Evaluation of Disease Resistance among 57 Varieties of Zinnia elegans

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 467a-467
Author(s):  
Linda Gombert ◽  
Susan Hamilton ◽  
Mark Windham

Fifty-seven of the most widely grown, commercially popular varieties of Zinnia elegans were evaluated for disease susceptibility under uniform field conditions. Plants were started from seed and transplanted into cell-packs to be grown on as bedding plants. They were later transplanted into the field and observed for development and progression of the diseases alternaria blight (Alternaria zinniae), powdery mildew (Erisyphe cichoracearum), and bacterial leaf and flower spot (Xanthomonas campestris pv. zinniae). Evaluations were performed throughout the growing season in order to rate each variety on its susceptibility to disease based upon severity of infection as well as portion of plant affected. Results will be presented on disease susceptibility and resistance of the 57 varieties evaluated.

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 466g-467
Author(s):  
Linda Gombert ◽  
Susan Hamilton ◽  
Mark Windham

The objective of this study was to determine if field irrigation practices affect the development and suppression of three diseases, alternaria blight (Alternaria zinniae), powdery mildew (Erisyphe cichoracearum) and bacterial leaf and flower spot (Xanthomonas campestris pv. zinniae), on Zinnia elegans. Many commercial growers will no longer produce this popular bedding plant and cut flower crop due to high incidence of these three diseases. Plants of 17 different varieties of Z. elegans were started from seed and transplanted into cell-packs to be grown on as bedding plants. They were later transplanted into the field and subjected to one of three watering regimes: natural rainfall plus overhead irrigation, natural rainfall plus sub-irrigation, and natural rainfall only. Weekly evaluations were performed to rate each variety on its susceptibility to disease based upon severity of infection as well as portion of plant affected. Results will be presented on irrigation method and its influence on disease susceptibility and resistance on the 17 varieties evaluated.


2001 ◽  
Vol 11 (1) ◽  
pp. 71-74 ◽  
Author(s):  
Linda Gombert ◽  
Mark Windham ◽  
Susan Hamilton

Fifty-seven cultivars of zinnia (Zinnia elegans Jacq.) were studied for 17 weeks to determine their resistance to alternaria blight (Alternaria zinniae Pape), powdery mildew (Erysiphe cichoracearum DC ex Merat) and bacterial leaf & flower spot [Xanthomonas campestris pv. zinniae (syn. X. nigromaculans f. sp. zinniae Hopkins & Dowson)]. A disease severity scale was used to determine acceptability for landscape use. At week 4, all cultivars were acceptable. At week 10, eleven cultivars were acceptable. At week 17, all cultivars were unacceptable. Ten cultivars had been killed by one or more pathogens by week 17. Only two cultivars showed any tolerance to any disease (powdery mildew) at week 17.


Plant Disease ◽  
2020 ◽  
Author(s):  
Yi-Ting Xiao ◽  
Yuan-Min Shen ◽  
Chao-Jen Wang ◽  
Tung-Ching Huang

Zinnia elegans L., known as common zinnia, is an annual flowering plant belonging to the Asteraceae family and native to North America. The plant has colorful flowers and is one of the popular ornamental bedding plants for gardening. In March 2020, powdery mildew symptoms were observed in a zinnia floral field with an incidence of >70% in Dacun Township, Changhua County, Taiwan. The symptoms were spotted on the stems, flower petals and leaves which appeared as irregular colonies and white patches on the surfaces. When disease progressed, most of the plant surfaces were covered by the white fungal colonies and became yellowish. Under microscopic examination, hyphal appressoria of the fungus were indistinct or slightly nipple-shaped. The conidiophores were unbranched, erect, straight, smooth to slightly rough, 75.0 to 200.0 × 10.0 to 15.0 µm (n=10), composed of a cylindrical, flexuous foot cell, 40.0 to 100.0 × 8.8 to 15.0 µm (n=10), and following 1 to 5 shorter cells. The conidia were ellipsoid to ovoid, 25.0 to 37.5 × 15.0 to 23.8 µm (n=60), with an average length-to-width ratio of 1.8 and contained fibrosin bodies. No chasmothecia were found. Three voucher specimens (TNM Nos. F0033680, F0033681, and F0033682) were deposited in the National Museum of Natural Science, Taichung City, Taiwan. To confirm the identification, the internal transcribed spacer (ITS) regions of the three specimens were amplified using primer pairs ITS1/PM6 and PM5/ITS4 (Shen et al. 2015) and sequenced from both ends. The resulting sequences were deposited in GenBank under Accession Nos. MT568609, MT568610, and MT568611. The sequences were identical to each other and shared a 100% identity with that of Podosphaera xanthii MUMH 338 on Z. elegans from Japan (Accession No. AB040355) (Ito and Takamatsu 2010) over a 475 bp alignment. Accordingly, the fungus was identified as P. xanthii (Castagne) U. Braun & Shishkoff (Braun and Cook 2012) based on its morphological and molecular characters. Pathogenicity was demonstrated through inoculation by gently pressing naturally infected leaves onto leaves of three healthy potted common zinnia that had been sprayed with 0.02% Tween 20. Additional three non-inoculated plants treated in the same way without inoculating the powdery mildew served as the controls. Powdery mildew colonies were observed on inoculated leaves after 10 days at room temperature, later the diseased leaves became yellowish and deteriorated. The morphological traits of the fungus on the inoculated leaves were similar to those of the first observed. In addition, the ITS sequence from a colony on the inoculated leaves was 100% identical to MT568609-MT568611, fulfilling the Koch’s postulates. All the controls remained symptomless. Z. elegans is known to be a host for different species of powdery mildew in the genus Erysiphe, Golovinomyces, and Podosphaera (Farr and Rossman 2020). In Taiwan, powdery mildew has been briefly reported on zinnia without detailed descriptions (Hsieh 1983). This study confirmed P. xanthii as a causal agent of powdery mildew in Taiwan and the awareness of the disease may benefit the floral industry. To our knowledge, this is the first confirmed report of P. xanthii on Z. elegans in Taiwan.


2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Krishna Bhattarai ◽  
Ana Conesa ◽  
Shunyuan Xiao ◽  
Natalia A. Peres ◽  
David G. Clark ◽  
...  

Abstract Background RNA sequencing has been widely used to profile genome-wide gene expression and identify candidate genes controlling disease resistance and other important traits in plants. Gerbera daisy is one of the most important flowers in the global floricultural trade, and powdery mildew (PM) is the most important disease of gerbera. Genetic improvement of gerbera PM resistance has become a crucial goal in gerbera breeding. A better understanding of the genetic control of gerbera resistance to PM can expedite the development of PM-resistant cultivars. Results The objectives of this study were to identify gerbera genotypes with contrasting phenotypes in PM resistance and sequence and analyze their leaf transcriptomes to identify disease resistance and susceptibility genes differentially expressed and associated with PM resistance. An additional objective was to identify SNPs and SSRs for use in future genetic studies. We identified two gerbera genotypes, UFGE 4033 and 06–245-03, that were resistant and susceptible to PM, respectively. De novo assembly of their leaf transcriptomes using four complementary pipelines resulted in 145,348 transcripts with a N50 of 1124 bp, of which 67,312 transcripts contained open reading frames and 48,268 were expressed in both genotypes. A total of 494 transcripts were likely involved in disease resistance, and 17 and 24 transcripts were up- and down-regulated, respectively, in UFGE 4033 compared to 06–245-03. These gerbera disease resistance transcripts were most similar to the NBS-LRR class of plant resistance genes conferring resistance to various pathogens in plants. Four disease susceptibility transcripts (MLO-like) were expressed only or highly expressed in 06–245-03, offering excellent candidate targets for gene editing for PM resistance in gerbera. A total of 449,897 SNPs and 19,393 SSRs were revealed in the gerbera transcriptomes, which can be a valuable resource for developing new molecular markers. Conclusion This study represents the first transcriptomic analysis of gerbera PM resistance, a highly important yet complex trait in a globally important floral crop. The differentially expressed disease resistance and susceptibility transcripts identified provide excellent targets for development of molecular markers and genetic maps, cloning of disease resistance genes, or targeted mutagenesis of disease susceptibility genes for PM resistance in gerbera.


HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 547a-547
Author(s):  
Geunhwa Jung ◽  
James Nienhuis ◽  
Dermot P. Coyne ◽  
H.M. Ariyarathne

Common bacterial blight (CBB), bacterial brown spot (BBS), and halo blight (HB), incited by the bacterial pathogens Xanthomonas campestris pv. phaseoli (Smith) Dye, Pseodomonas syringae pv. syringa, and Pseudomonas syringae pv. phaseolicola, respectively are important diseases of common bean. In addition three fungal pathogens, web blight (WB) Thanatephorus cucumeris, rust Uromyces appendiculatus, and white mold (WM) Sclerotinia sclerotiorum, are also destructive diseases attacking common bean. Bean common mosaic virus is also one of most major virus disease. Resistance genes (QTLs and major genes) to three bacterial (CBB, BBS, and HB), three fungal (WB, rust, and WM), and one viral pathogen (BCMV) were previously mapped in two common bean populations (BAC 6 × HT 7719 and Belneb RR-1 × A55). The objective of this research was to use an integrated RAPD map of the two populations to compare the positions and effect of resistance QTL in common bean. Results indicate that two chromosomal regions associated with QTL for CBB resistance mapped in both populations. The same chromosomal regions associated with QTL for disease resistance to different pathogens or same pathogens were detected in the integrated population.


2008 ◽  
Vol 74 (20) ◽  
pp. 6327-6332 ◽  
Author(s):  
Josselin Montarry ◽  
Philippe Cartolaro ◽  
François Delmotte ◽  
Jérôme Jolivet ◽  
Laetitia Willocquet

ABSTRACT Isolates of the causal ascomycete of grapevine powdery mildew, Erysiphe necator, correspond to two genetically differentiated groups (A and B) that coexist on the same host. This coexistence was analyzed by investigating temporal changes in the genetic and phenotypic structures of E. necator populations during three epidemics. Group A was present only at the start of the growing season, whereas group B was present throughout all three epidemics. Group A was less aggressive in terms of germination and infection efficiency but was more aggressive than group B in terms of the latency period, lesion diameter, and spore production. Our results are consistent with a temporal differentiation of niches, preventing recombination, and suggest an association between the disease level and the frequencies of genetic groups.


Author(s):  
Reginah Pheirim ◽  
Noren Singh Konjengbam ◽  
Mayurakshee Mahanta

Powdery mildew is caused by an obligate parasite Erysiphe pisi and considered as one of the most important constraints causing yield reductions in pea. Development and utilization of genetic resistance is acknowledged as the most effective, economic and environmental friendly method of control. Therefore, development of cultivars with improved resistance to biotic stresses is a primary goal of plant breeding programs throughout the world. Three monogenic sources er1, er2 and Er3 have been described to govern the powdery mildew disease resistance. Several markers have been reported linked to resistant genes at varying distances in different mapping populations. Genetic markers linked to the disease resistance gene make the breeding process more efficient for the use of Marker Assisted Selection (MAS) strategy to aid in obtaining a complete powdery mildew resistance in pea.


2021 ◽  
pp. 178-193
Author(s):  
Svetla Sofkova-Bobcheva ◽  
Ivelin Pantchev ◽  
Ivan Kiryakov ◽  
Petar Chavdarov ◽  
Yordan Muhovski ◽  
...  

Abstract Although historically a surplus food producer, Bulgarian agriculture has faced a downturn in recent decades. Local legume cultivars have lost favour with farmers and the canning industry, due to their low productivity in comparison with imported ones. Diseases and abiotic stresses are the most important factors limiting the production of edible legumes, costing farmers hundreds of euros in lost revenue each year. The overall objective of our ongoing bean mutation breeding programme was to enrich the gene pool of Phaseolus vulgaris L. and to develop genotypes resistant to Xanthomonas axonopodis pv. phaseoli (Smith) (Xap) and Pseudomonas savastanoi pv. phaseolicola (Burkh.) (Psp) using EMS. An elite line and common cultivar (an heirloom and a snap bean type) in Bulgaria, were selected as parents and the chemical mutagen EMS was used for generating mutations. In total, 1000 seeds were treated and the two generated M1 populations were grown in the field. All M2 mutant plants (1650 from initial line IP564 and 2420 from initial cultivar 'Mastilen 11b') were grown in field conditions and a number of phenotypic changes were observed on these mutated plants. They were also screened for Xap disease resistance via leaf artificial inoculation under greenhouse conditions. Individual plant selection was performed for the putatively resistant M2 plants. In the M3 generation these lines were screened using artificial inoculation with Xap and Psp pathogens (leaves and pods) under field conditions. Selected M3-M4 lines with confirmed disease resistance were tested for fresh pod quality. Yield tests were started in M4 and M5 generations and, according to their productivity performance, mutants were advanced to the M6/M7 generation for validation. The expression patterns of genes putatively involved in the resistance reactions towards two races of Psp were determined using qRT-PCR for the specific and reference genes. In conclusion, 50 plants with visible morphological changes and/or increased tolerance to the two targeted bacterial diseases were selected. A total of 20 advanced mutant bean lines are currently being evaluated for their competitiveness in multiple sites.


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