| plant-originated PR proteins |
accumulate in large amounts when |
plants are attacked by pathogens |
|
| VmR2 -siR1 expression |
reduced expression of |
apple SA signaling pathway-related genes, cytochrome production signaling pathway-related gene, ROS production-related gene, and immune-related transcription factor gene |
Malus domestica |
| cotton variety |
did not significantly influence |
heliocide levels |
Gossypium hirsutum |
| EtHAn:pEDV6-Pt9029 ΔSP |
significantly inhibits |
callose deposition |
Triticum aestivum |
| changes in volatile emissions |
imply |
NlVgN is not limited to direct defenses but involves volatile-mediated indirect defense |
Oryza sativa |
| chitosan treatment |
increases |
percentage of sieve plates with callose deposition in WT rice |
Oryza sativa |
| hub2-2 mutant |
shows weaker depolymerization of |
cortical microtubules (MTs) |
Arabidopsis thaliana |
| BPH phloem-feeding |
caused inhibition of |
callose deposition |
Oryza sativa |
| Gossypium hirsutum plants exposed to undamaged emitter plants |
contain lower levels of |
gossypol |
Gossypium hirsutum |
| flg22 treatment |
induces |
plant defense responses |
|
| NlVgN from egg surface |
induces |
considerably stronger responses in rice plants |
Oryza sativa |
| hub2-2 mutant |
shows slightly increased transcript levels of |
ARABIDOPSIS THALIANA PLANT AND FUNGI ATYPICAL DUAL-SPECIFICITY PHOSPHATASE 5 (AtPFA-DSP5, PFA-DSP5, AT5G16480) |
Arabidopsis thaliana |
| hub1-4 mutant |
eliminates |
hypersensitive response-like cell death |
Arabidopsis thaliana |
| NlVgN treatment of rice plants (twice) |
decreased |
hatching rate of BPH eggs |
Oryza sativa |
| salicylic acid (SA) |
is suggested to be important for |
protecting rice from oxidative damage during pathogen infections |
Oryza sativa |
| BPH oviposition alone |
has no effect on |
callose deposition on sieve plates of WT rice |
Oryza sativa |
| JA signaling |
positively regulates |
apple resistance to AVC |
Malus domestica; Valsa mali |
| Gossypium hirsutum plants exposed to damaged emitter plants |
contain marginally significantly higher levels of |
gossypol |
Gossypium hirsutum |
| wild-type Arabidopsis |
shows increased |
cell death |
Arabidopsis thaliana |
| depolymerization of cortical microtubules (MTs) |
increases with |
treatment time |
Arabidopsis thaliana |
| ARABIDOPSIS THALIANA PLANT AND FUNGI ATYPICAL DUAL-SPECIFICITY PHOSPHATASE 5 (AtPFA-DSP5, PFA-DSP5, AT5G16480) |
gene expression is induced by |
Verticillium dahliae (Vd) toxins |
Arabidopsis thaliana |
| basal immunity |
is activated by |
Arabidopsis thaliana |
Arabidopsis thaliana |
| ATP-induced resistance against necrotrophic pathogen |
is not likely mediated through |
noncanonical pathway |
|
| GRPs |
are involved in |
blocking virus movement |
|
| pectin-derived oligogalacturonides (OGs) |
are |
elicitors with activity in plant defense |
|
| BPH oviposition |
counteracted |
BPH phloem-feeding-induced inhibition of callose deposition |
Oryza sativa |
| (ML3, AT5G23820) mutants |
are hypersensitive to |
herbivore attack |
Arabidopsis thaliana |
| ubc1-1/ubc2-2 mutant |
eliminates |
hydrogen peroxide accumulation |
Arabidopsis thaliana |
| heterologous overexpression or exogenous treatment of Bg_9562 protein |
provides protection against |
Rhizoctonia solani |
Solanum lycopersicum |
| protein tyrosine phosphatase (PTP) genes |
could be regulated or act as |
target genes of histone (H2B, HTB2, AT5G22880) monoubiquitination (H2Bub) |
Arabidopsis thaliana |
| difference in responses to gravid BPH females and BPH nymphs |
is due to |
difference in source (quantities) of NlVgN and difference in damage inflicted |
|
| peptide 2-treated leaves |
have only |
few callose spots |
Solanum lycopersicum |
| MdPYL4-RNAi transgenic line |
exhibits reduced expression of |
MdPR4 |
Malus domestica |
| ER bodies |
release |
hydrolytic enzymes |
|
| hub1-4 mutant |
shows only slight disassembly of |
cortical microtubules (MTs) |
Arabidopsis thaliana |
| small amounts of NlVgN in 40 μl treatment solution |
did not affect |
performance of BPH |
Oryza sativa |
| phloem-feeding of gravid BPH |
significantly reduces |
callose deposition in chitosan-treated WT rice plants |
Oryza sativa |
| VmSpm1 |
regulates plant immunity by modulating |
JA signaling pathway through MdPYL4 degradation |
Malus domestica; Valsa mali |
| VmSpm1 overexpression in apple leaves |
decreases expression of |
MdWRKY40 |
Malus domestica |
| pattern recognition receptors (PRRs) |
regulate |
first active line of plant defense response |
Arabidopsis thaliana |
| (XLG2, AT4G34390) mutation |
compromises resistance to |
avirulent strain of Pst |
Arabidopsis thaliana |
| Bg_9562 overexpressing lines |
exhibit enhanced expression of |
defense genes |
Solanum lycopersicum |
| infestation by gravid BPH with phloem-feeding and oviposition |
has no significant effect on |
callose deposition of OsSUT2 mutants |
Oryza sativa |
| VmR2 -siR1 |
appears to target and suppress |
defense responses induced by MdLRP14 |
Malus domestica |
| VmR2 -siR1 |
suppresses |
apple resistance |
Malus domestica |
| MdPYL4-RNAi transgenic line |
exhibits reduced expression of |
MdCYP81F2 |
Malus domestica |
| ubc1-1 mutant |
shows reduced |
(AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) expression level |
Arabidopsis thaliana |
| phenylarsine oxide (PAO) |
increases |
depolymerization of cortical microtubules (MTs) |
Arabidopsis thaliana |
| hub2-2 mutant |
eliminates |
hydrogen peroxide accumulation |
Arabidopsis thaliana |
| ubc1-1 mutant |
eliminates |
hypersensitive response-like cell death |
Arabidopsis thaliana |
| plants |
can perceive |
prophage proteins |
|
| MdLRP14 overexpression |
enhances |
V. mali resistance in apple leaves |
Malus domestica |
| histone (H2B, HTB2, AT5G22880) monoubiquitination (H2Bub) |
is an important modification with a regulatory part in |
defense response to Verticillium dahliae toxins |
Arabidopsis thaliana |
| NlVgN treatment of rice plants (once) |
had no effect on |
any BPH performance parameter |
Oryza sativa |
| MdPYL4-RNAi transgenic line |
exhibits reduced expression of |
MdWRKY40 |
Malus domestica |
| BPH phloem-feeding |
can attenuate |
inhibition of BPH phloem-feeding by OsSUT2 mutants |
Oryza sativa |
| Arbuscular mycorrhizal fungi (AMF) colonization of roots |
enhance |
flavonoids |
|
| plant defenses against insects |
are |
inducible |
|
| exogenously applied Salicylic acid (SA) |
protects |
tobacco leaves against viral infection |
Nicotiana tabacum |
| reduced JA synthesis in MdPYL4-RNAi plants |
causes |
reduced resistance to V. mali |
Malus domestica; Valsa mali |
| harpin (HrpZ) |
can induce expression of |
(PSS1, AT3G59640) |
Arabidopsis thaliana |
| autophagy |
has been shown to be linked to |
induction of programmed cell death |
|
| (AGB1, ATAGB1, ELK4, AT4G34460) mutation |
leads to enhanced susceptibility to |
necrotrophic fungal pathogens |
Arabidopsis thaliana |
| suppression of H2O2 production |
impedes |
wheat disease resistance mechanisms |
Triticum aestivum |
| ubc1-1/ubc2-2 double mutant |
shows reduced |
(AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) expression level |
Arabidopsis thaliana |
| dynamics of microtubules |
plays an important part in |
defense response against Verticillium dahliae toxins |
Arabidopsis thaliana |
| 35S-ATL6 overexpression line |
shows enhanced callose deposition in response to |
flg22 |
Arabidopsis thaliana |
| biosynthesis of indole glucosinolates (IG) |
is central to |
Arabidopsis's defense to mite herbivory |
Arabidopsis thaliana |
| 2,3-trans-(+)-catechin and PAs produced in the tree in response to fungal infection |
can be considered |
chemical defense compounds |
Picea abies |
| flg22-induced reactive oxygen species (ROS) burst |
occurs within |
10 to 20 minutes |
Arabidopsis thaliana |
| BAK1-dependent recognition of aphid elicitors |
leads to |
immunity to green peach aphid (GPA) |
Arabidopsis thaliana |
| (BIK1, AT2G39660) mutants |
is not |
lesion mimic mutant |
Arabidopsis thaliana |
| (PSS1, AT3G59640) protein |
is induced in response to infection by |
multiple pathogens |
Arabidopsis thaliana |
| genes associated with lesion traits |
likely influence |
different and complementary mechanisms in a multifaceted defense response |
Arabidopsis thaliana |
| S. meliloti mutant strain unable to produce exopolysaccharides |
triggers induction of |
larger number of genes belonging to plant defense category |
Medicago truncatula |
| ubc1-1 mutant |
shows reduction of |
hydrogen peroxide (H2O2) production |
Arabidopsis thaliana |
| protein tyrosine phosphatase (PTP)-mediated signaling pathway |
was inferred to be |
a crucial mechanism for regulating the dynamics of microtubules |
Arabidopsis thaliana |
| ethylene (ET) |
is known to play a key role in |
cell death and plant response to pathogens and insects |
Arabidopsis thaliana |
| subsequent defense reactions |
include |
activation of defense-related genes |
|
| four lesion traits |
identify |
known defense mechanisms while also extending analysis to new pathways |
Arabidopsis thaliana |
| Verticillium dahliae toxins plus protein tyrosine kinase (PTK) inhibitor |
significantly decreased |
depolymerization of the cortical microtubules |
Arabidopsis thaliana |
| 3- to 10-kD fraction of green peach aphid (GPA)-derived extract |
induced |
reactive oxygen species (ROS) burst |
Arabidopsis thaliana |
| elevated basal salicylic acid (SA) |
was detected in |
(BIK1, AT2G39660) mutants |
Arabidopsis thaliana |
| genetic screening for Arabidopsis mutants with increased penetration by Bgh |
resulted in identification of |
PENETRATION1 (04C11, ATPEN1, PEN1, AT4G15340) gene |
Arabidopsis thaliana |
| bacterial PAMP HrpZ |
triggers |
hypersensitive response at infection site |
|
| (ATPAD4, PAD4, AT3G52430) |
is involved in |
basal resistance |
|
| Gγ subunit |
is |
positive regulator in disease resistance |
Arabidopsis thaliana |
| (ATFLS2, FLS2, AT5G63580) (EFR, AT5G20480) and (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) mutants |
showed no visible lesions |
lesion formation |
Arabidopsis thaliana |
| γ-thionin family domain-containing protein gene (LOC_Os02g07628) and defense in DEFL family gene (LOC_Os07g41290) |
showed 5.09- and 3.2-fold increases, respectively, in expression in |
developing seeds of HFL1 |
Oryza sativa |
| (ATEDS1, EDS1, AT3G48090) |
is involved in |
basal resistance |
|
| (XLG2, AT4G34390) mutation |
compromises resistance to |
non-host strain (PSP, PSP1, AT1G18640) |
Arabidopsis thaliana |
| xlg mutants (including double and triple mutants) |
do not show obvious differences from wt plants in resistance to |
A. brassicicola |
Arabidopsis thaliana |
| defense-associated responses |
characterized by production of |
salicylic acid (SA) |
|
| transcriptional activation of defense-related genes |
results in |
accumulation of pathogenicity-related (PR) proteins |
|
| lignification |
is one of the mechanisms to strengthen |
cell wall |
|
| thiamine |
complemented |
compromised defense of OsDR8-suppressing plants |
|
| obligate biotrophic oomycetes Hyaloperonospora arabidopsidis |
showed decreased reproduction on |
bak1-4 mutant plants |
Arabidopsis thaliana; Hyaloperonospora arabidopsidis |
| callose, phenolics, reactive oxygen species, and antimicrobial compounds in papillae |
act as physical and chemical barriers to |
pathogen invasion |
|
| PR genes/probesets |
are up-regulated starting at 3 hpi and increase in expression over time |
expression levels |
|
| carbon |
is crucial for |
plant immunity |
|
| (ATL31, CNI1, AT5G27420) |
contributes to |
resistance to fungal penetration |
Arabidopsis thaliana |
| ATP-activated JA signaling |
likely expedites |
plant defense responses against pathogen attacks |
|
| interference with de-repression of cell wall invertase activity |
increases |
pathogen sensitivity |
Arabidopsis thaliana |
| Phe pre-treatment |
reduces ROS production during |
plant defense response to Botrytis cinerea |
Chrysanthemum morifolium |
| MeATG8c overexpression |
alleviates the effect of |
MeHSP90.9 silencing |
Manihot esculenta |
| MeATG8c-silenced cassava leaves |
show significantly less |
MePR1 and MePR2 transcripts |
Manihot esculenta |
| hub1-4/hub2-2 double mutant |
shows only slight depolymerization of |
cortical microtubules (MTs) |
Arabidopsis thaliana |
| (BIK1, AT2G39660) mutants |
began to show |
apparent lesion spots approximately 5 d after aphid infestation |
Arabidopsis thaliana |
| Ca2+-mediated signaling |
evokes expression of |
pathogen-related genes |
|
| hub1-4 mutant |
shows reduction of |
hydrogen peroxide (H2O2) production |
Arabidopsis thaliana |
| hub1-4 mutant |
shows reduced |
(AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) expression level |
Arabidopsis thaliana |
| genistein (GN) |
decreases |
depolymerization of cortical microtubules (MTs) |
Arabidopsis thaliana |
| ARABIDOPSIS THALIANA PLANT AND FUNGI ATYPICAL DUAL-SPECIFICITY PHOSPHATASE 5 (AtPFA-DSP5, PFA-DSP5, AT5G16480) |
is important in |
response to Verticillium dahliae (Vd) toxins |
Arabidopsis thaliana |
| Verticillium dahliae toxins |
induces a more dramatic depolymerization of |
cortical microtubules |
Arabidopsis thaliana |
| fractions of green peach aphid (GPA)-derived extract smaller than 3 kD |
did not induce |
reactive oxygen species (ROS) burst |
Arabidopsis thaliana |
| plant defense response |
is reflected by |
reduced offspring production (antibiosis) |
|
| extracellular ATP |
acts as central signal in |
plant defense responses |
|
| Gβ mutation |
does not alter resistance to |
virulent or avirulent strains of P. syringae |
Arabidopsis thaliana |
| constitutive overexpression of (XLG2, AT4G34390) |
leads to constitutive expression of |
(CYP71B15, PAD3, AT3G26830) |
Arabidopsis thaliana |
| green peach aphid (GPA)-derived extract-induced reactive oxygen species (ROS) burst |
occurs after |
1 hour |
Arabidopsis thaliana |
| subsequent defense reactions |
include |
export of pathogenesis-related proteins |
|
| ATP addition |
induces resistance against |
Botrytis cinerea |
|
| salicylic acid (SA) and ethylene (ET) levels |
increased in |
wild-type and (BIK1, AT2G39660) plants upon aphid infestation |
Arabidopsis thaliana |
| pathogen with different growth strategies to optimize fitness |
would require |
plant to defend against local growth and growth geared toward spread of the pathogen |
Arabidopsis thaliana |
| histone (H2B, HTB2, AT5G22880) monoubiquitination (H2Bub) |
is a positive regulator of |
expression of protein tyrosine phosphatase (PTP) genes |
Arabidopsis thaliana |
| wild type |
showed no visible lesions |
lesion formation |
Arabidopsis thaliana |
| ethylene (ET) levels |
were measured in |
wild-type and (BIK1, AT2G39660) plants in the presence and absence of aphid feeding |
Arabidopsis thaliana |
| genes whose expression is influenced by a wide range of pathogens |
are identified from |
expression pattern analysis |
Oryza sativa |
| mixtures of Norway spruce monomeric flavan-3-ols and proanthocyanidins (PAs) |
has activity against |
C. polonica fungus |
Picea abies; Ceratocystis polonica |
| (SAG13, AT2G29350) expression |
shared a similar expression pattern with |
(ATPAD4, PAD4, AT3G52430) |
Arabidopsis thaliana |
| sucrose (Suc) treatment |
transcriptionally induces |
pathogenesis-related genes |
|
| pen1-1 loss-of-function mutant |
causes delayed formation of |
papillae |
Arabidopsis thaliana |
| (ATGPA1, GP ALPHA 1, GPA1, AT2G26300) mutant |
exhibited enhanced resistance to |
A. brassicicola |
Arabidopsis thaliana |
| (ATGPA1, GP ALPHA 1, GPA1, AT2G26300) mutant |
exhibited enhanced resistance to |
Fusarium oxysporum |
Arabidopsis thaliana |
| histone (H2B, HTB2, AT5G22880) monoubiquitination (H2Bub) |
is involved in regulating |
expression of key protein tyrosine phosphatase genes |
Arabidopsis thaliana |
| ubc1-1 mutant |
eliminates |
defense gene expression activation |
Arabidopsis thaliana |
| Verticillium dahliae toxins plus protein tyrosine phosphatase (PTP) inhibitor |
markedly increased |
depolymerization of the cortical microtubules |
Arabidopsis thaliana |
| papillae |
include |
reactive oxygen species |
|
| multiple environmental factors |
are employed to activate |
defense responses |
|
| hub1-4 mutant |
shows slightly increased transcript levels of |
ARABIDOPSIS THALIANA PROTEIN TYROSINE PHOSPHATASE 1 (ATPTP1, PTP1, AT1G71860) |
Arabidopsis thaliana |
| transcript levels of protein tyrosine phosphatase (PTP) genes, including (ATPTP1, PTP1, AT1G71860) and (AtPFA-DSP5, PFA-DSP5, AT5G16480) |
a slight increase was observed in |
mutants after Verticillium dahliae toxin treatment |
Arabidopsis thaliana |
| camalexin |
is toxic to |
green peach aphid (GPA) |
Arabidopsis thaliana; green peach aphid |
| Arabidopsis defenses |
have been associated with |
deterrence of insect herbivores |
Arabidopsis thaliana |
| gene-for-gene interaction |
induces responses similar to |
elicitor-induced responses |
|
| victorin |
induces |
respiratory burst |
|
| PR1b |
is |
rice defense gene |
Oryza sativa |
| 3-methyladenine (3-MA) treatment |
alleviates the effects of |
MeATG8b overexpression |
Manihot esculenta |
| MeATG8b overexpression |
alleviates the effect of |
MeHSP90.9 silencing |
Manihot esculenta |
| MeATG8b-silenced cassava leaves |
show significantly less |
callose depositions |
Manihot esculenta |
| MeRAR1 overexpression |
displays significantly more |
callose depositions |
Manihot esculenta |
| MeHSP90.9-MeSGT1-MeRAR1 chaperone complex |
is essential for |
autophagy signaling-mediated disease resistance |
Manihot esculenta |
| ubc1-1/ubc2-2 double mutant |
shows reduction of |
hydrogen peroxide (H2O2) production |
Arabidopsis thaliana |
| histone (H2B, HTB2, AT5G22880) monoubiquitination (H2Bub) |
may be positive regulator of |
expression of protein tyrosine phosphatase (PTP) genes |
Arabidopsis thaliana |
| histone (H2B, HTB2, AT5G22880) monoubiquitination (H2Bub) |
has a positive regulatory role in |
defense response against Verticillium dahliae toxins |
Arabidopsis thaliana |
| (SIB1, AT3G56710) |
simulates the DNA-binding and transcriptional activity of |
(ATWRKY33, WRKY33, AT2G38470) |
Arabidopsis thaliana |
| victorin |
induces |
ethylene production |
|
| pathogenesis-related (PR) genes |
are |
hallmark of plant defense response |
|
| W-box DNA cis-element |
is often overrepresented within promoters of |
up-regulated defense genes |
Arabidopsis thaliana |
| (ATWRKY11, WRKY11, AT4G31550) and (ATWRKY17, WRKY17, AT2G24570) |
are negative regulators of |
(ATKC1, AtLKT1, KAT3, KC1, AT4G32650) |
Arabidopsis thaliana |
| MeHSP90.9 overexpression |
displays significantly more |
callose depositions |
Manihot esculenta |
| virus-induced changes in plant volatile release |
requires identification of |
molecular basis |
|
| (CYP705A1, AT4G15330) and arabidiol synthase gene ABDS transcript levels |
increase when roots are infected with |
root-rot pathogen Pythium irregulare |
Arabidopsis thaliana |
| Metabolomics analysis of Brachypodium distachyon roots |
revealed |
initial defense activation by beneficial Azospirillum brasilense |
Brachypodium distachyon |
| disease susceptibility responses to ToxA |
are similar to |
defense responses typically associated with resistance |
Triticum aestivum |
| post-translational regulation of cell wall invertase (INV) activity |
participates in |
plant defense |
|
| spray inoculation of bacteria onto (AtRIN4, RIN4, AT3G25070) (RPM1, RPS3, AT3G07040) (RPS2, uS2C, ATCG00160) plants |
resulted in significantly enhanced |
disease resistance |
Arabidopsis thaliana |
| lignification |
occurs during |
plant defense response |
|
| PAL |
is |
rice defense gene |
Oryza sativa |
| victorin |
induces |
phytoalexin accumulation |
|
| Pst infection |
suppressed |
callose deposition |
Arabidopsis thaliana |
| Arabidopsis top mutants |
are more susceptible to |
P. syringae pv. tomato DC3000 avrRpt2 and avrRpm1 |
Arabidopsis thaliana |
| MeHSP90.9 |
interacts with |
suppressor of the G2 allele of (ASK1, ATSKP1, SKP1, SKP1A, UIP1, AT1G75950) (MeSGT1) |
Manihot esculenta |
| MePR1 and MePR2 |
positively modulate |
plant disease resistance |
Manihot esculenta |
| acarbose-mediated increase in susceptibility |
is independent of |
salicylic acid-regulated defense pathway |
Arabidopsis thaliana |
| (AtRIN4, RIN4, AT3G25070) |
genetically acts as negative regulator of |
disease resistance |
|
| pathogen infection |
causes repression of |
invertase inhibitor expression |
Arabidopsis thaliana |
| released NLR proteins |
activate |
hypersensitive responses |
Zea mays |
| aphid-induced changes in plant volatile release |
requires identification of |
molecular basis |
|
| (CAMTA3, SR1, AT2G22300) loss-of-function mutants |
are hyper-resistant to |
bacterial pathogens |
Arabidopsis thaliana |
| MeRAR1 |
is upregulated upon |
pathogen infection |
Manihot esculenta |
| MeATG12 overexpression |
alleviates the effect of |
geldanamycin (GDA) treatment |
Manihot esculenta |
| MeATG8c overexpression |
displays significantly more |
callose depositions |
Manihot esculenta |
| 3-methyladenine (3-MA) treatment |
alleviates the effect of |
MeHSP90.9 overexpression on MePR1/2 transcripts |
Manihot esculenta |
| camalexin |
accumulates upon infection with |
plant pathogens |
Arabidopsis thaliana |
| non-uniform pathogen-induced modification |
may result in compartmentalized |
host response |
|
| MeATGs-mediated autophagy |
functions downstream of and is essential for |
MeHSP90.9-MeSGT1-MeRAR1 chaperone complex-mediated disease defense response |
Manihot esculenta |
| salicylic acid (SA) |
induces rapid expression of |
WRKY genes |
|
| Arabidopsis thaliana lms-1 pad3-1 pmr4-1 mutants |
were previously shown to be susceptible when |
wounded |
Arabidopsis thaliana |
| single avirulent larva |
induces changes leading to minimal staining in |
resistant H9-Iris plants |
|
| GDSL-motif lipase/hydrolase mRNA |
shows sudden 51-fold increase at 1 DAH in resistant plants |
resistant plants at 1 DAH |
|
| polygalacturonase inhibitor |
displays differential expression |
mRNA levels |
|
| bacterial multiplication |
is significantly increased in |
(FHY2, FRE1, HY8, PHYA, AT1G09570) (HY3, OOP1, PHYB, AT2G18790) mutant compared with wild-type under continuous light (CL) |
Arabidopsis thaliana |
| MeSGT1-silenced cassava leaves |
show significantly less |
MePR1 and MePR2 transcripts |
Manihot esculenta |
| 3-methyladenine (3-MA) treatment |
eliminates the difference in |
flg22-induced reactive oxygen species (ROS) burst |
Manihot esculenta |
| lichenases |
are down-regulated |
expression levels |
|
| invaders |
are able to bypass |
defense response |
|
| induced accumulation of sakuranetin |
was detected in |
leaves infected by Xanthomonas oryzae |
Oryza sativa |
| diferulates |
are involved in |
plant protection against pathogen invasion |
|
| defense-associated responses |
characterized by production of |
jasmonic acid (JA) |
|
| (CAMTA3, SR1, AT2G22300) |
may regulate transcriptionally |
WRKY genes |
Arabidopsis thaliana |
| callose deposition at sieve plates and plasmodesmata |
is a common defense in response to |
pathogens and insect feeding |
|
| aspartic protease Constitutive Disease Resistance 1 |
generates |
systemin-like peptides |
Arabidopsis thaliana |
| source tissues |
are turned into |
strong carbohydrate sink |
|
| Phe pre-treatment |
results in significantly lower ROS accumulation after infection compared to |
non-treated flowers |
Chrysanthemum morifolium |
| MeSGT1 |
is upregulated upon |
pathogen infection |
Manihot esculenta |
| general downstream responses |
include |
expression of digestion inhibitors |
|
| plant resistance |
is induced by |
pathogen infection |
|
| ROS |
are major signaling molecules that have repeatedly linked |
defense and proteolytic pathways |
Arabidopsis thaliana |
| Phenylalanine ammonia lyase 1 (AevPAL1) overexpression lines 15 and 18 |
show significantly less |
number of cereal cysts formed in soil |
Triticum aestivum |
| pure HAMPs |
frequently activates |
general downstream responses |
|
| wild-type Arabidopsis |
shows strongly induced |
(AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) expression level |
Arabidopsis thaliana |
| hub2-2 mutant |
eliminates |
defense gene expression activation |
Arabidopsis thaliana |
| transcript levels of protein tyrosine phosphatase (PTP) genes, including (ATPTP1, PTP1, AT1G71860) and (AtPFA-DSP5, PFA-DSP5, AT5G16480) |
were strongly increased in the wild type after Verticillium dahliae toxin treatment |
wild type plants after Verticillium dahliae toxin treatment |
Arabidopsis thaliana |
| pattern recognition receptors (PRRs) |
are proposed to be involved in |
nonhost resistance in plant species distantly related to the natural host |
Arabidopsis thaliana |
| synergistic relationship between ATP and JA |
is involved in |
plant pathogen resistance |
|
| genes controlling cell wall modification |
play a role in |
plant defense strategies to contain the infected area |
Arabidopsis thaliana |
| Gβ subunit |
is |
positive regulator in disease resistance |
Arabidopsis thaliana |
| 3-methyladenine (3-MA) treatment |
decreases |
disease resistance |
Manihot esculenta |
| defense responses |
includes |
generation of reactive oxygen species |
|
| plants |
perceive |
herbivore attack |
|
| disease susceptibility responses to ToxA |
are similar to responses in |
classical gene-for-gene interaction |
Triticum aestivum |
| (ATWRKY7, WRKY7, AT4G24240) |
is suggested to have negative regulatory role in |
plant defense responses against bacterial pathogens |
Arabidopsis thaliana |
| paralogous genes |
are expressed when plants are stimulated by |
pathogen infection |
|
| Phenylalanine ammonia lyase 1 (AevPAL1) overexpression lines 15 and 18 |
show significantly less |
number of cereal cyst nematodes (CCNs) penetrating into roots at 3 dpi |
Triticum aestivum |
| Rp1-D |
confers race-specific resistance to |
Puccinia sorghi |
Zea mays |
| storage tissue location and in situ release |
can confer |
selectivity to insects |
|
| TIBA treatment of axr1-12 and axr2-1 mutants and NahG plants |
does not result in further enhancement of susceptibility to |
Pectobacterium cucumerina |
Arabidopsis thaliana; Pectobacterium cucumerina |
| treatment of detached leaves with Pseudomonas spp. |
results in significant reduction of |
grey mould disease |
Vitis vinifera |
| kaempferol 1 (kaempferol 3-O-[6"-O-rhamnosyl-glucoside]-7-O-rhamnoside) |
exhibited steady-state level in |
both PI and PU tissues after infection |
Arabidopsis thaliana |
| Capsicum chinense (AtPR4, HEL, PR-4, PR4, AT3G04720) protein |
accumulates during |
necrogenic reaction induced by Potato virus X |
Capsicum chinense |
| glucanases |
belong to family of |
β-1,3-glucanases (glucan endo-1,3-β-glucosidases) |
|
| (ATWRKY11, WRKY11, AT4G31550) and (ATWRKY17, WRKY17, AT2G24570) |
are negative regulators of |
(ATWRKY70, WRKY70, AT3G56400) |
Arabidopsis thaliana |
| invertase inhibition |
impacts |
spatial and temporal dynamics of repression of photosynthesis |
Arabidopsis thaliana |
| Xanthomonas oryzae infection |
enhanced expression of |
genes encoding biosynthetic enzymes such as chalcone synthase and phenylalanine ammonia-lyase |
Oryza sativa |
| genes mediating lesion phenotype via plant defense machinery interaction |
mediate phenotype via interaction with |
plant defense machinery |
Arabidopsis thaliana; Zea mays; Oryza sativa |
| paralogous genes |
are expressed when plants are stimulated by |
herbivory |
|
| microbial pathogenicity |
understanding is essential to improve |
plant biotechnologies and crop protection |
|
| rice qualitative resistance to Xanthomonas oryzae pv. oryzae (Xoo) |
is based on |
major disease resistance (MR) genes |
Oryza sativa |
| general downstream responses |
include |
oxidative stress |
|
| GmGBP dual functionality (binding and endoglycosidic activity) |
allows |
GmGBP to potentially release fragments from microbial cell walls that it can recognize, thereby initiating defense responses |
Glycine max |
| (ATRP1, RP1, AT4G21210) |
is |
nucleotide binding Leu-rich-repeat (NLR) protein |
Zea mays |
| 13-HPOT |
seems to be accumulated, perhaps as |
protective compound or signal molecule |
|
| Rp1-D21 |
confers |
autoactive lesion phenotype |
Zea mays |
| Arabidopsis plants lacking chaperonin 60 subunit β 1 (CPN60B, Cpn60beta1, CPNB1, LEN1, AT1G55490) |
express |
SAR in the absence of pathogens |
Arabidopsis thaliana |
| community collapse |
leads to |
loss of plant protection |
|
| plant extracellular vesicles (EVs) |
play a role in |
defense response against infecting pathogens |
|
| endogenous high salicylic acid (SA) level |
is consistent with |
improved cereal cyst nematode (CCN) resistance in Phenylalanine ammonia lyase 1 (AevPAL1)-transgenic wheat |
Triticum aestivum |
| oxidative burst |
is |
one of the fastest reactions |
|
| 13-hydroxide of linolenic acid (13-HOT) |
treatment induces expression of |
pathogenesis-related protein |
|
| MeRAR1-silenced cassava leaves |
show significantly less |
callose depositions |
Manihot esculenta |
| MeATG8c overexpression |
displays higher |
MePR1 and MePR2 transcripts |
Manihot esculenta |
| MeATG8c-silenced cassava leaves |
show significantly lower levels of |
flg22-induced reactive oxygen species (ROS) burst |
Manihot esculenta |
| ZmMC9 |
does not suppress |
HR in N. benthamiana mediated by Rp1-D21 |
Nicotiana benthamiana |
| 3-methyladenine (3-MA) treatment |
alleviates the effects of |
MeATG12 overexpression |
Manihot esculenta |
| MeATG8e-silenced cassava leaves |
show significantly lower levels of |
flg22-induced reactive oxygen species (ROS) burst |
Manihot esculenta |
| pathogen infection |
disrupts |
protein interaction |
Zea mays |
| chitinase (AtPR4, HEL, PR-4, PR4, AT3G04720) |
is |
protein family represented on microarray |
|
| camalexin |
does not contribute to resistance against |
biotrophs |
Arabidopsis thaliana |
| monosaccharide transporters |
are presumed to be recruited to provide energy to |
fight invasion |
|
| systemin-like peptides |
induce |
plant defense response and systemic acquired resistance (SAR) |
Arabidopsis thaliana |
| active defense responses |
restrict |
pathogen entry |
|
| pathogen elicitors |
induces rapid expression of |
WRKY genes |
|
| Arabidopsis (ATWRKY70, WRKY70, AT3G56400) mutations |
enhance plant susceptibility to |
Erwinia carotovora |
Arabidopsis thaliana |
| priming |
is |
enhanced capacity to express infection-induced basal defences |
|
| elicitor molecules |
enhance resistance against |
Plasmopara viticola |
Vitis vinifera |
| V. rupestris cell line |
shows faster peak response to |
Harpin elicitor |
Vitis rupestris |
| MeRAR1-silenced cassava leaves |
show significantly less |
MePR1 and MePR2 transcripts |
Manihot esculenta |
| MeRAR1 overexpression |
displays higher |
MePR1 and MePR2 transcripts |
Manihot esculenta |
| MeHSP90.9 overexpression |
confers improved |
disease resistance |
Manihot esculenta |
| MeHSP90.9 chaperone complex-MeATGs module |
mediates |
immune responses |
Manihot esculenta |
| aphid salivary proteins |
inhibit |
plant defenses |
|
| (ATWRKY25, WRKY25, AT2G30250) overexpression |
enhances susceptibility to |
bacterial pathogen |
Arabidopsis thaliana |
| (BARS1, PEN2, AT4G15370) |
is proposed to activate |
toxin that poisons fungal penetration pegs |
Arabidopsis thaliana |
| phytoalexins |
were examined in |
leaves of intact plantlets |
Vitis vinifera |
| spatial differences in secondary metabolite accumulation |
are largely |
quantitative rather than qualitative |
Arabidopsis thaliana |
| ROS accumulation in (CAT2, AT4G35090) and Col-0 |
was analyzed in |
response to bacterial infection |
Arabidopsis thaliana |
| cryptogein |
has effects on |
hypersensitive response in tobacco |
Nicotiana tabacum |
| JA and ET |
may play a positive role in |
some aspects of Arabidopsis responses to P. syringae |
Arabidopsis thaliana |
| screening of mutant banks of Arabidopsis thaliana |
has allowed unraveling of |
mechanisms plants use to defend against microbe attack |
Arabidopsis thaliana |
| hypersensitive reaction (HR) |
involves formation of |
necrotic local lesions |
Capsicum chinense |
| xyloglucanase XEG1 |
binding to RXEG1 triggers |
cell death |
|
| stilbenic compounds |
are accumulated in response to |
elicitors |
Vitis vinifera |
| monosaccharide transporters |
play roles in |
plant defense response |
|
| Heterodera schachtii syncytium |
may establish a strong carbohydrate sink independently from |
general plant defense response pathway |
Arabidopsis thaliana |
| Pst (ΔavrPtoB) complemented with AvrPtoB WT or AvrPtoB S335A infection |
exhibited levels of callose deposition similar to |
Pst infection |
Arabidopsis thaliana |
| burst in ROS synthesis |
modifying proteins for degradation and prompting |
retrograde defense signaling |
Arabidopsis thaliana |
| pathogen inoculation |
rapidly activates |
PAMP-induced defense responses |
Arabidopsis thaliana |
| aniline-blue staining pattern of Ler-0 (which does not contain (RLM1, AT1G64070) Col) |
showed no difference compared to |
aniline-blue staining pattern of Col-0 |
Arabidopsis thaliana |
| increased penetration frequency of mutant |
indicates independence from |
resistance genes (RLM1, AT1G64070) Col and RLM2 Ler |
Arabidopsis thaliana |
| L. maculans fungal mutant A22 |
elicited stronger hypersensitive response than |
wild-type L. maculans isolate (IBCN18) |
Leptosphaeria maculans; Arabidopsis thaliana |
| increased deposition of aniline-blue-staining material |
indicates |
hypersensitive response |
Arabidopsis thaliana; Leptosphaeria maculans |
| sinapoyl malate content decrease |
was not |
significant |
Arabidopsis thaliana |
| sinapoyl malate levels |
remained unchanged |
between Col-0 and (CAT2, AT4G35090) mutants |
Arabidopsis thaliana |
| resistant plants |
have smaller neutral red staining features than |
susceptible plants |
|
| a single dominant gene in A17 |
controls |
BGA-induced lesion response |
Medicago truncatula |
| MeATG12 overexpression |
displays significantly more |
callose depositions |
Manihot esculenta |
| pathogen effectors |
trigger |
plant immunity |
|
| geldanamycin (GDA) treatment |
decreases |
disease resistance |
Manihot esculenta |
| salicylic acid (SA) |
is involved in |
plant defense responses to nematodes |
|
| plants |
perceive |
injury |
|
| rearrangement of the cortical microtubule (MT) network |
has been observed during |
pathogenic attack |
|
| Arabidopsis (ATWRKY70, WRKY70, AT3G56400) mutations |
enhance plant susceptibility to |
Erysiphe cichoracearum |
Arabidopsis thaliana |
| (ATWRKY18, WRKY18, AT4G31800) (ATWRKY40, WRKY40, AT1G80840) and (ATWRKY60, WRKY60, AT2G25000) |
function partially redundantly as negative regulators in plant resistance against |
fungal pathogen Erysiphe cichoracearum |
Arabidopsis thaliana |
| wounding |
triggers production of |
phytoalexins |
|
| defence responses in grapevine |
comprise |
oxidative burst |
Vitis vinifera |
| 4-hydroxybenzoylcholine |
was exception to |
indolic compounds in cluster A |
Arabidopsis thaliana |
| PMMoV-S (Spanish strain) |
induces |
hypersensitive reaction (HR) |
Capsicum chinense |
| Arabidopsis (ATWRKY70, WRKY70, AT3G56400) mutations |
enhance plant susceptibility to |
necrotrophic pathogens |
Arabidopsis thaliana |
| Arabidopsis (ATWRKY11, WRKY11, AT4G31550) mutations |
enhance basal plant resistance to |
virulent Pseudomonas syringae strains |
Arabidopsis thaliana |
| grapevine plants |
express defence mechanisms in response to |
elicitor molecules |
Vitis vinifera |
| stilbenic compounds |
are accumulated in response to |
UV radiation |
Vitis vinifera |
| inducible plant defence responses |
may activate |
resistance |
|
| total SA levels in PU tissues |
showed lower but significant increase at |
24 hpi |
Arabidopsis thaliana |
| malate efflux from roots triggered by foliar infection with Pseudomonas syringae |
is triggered by |
foliar infection with Pseudomonas syringae |
Arabidopsis thaliana |
| barley HvWRKY2 |
function as PAMP-inducible suppressors of |
basal defense |
Hordeum vulgare |
| phytoalexins |
were examined in |
suspension-cultured cells of grapevine |
Vitis vinifera |
| three kaempferol derivatives and sinapoyl malate |
belonged to |
cluster C |
Arabidopsis thaliana |
| +3 leaves fed with 500 μM scopoletin |
developed significantly smaller lesions than |
control leaves |
Nicotiana attenuata |
| SA-mediated defence responses and JA/ET pathway |
utilize |
separate signal pathways |
|
| ethylene (ET) |
is responsible for elicitation of |
defences against herbivores |
|
| extracellular alkalinization |
is |
earliest physiological response |
|
| induction of AtWRKY33-mediated defence genes |
takes place in |
infected plant cells and surrounding areas |
Arabidopsis thaliana |
| caffeoyl CoA O-methyltransferase (CCoAOMT) and hydroxycinnamoyltransferase |
work as guardees in the plant defense response through formation of a complex with |
(ATRP1, RP1, AT4G21210) |
Zea mays |
| R gene recognition of effectors |
triggers |
defense responses |
|
| associated symbiotic organisms |
can enhance |
plant resistance to biotic stresses |
|
| generation of (AOS, CYP74A, DDE2, AT5G42650) |
is one of |
earliest events produced in cell suspension cultures in response to rhizobacterial elicitors |
Vitis vinifera |
| hydrogen peroxide |
is needed for |
strengthening of the cell walls and cell wall protein cross-linking |
|
| cv. 'Pinot Noir' cell line |
shows delayed peak response to |
Harpin elicitor |
Vitis vinifera |
| guard cell collapse |
was never observed in |
this study |
Arabidopsis thaliana |
| unknown compounds with Rt 29.15 min, Rt 30.87 min, and Rt 31.36 min |
were only detected in |
PI tissues |
Arabidopsis thaliana |
| most metabolites induced at 10 hpi in cluster B |
were also induced at |
24 hpi |
Arabidopsis thaliana |
| accumulation of tryptophan |
was less abundant in |
PI tissues of (CAT2, AT4G35090) leaves than in PI tissues of Col-0 leaves |
Arabidopsis thaliana |
| local pre-inoculation with Pseudomonas fluorescens CHA0 |
prevented |
reduction in plant biomass in response to Fusarium graminearum infection |
Hordeum vulgare |
| (ATWRKY18, WRKY18, AT4G31800) (ATWRKY40, WRKY40, AT1G80840) and (ATWRKY60, WRKY60, AT2G25000) |
function partially redundantly as negative regulators in plant resistance against |
biotrophic bacterial pathogen Pseudomonas syringae |
Arabidopsis thaliana |
| wounding |
triggers production of |
oxidative compounds |
|
| defence responses in grapevine |
comprise |
accumulation of host-synthesized phytoalexins |
Vitis vinifera |
| hydrogen peroxide |
can diffuse across cell membranes and has been implicated in |
signalling for the establishment of downstream plant immunity events |
|
| clusters A and B |
regrouped |
secondary metabolites mainly induced in PI tissues |
Arabidopsis thaliana |
| camalexin levels |
reached |
3.04 and 6.72 μg g⁻¹ FW at 10 hpi and 24 hpi respectively |
Arabidopsis thaliana |
| plants |
defend themselves against |
pathogens |
|
| phenylalanine and adenosine |
were previously not described in |
Arabidopsis infected leaves |
Arabidopsis thaliana |
| scopolin content |
was 1.6-fold more abundant in |
PU tissues of (CAT2, AT4G35090) mutants than in PU tissues of Col-0 wild-type |
Arabidopsis thaliana |
| distribution and function of SMs in plants attacked by pathogens or herbivores |
are generally related to |
resistance and/or signalling |
|
| Pseudomonas fluorescens CHA0 |
prevents reduction in biomass of |
barley shoots |
Hordeum vulgare |
| chitinases |
is induced in plants upon |
fungal infection |
|
| resistance in Arabidopsis thaliana in L. maculans interaction |
is independent of |
ethylene signaling |
Arabidopsis thaliana |
| crude cell extracts of bacteria |
are capable of reducing |
necrotic lesions in leaves |
Vitis vinifera |
| flagellin |
has been demonstrated to act in similar way as |
MAMPs |
|
| low background NO production by suspension-cultured cells |
increased significantly when |
cells were exposed to the elicitor |
Nicotiana tabacum |
| non-pathogenic rhizobacteria |
can trigger |
induced resistance |
|
| induced resistance |
is effective against |
several, but not all pathogens |
|
| indole-3-carboxylic acid β-D-glucopyranosyl ester (I3CAGlc) |
increased gradually from |
10 h to 24 h after Pst-AvrRpm1 inoculation |
Arabidopsis thaliana |
| significant differences in secondary metabolite distribution |
were specifically in |
PI tissues |
Arabidopsis thaliana |
| MeSGT1 overexpression |
displays higher |
MePR1 and MePR2 transcripts |
Manihot esculenta |
| 3-methyladenine (3-MA) |
represses |
callose accumulation |
Manihot esculenta |
| Phenylalanine ammonia lyase 1 (AevPAL1)-silenced plants |
show significantly repressed |
pathogenesis related (PR) gene expression in roots |
Aegilops variabilis |
| Phenylalanine ammonia lyase (PAL) expression with cereal cyst nematode (CCN) treatment |
is obviously induced by |
cereal cyst nematode (CCN) treatment at 3 dpi |
Triticum aestivum |
| VvMC2 and VvMC5 |
enhanced |
HR elicited by bacterial harpin |
Vitis vinifera |
| (ATMC1, AtMCP1b, ATMCPB1, LOL3, MC1, MCP1b, AT1G02170) |
acts as positive regulator of |
HR induced by different pathogens |
Arabidopsis thaliana |
| viruses that are acquired rapidly by aphids |
induce |
volatile release |
|
| plants |
resist |
microbe invasions |
|
| barley HvWRKY1 |
function as PAMP-inducible suppressors of |
basal defense |
Hordeum vulgare |
| certain stress-induced regulatory genes such as (ATWRKY48, WRKY48, AT5G49520) |
have |
negative role in basal disease resistance |
Arabidopsis thaliana |
| OGs-induced expression of (ATPGIP1, PGIP1, AT5G06860) |
is independent of |
ethylene (ET) signaling |
Arabidopsis thaliana |
| stilbenic compounds |
are selectively accumulated in |
leaves and grape skins |
Vitis vinifera |
| Pseudomonas aeruginosa 7NSK2 |
reduces symptoms of |
Botrytis cinerea |
Vitis vinifera |
| live cells of P. aeruginosa 7NSK2 mutant KMPCH-567 |
does not provoke disease reduction |
Botrytis cinerea infection |
Vitis vinifera |
| eight unknown compounds of cluster D |
showed particular trends |
in PI and PU tissues |
Arabidopsis thaliana |
| total SA levels |
increased in |
PI tissues reaching 13.02 μg g⁻¹ FW at 24 hpi |
Arabidopsis thaliana |
| scopoletin |
was not detected in |
untreated leaves |
Arabidopsis thaliana |
| glucoside form of coumarin derivative |
was |
pre-existing form before infection |
Arabidopsis thaliana |
| scopoletin and scopolin levels |
remained quite low compared with |
SA and camalexin levels |
Arabidopsis thaliana |
| growth conditions or mock infiltrations |
do not cause |
spontaneous formation of lesions in (CAT2, AT4G35090) |
Arabidopsis thaliana |
| unknown compounds with Rt of 29.15 min and Rt of 30.87 min |
were less abundant in |
PI tissues of (CAT2, AT4G35090) leaves than in PI tissues of Col-0 leaves |
Arabidopsis thaliana |
| chitinases |
participates in plant defence against |
pathogenic fungi |
|
| microbes |
must avoid recognition and defense responses of |
plant |
|
| (CAT2, AT4G35090) mutant grown in short days |
is |
useful model system to explore endogenous oxidative stress interactions with pathogenesis responses |
Arabidopsis thaliana |
| virus-induced silencing of three WRKY genes |
compromises |
N-gene-mediated resistance to tobacco mosaic virus |
Nicotiana tabacum |
| successful penetration events through stomatal apertures |
were stopped due to |
defence response in mesophyll layer |
Arabidopsis thaliana |
| cv. 'Pinot Noir' cells treated with increased Harpin concentration |
shows accelerated and higher amplitude response |
extracellular alkalinization |
Vitis vinifera |
| chitinases |
inhibits |
fungal growth |
|
| callose deposition in epidermal and mesophyll tissues |
is not observed in |
epidermal and mesophyll tissues |
Cucumis melo |
| insect itself |
influences |
plant response after insect infestation |
Solanum tuberosum L. |
| suppressor of the G2 allele of (ASK1, ATSKP1, SKP1, SKP1A, UIP1, AT1G75950) (MeSGT1) |
interacts with |
Mla12 resistance 1 (MeRAR1) |
Manihot esculenta |
| (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) |
is |
defense-related gene |
Arabidopsis thaliana |
| Rp1-dp2 and Rp1-D |
do not confer |
HR phenotype |
Nicotiana benthamiana |
| CaMC9 |
plays positive role in |
pathogen-induced cell death |
Capsicum annuum |
| WT plants treated with 5 μM TIBA |
shows susceptibility level similar to |
control axr1-12 and axr2-1 mutants and NahG plants |
Arabidopsis thaliana |
| (ATWRKY70, WRKY70, AT3G56400) mutants |
are compromised in |
RPP4-mediated disease resistance to Hyaloperonospora parasitica |
Arabidopsis thaliana |
| pmr4-1 mutant |
is susceptible to |
L. maculans infection |
Arabidopsis thaliana |
| chitinases and glucanases |
are examples of |
pathogenesis-related (PR) proteins with hydrolytic activity |
Vitis vinifera |
| 14 compounds |
were diminished in |
PI tissues compared with PU tissues |
Arabidopsis thaliana |
| scopolin |
was present in |
appreciable amounts in untreated leaves |
Arabidopsis thaliana |
| (ATEBP, EBP, ERF72, RAP2.3, AT3G16770) |
is inducible by |
infection with Botrytis cinerea |
Arabidopsis thaliana; Botrytis cinerea |
| callose deposition in cell walls |
is not induced by |
absence of intracellular punctures by Aphis gossypii |
Cucumis melo |
| Leptinotarsa decemlineata Say |
induces differential changes in |
oxylipin synthesis |
Solanum tuberosum L. |
| MeRAR1 overexpression |
confers improved |
disease resistance |
Manihot esculenta |
| SA-mediated defence responses and JA/ET pathway |
have considerable overlap in |
cross-communicating defence processes |
|
| jasmonic acid (JA) |
is responsible for elicitation of |
defences against herbivores |
|
| oxidizer column-based NO detector |
showed |
increase in NO production by cryptogein-treated suspension-cultured cells of tobacco |
Nicotiana tabacum |
| DAF-FM |
showed |
increase in NO production by cryptogein-treated suspension-cultured cells of tobacco |
Nicotiana tabacum |
| axr2-1 mutant |
exhibits enhanced susceptibility to |
necrotrophic fungi |
Arabidopsis thaliana |
| pathogen-induced WRKY proteins |
function as important positive regulators of |
plant disease resistance |
|
| pen2-1 mutant of Arabidopsis thaliana |
is defective in |
non-host responses to several pathogens |
Arabidopsis thaliana |
| localized trypan-blue-staining material |
appears in |
mutants lms1 pmr4-1 |
Arabidopsis thaliana |
| total SA levels in PU tissues at 24 hpi |
were |
2-fold higher than in MU tissues and 6-fold lower than in PI tissues |
Arabidopsis thaliana |
| camalexin levels in PU tissues |
were rather low at |
10 hpi |
Arabidopsis thaliana |
| hypersensitive reaction (HR) |
results in restriction of |
virus at primary infection sites |
Capsicum chinense |
| localized fluorescence after aniline-blue staining |
suggests importance of |
callose in resistance response to L. maculans |
Arabidopsis thaliana |
| resistance in Arabidopsis thaliana in L. maculans interaction |
is independent of |
salicylic acid signaling |
Arabidopsis thaliana |
| Pseudomonas putida WCS358 |
did not induce resistance in |
radish |
|
| unknown compound with Rt of 32.65 min |
is suggested to have |
early role in PI tissues |
Arabidopsis thaliana |
| spatial patterns of (ATICS1, EDS16, ICS1, SID2, AT1G74710) and (CYP71B15, PAD3, AT3G26830) expression |
in PI and PU tissues are similar to |
those of SA and camalexin accumulation |
Arabidopsis thaliana |
| Myzus persicae infestation |
induces |
appearance of autofluorescence and deposition of lignin |
Cucumis melo |
| nitric oxide (NO) |
plays a role in |
disease resistance |
|
| parasite endophyte encapsulated in lignin |
prevents the parasite from abstracting |
almost any of the host's resources |
Leucanthemum vulgare; Rhinanthus minor |
| passive barriers |
restrict |
pathogen entry |
|
| (ATWRKY29, WRKY29, AT4G23550) gene overexpression |
constitutively activates |
plant defense response against bacteria |
Arabidopsis thaliana |
| Arabidopsis thaliana |
contains |
49 out of 72 WRKY genes differentially regulated after pathogen infection or SA treatment |
Arabidopsis thaliana |
| (ATWRKY48, WRKY48, AT5G49520) |
is highly responsive to |
avirulent strain of Pseudomonas syringae |
Arabidopsis thaliana |
| accumulation of secondary metabolites belonging to cluster B |
was induced earlier than |
that of cluster A |
Arabidopsis thaliana |
| unknown compounds with Rt of 29.15 min and Rt of 30.87 min |
were not detected in |
PU tissues |
Arabidopsis thaliana |
| incompatible interaction |
is |
resistant H9-Iris wheat infested with Biotype L larvae |
|
| GhNDR1 |
improves |
cotton (G. hirsutum) resistance to V. dahliae |
Gossypium hirsutum |
| NbWRKY8 |
positively regulates |
genes involved in biosynthesis of isoprenoid phytoalexins |
Nicotiana benthamiana |
| events observed in resistant and susceptible genotypes after Myzus persicae infestation |
should be triggered in response to |
cell damage |
Cucumis melo |
| callose deposition in cell walls |
is observed in |
aphid resistant and susceptible melon genotypes |
Cucumis melo |
| Myzus persicae Sulzer |
induces differential changes in |
volatile compound release |
Solanum tuberosum L. |
| failure of haustorium formation in (ATMTK, MTK, MTK1, AT1G49820) plants |
was associated with augmented frequencies of |
effective cell wall apposition (CWA) |
Hordeum vulgare; Blumeria graminis f. sp. hordei |
| PR genes expression |
significantly increased in GP and Mtk plants upon |
fungal inoculation |
Hordeum vulgare |
| cell suspension challenged with Bacillus phytofirmans PsJN |
shows no cell death over |
time-course |
Vitis vinifera |
| trypan-blue staining |
indicates intense hypersensitive response in |
mutant pen1-1 |
Arabidopsis thaliana |
| killed cells of P. aeruginosa 7NSK2 mutant KMPCH-567 |
induce slight but significant protective effect against |
Botrytis cinerea |
Vitis vinifera |
| 10 compounds |
showed no change in |
PI and PU tissues |
Arabidopsis thaliana |
| Capsicum chinense (AtPR4, HEL, PR-4, PR4, AT3G04720) protein |
is induced during |
compatible interaction |
Capsicum chinense |
| single virulent larva |
induces larger area of permeability on |
susceptible plant |
|
| resistant plants at 3 DAH |
have red stain restricted to epidermal cells and vascular bundles |
epidermal cells and vascular bundles |
|
| plant responses to herbivory |
include |
JA-mediated responses |
|
| (ATEXO70B2, EXO70B2, AT1G07000) |
has more important role in |
cell wall apposition formation related to plant defence |
Arabidopsis thaliana |
| GhMKK2 |
improves |
cotton (G. hirsutum) resistance to V. dahliae |
Gossypium hirsutum |
| plant responses to herbivory |
include |
SA-mediated responses |
|
| perception of PAMPs or effectors |
initiates |
series of physiological processes |
|
| aphid infestation |
induces activity of |
phenylalanine ammonia-lyase |
|
| appearance of autofluorescence and deposition of lignin |
occurs |
24 h after Myzus persicae infestation |
Cucumis melo |
| wheat cultivar Xingzi9104 seedlings inoculated with Pst avirulent race CYR23 |
exhibit |
immune or few necrotic flecks phenotype (Scale 0–1) |
Triticum aestivum |
| pea plants (Pisum sativum) colonized by R. leguminosarum (strain P.SOM) |
exhibit significantly greater resistance to |
root holoparasite Orobanche crenata |
Pisum sativum; Rhizobium leguminosarum; Orobanche crenata |
| trypan-blue staining |
indicates intense hypersensitive response in |
mutant pen2-1 |
Arabidopsis thaliana |
| induced resistance |
is |
enhanced defensive capacity of plants |
|
| compound (12) |
showed diminished levels in |
PI tissues compared with PU tissues |
Arabidopsis thaliana |
| scopoletin and scopolin levels |
compared with |
mock treatments |
Arabidopsis thaliana |
| Nicotiana tabacum cv Xanthi cells in 24-well plates |
treated with |
cryptogein |
Nicotiana tabacum |
| fluorescent probes |
demonstrated |
rapid burst of NO production in response to cryptogein treatment |
Nicotiana tabacum |
| Arabidopsis thaliana |
has proven valuable for |
dissecting mechanisms of non-host resistance of plants |
Arabidopsis thaliana |
| aniline-blue staining |
enables determination of |
callose accumulation |
Arabidopsis thaliana |
| accumulation of secondary metabolites belonging to cluster B |
was observed mainly in |
PI tissues |
Arabidopsis thaliana |
| free SA accumulation rate |
was |
2-fold lower |
Arabidopsis thaliana |
| secondary metabolite distribution |
was examined in |
leaves of CATALASE2-deficient plants (CAT2, AT4G35090) infected with Pst-AvrRpm1 |
Arabidopsis thaliana |
| lectins and basic secretory proteins |
are increased in abundance in |
flax |
Linum usitatissimum |
| Leucanthemum vulgare |
encapsulating |
parasite endophyte in lignin |
Leucanthemum vulgare; Rhinanthus minor |
| proposed name AIN |
stands for |
Acyrthosiphon-induced necrosis |
Medicago truncatula |
| BPH oviposition |
counteracts |
suppression by BPH phloem-feeding of callose deposition |
Oryza sativa |
| VmR2 -siR1 expression |
inhibits |
MdLRP14 -enhanced resistance |
Malus domestica |
| MdLRP14 overexpression |
accumulated increased |
callose |
Malus domestica |
| MdPYL4 |
positively regulates |
apple resistance to V. mali |
Malus domestica; Valsa mali |
| wild-type Arabidopsis |
displays dramatic depolymerization of |
cortical microtubules (MTs) |
Arabidopsis thaliana |
| ubc1-1/ubc2-2 mutant |
eliminates |
defense gene expression activation |
Arabidopsis thaliana |
| effect of NlVgN-induced defenses on hatching rate |
was observed in |
plants expressing NlVgN |
Oryza sativa |
| hub2-2 mutant |
eliminates |
hypersensitive response-like cell death |
Arabidopsis thaliana |
| phloem-feeding by gravid BPH without oviposition ability |
reduces |
callose deposition in OsSUT2 mutants to the same level as WT rice |
Oryza sativa |
| differentially expressed genes |
were identified in |
Arabidopsis following infection with three pathogens |
Arabidopsis thaliana |
| caterpillar attack |
redirects metabolic flux away from growth and into |
defensive compounds |
|
| phospho-mimicking NcWRKY8 mutant |
overexpression induced |
expression of defence genes |
Nicotiana benthamiana |
| (ATCNGC4, CNGC4, DND2, HLM1, AT5G54250) mutant |
is also known as |
dnd2-1 |
|
| VmR2 -siR1 expression |
decreased |
reactive oxygen species (ROS) and callose |
Malus domestica |
| heliocide levels |
were not significantly different between |
plants exposed to damaged emitters and plants exposed to undamaged emitters |
Gossypium hirsutum |
| infiltration at higher cell density (10^7 CFU ml^−1) |
induces |
callose deposition |
Solanum lycopersicum |
| Pti4/5/6-overexpressing (Pti4/5/6-OE) lines |
displayed escalated |
PR expression |
Solanum lycopersicum |
| STTM- VmR2 -siR1-2 inoculation |
significantly induces |
apple defense-related genes |
Malus domestica |
| induction of negative regulator in response to signal molecules |
contributes to |
fine-tuning of defense responses |
Arabidopsis thaliana |
| pskr1-3 mutant |
reduces |
bacterial growth |
Arabidopsis thaliana |
| PSKα and probably (PSY1, AT5G58650) signaling |
act in a negative regulatory loop to prevent |
over-responsiveness to PAMPs |
Arabidopsis thaliana |
| (ACH1, ATNRT2.1, ATNRT2:1, LIN1, NRT2, NRT2.1, NRT2:1, NRT2;1AT, AT1G08090) mutant |
displays altered |
effector-triggered susceptibility |
Arabidopsis thaliana |
| caterpillar LS added to wounded plant tissues |
may suppress and/or delay |
plant responses |
Arabidopsis thaliana |
| fungal growth |
grew and spread outside the zone of inoculation in |
pskr1-2 and pskr1-3 plants |
Arabidopsis thaliana |
| defense-related phenotypes |
are due to direct effects of |
PSKα signaling |
Arabidopsis thaliana |
| partial character of the complementation |
may also support |
the impact of the second receptor (PSY1R, AT1G72300) which is not restored in these plants |
Arabidopsis thaliana |
| reactive oxygen species (ROS) |
can be used to monitor |
extent of pathogen ingress |
Arabidopsis thaliana |
| ubc1-1 mutant |
eliminates |
hydrogen peroxide accumulation |
Arabidopsis thaliana |
| Bg_9562-treated WT tomato leaves |
show |
large number of callose spots during 1 and 2 dpi |
Solanum lycopersicum |
| oxidative burst |
is |
earliest physiological response |
|
| biotrophic pathogens |
suppress |
host defence |
|
| scopoletin |
increases its level dramatically after |
fungal challenge |
|
| necrotrophic pathogens |
are controlled by |
JA/ET pathway |
|
| transcript levels of (ATWRKY33, WRKY33, AT2G38470) |
are induced rapidly and strongly in response to |
defence-associated stimuli |
Arabidopsis thaliana |
| btl1 mutant |
showed reduced accumulation of |
PATHOGENESIS-RELATED 1 (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) |
|
| biological processes associated with stress responses |
include |
production of antimicrobial compounds (e.g. phytoalexins) |
|
| ethylene (ET) |
is responsible for elicitation of |
defences against necrotrophic pathogens |
|
| uncontrolled activation of downstream signaling events |
contributes to |
defense gene induction |
|
| root growth inhibition assay |
measures |
root growth inhibition |
Arabidopsis thaliana |
| herbivory |
induces |
plant production of volatile compounds |
Plantae |