (PLRV), Tomato severe rugose virus (ToSRV), and Potato virus Y (PVY). Total RNA was extracted separately from each tuber and used for reverse transcription (RT)-PCR using the HS-11/HS-12 primer pair, which amplifies a fragment of 587 bp from the highly conserved region of the heat shock protein (HSP-70) homolog gene reported for ToCV. The RT-PCR product was subsequently tested by nested-PCR for detection of ToCV with specific primers ToC-5/ToC-6 (2). Amplicons of 463 bp, amplified from total RNA separately extracted from three tubers, were purified and directly sequenced. Comparisons among the three consensus sequences of 448 bp (GenBank Accession Nos. JQ288896, JQ288897, and JQ288898) revealed respectively, 98, 100, and 100% identity with the reported sequence of a tomato isolate of ToCV from Brazil (GenBank Accession No. EU868927) (1). For ToSRV detection, total DNA was extracted from two tubers and a fragment of approximately 820 bp was amplified by PCR with specific primers (3). PLRV and PVY were indexed in two and three tubers, respectively, by double-antibody sandwich-ELISA (SASA, Edinburg, Scotland). Virus-free B. tabaci biotype B were separately transferred to potato and tomato leaves infected with ToCV for an acquisition access period of 24 h. Groups of 30 viruliferous whitefly were transferred to four, young, sprout-grown potato plants cv. Ágata (two plants per virus isolate) for 24-h inoculation access period. After 37 days of inoculation, one plant inoculated with the potato and tomato isolates of ToCV, respectively exhibited symptoms of leaf roll and interveinal chlorosis on order leaves, which were similar to that induced by PLRV. Experimental infection of potato plants with ToCV, which induced leaf roll symptoms resembling PLRV infection, was reported in the United States by Wisler et al. (4). The potato isolate of ToCV was also transmitted by B. tabaci to one of two inoculated tomato plants. The presence of ToCV in all inoculated plants was detected by nested-RT-PCR as described above. To our knowledge, this is the first report on detection of ToCV in field potato plants in the world. Considering that ToCV occurs in innumerous countries around the world, it is transmitted by a cosmopolitan insect, and it induces symptoms similar to PLRV, this finding triggers an alert to field dependent seed-potato multiplication, virus inspector, and certification system. References: (1) J. C. Barbosa et al. Plant Dis. 92:1709, 2008. (2) C. I. Dovas et al. Plant Dis. 86:1345, 2002. (3) F. R. Fernandes et al. Trop. Plant Pathol. 35:43, 2010. (4) G. C. Wisler et al. Plant Dis. 82:270, 1998.

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First Report of Tomato chlorosis virus in Tomato on Mauritius Island

Plant Disease ◽

10.1094/pdis-93-1-0111a ◽

2009 ◽

Vol 93 (1) ◽

pp. 111-111 ◽

Cited By ~ 9

Author(s):

J. M. Lett ◽

M. Hoareau ◽

B. Reynaud ◽

A. Saison ◽

B. Hostachy ◽

...

Keyword(s):

Vector System ◽

Reunion Island ◽

Hsp70 Gene ◽

Tomato Plants ◽

Interveinal Chlorosis ◽

Cp Gene ◽

Pcr Products ◽

Réunion Island ◽

Plant Pathol ◽

Tomato Chlorosis Virus

In February of 2007, a virus disease survey on tomato plants (Solanum lycopersicum) in greenhouses and open fields was conducted on the island of Mauritius at the request of the Agricultural Research and Extension Unit (AREU), sponsored by the European Union, and funded by the Programme Régional de Protection des Végétaux (PRPV). Yellowing symptoms on the lower and middle leaves of tomato plants and whiteflies (Bemisia tabaci) were observed in greenhouses in Pailles, located in the north region of the island. The interveinal chlorosis pattern of the discolored leaves was similar to symptoms described for Tomato chlorosis virus (ToCV; genus Crinivirus) detected on tomato in 2004 on Reunion Island (1), suggesting the possible involvement of the same virus. Six symptomatic tomato leaf samples were collected from separate plants in the Pailles greenhouses. Total RNA was extracted from these samples with the Qiagen (Courtaboeuf, France) RNeasy Plant Mini Kit. Reverse transcription-PCR was used for molecular diagnosis, independently using two sets of specific ToCV primers. The first set of primers, ToCV-172 and ToCV-610, was designed to amplify the highly conserved region of the heat shock protein 70 (HSP70) gene (2). The second set of primers was designed to amplify the coat protein (CP) gene (forward-CP-ToCV-4384: 5′-ATCCTCTGGTTAGACCGTTAG-3′ and reverse as in Segev et al. [3]). PCR products of the expected size (439 and 725 bp, respectively) were observed for the six samples from the greenhouse from Pailles. For each set of primers, two PCR products obtained from two different samples were cloned using the pGEM-T Easy Vector system (Promega, Madison, WI) and sequenced (Macrogen, Seoul, Korea). The two HSP70 sequences (GenBank-EMBL-DDBJ Accession Nos. AM884013 and AM884014) and the two CP sequences (FM206381 and FM206382) had 100% nucleotide identities (DNAMAN; Lynnon BioSoft, Quebec City, Canada). The highest nucleotide identities of the 439-bp fragment of HSP70 gene (NCBI, BLASTn) were 97% with ToCV isolates from France (DQ355214, DQ355215, and DQ355216), Florida (AY903448), Italy (AM231038 and AY048854), Mayotte Island (AM748818), Portugal (AF234029), and Reunion Island (AM748816). Similarly, the highest nucleotide identities (98%) were obtained with ToCV isolates from France (EU625350) and Spain (DQ136146), with the 725-bp fragments of CP gene. Interestingly, ToCV isolates from Mauritius and Reunion are as divergent as isolates from the rest of the world, which suggests the possibility of different introductions. In conclusion, observed symptoms and laboratory results based on two different regions of the genome confirm the presence of ToCV in symptomatic tomatoes on the island of Mauritius, for the first time to our knowledge. The visual survey carried out in June of 2008 confirmed the presence of typical interveinal chlorosis symptoms in other greenhouses, requiring further studies to assess the incidence of ToCV on tomato crops. References: (1) H. Delatte et al. Plant Pathol. 55:289, 2006. (2) D. Louro et al. Eur. J. Plant Pathol. 106:589, 2000. (3) L. Segev et al. Plant Dis. 88:1160, 2004.

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First Report of Koch's Postulates Completion of Sudden Death Syndrome of Soybean in Argentina

Plant Disease ◽

10.1094/pdis.2003.87.4.447b ◽

2003 ◽

Vol 87 (4) ◽

pp. 447-447 ◽

Cited By ~ 1

Author(s):

M. Scandiani ◽

D. Ruberti ◽

R. Pioli ◽

A. Luque ◽

L. Giorda

Keyword(s):

Sudden Death ◽

Fusarium Solani ◽

Colony Growth ◽

Positive Control ◽

Sudden Death Syndrome ◽

Symptom Development ◽

Koch’S Postulates ◽

Interveinal Chlorosis ◽

Soil Infestation ◽

Koch's Postulates

Foliage symptoms on soybean resembling those of sudden death syndrome were detected in Argentina during 1991 and 1992 in the Pampas Region and during 1992 and 1993 in the Northwest Region. Isolations were made in 1999, 2000, and 2001 from soybean plants (Glycine max (L.) Merr.) showing these symptoms. Five isolates of fungi obtained from taproot tissue and blue sporulation on taproot exteriors were selected for further evaluation. These isolates were plated on potato dextrose agar supplemented with streptomycin (PDAS). Based on the spore morphology, colony growth rate, morphology and pigmentation on PDAS, and lack of microconidia (1) five isolates were identified as Fusarium solani f. sp. glycines. Soybean cvs. Ripley, Spencer, Pioneer 9492RR, and A6445 RG were inoculated in greenhouse tests with each of the isolates using toothpick and soil infestation methods for a total of six experiments. Isolate 171 provided by J. Rupe (University of Arkansas, Fayetteville) was tested as a positive control. Foliar symptoms typical of sudden death syndrome and similar to those in the field were observed 14 and 25 days, respectively, after inoculations using the toothpick and soil infestation methods. Lesions produced on leaves averaged 3.6 for all five isolates and 4 for the reference strain using a disease severity scale where: 1 = no symptoms; 2 = slight symptom development with mottling and mosaic on leaves (1 to 20% foliage affected); 3 = moderate symptom development with interveinal chlorosis and necrosis on foliage (21 to 50% foliage affected); 4 = heavy symptom development with interveinal chlorosis and necrosis (51 to 80% foliage affected); and 5 = severe interveinal chlorosis and necrosis (81 to 100% foliage affected). Noninoculated controls were symptomless. Differences in virulence were observed among the isolates. Based on disease symptoms in the greenhouse and cultural morphology on PDAS, the isolates were classified as Fusarium solani f. sp. glycines. Isolates recovered from symptomatic plants resembled Fusarium solani f. sp. glycines on PDAS and peptone/p-chloro-nitrobenzene agar amended with streptomycin, confirming Koch's postulates. Fusarium solani f. sp. glycines was recovered from 60% of inoculated plants. Reference: (1) K. W. Roy et al. Plant Dis. 81:1100,1997.

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