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plant-pathogen interaction

12215 relationships annotated with this phrase. Showing first 500 of 12215.
Source entity Relationship Target entity Species
LRR domains interact directly with effectors
pathogenic effectors targeting ROS scavenging proteins causes suppression of plant immunity
Avr9B triggers Cf-9B-independent cell death response Nicotiana benthamiana
p35S:PB1CP-3xHA lines showed no difference in bacterial growth of Pseudomonas syringae pv cilantro (Pci) 0788-9 Arabidopsis thaliana
Colletotrichum higginsianum relies on penetrating plant cell wall and invaginating into cell Arabidopsis thaliana
pathogens utilize diverse strategies including secretion of varied effectors subversion of plant defense responses
CfCE54 does not trigger strong response upon co-expression with Cf-9C Nicotiana tabacum
pathogen taxon explains variation in effects of AMF inoculation on aboveground plant pathogens
Fulvia fulva strain P31 causes disease on MM-Cf-9 plants Fulvia fulva; Solanum lycopersicum
fungal effector AvrPiz-t exploited ROD1-CatB mechanism
meta-analysis and glasshouse experiments emphasize importance of biological context in understanding how aboveground pathogens respond to AMF inoculation
Avr9B triggers chlorosis and/or small patch of cell death Nicotiana tabacum
changes in secondary chemicals and foliar nutrition may be possible explanation for inhibitory effect on necrotrophic pathogens
TW65_01570 is not recognised by Cf-9B Solanum lycopersicum
Fusarium oxysporum f. sp. lycopersici (Fol) invades tomato plants through vascular bundles Solanum lycopersicum; Fusarium oxysporum f. sp. lycopersici
young Nicotiana benthamiana plants are highly susceptible to Agrobacterium tumefaciens Nicotiana benthamiana
Ogliarola salentina cultivar is highly susceptible to Xylella fastidiosa infection Olea europaea
Avr9B-like proteins from S. lycopersici and P. fuligena trigger strong cell death response in absence of Cf-9B in N. benthamiana Nicotiana benthamiana
intrinsic properties of host plants, AMF, and plant pathogens may shape disease impact across ecosystems
sequence modifications in secreted pathogen proteins circumvent host defense responses
fungal sRNAs can act as potent virulence factors by infiltrating the host and suppressing plant disease resistance responses Botrytis cinerea
repeat region of Avr9B is not required for Cf-9B-dependent and Cf-9B-independent responses in N. tabacum Nicotiana tabacum
Glomus had stronger negative effects on pathogens
infected roots produces toxins that cause foliar (SDS, AT1G14750) Glycine max
Alternaria citri produces polygalacturonase that acts as virulence factor in interaction with citrus Citrus spp.
directed growth along the vasculature could enable pathogen isolates to move systemically through the vasculature of the plant Arabidopsis thaliana
pathogen effectors promote pathogen nutrition acquisition and reproduction
repertoire of effectors present in a pathogen largely defines compatibility with host genotype
virulence toward Rpv3.1 was associated with deletion of g164 and g165 Plasmopara viticola; Vitis vinifera
PB1CP negatively regulates resistance against Colletotrichum higginsianum Arabidopsis thaliana
Aboveground pathogens primarily affect photosynthesis
inoculation with mixture of AMF species may have different effect on pathogens than inoculation with single AMF species
arbuscular mycorrhizal fungi (AMF) inoculation negatively affects aboveground plant pathogens
CfCE54 from strain 0WU triggers Cf-9B-dependent cell death response Nicotiana tabacum
AvrPiz-t exploitation of ROD1-CatB mechanism promotes pathogen virulence
arbuscular mycorrhizal fungi (AMF) inoculation did not affect biotroph-mediated diseases
Arabidopsis thaliana / Botrytis cinerea (Botrytis) pathosystem is used as model system for studying plant-pathogen interactions Arabidopsis thaliana; Botrytis cinerea
secreted version of Avr9B with repeat region deleted maintained ability to trigger Cf-9B-independent chlorosis/cell death and Cf-9B-dependent cell death response Nicotiana tabacum
AMF inoculation exerted contrasting effects on different viruses
wheat blast disease is caused by M. oryzae Triticum aestivum; Magnaporthe oryzae
Cf-9B-independent cell death response triggered by Avr9B in N. benthamiana is not dependent on (EVR, SOBIR1, AT2G31880) Nicotiana benthamiana
p35S:PB1CP-3xHA lines showed no difference in bacterial growth of Pseudomonas syringae pv tomato (Pto) DC3000 COR− Arabidopsis thaliana
mechanisms underlying host range are not exclusive from qualitative resistance and quantitative resistance mechanisms
WT-GmBIR1 overexpression significantly increases plant susceptibility to SCN Glycine max
structural variations at avrRpv3.1 locus result in breakdown of Rpv3.1 resistance Plasmopara viticola; Vitis vinifera
MdLRP14 -OE exhibits smaller lesion areas upon V. mali infection Malus domestica
CfCE54 is Avr9B Fulvia fulva
effector proteins from avrRpv3.1 locus can effectively induce Rpv3.1-dependent cell death Vitis vinifera
Higher nitrogen (N) content in plant tissues suppresses necrotrophs such as Alternaria spp. and Fusarium spp.
necrotrophic, soil-borne fungal and oomycete pathogens represent most pathogens driving conspecific negative density dependence
rice blast disease is caused by M. oryzae Oryza sativa; Magnaporthe oryzae
g166h exhibited more consistent induction of cell death across experiments Vitis vinifera
GmBIR1 is upregulated in soybean cyst nematode (SCN) infection sites Glycine max
plant pathogens requires circumvention of host defense responses
effector proteins modulate host immune responses
RESPIRATORY BURST OXIDASE HOMOLOG D (ATRBOHD, DELT1, RBOHD, AT5G47910) plays an important role in resistance against Colletotrichum higginsianum Arabidopsis thaliana
positive effect of AMF inoculation through enhancing plant nitrogen acquisition may counterbalance negative effect of AMF inoculation through enhancing SA-dependent responses
PHYTOALEXIN DEFICIENT 3 (CYP71B15, PAD3, AT3G26830) expression is required for oligogalacturonide (OG)-induced protection against Botrytis cinerea Arabidopsis thaliana
further validation studies could reveal more plant genes that have a greater effect on quantitative resistance Arabidopsis thaliana
leaf shape influences disease progression
pb1cp mutants showed no difference in bacterial growth of Pseudomonas syringae pv cilantro (Pci) 0788-9 Arabidopsis thaliana
protection response induced by elf18 examined against Botrytis cinerea Arabidopsis thaliana
pathogen life history explains variation in effects of AMF inoculation on aboveground plant pathogens
delayed papilla formation results in increased Bgh infection Arabidopsis thaliana
fungal pathogen remains in infected roots Glycine max
variation in lesion eccentricity trait is highly dependent on interaction of plant and pathogen genotypes Arabidopsis thaliana
Cotton Verticillium wilt is caused by Verticillium dahliae Gossypium hirsutum
lesion eccentricity is controlled by variation in both pathogen and host genes Arabidopsis thaliana
lesion color is a potentially key aspect of plant-pathogen interaction for vegetable and fruit crops
sprayed inoculations revealed interactions between the lesions such that outgrowth was limited Arabidopsis thaliana
T-DNA insertion line SALK_090245C is susceptible to Phytophthora sojae Arabidopsis thaliana
Puccinia striiformis uses similar strategy to break down wheat resistance Triticum aestivum; Puccinia striiformis
specific spore concentration allows for high efficiency of lesion establishment with modest outgrowth Arabidopsis thaliana
bacterial suspensions at 5 × 10^4 cfu ml^−1 Pst is used for in-planta growth assays Arabidopsis thaliana
Pseudomonas syringae pv tomato strain DC3000 (Pst DC3000) infection modulates host responses through coronatine (COR) and the action of numerous type III effectors and programmed cell death responses
pathogen genotypes B05.10 and Supersteak show negative correlation between lesion size and eccentricity Arabidopsis thaliana
(ACD6, DEG16, AT4G14400) is the only gene associated solely with lesion greenness Arabidopsis thaliana
understanding the complete network of genes that are critical for this interaction requires a diverse range of strategies Arabidopsis thaliana
plant glutaredoxins (GRXs) were recently shown to be involved in plant/pathogen interactions
treatment with oligogalacturonides (OGs) prompts (primes) tissue to produce camalexin either more rapidly and/or at higher levels in response to Botrytis cinerea Arabidopsis thaliana
unidentified Guy11 effector(s) may be secreted to rice cells Oryza sativa; Magnaporthe oryzae
bacterial diseases such as bacterial blight of rice tend to be more serious in tropical Asia Oryza sativa
diverse field infection strategies of this pathogen means that there is no single optimal system to find the important genes
Pseudomonas syringae pv. maculicola (Psm) is pathogen used in in-planta growth assays Arabidopsis thaliana
Botrytis cinerea produces polygalacturonase that acts as virulence factor in interaction with tomato Solanum lycopersicum
Guy11 strain has evolved successful machinery to ward off the host defense and invade its host Magnaporthe oryzae
success of the pathogen in the host-pathogen interaction would depend on combination of the ability to infect local tissue and to move rapidly to distal tissue
Pseudomonas syringae pv. tomato (Pst) is pathogen used in in-planta growth assays Arabidopsis thaliana
atl31-1 atl6-1 double knockout mutant causes increased susceptibility to Pseudomonas syringae pv tomato (Pst) DC3000 Arabidopsis thaliana
miR319-mediated silencing of OsTCP21 reveals common host resistance-suppressing strategy employed by various pathogens
color and shape of the developing lesion is genetically determined by variation in the host and in the pathogen and the interaction of genetic variation in the two organisms
most studies of quantitative resistance omit lesion shape and color
all anp mutants exhibited basal susceptibility to Botrytis cinerea similar to wild type Arabidopsis thaliana
(PHYE, AT4G18130) plays a role in lesion size Arabidopsis thaliana
eccentric lesions tend to be smaller Arabidopsis thaliana
Pseudomonas syringae pv. tomato (Pst) avrRpt2 is pathogen used in in-planta growth assays Arabidopsis thaliana
correlation between OsTCPs and ROS is also observed in rice infected by Guy11 Oryza sativa; Magnaporthe oryzae
sulfur transporter functions specifically in lesion size Arabidopsis thaliana
single and double anp mutants were not protected by treatment with oligogalacturonides (OGs) or elf18 Arabidopsis thaliana
all three ANPs are required for elicitor-induced protection against Botrytis cinerea Arabidopsis thaliana
heritability of lesion eccentricity for plant-pathogen interaction is 11.1% Arabidopsis thaliana
most studies of quantitative resistance focus on pathogen biomass or lesion size measurements
protection response induced by oligogalacturonides (OGs) examined against Botrytis cinerea Arabidopsis thaliana
(COI1, AT2G39940) is associated with lesion greenness Arabidopsis thaliana
(LecRK-IX.2, AT5G65600) mutant plants are equally susceptible to Pst (ΔavrPtoB) Arabidopsis thaliana
Zea mays (maize) interacts with aflatoxin B1 (AFB1) Zea mays
defective protection in anp mutants was rescued in complemented (ANP3, AtANP3, MAPKKK12, NP3, AT3G06030) mutants expressing wild-type copy of gene Arabidopsis thaliana
lesion size trait is genetically determined by variation in the host and in the pathogen and the interaction of genetic variation in the two organisms
pathogen and MG132 co-treatment mixture is immediately infiltrated into Arabidopsis leaves Arabidopsis thaliana
gene-for-gene resistance will lead to compatible or incompatible interaction
differentially phosphorylated proteins in WT-GmBIR1 and KD-GmBIR1 achieve mostly unique downstream signaling in WT-GmBIR1 and KD-GmBIR1 response to SCN infection Glycine max
m6A-associated genes related to plant-pathogen interaction Arachis hypogaea
MdLRP14 -RNAi exhibits significantly larger lesion areas upon V. mali infection Malus domestica
brassinosteroids (BRs) favoured fungal infection Oryza sativa
transgenic lines overexpressing (MIR398B, AT5G14545) show hypersensitivity to avirulent strain Pseudomonas syringae DC3000 hrcC− Arabidopsis thaliana
atl31-1 single knockout mutant does not cause increased susceptibility to Pseudomonas syringae pv tomato (Pst) DC3000 Arabidopsis thaliana
active infections can affect many different traits within the plant host
acarbose co-infiltration in cpr6 mutant results in approximately 400% increase in bacterial growth Arabidopsis thaliana; Pseudomonas syringae
plant stress caused by pathogens reduces agricultural yields
genes with PAV variations were dramatically enriched in plant–pathogen interaction pathway (related to disease resistance; ko04626) Boehmeria nivea
Leptospaeria maculans is causal agent of foliar disease of oilseed rape Leptospaeria maculans
fungal pathogens repeatedly defeat crop resistance
pathogenic microbes have threatened plant survival
co-infiltration of acarbose and Pseudomonas syringae results in more prominent growth of bacteria Arabidopsis thaliana
antisense-mediated transcriptional silencing of cell wall invertase (cwInv) does not interfere with growth of fungal pathogen Nicotiana tabacum
calcium-dependent protein kinase upregulated in field non-acclimation (F-NA) sample
gibberellin (GA) treatment enhanced resistance in a concentration-dependent manner fungal infection resistance Oryza sativa
approximately 100 rice MR genes conferring resistance to Magnaporthe oryzae confer resistance to Magnaporthe oryzae Oryza sativa
secreted effector proteins dampen plant defense responses
acarbose co-treatment in (ATICS1, EDS16, ICS1, SID2, AT1G74710) mutant results in approximately 600% higher bacterial growth compared to bacteria-alone treatment in (ATICS1, EDS16, ICS1, SID2, AT1G74710) mutant Arabidopsis thaliana; Pseudomonas syringae
P. syringae type III effectors and phytotoxin coronatine can augment COI1-dependent pathway in plants Pseudomonas syringae
(LecRK-IX.2, AT5G65600) mutant plants are more susceptible to Pst Arabidopsis thaliana
calcium-binding protein upregulated in field non-acclimation (F-NA) sample
down-regulation of endogenous invertase inhibitor occurs during pathogen infection Arabidopsis thaliana
cell death role in plant-pathogen interactions depends on both the pathogen and its stage of growth
Gh_A12G0912 is induced by Pseudomonas syringae effector AvrB Gossypium hirsutum; Pseudomonas syringae
rice NB-LRR-type proteins play important roles in resistance to Magnaporthe oryzae Oryza sativa
acarbose-mediated increase of susceptibility is mediated by SA-independent mechanism Arabidopsis thaliana
up-regulation of cell wall invertase (cwInv) occurs during plant-pathogen interactions
competition between (LecRK-IX.2, AT5G65600) degradation and AvrPtoB phosphorylation exists in plant-pathogen interaction Arabidopsis thaliana
Pseudomonas syringae growth can be monitored in agromonas assay using both infiltration and spray inoculation Nicotiana benthamiana
plant-pathogen interaction involves molecular mechanisms of infection and defence
direct manipulation of PM H+-ATPase activity by pathogens suggests PM H+-ATPases perform multiple roles in susceptible and resistant interactions
phenotypic assays involved infection assays with different strains of the plant pathogenic bacterium Pseudomonas syringae Arabidopsis thaliana; Pseudomonas syringae
nitrile moiety can create a different covalent modification of both cysteine and serine residues
mock inoculations with water is control for pathogen infiltration assays Arabidopsis thaliana
relationships among cytoskeleton, endomembrane system, and pathogens could lead to new approaches to engineer broad-spectrum pathogen resistance
acarbose effect in (ATICS1, EDS16, ICS1, SID2, AT1G74710) mutant is similar to acarbose effect in wild-type Arabidopsis thaliana
AlphaFold 3 added functionality will prove useful to unravel extracellular plant-pathogen interactions
land plants face microbial pathogens
FLS2-flg22-BAK1 complex is resolved extracellular complex
genetic dispensability of (AXR1, AT1G05180) and (AXR2, IAA7, AT3G23050) in (CHS2, RPP4, AT4G16860) resistance suggests that SCF-mediated ubiquitination does not play a major role in restriction of biotrophic pathogens Arabidopsis thaliana
invading pathogens may actively promote expression of negative regulators through the action of certain secreted effector proteins Pseudomonas syringae
agromonas method quantifies Pseudomonas syringae growth Nicotiana benthamiana; Pseudomonas syringae
Passalora fulva is causal agent of foliar disease of tomato Passalora fulva
mobile RNAs form key components of plant responses to pathogens
non-vascular/non-seed bryophytes is used to address fundamental questions on plant health
salicylic acid (SA) application promoted pathogenicity of a necrotrophic fungal pathogen
CERK1-chitin complex is resolved extracellular complex
(ATICS1, EDS16, ICS1, SID2, AT1G74710) mutant shows higher bacterial growth when treated with acarbose and Pseudomonas syringae
Maize Rxo1 confers resistance to Burkholderia andropogonis Zea mays
Zymoseptoria tritici is causal agent of foliar disease of wheat Zymoseptoria tritici
dn-OPDA treatment inhibited pathogenicity of a necrotrophic fungal pathogen
agromonas assay allows the study of available repertoire of Pseudomonas syringae mutants and strains Pseudomonas syringae
secondary metabolite toxins play a role in triggering plant defence responses
plant molecules and processes can be co-opted to promote infection
Mycosphaerella fijiensis is causal agent of foliar disease of banana Mycosphaerella fijiensis
rice is pathosystem with Xanthomonas oryzae pv. oryzae
MR genes confer resistance to Xanthomonas oryzae pv. oryzae (Xoo) Oryza sativa
Botrytis cinerea infection was followed by viewing disease symptoms
levels of secondary metabolites in cluster C were either not affected or decreased during infection Arabidopsis thaliana
effector proteins modulate plant innate immunity
plant pathogenic fungi cause crop diseases
complex signaling networks result in susceptibility or resistance
combination of substrate identification approaches and genetically encoded sensors enables answering of questions regarding role of pathogen apoplastic proteases in shaping plant–pathogen interactions
single-cell RNA sequencing has been applied to study Arabidopsis thaliana infections with Colletotrichum higginsianum Arabidopsis thaliana; Colletotrichum higginsianum
transformants A22c11, A22c12, and A22c18 caused hypersensitive response on Arabidopsis thaliana Col-0 similar to isolate A22 Leptosphaeria maculans; Arabidopsis thaliana
plants face diverse microbial pathogens
gene-for-gene recognition results in incompatible interaction
Small molecules in the apoplast are abundant in apoplast
single carbon or oxygen modifications to a core terpene alter effector regulation
chloroplasts and peroxisomes gather near haustorium upon P. infestans infection
(ATSAGT1, GT, SAGT1, SGT1, UGT74F2, AT2G43820) and (ATRAR1, PBS2, RAR1, RPR2, AT5G51700) do not help to restrict necrotrophic fungal infection Arabidopsis thaliana
(ATSGT1B, EDM1, ETA3, RPR1, SGT1B, AT4G11260) mutant correlates with increased colonization of leaves compared to wild-type Col-0 Arabidopsis thaliana
genetic additivity of (ATSGT1B, EDM1, ETA3, RPR1, SGT1B, AT4G11260) axr1-3 mutants points to minor but detectable contribution of (AXR1, AT1G05180) to oomycete resistance Arabidopsis thaliana
constitutive overexpression of (ATWRKY48, WRKY48, AT5G49520) manifests as development of disease symptoms Arabidopsis thaliana
P. syringae type III effector can compromise defense-related callose deposition in the host cell wall Pseudomonas syringae
powdery mildew fungi induce re-organization of host cell architecture and physiology
RXEG1-XEG1-BAK1 complex is resolved extracellular complex
Fusarium oxysporum or Verticillium longisporum might synthesize jasmonoyl-isoleucine (JA-Ile) or JA-Ile mimic Arabidopsis thaliana
Alternaria alternata f. sp. mali strain (ALT1, AT1G35290) causes Alternaria leaf spot Malus domestica
Verticillium dahlia causes economically important wilt disease in several crops Verticillium dahlia
terpenes likely have different mechanistic targets
effectors are powerful tools to modulate plant defence and developmental processes
seedlings on chemical-free MS plates are inoculated with Pseudomonas cucumerina suspension or water
certain virulence factors from the bacterial pathogen promote parasitism Pseudomonas syringae
salicylic acid (SA) accumulates in compatible interactions
fully expanded leaves (+3 leaves) are more susceptible to Alternaria alternata Nicotiana attenuata
+3 leaves are more susceptible to Alternaria alternata Nicotiana attenuata
glucose transport is enhanced after infection wheat–powdery mildew interaction Triticum aestivum; Blumeria graminis
Pseudomonas syringae pv. tomato DC3000 polymutants can be tested in agromonas assays Nicotiana benthamiana
positive contribution of auxin signaling to defense against necrotrophic fungi may render this pathway vulnerable to manipulation by pathogens Arabidopsis thaliana
metabolite profiling method was used for Arabidopsis leaves infected with Pseudomonas Arabidopsis thaliana; Pseudomonas syringae
MS medium-grown plants were inoculated with Botrytis cinerea
wild-type virulent and avirulent Pst DC3000 strains enhance (ATWRKY48, WRKY48, AT5G49520) expression Pseudomonas syringae
vascular wilt diseases occur in a wide range of host crops
invertase activity is increased in plant–biotroph interactions
soil-grown plants were inoculated by drop inoculation with 5 μl of 4 × 10^5 spores ml^-1 Pectobacterium cucumerina suspension
increase in hypersensitive response was associated with increase in fungal biomass Leptosphaeria maculans; Arabidopsis thaliana
type III effector proteins from P. syringae suppress hypersensitive cell death of plant host cells Pseudomonas syringae
Pst DC3000 hrcC mutant strain defective in the type III secretion system did not enhance (ATWRKY48, WRKY48, AT5G49520) expression Pseudomonas syringae
Hyaloperonospora parasitica isolate Emwa1 was used for plant inoculation
flavonoids contribute to plant defence Fragaria × ananassa
Arabidopsis is non-host for Phytophthora infestans Arabidopsis thaliana
seven MR genes (Xa1, Xa3/Xa26, xa5, xa13, Xa21, xa25, and Xa27) against Xoo indicate functional diversity in rice–Xoo interactions Oryza sativa
disease-causing microbes have evolved to coopt cytoskeleton and endomembrane
Arabidopsis thaliana can be useful model for the study of plant-pathogen interaction in a Rosaceae plant Arabidopsis thaliana
lesion areas in leaves of transgenic line were statistically significantly larger than lesion areas on parental leaves Fragaria × ananassa
inoculation of Arabidopsis with grey mould fungus Botrytis cinerea resulted in necrotic lesions Arabidopsis thaliana
Pseudomonas syringae pv. syringae B728a mutants can be tested in agromonas assays Nicotiana benthamiana
plant microbiome structure changes upon infection may reflect changes made to habitat by pathogen
Nucleic acids in the apoplast are present in apoplast
strong up-regulation of VvSWEET4 upon infection with B. cinerea Vitis vinifera; Botrytis cinerea
production of SA precursors is major function of PAL in resistance of Arabidopsis to Hyaloperonospora arabidopsidis (Hpa) Arabidopsis thaliana
rar1-10 mutant shows similar reduction in plant fresh weight to wild-type Ler upon Pseudomonas cucumerina infection Arabidopsis thaliana
disease rating scale includes severe tissue maceration
disease rating scale includes necrosis
35S:NS-Vitis3 strawberry line was tested for susceptibility to fungal infection Fragaria × ananassa
(ATSGT1B, EDM1, ETA3, RPR1, SGT1B, AT4G11260) axr1-3 double mutant shows increased susceptibility to Hyaloperonospora parasitica Emwa1 Arabidopsis thaliana
inoculated plants had measured average disease rating at different dpi
certain virulence factors from the bacterial pathogen may actively promote expression of negative regulatory genes such as (ATWRKY48, WRKY48, AT5G49520) Pseudomonas syringae
tobacco is generally more susceptible to disease in early than in late phases to Phytophthora parasitica Nicotiana tabacum; Phytophthora parasitica
BSMV-TaSYP132 pre-infected wheat leaves showed increased number and size of necrotic spots on wheat leaves inoculated with Pst avirulent race CYR23 Triticum aestivum
Oy-0 is clearly more susceptible than Col-0 Arabidopsis thaliana
Pst DC3000 inoculated plants were assessed for bacterial populations Arabidopsis thaliana; Pseudomonas syringae
(AGP17, ATAGP17, AT2G23130) might influence Agrobacterium binding Arabidopsis thaliana
(ATEXO70B2, EXO70B2, AT1G07000) mutants show increase in abnormal papilla formation with unusual wide halo upon inoculation with Blumeria graminis f. sp. hordei Arabidopsis thaliana
wrky75At22 mutant plants behave differently from wild-type plants in both compatible and incompatible interactions Arabidopsis thaliana
VIGS has been successfully used on leaves to decipher plant responses to pathogens
transcriptomic study aims to characterize grapevine responses to Eutypa lata infection Vitis vinifera
aphid stylet interaction with plant cells is similar to pathogen–plant cells interaction during infection
pathogen-triggered changes in metabolite levels may reflect plant responses and pathogen requirements
root CWINV activity in Vicia faba was affected by shoot pathogen Uromyces fabae Vicia faba; Uromyces fabae
young leaves of tobacco are highly resistant to Alternaria alternata Nicotiana tabacum
increased permeability of host cells induced by chitosan could facilitate infection by enabling fungal products to enter host cells
DELLA proteins promote resistance to necrotrophs Arabidopsis thaliana
(GAI, RGA2, AT1G14920) mutant shows elevated resistance to Alternaria brassicicola Arabidopsis thaliana
degradation of DELLAs and disabling of JA-mediated necrotroph resistance results concomitantly in loss of DELLA-mediated growth restraint Arabidopsis thaliana
IPO 2679 complemented with CfCE54 restores avirulence of IPO 2679 on mature Cf-9 plants Fulvia fulva; Solanum lycopersicum
plant growth type explains variation in effects of AMF inoculation on aboveground plant pathogens
negative effects were most commonly observed with necrotrophic pathogens
complex role of programed cell death in plant disease is believed to be due to fact that genes commonly associated with resistance confer susceptibility
Albugo is causal agent of white blister rust Brassicaceae
callose deposition differences reflects different effect on Meloidogyne graminicola infection Oryza sativa; Meloidogyne graminicola
viral systems illustrate complexity of interactions in age-related resistance
absence of avrRpv3.1 genes correlates with strains' virulence on Rpv3.1+ grapevine cultivars Plasmopara viticola; Vitis vinifera
(ATRBOHD, DELT1, RBOHD, AT5G47910) phosphorylation at S343 and S347 is crucial for resistance against Colletotrichum higginsianum Arabidopsis thaliana
microbial pathogens reduce host plant fitness
pathogen life history should be included in frameworks used to predict plant-microorganism interactions
miRNAs and their targets have regulatory effects on pathogen infection
elevated [CO2]-treated leaves are much more susceptible to Botrytis cinerea Solanum lycopersicum
infection assays is performed using seedling flood inoculation assays Arabidopsis thaliana; Pseudomonas syringae
Col-0 displays increased hydathode resistance to Xcc compared with Oy-0 Arabidopsis thaliana
(ATCML9, CAM9, CML9, AT3G51920) overexpression lines (OE-CC-2 and OE-CC-5) exhibit significantly enhanced bacterial growth in response to Pseudomonas syringae pv. phaseolicola (Pph) 1448a Arabidopsis thaliana
higher foliar nitrogen concentrations promote infections by biotrophic pathogen
tomato is host for Fusarium oxysporum f. sp. lycopersici (Fol) Solanum lycopersicum; Fusarium oxysporum f. sp. lycopersici
arbuscular mycorrhizal fungi (AMF) inoculation dramatically decreases necrotroph impact
+ AVR-Pikp:AVR-Pik and + AVR-Pikp:Ak:mCherry fail to cause disease in rice cultivar Kanto51 (Pik+) Magnaporthe oryzae; Oryza sativa
wat1-1 Pro35S:AFB1-myc transgenic line exhibits partially restored susceptibility to Ralstonia solanacearum Arabidopsis thaliana
BG-pEDV-AVR-Pii and BG-pEDV show no significant difference in bacterial numbers in Nicotiana benthamiana leaves Burkholderia glumae; Nicotiana benthamiana
fungal cell wall is initial barrier between the two organisms
environmental conditions influence quantitative interaction between grapevine and downy mildew Vitis vinifera; Plasmopara viticola
deletion in the (NAI1, AT2G22770) promoter is associated with increased susceptibility to the mutualistic fungus Piriformospora parasitica Arabidopsis thaliana
plant monosaccharide transporter expression is increased in plant–biotroph interactions
Constitutive overexpression of CaPAL1 in Arabidopsis conferred reduced susceptibility to Pseudomonas syringae pv. tomato (Pst) Arabidopsis thaliana
BSMV-TaNPSN11 pre-infected wheat leaves showed increased number and size of necrotic spots on wheat leaves inoculated with Pst avirulent race CYR23 Triticum aestivum
whole-plant inoculation experiment reveals increased infection in elevated [CO2]-treated plants Solanum lycopersicum
systemic changes in INV and SUS activity have frequently been described during plant–pathogen interactions
CaPAL1 silencing promoted Xcv growth Capsicum annuum
Pseudomonas syringae infection in pTRV:NPR1-silenced plants causes much more severe symptoms than in pTRV:0 plants Solanum lycopersicum
bacterial growth analysis is used to measure Pseudomonas syringae growth Solanum lycopersicum
sensitized ROS- and SA-mediated responses in GhFMO1-expressing plants might be responsible for susceptibility to V. dahliae Nicotiana tabacum
CaPAL1-silenced pepper plants exhibited increased susceptibility to Xcv infection Capsicum annuum
Bacterial growth in Arabidopsis is measured by bacterial colony forming unit (CFU) counting Arabidopsis thaliana; Pseudomonas syringae pv. tomato DC3000
Botrytis cinerea challenge enhances glucose transport Pinus
pathogen infection has been shown to lead to changes in expression of many genes involved in amino acid metabolism and transport
Microscopic examination of lesions (monitored by trypan blue) revealed lesions spread beyond fungal infection foci in (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) lines but remained restricted to inoculation sites in Col-0 Arabidopsis thaliana
(ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) is not a spontaneous lesion-mimic mutant of the lsd class indicates susceptibility to fungal infection is unlikely to be due to enhanced saprophytic growth base Arabidopsis thaliana
AvrPtoB was initially identified through activation of hypersensitive resistance in tomato cultivars expressing Pto kinase Solanum lycopersicum
Pseudomonas syringae effector AvrPto blocks innate immunity
ABA distribution pattern at least partially contributed to age-dependent susceptibility Nicotiana attenuata
irAOC plants were more susceptible to Alternaria alternata Nicotiana attenuata
GhFMO1 (flavin-dependent monooxygenase 1) overexpression aggravated Verticillium wilt symptoms in tobacco Nicotiana tabacum
pattern-triggered immunity (PTI) is sufficient to limit infection by non-adapted pathogens
TaSYP132 transcriptional regulation in wheat response to Puccinia striiformis f. sp. tritici (Pst) Triticum aestivum
pTRV:PI-silenced plants do not exhibit altered resistance to Pseudomonas syringae Solanum lycopersicum
wat1-1 jar1-1 double mutant exhibits similar resistance to Ralstonia solanacearum Arabidopsis thaliana
leaves from double and single mutant top lines inoculated with pathogens Arabidopsis thaliana
(AtGBF1, GBF1, AT4G36730) binding in the (ATPAD4, PAD4, AT3G52430) intron is enhanced upon Pseudomonas syringae pv. maculicola ES4326 (Psm) inoculation Arabidopsis thaliana
aberrant response in (ATPSAT1, ERP1, PSAT1, AT1G04010) mutant is observed after infection by non-adapted pathogen Phytophthora infestans Arabidopsis thaliana
Filipin staining of barley leaf epidermal cells infected with Blumeria graminis shows enrichment of sterols at sites of pathogen attack Hordeum vulgare
Ralstonia solanacearum growth is strongly decreased in wat1-3 mutant Arabidopsis thaliana
wat1-3 mutant is as susceptible as Col-0 to Pseudomonas syringae pv. tomato (Pst) Arabidopsis thaliana
Sasa2 WT and all transformants successfully infect rice cultivar Moukoto (Pik−, Pii−) Magnaporthe oryzae; Oryza sativa
transcriptomic study describes grapevine response after infection by Eutypa lata Vitis vinifera
young source–sink transition leaves are more resistant to Alternaria alternata Nicotiana attenuata
Constitutive overexpression of CaPAL1 in Arabidopsis conferred increased basal resistance to infection by the obligate biotrophic oomycete Hpa Arabidopsis thaliana
reduction of wax content in (ACBP, ACBP1, AtACBP1, AT5G53470) mutant could have caused greater susceptibility to Botrytis infection Arabidopsis thaliana
whole-plant inoculation protocol provides more reliable and reproducible system than detached leaf-based infection studies Solanum lycopersicum
impaired response to elicitors in anp single mutants likely causes lack of protection against Botrytis cinerea Arabidopsis thaliana
location of the droplet by the midrib facilitated measurement of preferential growth along the primary but not the secondary vasculature Arabidopsis thaliana
X. oryzae pv. oryzae induces otherwise developmentally regulated host genes Oryza sativa
BSMV-TaNPSN13 pre-infected wheat leaves showed increased number and size of necrotic spots on wheat leaves inoculated with Pst avirulent race CYR23 Triticum aestivum
Pseudomonas syringae growth is in good agreement with disease symptom Solanum lycopersicum
T-DNA insertion line SALK_148857C is susceptible to Phytophthora sojae Arabidopsis thaliana
(04C11, ATPEN1, PEN1, AT4G15340) acts at prehaustorial level Arabidopsis thaliana
(ATPAD4, PAD4, AT3G52430) is associated with lesion greenness Arabidopsis thaliana
individual SNPs appeared to have small effects Arabidopsis thaliana
further validation studies could fill gaps in our knowledge of the cellular mechanisms involved in lesion traits and pathogen virulence Arabidopsis thaliana
35S-ATL31 overexpression line shows enhanced resistance to Pseudomonas syringae pv tomato (Pst) DC3000 Arabidopsis thaliana
(ATGSL05, ATGSL5, EED3, GSL05, GSL5, PMR4, AT4G03550) or (ATGSL06, ATGSL6, CALS1, GSL06, GSL6, AT1G05570) gene expression show no major changes in response to Phytophthora infestans Arabidopsis thaliana
(AtSERPIN1, SERPIN1, AT1G47710) mutant plants accelerates growth of Botrytis cinerea Arabidopsis thaliana; Botrytis cinerea
Phytophthora species and related oomycetes seriously affect crop yield
sugar transport and partitioning are affected following infection with biotrophic fungal and oomycete pathogens
transgenic lines overexpressing (MIR398B, AT5G14545) show hypersensitivity to virulent strain Pseudomonas syringae DC3000 Arabidopsis thaliana
anp mutants examined for susceptibility to Botrytis cinerea Arabidopsis thaliana
droplet placed near the primary vasculature ensured that this would create an elliptical growth pattern allowing easy measurement of eccentricity Arabidopsis thaliana
bacterial suspensions at 1 × 10^5 cfu ml^−1 Pst avrRpm1 is used for in-planta growth assays Arabidopsis thaliana
SynComA without Aeromicrobium fastidiosum I01 observed variable decrease in the resistance of the plant to infection Arabidopsis thaliana
structural variations at avrRpv3.1 locus in different geographical strains confirm involvement in breakdown of Rpv3.1 resistance Plasmopara viticola; Vitis vinifera
genes g164 and g165 are most promising candidates to be cognate Rpv3.1 avirulence genes Plasmopara viticola
pathogenic effectors could specifically target proteins associated with ROS scavenging
DG7 transformants expressing wild-type AvrPib allele were incompatible on cultivar BL1 Magnaporthe oryzae; Oryza sativa
spraying inoculation approach obtained similar results Magnaporthe oryzae; Oryza sativa
Bacterial inoculum is prepared at 5 × 10^6 CFU/mL concentration Pseudomonas syringae pv. tomato DC3000
Tn5:lux strains used to evaluate plant immunity level in Arabidopsis lines Arabidopsis thaliana
(RPM1, RPS3, AT3G07040) gene encodes resistance to Pseudomonas syringae Arabidopsis thaliana
individual gene validation efforts showed that most of these individual genes can have 25% or larger effects on the trait Arabidopsis thaliana
no gene affected all of these lesion traits Arabidopsis thaliana
GWA on lesion traits requires polygenic models, like the ridge regression approach Arabidopsis thaliana
CFU counting assay measures bacterial colonization Pseudomonas protegens; Arabidopsis thaliana
Pst DC3000 inoculated plants were covered with plastic lid to maintain high humidity Arabidopsis thaliana; Pseudomonas syringae
P. parasitica is soil fungus with spores that infect tobacco roots Phytophthora parasitica
Verticillium dahliae is responsible for vascular wilt diseases
AtWRKY26 mutants show no enhanced susceptibility to necrotrophic pathogens Arabidopsis thaliana
(ATCML9, CAM9, CML9, AT3G51920) restricts susceptibility to virulent Pto DC3000 Arabidopsis thaliana
(ATMED14, MED14, SWP, AT3G04740) and (AtSFR6, GLH2, IEN1, MED16, SFR6, YID1, AT4G04920) play positive role in resistance to Pst DC3000/ avrRpt2 Arabidopsis thaliana
Gibberella might secrete gibberellin (GA) as a virulence factor to degrade DELLAs and disable JA-mediated necrotroph resistance Gibberella fujikuroi
Infection with the virulent fungus Botrytis cinerea caused complete decay of (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) plants Arabidopsis thaliana
reduced HR in BG-pEDV-AVR-Pik is not caused by reduction of bacterial numbers Nicotiana benthamiana
suppression of TaADF7 expression resulted in weakened ROS accumulation in the wheat–Pst incompatible interaction Triticum aestivum
core effector PhRXLR-C01 is proposed as AVR component of AVR/R couple Helianthus annuus L.
effect of AvrRpt2, AvrRpm1, or (AtRIN4, RIN4, AT3G25070) levels on plant defense correlates with growth of P. syringae Pseudomonas syringae
M. oryzae isolate Sasa2 transformed with AVR-Pikp:signal peptide(sp):HA:AVR-Pik and AVR-Piip:sp:HA:AVR-Pii are used in rice inoculation assay Magnaporthe oryzae; Oryza sativa
(RD21, RD21A, AT1G47128) silencing resulted in increase in number of lesions in Botrytis cinerea infection Arabidopsis thaliana; Botrytis cinerea
Pseudomonas syringae pv. phaseolicola (Pph) is pathogen of Phaseolus vulgaris (bean) Pseudomonas syringae pv. phaseolicola
Ralstonia solanacearum effector PopP2 targets multiple WRKY transcription factors Arabidopsis thaliana
Pseudomonas syringae pv. tomato DC30000 (Pst DC3000) multiplies approximately 100-fold more in ARABIDOPSIS PROFILIN 3 mutant (PFN3, PRF3, AT5G56600) Arabidopsis thaliana; Pseudomonas syringae
cml9-1 knockout mutant exhibits enhanced susceptibility to Pseudomonas syringae pv. maculicola (Pma) Arabidopsis thaliana
(TBL10, AT3G06080) mutant exhibits similar level of susceptibility to Botrytis cinerea Arabidopsis thaliana
knock-down of GbTSA1 improves cotton resistance to V. dahliae Gossypium barbadense
T6SS can directly influence plants
bacterial suppression of stomatal defense is common phenomenon in plant-bacterium interactions
Nicotiana tabacum does not follow the general pattern of increased early susceptibility to Alternaria alternata Nicotiana tabacum; Alternaria alternata
competition for sugar at the plant–microbe interface is controlled by membrane transporters
TaNPSN12 transcriptional regulation in wheat response to Puccinia striiformis f. sp. tritici (Pst) Triticum aestivum
Arabidopsis accession Col-0 is partially resistant Arabidopsis thaliana
chlorophyll fluorescence parameters are affected in plant-pathogen interactions
post-translational inhibition of cell wall invertase (cwInv) activity by acarbose results in more pronounced growth of bacterial pathogen Arabidopsis thaliana
Pst (avrPtoB S335A) infection showed slightly less but not significantly different bacterial titer from that of Pst Arabidopsis thaliana
LecRK-IX.2-overexpression plants displayed enhanced disease resistance to Pst Arabidopsis thaliana
WRKY transcription factor 33 upregulated in field non-acclimation (F-NA) sample
Col-0 is generally considered to be susceptible host for Xcc8004 ΔxopAC Arabidopsis thaliana
KD-GmBIR1 overexpression shows remarkable increase in plant resistance to SCN Glycine max
175 differentially phosphorylated peptides are identified in infected WT-GmBIR1 roots compared with noninfected WT-GmBIR1 roots Glycine max
plant vascular system can be disrupted by invading pathogens, especially plant viruses Arabidopsis thaliana
Avr9B-like protein from Pseudocercospora fuligena (HII31_03919) triggers chlorotic response Nicotiana tabacum
cell death responses triggered by Avr9B-like proteins in N. benthamiana are not dependent on (EVR, SOBIR1, AT2G31880) Nicotiana benthamiana
Cluster 2 genes (Nitrate-C2; 4881 genes) are enriched in pathways of plant-pathogen interaction, autophagy, and signaling responses Lotus japonicus
Cf-9B-mediated resistance was overcome second Fulvia fulva; Solanum lycopersicum
jasmonic acid-mediated immunity occurs during Plasmodiophora brassicae secondary infection Brassica napus; Arabidopsis thaliana; Brassica rapa; Brassica oleracea
species-specific impacts of mycorrhizal fungal species on their hosts may explain reduction in effects of AMF inoculation as diversity increases
PevD1ox and ORE1ox plants exhibit more severe disease symptoms Arabidopsis thaliana
massive callose depositions in the mesophyll cell layer are formed in response to inoculation with invasive filamentous pathogens Arabidopsis thaliana
effector protein PTTG_04779 is identified as candidate protein for AvrLr19 Puccinia striiformis f. sp. tritici
movement of hyphae from host root cortex to xylem vessels is critical for disease progression Fusarium oxysporum f. sp. lycopersici; Solanum lycopersicum
pathogen life history included in studies of how AMF inoculation affects plant diseases, will enable better prediction of disease occurrences
effector recognition by resistance proteins defines compatibility with host genotype or host species
100 differentially phosphorylated peptides are identified in infected KD-GmBIR1 roots compared with noninfected KD-GmBIR1 roots Glycine max
Magnaporthe oryzae needs to overcome host immunity Magnaporthe oryzae
hyphal growth in infected roots is characterized by centripetal growth towards the stele Fusarium oxysporum f. sp. lycopersici; Solanum lycopersicum
(ATRBOHD, DELT1, RBOHD, AT5G47910) mutants showed increased lesion diameters Arabidopsis thaliana
(ATRBOHD, DELT1, RBOHD, AT5G47910) pRBOHD:3xFLAG-gRBOHD S343A/S347A transgenic plants showed increased lesion diameters Arabidopsis thaliana
repertoire of effectors present in a pathogen largely defines compatibility with host species
Fulvia fulva strain P31 was inoculated onto mature MM-Cf-0 and MM-Cf-9 tomato plants Fulvia fulva; Solanum lycopersicum
AMF inoculation may facilitate biotrophic pathogens
effects of AMF inoculation on plant resistance are reduced as AMF diversity increases
5-weeks-old WT Arabidopsis plants were placed in 1μM Ascr2 or Ascr18 solution Arabidopsis thaliana
suppression of JA synthesis component genes suggests Guy11 infection can suppress the expression of these genes and evade the JA-mediated rice defense response Oryza sativa; Magnaporthe oryzae
Fusarium wilt is caused by Fusarium oxysporum (F. oxysporum) Fusarium oxysporum
PpE18 interacted with NbAPX3-1 Nicotiana benthamiana
pb1cp mutants showed no difference in bacterial growth of Pseudomonas syringae pv tomato (Pto) DC3000 COR− Arabidopsis thaliana
p35S:PB1CP-3xHA lines showed larger lesion diameters Arabidopsis thaliana
TRV::GhORE1 plants exhibits lower percentage of wilting plants Gossypium hirsutum
PevD1 interacts with (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) Arabidopsis thaliana
phytoplasma is a phloem invading pathogen plants
no significant effects were observed with biotrophic pathogens
carborundum is routinely used to aid screening of plant susceptibility for pathogens
Alternanthera philoxeroides developed distinct rhizosphere fungal pathogens Alternanthera philoxeroides; China
HII31_03919 does not trigger cell death response when co-expressed with Cf-9B Nicotiana tabacum
Rpv3.1-mediated resistance is conferred by Rpv3.1 locus Vitis vinifera
specific single-stranded ribonuclease effectors mediate plant–microbe interaction Colletotrichum orbiculare; Cucumis sativus
pb1cp mutants showed smaller lesion diameters Arabidopsis thaliana
88 phosphopeptides show increased abundance in infected root samples relative to noninfected control root samples Glycine max
diminished pathogen control over host resistance genes enables plants to mount specialized resistance against the disease
W97C mutation in Avr9B enables evasion of recognition by Cf-9B Fulvia fulva; Solanum lycopersicum
transient expression assays demonstrated that all genes induced cell death in Regent but not in Syrah Vitis vinifera
microbial pathogens reduce host plant photosynthesis
arbuscular mycorrhizal fungi (AMF) inoculation does not affect biotroph impact
specific AMF genera had stronger negative effects on pathogens
this research deepened understanding of plant-pathogen interactions
germination of dormant conidia in soil leads to fungal hyphae adhering to and invading tomato roots Fusarium oxysporum f. sp. lycopersici; Solanum lycopersicum
AMF genus explains variation in effects of AMF inoculation on aboveground plant pathogens
type III secretion system-dependent translocation of Bg_9562 into host apoplast is important for elicitation of immune responses during colonization of NGJ1 Solanum lycopersicum; Burkholderia gladioli
W97C mutant of Avr9B is unable to trigger Cf-9B-dependent cell death response Nicotiana tabacum
breakdown of Rpv3.1 resistance correlates with deletion of genes within avrRpv3.1 locus Plasmopara viticola; Vitis vinifera
ABA receptors are involved in plant-pathogen interactions
wat1-3 mutant exhibits delay in symptom development (leaf wilting) Arabidopsis thaliana
Ralstonia solanacearum growth is strongly decreased in wat1-1 mutant Arabidopsis thaliana
(RD21, RD21A, AT1G47128) mutant plants compromises growth of Botrytis cinerea Arabidopsis thaliana; Botrytis cinerea
Botrytis cinerea can grow better in HR-induced plants
wild-type plants challenged with Pseudomonas syringae DC3000 (avrRpt2)
acarbose co-treatment in (ATICS1, EDS16, ICS1, SID2, AT1G74710) mutant further increases bacterial growth Arabidopsis thaliana; Pseudomonas syringae
12 phosphopeptides show decreased abundance in infected root samples relative to noninfected control root samples Glycine max
VmR2-siR1 targeted novel disease resistance-related gene in apple Malus domestica
PpE18 is required for full pathogenicity of P. parasitica Phytophthora parasitica
AVR-Pii is avirulence effector protein Magnaporthe oryzae
line that overexpress (AtSERPIN1, SERPIN1, AT1G47710) compromised growth of necrotrophic fungi Arabidopsis thaliana
Plant pathogenic nematodes cause serious damage to crop plants
BG-pEDV-AVR-Pik shows significantly lower bacterial growth than BG-pEDV (empty vector) Burkholderia glumae; Oryza sativa
(ATPME3, OZS2, PME3, AT3G14310) interacts with and is possibly targeted by cellulose-binding protein from parasitic nematode Heterodera schachtii Arabidopsis thaliana; Heterodera schachtii
(AtSFR6, GLH2, IEN1, MED16, SFR6, YID1, AT4G04920) plants are more susceptible to Pst DC3000/ avrRpt2 Arabidopsis thaliana
+ AVR-Piip:AVR-Pii and + AVR-Piip:Ai:mCherry fail to infect rice cultivar Kakehashi (Pii+) Magnaporthe oryzae; Oryza sativa
top mutants exhibited WT levels of growth in the case of infections with avirulent Pst avrRpm1 or Pst avrPphB, virulent P. syringae pv. maculicola, or the defective P. syringae ∆hrcC strain Arabidopsis thaliana; Pseudomonas syringae
wild-type Arabidopsis thaliana shows no noticeable change in disease resistance with ARABIDOPSIS PROFILIN 3 overexpression line (AtPRF3-OE) Arabidopsis thaliana
enhanced response in (ATPSAT1, ERP1, PSAT1, AT1G04010) mutant does not correlate with obvious alterations in the growth of the pathogen Arabidopsis thaliana
cystatin CC9 is transcriptionally induced upon penetration by Ustilago maydis strains secreting effector protein (ATPEP1, PEP1, PROPEP1, AT5G64900) Zea mays; Ustilago maydis
28-day-old Col-0 and T3 transgenic plants were inoculated with V. dahliae Arabidopsis thaliana; Verticillium dahliae
AVR-Pik is avirulence effector protein Magnaporthe oryzae
Blumeria graminis inoculation shows no differences in cell death Arabidopsis thaliana
PMU genes include effectors that modulate plant development
ROS regulation appears to be critical battleground between plants and pathogens
V. dahliae acquires nutrients released from senescent leaves Verticillium dahliae
(PMR5, TBL44, AT5G58600) tbr1 double mutant was more susceptible to all strains of Botrytis cinerea except UKRazz
PthXo1 induces Xa13 expression Xanthomonas oryzae
composition of microbial communities can influence disease
Verticillium wilt is first observed on upland cotton Gossypium hirsutum
wat1-1 (AMT1, ASA1, JDL1, TRP5, WEI2, AT5G05730) double mutant does not exhibit partial restoration of susceptibility to Verticillium dahliae Arabidopsis thaliana
Sasa2 WT and all five strains successfully infect susceptible rice cultivar Moukoto (Pik−, Pii−) Magnaporthe oryzae; Oryza sativa
top mutant lines challenged with several strains of Pseudomonas syringae DC3000 Arabidopsis thaliana; Pseudomonas syringae
aberrant response in (ATPSAT1, ERP1, PSAT1, AT1G04010) mutant is observed after infection by non-adapted pathogen Blumeria graminis Arabidopsis thaliana
(AP-3 beta, PAT2, WAT1, AT3G55480) mutant maintains resistance when pathogen is injected into central leaf vein (vascular system) Arabidopsis thaliana
protease-protease inhibitor interactions are not just important feature shaping the fate of plant-pathogen associations
this research documented mechanism by which P. parasitica attacks host plant to promote infection Phytophthora parasitica
Funneliformis had stronger negative effects on pathogens
new auxin maxima is imperative for symptom onset Arabidopsis thaliana
diverse cargo delivered to microbial contact sites combat invading microbes
plant-pathogenic filamentous eukaryotes from three different phyla infect plant hosts that include monocots and dicots
(AtSERPIN1, SERPIN1, AT1G47710) mutant plants accelerates growth of Sclerotinia sclerotiorum Arabidopsis thaliana; Sclerotinia sclerotiorum
(ANP2, MAPKKK2, NP2, AT1G54960) (ANP3, AtANP3, MAPKKK12, NP3, AT3G06030) double mutant was more resistant Arabidopsis thaliana
suppression of miR319-mediated JA signaling may be counter defense mechanism conserved among many plant/pathogen systems
Cf-9C was overcome first Fulvia fulva; Solanum lycopersicum
Phytophthora sojae is not able to penetrate ecotype Col-0 Arabidopsis thaliana
GWA within the Arabidopsis accessions and subsequent mutant validation studies showed that four lesion traits had a blend of distinct and overlapping genetic mechanisms Arabidopsis thaliana
bacterial suspensions at 2 × 10^5 cfu ml^−1 (PSP, PSP1, AT1G18640) is used for in-planta growth assays Arabidopsis thaliana
CRY1-ovx plants show reduced bacterial growth of virulent Pseudomonas syringae DC3000
partial phosphorylation of AvrPtoB resulted in AvrPtoB virulence was only partially reduced during pathogen infection Arabidopsis thaliana
calmodulin up- or downregulated in field non-acclimation (F-NA) sample
mitogen-activated protein kinase (MAPK) 6 has been shown to be required for oligogalacturonide (OG)- and flg22-induced resistance to Botrytis cinerea Arabidopsis thaliana
broader life history studies of plant-pathogen interactions in the field could identify the potential ecological or evolutionary drivers of these traits Arabidopsis thaliana
Colletotrichum higginsianum infection process increases likelihood of ROS exposure Arabidopsis thaliana
effectors play deterministic roles in outcome of plant–pathogen interactions
knock-down of GbICS1 makes plants more susceptible to V. dahliae Gossypium barbadense
OsTPS19 RNA interference (RNAi) lines were more susceptible to Magnaporthe oryzae rice (Oryza sativa)
defective protection in anp mutants was also rescued in complemented (ANP2, MAPKKK2, NP2, AT1G54960) (ANP3, AtANP3, MAPKKK12, NP3, AT3G06030) double mutant expressing wild-type Arabidopsis thaliana
(PSS1, AT3G59640) may act at prehaustorial and posthaustorial levels Arabidopsis thaliana
generation of visual traits can identify genes not known to influence lesion size
preferential growth along the primary vasculature implies shift from general radial outward growth to directed growth along the leaf midrib Arabidopsis thaliana
findings of this study suggest that there are potentially unrecognized mechanisms that may be important for plant-pathogen interactions Arabidopsis thaliana
Phytophthora sojae can penetrate single cells of pen1-1 mutant Arabidopsis thaliana
35S-ATL6 overexpression line shows enhanced resistance to Pseudomonas syringae pv tomato (Pst) DC3000 Arabidopsis thaliana
moving the droplet away from the midrib would still allow for measuring preferential growth Arabidopsis thaliana
four candidate genes can influence rice phenotype in interaction with Xoo or M. grisea Oryza sativa
Avr9B-like protein from Stemphylium lycopersici (TW65_01570) triggers strong cell death response Nicotiana tabacum
corresponding wild-type genotypes were protected by treatment with oligogalacturonides (OGs) or elf18 Arabidopsis thaliana
(LUX, PCL1, AT3G46640) functions specifically in lesion size Arabidopsis thaliana
atl6-1 single knockout mutant does not cause increased susceptibility to Pseudomonas syringae pv tomato (Pst) DC3000 Arabidopsis thaliana
coronatine (COR) treatment does not cause tissue damage or attacker-derived effector molecules
eccentric lesions are associated with preferential growth along the primary vasculature Arabidopsis thaliana
candidate genes that were tested using insertional mutants affected more than one aspect of the plant-pathogen interaction Arabidopsis thaliana