gall tissue
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2019 ◽  
Vol 48 (5) ◽  
pp. 1138-1148
Author(s):  
Austin M Thomas ◽  
Ray S Williams ◽  
Robert F Swarthout

AbstractMany plants use terpenoids and other volatile compounds as semiochemicals. Reception of plant volatiles by conspecifics may trigger a defensive phytochemical response. These same compounds can also function as host recognition signals for phytophagous insects. In this experiment, we find that when the specialist gall-forming fly Eurosta solidaginis (Fitch; Diptera: Tephritidae) attacks its tall goldenrod (Solidago altissima (L.; Asterales: Asteraceae)) host plant, the fly indirectly induces a phytochemical response in nearby tall goldenrod plants. This phytochemical response may, in turn, act as a positive signal attracting the goldenrod specialist aphid Uroleucon nigrotuberculatum (Olive; Hemiptera: Aphididae). Laboratory-based experiments exposing ungalled tall goldenrod plants to the volatiles released by E. solidaginis galls demonstrated a consistent increase in foliar terpenoid concentrations in ungalled plants. Analysis of tall goldenrod stem and gall tissue chemistry revealed induction of terpenoids in gall tissue, with a simultaneous decrease in green leaf volatile concentrations. Field experiments demonstrated a consistent spatial relationship in tall goldenrod foliar terpenoid concentrations with distance from an E. solidaginis gall. Both laboratory and field experiments establish consistent induction of the terpene β-farnesene, and that this compound is a strong positive predictor of U. nigrotuberculatum aphid presence on goldenrod plants along with plant biomass and several other foliar terpenoids. These findings suggest E. solidaginis induced phytochemistry, especially β-farnesene, may be acting as a kairomone, driving aphid distribution in the field.


2018 ◽  
Author(s):  
Stefan Ciaghi ◽  
Arne Schwelm ◽  
Sigrid Neuhauser

AbstractBackgroundClubroot disease caused by Plasmodiophora brassicae (Phytomyxea, Rhizaria) is one of the economically most important diseases of Brassica crops. The formation of hypertrophied roots accompanied by altered metabolism and hormone homeostasis is typical for infected plants. Not all roots of infected plants show the same phenotypic changes. While some roots remain uninfected, others develop galls of diverse size. The aim of this study was to analyse and compare the intra-plant heterogeneity of P. brassicae root galls and symptomless roots of the same host plants (Brassica oleracea var. gongylodes) collected from a commercial field in Austria using transcriptome analyses.ResultsTranscriptomes were markedly different between symptomless roots and gall tissue. Symptomless roots showed transcriptomic traits previously described for resistant plants. Genes involved in host cell wall synthesis and reinforcement were up-regulated in symptomless roots indicating elevated tolerance against P. brassicae. By contrast, genes involved in cell wall degradation and modification processes like expansion were up-regulated in root galls. Hormone metabolism differed between symptomless roots and galls. Brassinosteroid-synthesis was down-regulated in root galls, whereas jasmonic acid synthesis was down-regulated in symptomless roots. Cytokinin metabolism and signalling were up-regulated in symptomless roots with the exception of one CKX6 homolog, which was strongly down-regulated. Salicylic acid (SA) mediated defence response was up-regulated in symptomless roots, compared with root gall tissue. This is probably caused by a secreted benzoic acid salicylic acid methyl transferase from the pathogen (PbBSMT), which was one of the highest expressed pathogen genes in gall tissue. The PbBSMT derived Methyl-SA potentially leads to increased pathogen tolerance in uninfected roots.ConclusionsInfected and uninfected roots of clubroot infected plants showed transcriptomic differences similar to those previously described between clubroot resistant and susceptible hosts. The here described intra-plant heterogeneity suggests, that for a better understanding of clubroot disease targeted, spatial analyses of clubroot infected plants will be vital in understanding this economically important disease.


Data in Brief ◽  
2017 ◽  
Vol 14 ◽  
pp. 793-803
Author(s):  
George Washburn ◽  
Sunshine A. Van Bael
Keyword(s):  

2017 ◽  
Vol 81 (6) ◽  
pp. 1069-1077 ◽  
Author(s):  
Mami Takei ◽  
Shinsaku Ito ◽  
Keisuke Tanaka ◽  
Taichiro Ishige ◽  
Yoshihito Suzuki
Keyword(s):  

2012 ◽  
Vol 145 (3) ◽  
pp. 238-249 ◽  
Author(s):  
M.O. Harris ◽  
T.P. Freeman ◽  
K.M. Anderson ◽  
J.P. Harmon ◽  
J.A. Moore ◽  
...  

2010 ◽  
Vol 70 (3 suppl) ◽  
pp. 723-728 ◽  
Author(s):  
GW. Fernandes ◽  
MS. Coelho ◽  
U. Lüttge

Leaf galls induced by a still undescribed new species of Cecidomyiidae (Diptera) are frequent on leaves of Clusia arrudae Planchon & Tirana (Clusiaceae) in the rupestrian fields at 1400 m a.s.l. in Serra do Cipó, Minas Gerais, Brazil. Galls were 7.1 ± 0.7 mm in diameter, one chambered with only one larva inside. Gall tissue is green and soft. Assessments of photosynthetic capacity using chlorophyll-a fluorescence measurements revealed that photosynthetic performance of gall tissue and healthy leaf tissue were rather similar. Hence, the morphological changes due to gall development were not associated with significant changes in the photosynthetic capacity of the tissue.


HortScience ◽  
1993 ◽  
Vol 28 (8) ◽  
pp. 782-785 ◽  
Author(s):  
M.E. Valverde ◽  
P. Fallah Moghaddam ◽  
M.S. Zavala-Gallardo ◽  
J.K. Pataky ◽  
O. Paredes-Lopez ◽  
...  

Ear gall development was evaluated after inoculating sweet corn (Zea mays L.) hybrids with Ustilago maydis (DC) Corda by injecting sporidial suspensions into silk channels when silks had emerged ≈3 to 6 cm from ear shoots. Gall incidence was ≈35% in two inoculation trials. About 0.5% of the noninoculated control plants was infected. Gall weight increased ≈250% to 500% between 14 and 21 days after inoculation, reaching a maximum of ≈280 to 600 g. Gall tissue was nearly 100% black and had lost its spongy integrity 19 to 21 days after inoculation, when mycelial cells formed powdery teliospores. A 1- or 2-day harvest window during which huitlacoche yield and quality were optimized corresponded to the time at which 60% to 80% of the gall tissue was black. The optimal huitlacoche harvest time varied among hybrids from 17 to 19 days after inoculation, but we suspect that optimal harvest time varies from ≈15 to 24 days after inoculation, depending on the growth stage at which the host is inoculated and the environmental conditions following inoculation. Differences among sweet corn hybrids in gall incidence, gall size, and coverage of mature galls by husk leaves were observed and could be used to select sweet corn hybrids that are well suited for producing huitlacoche.


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