scholarly journals Apoplastic pH Signaling in Barley Leaves Attacked by the Powdery Mildew Fungus Blumeria graminis f. sp. hordei

2004 ◽  
Vol 17 (1) ◽  
pp. 118-123 ◽  
Author(s):  
Hubert H. Felle ◽  
Almut Herrmann ◽  
Stefan Hanstein ◽  
Ralph Hückelhoven ◽  
Karl-Heinz Kogel
Keyword(s):  
Powdery Mildew ◽  
Hypersensitive Reaction ◽  
Blumeria Graminis ◽  
Short Term ◽  
Hordeum Vulgare L ◽  
Powdery Mildew Fungus ◽  
Apoplastic Ph ◽  
Host Defense Response ◽  
Barley Leaves

To investigate apoplastic responses of barley (Hordeum vulgare L.) to the barley powdery mildew fungus Blumeria graminis f. sp. hordei, noninvasive microprobe techniques were employed. H+- and Ca2+-selective microprobes were inserted into open stomata of barley leaves inoculated with Blumeria graminis f. sp. hordei race A6 conidia. Resistance gene-mediated responses of barley genotype Ingrid (susceptible parent line) and the near-isogenic resistant Ingrid backcross lines (I-mlo5, I-Mla12, and I-Mlg) were continuously monitored from 20 min to 4 days after inoculation. The main events were categorized as short-term responses around 2 h after inoculation (hai), intermediate responses around 8 and 12 hai, and long-term responses starting between 21 and 24 hai. Short-term responses were rapid transient decreases of apoplastic H+- and Ca2+ activities that lasted minutes only. Kinetics were similar for all genotypes tested, and thus, these short-term responses were attributed as nonspecific first encounters of fungal surface material with the host plasma membrane. This is supported by the observation that a microinjected chitin oligomer (GlcNAc)8 yielded similar apoplastic alkalinization. Intermediate responses are trains of H+ (increase) spikes that, being different in susceptible Ingrid and penetration-resistant I-mlo5 (or I-Mlg), were interpreted as accompanying specific events of papillae formation. Long-term events were massive slow and long-lasting alkalinizations up to two pH units above control. Since these latter changes were only observed with near-isogenic hypersensitive reaction (HR)-mounting genotypes I-Mla12 and I-Mlg but not with I-mlo5 or, to a smaller extent, with susceptible Ingrid, both lacking significant rates of HR, they were rated as cell death specific. It is concluded that apoplastic pH changes are important indicators of host-pathogen interactions that correlate with both the different stages of fungal development and the different types of host defense response.

scholarly journals The Mycorrhiza Fungus Piriformospora indica Induces Fast Root-Surface pH Signaling and Primes Systemic Alkalinization of the Leaf Apoplast Upon Powdery Mildew Infection

2009 ◽  
Vol 22 (9) ◽  
pp. 1179-1185 ◽  
Author(s):  
Hubert H. Felle ◽  
Frank Waller ◽  
Alexandra Molitor ◽  
Karl-Heinz Kogel
Keyword(s):  
Powdery Mildew ◽  
Piriformospora Indica ◽  
Plant Responses ◽  
Hordeum Vulgare L ◽  
Powdery Mildew Fungus ◽  
Surface Ph ◽  
Apoplastic Ph ◽  
Elicitor Response ◽  
Ph Increase ◽  
Leaf Apoplast

We analyze here, by noninvasive electrophysiology, local and systemic plant responses in the interaction of barley (Hordeum vulgare L.) with the root-colonizing basidiomycete Piriformospora indica. In the short term (seconds, minutes), a constant flow of P. indica chlamydospores along primary roots altered surface pH characteristics; whereas the root-hair zone transiently alkalized—a typical elicitor response—the elongation zone acidified, indicative of enhanced H+ extrusion and plasma membrane H+ ATPase stimulation. Eight to 10 min after treating roots with chlamydospores, the apoplastic pH of leaves began to acidify, which contrasts with observations of an alkalinization response to various stressors and microbe-associated molecular patterns (MAMPs). In the long term (days), plants with P. indica-colonized roots responded to inoculation with the leaf-pathogenic powdery mildew fungus Blumeria graminis f. sp. hordei with a leaf apoplastic pH increase of about 2, while the leaf apoplast of noncolonized barley responded to B. graminis f. sp. hordei merely with a pH increase of 0.8. The strong apoplastic pH response is reminiscent of B. graminis f. sp. hordei–triggered pH shifts in resistance gene–mediated resistant barley leaves or upon treatment with a chemical resistance inducer. In contrast, the MAMP N-acetylchito-octaose did not induce resistance to B. graminis f. sp. hordei and did not trigger the primed apoplastic pH shift. We speculate that the primed pH increase is indicative of and supports the potentiated systemic response to B. graminis f. sp. hordei–induced by P. indica in barley.

scholarly journals Disruption of barley immunity to powdery mildew by an in-frame Lys-Leu deletion in the essential protein SGT1

Genetics ◽  
2020 ◽  
Vol 217 (2) ◽  
Author(s):  
Antony V E Chapman ◽  
Matthew Hunt ◽  
Priyanka Surana ◽  
Valeria Velásquez-Zapata ◽  
Weihui Xu ◽  
...  
Keyword(s):  
Powdery Mildew ◽  
Fungal Pathogens ◽  
Novel Mutation ◽  
Exome Capture ◽  
Resistance Locus ◽  
Hordeum Vulgare L ◽  
Powdery Mildew Fungus ◽  
Pathogen Effectors ◽  
Cell Processes ◽  
Disease Resistances

Abstract Barley (Hordeum vulgare L.) Mla (Mildew resistance locus a) and its nucleotide-binding, leucine-rich-repeat receptor (NLR) orthologs protect many cereal crops from diseases caused by fungal pathogens. However, large segments of the Mla pathway and its mechanisms remain unknown. To further characterize the molecular interactions required for NLR-based immunity, we used fast-neutron mutagenesis to screen for plants compromised in MLA-mediated response to the powdery mildew fungus, Blumeria graminis f. sp. hordei. One variant, m11526, contained a novel mutation, designated rar3 (required for Mla6 resistance3), that abolishes race-specific resistance conditioned by the Mla6, Mla7, and Mla12 alleles, but does not compromise immunity mediated by Mla1, Mla9, Mla10, and Mla13. This is analogous to, but unique from, the differential requirement of Mla alleles for the co-chaperone Rar1 (required for Mla12 resistance1). We used bulked-segregant-exome capture and fine mapping to delineate the causal mutation to an in-frame Lys-Leu deletion within the SGS domain of SGT1 (Suppressor of G-two allele of Skp1, Sgt1ΔKL308–309), the structural region that interacts with MLA proteins. In nature, mutations to Sgt1 usually cause lethal phenotypes, but here we pinpoint a unique modification that delineates its requirement for some disease resistances, while unaffecting others as well as normal cell processes. Moreover, the data indicate that the requirement of SGT1 for resistance signaling by NLRs can be delimited to single sites on the protein. Further study could distinguish the regions by which pathogen effectors and host proteins interact with SGT1, facilitating precise editing of effector incompatible variants.

scholarly journals The Ambivalence of the Barley Mlo Locus: Mutations Conferring Resistance Against Powdery Mildew (Blumeria graminis f. sp. hordei) Enhance Susceptibility to the Rice Blast Fungus Magnaporthe grisea

1999 ◽  
Vol 12 (6) ◽  
pp. 508-514 ◽  
Author(s):  
Birgit Jarosch ◽  
Karl-Heinz Kogel ◽  
Ulrich Schaffrath
Keyword(s):  
Powdery Mildew ◽  
Rice Blast ◽  
Magnaporthe Grisea ◽  
Durable Resistance ◽  
Rice Blast Fungus ◽  
Blumeria Graminis ◽  
Negative Regulator ◽  
Powdery Mildew Fungus ◽  
Mesophyll Cells ◽  
Blast Fungus

Recessive alleles of the barley Mlo locus confer non-race-specific resistance against the powdery mildew fungus Blumeria graminis f. sp. hordei (Bgh). Recently the Mlo gene has been isolated and it was suggested that the Mlo product is a negative regulator of cell death. Thus, loss of function can precondition cells to a higher responsiveness for the onset of multiple defense functions. Here, we document an enhanced susceptibility of barley mlo mutants to the rice blast fungus Magnaporthe grisea. The disease phenotype is independent of the barley cultivar in which the mlo allele has been introgressed and occurs in equal amounts in barley backcross lines of cv. Ingrid carrying the mlo-1, mlo-3, or mlo-5 allele. Ror genes, which are required for the full expression of mlo resistance in barley against Bgh, do not affect the specific mlo-mediated phenotype observed after M. grisea infection. Formation of an effective papilla restricts blast development in epidermal cells of Mlo plants. In contrast, papillae are mostly penetrated in mlo mutants and, as a consequence, the fungus spreads into adjacent mesophyll cells. Both wild-type plants and mlo mutants did not differ in perception of a purified elicitor derived from M. grisea. Thus, we hypothesize that a functional Mlo protein is a prerequisite for penetration resistance of barley to fungal pathogens like M. grisea. The benefit of mlo alleles for durable resistance in barley and a proposed role of mlo-type-mutations in rice are discussed.

scholarly journals Multivesicular compartments proliferate in susceptible and resistant MLA12-barley leaves in response to infection by the biotrophic powdery mildew fungus

2006 ◽  
Vol 172 (3) ◽  
pp. 563-576 ◽  
Author(s):  
Qianli An ◽  
Katrin Ehlers ◽  
Karl-Heinz Kogel ◽  
Aart J. E. van Bel ◽  
Ralph Hückelhoven
Keyword(s):  
Powdery Mildew ◽  
Powdery Mildew Fungus ◽  
Barley Leaves

Impact of proquinazid on appressorial development of the barley powdery mildew fungus Blumeria graminis f.sp hordei

2009 ◽  
Vol 94 (2-3) ◽  
pp. 127-132 ◽  
Author(s):  
Sally R. Gilbert ◽  
Hans J. Cools ◽  
Bart A. Fraaije ◽  
Andy M. Bailey ◽  
John A. Lucas
Keyword(s):  
Powdery Mildew ◽  
Blumeria Graminis ◽  
Powdery Mildew Fungus ◽  
Barley Powdery Mildew

scholarly journals Selections from barley landrace collected in Libya as new sources of effective resistance to powdery mildew (Blumeria graminis f.sp. hordei)

2011 ◽  
Vol 48 (No. 5) ◽  
pp. 217-223 ◽  
Author(s):  
J.H. Czembor ◽  
H.J. Czembor
Keyword(s):  
Powdery Mildew ◽  
Powdery Mildew Resistance ◽  
Agricultural Research ◽  
Genetic Resistance ◽  
Recessive Gene ◽  
Blumeria Graminis ◽  
Hordeum Vulgare L ◽  
Mildew Resistance ◽  
Barley Landrace ◽  
Barley Powdery Mildew

Powdery mildew on barley (Hordeum vulgare L.) caused by the pathogen Blumeria graminis f.sp. hordei occurs worldwide and can result in severe yield loss. Because agronomical methods to control the disease are not completely effective, cultivars with genetic resistance are needed. Therefore, there is a need to describe new sources of genes that confer resistance to barley powdery mildew. This study was conducted to determine the genetic basis of resistance to powdery mildew in three selections 995-1-1, 995-1-2, 995-1-3 from barley landrace 995 (ICB 112840) collected in Al Aziziyah district, Tripolitania, Libya. Landrace originated from InternationalCenter for Agricultural Research in the Dry Areas – ICARDA, Aleppo, Syria. To determine the number of genes, the types of genes action and the gene loci in tested lines two types of crosses were made: (1) the lines were crossed to the susceptible cultivar Pallas, (2) the lines were crossed with Pallas isoline P22 carrying gene mlo5. The parents and progeny F2 were evaluated with isolate R303.1 for the powdery mildew resistance. Based on segregation ratios we found that resistance in these three selections was determined by a single recessive gene allelic to the Mlo locus occurring in Pallas isoline P22. In addition tested lines showed resistance reaction type 0(4) characteristic only for genes mlo. The value of new identified sources of highly effective powdery mildew resistance to breeding programs and barley production is discussed.

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