Search

A legume survey in Story County was conducted to characterize legume viruses present in Iowa and potentially problematic to soybeans. Symptomatic (chlorosis, leaf curl, or vein banding) and non-symptomic leaves were selected from Apios americana, Cyamopsis tetragonolobus, Desmodium spp., Glycine max, Lablab purpureus, Lotus japonicus, Phaseolus coccineus, Phaseolus vulgaris, Vicia faba, Vigna ungulculata, and Chenopodium quinoa (an indicator species), and sent to Agdia Inc. for their Crop Screen: "Bean (Soybean)" tests. Cowpea mosaic virus (in L. purpureus), Southern bean mosaic virus (in A. americana), Soybean dwarf virus (in L. purpureus), and Tobacco streak virus (in Desmodium spp.) were identified. In addition, P. vulgaris was found positive in the serological Potyvirus group test, and was further characterized using reverse transcription (RT)-PCR using total RNA (Qiagen RNeasy extraction kit) from symptomatic leaves. A ~1-kb fragment of virus genome was amplified using degenerate primers, forward: 5' TGYGTNGAYGAYYTYAAYAA 3' (3) and reverse: 5' TCRTARAARTCRAAIGCRTAICKIG 3' (2). The closest GenBank BLAST hits for the sequence were BCMV strain NL1 (GenBank Accession No. AY112735) and BCMV MS1 (EU761198), both at 97% identity. RNA sequencing using an Illumina HiSeq 2500 (100 base paired ends) allowed construction of a nearly complete viral sequence from positions 38 to 10,037 nt (KM023744). This showed 99% similarity to BCMV-NL1 (AY112735) and 98% similarity to BCMV MS1 (EU761198). The BCMV isolate was recovered on the P. vulgaris cv. Taos Red and tested against a panel of Phaseolus, Glycine, and other hosts. Symptomatic hosts (vein-banding, mosaic, stunting, and leaf curl) were P. vulgaris cvs. Starlight, Tohono O'odham vaya Amarillo, Black Valentine Stringless, Sutter Pink, Hidatsa red, Stringless Green Refugee, Burpees Stringless Improved Bush, Princess d'Artois, Princess Double de Holland, and Dubelle Witte. Asymptomatic hosts included P. vulgaris cvs. Sierra, Great Northern Tara, Tara, and Vigna radiata. Non-host plants were P. vulgaris cvs. Michelite 62, Great Northern UI 31, Great Northern UI 123, Pure Gold Wax, Top Crop, Redlands Greanleaf B, Red Mexican UI 34, Imuna, Monroe, Pinto UI 114, Widusa, Othello, Sacramento, Red Kidney, Provider, Black Turtle Soup, Victor, and Witte boon, G. max cv. Williams, Cucumis sativus cv. Straight 8, Solanum lycopericum cv. Reine des Hatives, Vicia faba, Pisum sativum var. macrocarpon, V. unguiculata, and A. americana. The host range of the BCMV isolate on common bean differential species concurred with pathogenicity group I (1) and agreed with assignment as strain NL1. To our knowledge, this is the first complete characterization of a pathotype I strain NL1 of BCMV in the United States, combining biological typing and whole genome sequencing. References: (1) R. E. Klein et al. Plant Dis. 76:1263, 1992. (2) H. Yamamoto et al. J. Gen. Plant Pathol. 74:97, 2008. (3) L. Zheng et al. PLoS One 3:e1586, 2008.

The recent introduction of the colonizing soybean aphid (Aphis glycines) to soybean in the northern United States has raised concern for potential increased disease caused by the nonpersistently aphid-transmitted Soybean mosaic virus (SMV). This study was conducted to examine the potential integration of host plant resistance and insecticide tactics for control of virus disease. Research from four location-years demonstrated that foliar application of the pyrethroid insecticide lambda-cyhalothrin (Warrior) or the organophosphate chlorpyrifos (Lorsban 4E) timed to suppress soybean aphid populations does not reduce SMV. Therefore, the introduction of a colonizing aphid to the array of migratory noncolonizing aphids that transmit SMV does not result in potential for disease control through vector suppression by foliar insecticides. Treatment also did not result in management of Bean pod mottle virus (BPMV), transmitted by the bean leaf beetle (Cerotoma trifurcata), presumably because of issues related to different phenologies of the insect vectors. Soybean cultivars with the lowest virus titer in seed produced the highest grain yield and, thus, were rated as field tolerant compared with cultivars with the highest virus titer in seed. Host plant resistance, not vector control, is the most effective tactic to control SMV.

A survey of Bean pod mottle virus (BPMV) in Iowa counties was conducted and the virus was found throughout the state. A long-term monitoring study (1989 to 2002) of the main BPMV vector, the bean leaf beetle, Cerotoma trifurcata, indicated that, in 2002, populations reached the highest abundance recorded in 14 years. Three potential sources for an early season primary inoculum source were found: (i) soybean (Glycine max) seed, (ii) overwintered bean leaf beetles, and (iii) alternate BPMV host plants. Examination of 5,804 and 8,064 soybean seedlings of two cultivars yielded 0 and 3 seedlings, respectively, infected with BPMV. In a separate test, BPMV was detected in mottled and nonmottled soybean seed. Some mottled seed did not contain BPMV, indicating that soybean seed coat mottling is an unreliable indicator for presence of the virus in seed. Of 194 naturally overwintered bean leaf beetles, only 1 transmitted BPMV to soybean. BPMV was detected serologically only in 1 alternate host, Desmodium canadense, out of 23 naturally occurring plant species collected from the field. The three inoculum sources discovered in Iowa in this study could be important primary sources when vector populations are high and indicate starting points for future epidemiological investigations.

The recent discovery of the soybean aphid, Aphis glycines Matsamura, in the North Central region of the United States is significant because it is the first time that a soybean-colonizing aphid has been detected in the New World. Although the aphid has the potential to cause physiological loss of up to 52% on soybeans (4), it can also transmit Soybean mosaic virus (SMV). Transmission of Alfalfa mosaic virus (AMV) has not been reported. SMV, and less commonly AMV, are found in soybeans in the North Central states and are transmitted by numerous aphids in a nonpersistent manner (2; Grau, unpublished). For SMV, potential exists for specificity of transmission between virus strain and aphid species (3). For these reasons, it was important to determine if an endemic isolate of these viruses could be transmitted by this introduced species of aphid in the North Central region. Transmission experiments were conducted as described (3), using 3, 5, and 10 aphids per plant. Ten plants of the soybean cultivar Williams 82 were used for each treatment. To preclude confounding results by possible seed transmission, plants used in all tests were grown from seeds harvested from virus-indexed plants grown in the greenhouse. For experiments involving SMV, the aphid-transmissible field isolate Al5 (GeneBank Accession no. AF242844) and, as a negative control, the non-aphid transmissible isolate N (GeneBank Accession no. D500507) were used. For experiments involving AMV, a field isolate of AMV, confirmed by ELISA and host range, was used. The aphid species Myzus persicae was maintained on broad bean and A. glycines was maintained on virus-free soybean. The protocol for transmission studies of AMV was identical to that used in the SMV study, except only A. glycines was tested. For experiments, plants were periodically observed for symptom development and tested by ELISA 4 to 5 weeks after inoculation access. No transmission of SMV-N occurred in any tests, which together involved 180 aphids each of M. persicae or A. glycines. For the Al5 isolate, transmission efficiencies of 30, 50, and 50% were obtained with 3, 5, and 10 individuals, respectively, of M. persicae per plant. Efficiencies for A. glycines were 30, 40, and 40%. Transmission levels by the two aphid species did not differ significantly (t-test, P = 0.01). For AMV, corresponding transmission efficiencies were 0, 0, and 20%. The data suggest that the introduced A. glycines can be an efficient vector of SMV, but a less efficient vector of AMV, in the North Central region. Transmission of AMV by M. persicae has been documented (1) but was not examined in this study. Transmission of SMV and AMV by A. glycines is of concern because it may increase SMV and AMV incidence. With the recent outbreak of Bean pod mottle virus (BPMV) in the region, the potential for synergism of SMV and BPMV is increased (2). References: (1) M. B. Castillo and G. G. Orlob. Phytopathology 56:1028, 1966. (2) G. L. Hartman et al., eds. 1999. Compendium of Soybean Diseases, 4th Ed. American Phytopathological Society, St. Paul, MN. (3) B. S. Lucas and J. H. Hill. Phytopathol. Z. 99:47, 1980. (4) C. L. Wang et al. Plant Prot. 20:12, 1994.

The relationship between the amount of foliar disease on maize plants and seed contamination by the causal bacterium, Pantoea stewartii, was studied by comparing disease severity on adult plants with results from laboratory seed tests. Seventy-seven naturally infected maize lines (25 in 1990 and 52 in 1992) were selected and assigned to one of six disease severity classes based on the percentage of ear leaf tissue killed by Stewart's wilt: trace to 2%, 6 to 14%, 25 to 34%, 35 to 49%, 50 to 74%, and 75 to 100%. Ears were harvested from 10 to 20 plants representative of the disease class for each maize line, and seeds were tested by enzyme-linked immunosorbent assay (ELISA) of bulk-seed samples. Seed infection percentages were estimated from the bulk-test results by using statistical equations for group testing. The accuracy of the bulk-seed method for estimating seed infection was validated by comparison with 300-kernel single-seed tests. Infected seed was detected only from seed of plants with ≥25% disease severity; however, 45 of 63 such seed lots had no infection. Three seed lots had >5% infected seeds, all from plants with >50% disease severity. The results suggest a possible threshold level between 15 and 25% disease severity for Stewart's wilt on leaves before bacteria are detected in seed. This study describes a relatively simple method for estimating the incidence of infected seeds in a seed lot and contributes additional evidence to indicate that the chance of spreading P. stewartii from U.S.-produced maize seeds is low.

Seed transmission of Pantoea stewartii was evaluated by assays of more than 76,000 plants in greenhouse and field grow-out trials. Fourteen P. stewartii-infected seed lots were obtained from two dent corn inbreds and two sweet corn cultivars that were inoculated with either a rifampicin and nalidixic acid-resistant strain (rif-9A) or a wild-type strain (SS104) of P. stewartii. Four additional seed lots were collected from naturally infected inbreds. Percentages of infected kernels ranged from 0.8 to 72%, as determined by agar plating or by individual-kernel enzyme-linked immunosorbent assay (ELISA). Plants grown from this seed were assayed by a stem-printing technique that consisted of cutting and pressing a cross-section of each stem onto agar media. Prints were examined for development of P. stewartii colonies after 24 and 48 h. The transmission rate from seed produced on the inoculated plants was 0.066% (28 of 42,206 plants), based on all seedlings assayed. Transmission was estimated to be 0.14% from infected kernels. The transmission rate from seed produced on naturally infected plants was 0.0029% (1 of 34,924 plants), based on all seedlings, and 0.022% from infected kernels. Seed transmission occurred significantly less often (P = 0.034) from seed produced on naturally infected plants than from seed produced on inoculated plants, probably due to greater kernel damage caused by ear shank inoculation. The rarity of seed transmission of P. stewartii from heavily infected seed lots that would ordinarily be rejected due to poor germination suggests that the likelihood of seed transmission from good quality commercial seed corn is virtually nonexistent.