scholarly journals Genomics-enabled analysis of the emergent disease cotton bacterial blight

2017 ◽  
Author(s):  
Anne Z. Phillips ◽  
Jeffrey C. Berry ◽  
Mark C. Wilson ◽  
Anupama Vijayaraghavan ◽  
Jillian Burke ◽  
...  
Keyword(s):  
Rna Sequencing ◽  
Resistance Genes ◽  
Bacterial Blight ◽  
Durable Resistance ◽  
Gene List ◽  
Susceptibility Gene ◽  
The United States ◽  
Transcription Activator ◽  
Xanthomonas Citri ◽  
Putative Gene

AbstractCotton bacterial blight (CBB), an important disease of (Gossypium hirsutum) in the early 20th century, had been controlled by resistant germplasm for over half a century. Recently, CBB re-emerged as an agronomic problem in the United States. Here, we report analysis of cotton variety planting statistics that indicate a steady increase in the percentage of susceptible cotton varieties grown each year since 2009. Phylogenetic analysis revealed that strains from the current outbreak cluster with race 18 Xanthomonas citri pv. malvacearum (Xcm) strains.Illumina based draft genomes were generated for thirteen Xcm isolates and analyzed along with 4 previously published Xcm genomes. These genomes encode 24 conserved and nine variable type three effectors. Strains in the race 18 clade contain 3 to 5 more effectors than other Xcm strains. SMRT sequencing of two geographically and temporally diverse strains of Xcm yielded circular chromosomes and accompanying plasmids. These genomes encode eight and thirteen distinct transcription activator-like effector genes. RNA-sequencing revealed 52 genes induced within two cotton cultivars by both tested Xcm strains. This gene list includes a homeologous pair of genes, with homology to the known susceptibility gene, MLO. In contrast, the two strains of Xcm induce different clade III SWEET sugar transporters. Subsequent genome wide analysis revealed patterns in the overall expression of homeologous gene pairs in cotton after inoculation by Xcm. These data reveal host-pathogen specificity at the genetic level and strategies for future development of resistant cultivars.Author SummaryCotton bacterial blight (CBB), caused by Xanthomonas citri pv. malvacearum (Xcm), significantly limited cotton yields in the early 20th century but has been controlled by classical resistance genes for more than 50 years. In 2011, the pathogen re-emerged with a vengeance. In this study, we compare diverse pathogen isolates and cotton varieties to further understand the virulence mechanisms employed by Xcm and to identify promising resistance strategies. We generate fully contiguous genome assemblies for two diverse Xcm strains and identify pathogen proteins used to modulate host transcription and promote susceptibility. RNA-Sequencing of infected cotton reveals novel putative gene targets for the development of durable Xcm resistance. Together, the data presented reveal contributing factors for CBB re-emergence in the U.S. and highlight several promising routes towards the development of durable resistance including classical resistance genes and potential manipulation of susceptibility targets.

scholarly journals Physiologic Specialization of Puccinia triticina on Wheat in the United States in 2004

Plant Disease ◽  
2006 ◽  
Vol 90 (9) ◽  
pp. 1219-1224 ◽  
Author(s):  
J. A. Kolmer ◽  
D. L. Long ◽  
M. E. Hughes
Keyword(s):  
United States ◽  
Leaf Rust ◽  
Great Plains ◽  
Resistance Genes ◽  
Durable Resistance ◽  
Puccinia Triticina ◽  
Leaf Rust Resistance ◽  
The United States ◽  
Virulence Phenotype ◽  
Common Phenotype

Collections of Puccinia triticina were obtained from rust-infected wheat leaves by cooperators throughout the United States and from surveys of wheat fields and nurseries in the Great Plains, Ohio Valley, southeast, California, and Pacific Northwest, in order to determine the virulence of the wheat leaf rust population in 2004. Single uredinial isolates (757 in total) were derived from the collections and tested for virulence phenotype on lines of Thatcher wheat that are near-isogenic for leaf rust resistance genes Lr1, Lr2a, Lr2c, Lr3a, Lr9, Lr16, Lr24, Lr26, Lr3ka, Lr11, Lr17a, Lr30, LrB, Lr10, Lr14a, Lr18, Lr21, and Lr28, and winter wheat lines with genes Lr41 and Lr42. In the United States in 2004, 52 virulence phenotypes of P. triticina were found. Virulence phenotype MCDSB, selected by virulence to resistance genes Lr17a and Lr26, was the most common phenotype in the United States and was found in all wheat growing areas. Virulence phenotype TBBGG, with virulence to Lr2a, was the second most common phenotype and was found primarily in the spring wheat region of the north-central states. Virulence phenotype MBDSB, which has virulence to Lr17a, was the third most common phenotype and was found in all wheat growing areas except California. Phenotype TNRJJ, with virulence to genes Lr9, Lr24, and Lr41, was the fourth most common phenotype and occurred in the southeastern states and throughout the Great Plains region. Virulence phenotypes avirulent to a second gene in the Thatcher differential line with Lr1 increased in frequency in the United States in 2004. The highly diverse population of P. triticina in the United States will continue to present a challenge for the development of wheat cultivars with effective durable resistance.

scholarly journals Pan-Genome Analysis of Effectors in Korean Strains of the Soybean Pathogen Xanthomonas citri pv. glycines

2021 ◽  
Vol 9 (10) ◽  
pp. 2065
Author(s):  
In-Jeong Kang ◽  
Kyung Seok Kim ◽  
Gwyn Beattie ◽  
Jung-Wook Yang ◽  
Kee Hoon Sohn ◽  
...  
Keyword(s):  
Genome Analysis ◽  
Type Iii Secretion ◽  
The United States ◽  
Comparative Genome Analysis ◽  
Transcription Activator ◽  
Xanthomonas Citri ◽  
Carbohydrate Active Enzymes ◽  
Soybean Cultivars ◽  
Binding Domains ◽  
Effector Binding

Xanthomonas citri pv. glycines is a major pathogen of soybean in Korea. Here, we analyzed pathogenicity genes based on a comparative genome analysis of five Korean strains and one strain from the United States, 8ra. Whereas all six strains had nearly identical profiles of carbohydrate-active enzymes, they varied in diversity and number of candidate type III secretion system effector (T3SE) genes. The five Korean strains were similar in their effectors, but differed from the 8ra strain. Across the six strains, transcription activator-like effectors (TALEs) showed diverse repeat sizes and at least six forms of the repeat variable di-residue (RVD) sequences, with differences not correlated with the origin of the strains. However, a phylogenetic tree based on the alignment of RVD sequences showed two distinct clusters with 17.5 repeats, suggesting that two distinct 17.5 RVD clusters have evolved, potentially to adapt Xcg to growth on distinct soybean cultivars. The predicted effector binding elements of the TALEs fell into six groups and were strongly overlapping in sequence, suggesting evolving target specificity of the binding domains in soybean cultivars. Our findings reveal the variability and adaptability of T3SEs in the Xcg strains and enhance our understanding of Xcg pathogenicity in soybean.

scholarly journals Identification of virulence tal gene in the cotton pathogen, Xanthomonas citri pv. malvacearum strain Xss-V2-18

2020 ◽  
Author(s):  
Fazal Haq ◽  
Syed Mashab Ali Shah ◽  
Shiwang Xie ◽  
Kunxuan Huang ◽  
Wenxiu Ma ◽  
...  
Keyword(s):  
Virulent Strain ◽  
Evolutionary Relationship ◽  
The United States ◽  
In Planta ◽  
Dna Encoding ◽  
Transcription Activator ◽  
Xanthomonas Citri ◽  
Suicide Vector ◽  
In Trans ◽  
Highly Virulent

Abstract Background Bacterial blight of cotton (BBC), which is incited by Xanthomonas citri pv. malvacearum ( Xcm ), is a destructive disease in cotton. Transcription activator-like effectors (TALEs), encoded by tal -genes, play critical roles in the pathogenesis of xanthomonads. Characterized strains of cotton pathogenic Xcm harbor 6-13 different tal genes and only one of them is functionally decoded. Further identification of novel tal genes in Xcm strains with virulence contributions are prerequisite to decipher the Xcm -cotton interactionsResults In this study, we identified six tal genes in Xss-V 2 -18, a highly-virulent strain of Xcm from China, and assessed their role in BBC. RFLP-based Southern hybridization assays indicated that Xss-V 2 -18 harbors the six tal genes on a plasmid. The plasmid-encoded tal genes were isolated by cloning Bam HI fragments and screening clones by colony hybridization. The tal genes were sequenced by inserting a Tn 5 transposon in the DNA encoding the central repeat region (CRR) of each tal gene. Xcm TALome evolutionary relationship based on TALEs CRR revealed relatedness of Xss-V 2 -18 to MSCT1 and MS14003 from the United States. However, Tal2 of Xss-V 2 -18 differs at two repeat variable diresidues (RVDs) from Tal6 and Tal26 in MSCT1 and MS14003, respectively, inferred functional dissimilarity. The suicide vector pKMS1 was then used to construct tal deletion mutants in Xcm Xss-V 2 -18. The mutants were evaluated for pathogenicity in cotton based on symptomology and growth in planta . Four mutants showed attenuated virulence and all contained mutations in tal2 . One tal2 mutant designated M2 was further investigated in complementation assays. When tal2 was introduced into Xcm M2 and expressed in trans , the mutant was complemented for both symptoms and growth in planta , thus indicating that tal2 functions as a virulence factor in Xcm Xss-V 2 -18.Conclusions Overall, the results demonstrated that Tal2 is a major pathogenicity factor in Xcm strain Xss-V 2 -18 that contributes significantly in BBC. This study provides a foundation for future efforts aimed at identifying susceptibility genes in cotton that are targeted by Tal2.

scholarly journals Cloning of the rice Xo1 resistance gene and interaction of the Xo1 protein with the defense-suppressing Xanthomonas effector Tal2h

2020 ◽  
Author(s):  
Andrew C. Read ◽  
Mathilde Hutin ◽  
Matthew J. Moscou ◽  
Fabio C. Rinaldi ◽  
Adam J. Bogdanove
Keyword(s):  
Resistance Gene ◽  
Resistance Genes ◽  
Bacterial Blight ◽  
Rice Variety ◽  
Susceptible Variety ◽  
Xanthomonas Oryzae ◽  
Physical Interaction ◽  
Bacterial Leaf Streak ◽  
Transcription Activator ◽  
Rice Leaves

AbstractThe Xo1 locus in the heirloom rice variety Carolina Gold Select confers resistance to bacterial leaf streak and bacterial blight, caused by Xanthomonas oryzae pvs. oryzicola and oryzae, respectively. Resistance is triggered by pathogen-delivered transcription activator-like effectors (TALEs) independent of their ability to activate transcription, and is suppressed by variants called truncTALEs common among Asian strains. By transformation of the susceptible variety Nipponbare, we show that one of 14 nucleotide-binding, leucine-rich repeat (NLR) protein genes at the locus, with a zfBED domain, is the Xo1 gene. Analyses of published transcriptomes revealed that the Xo1-mediated response is similar to those of NLR resistance genes Pia and Rxo1 and distinct from that associated with induction of the executor resistance gene Xa23, and that a truncTALE dampens or abolishes activation of defense-associated genes by Xo1. In Nicotiana benthamiana leaves, fluorescently-tagged Xo1 protein, like TALEs and truncTALEs, localized to the nucleus. And, endogenous Xo1 specifically co-immunoprecipitated from rice leaves with a pathogen-delivered, epitope-tagged truncTALE. These observations suggest that suppression of Xo1-function by truncTALEs occurs through direct or indirect physical interaction. They further suggest that effector co-immunoprecipitation may be effective for identifying or characterizing other resistance genes.

scholarly journals Races of Puccinia striiformis f. sp. tritici in the United States in 2011 and 2012 and Comparison with Races in 2010

Plant Disease ◽  
2016 ◽  
Vol 100 (5) ◽  
pp. 966-975 ◽  
Author(s):  
Anmin Wan ◽  
Xianming Chen ◽  
Jonathan Yuen
Keyword(s):  
United States ◽  
Stripe Rust ◽  
Resistance Genes ◽  
Puccinia Striiformis ◽  
Single Gene ◽  
Durable Resistance ◽  
The United States ◽  
Western United States ◽  
Adult Plant ◽  
Low Frequencies

Stripe rust, caused by Puccinia striiformis f. sp. tritici, is one of the most important diseases on wheat in the United States. In 2011, severe wheat stripe rust caused extensive application of fungicides in the western United States, and the disease was more widespread and caused more yield loss in the eastern United States in 2012. In this study, we characterized virulences and identified races of P. striiformis f. sp. tritici by testing the stripe rust samples collected throughout the United States in 2011 and 2012 on a set of 18 Yr single-gene differentials. In 2011, 35 races were identified from 349 viable samples collected from 19 states of the United States and Ontario province of Canada, with PSTv-11 (35.5%), PSTv-37 (12.6%), PSTv-14 (11.8%), PSTv-4 (5.4%), and PSTv-34 (3.4%) as the top five predominant races. In 2012, 23 races were identified from 341 viable samples collected from 24 states of the United States and Ontario of Canada, with PSTv-37 (47.5%), PSTv-11 (11.7%), PSTv-14 (10.0%), PSTv-52 (9.4%), and PSTv-48 (4.4%) as the top five predominant races. Nationally, PSTv-37, PSTv-52, and PSTv-34 were most widely distributed, while PSTv-11, PSTv-14, PSTv-4, and PSTv-48 were mostly detected in the western United States. High frequencies (>80%) were detected for virulences to Yr6, Yr7, Yr8, Yr9, Yr17, Yr27, Yr44, and YrExp2; moderate frequencies (20 to 80%) for virulences to Yr1, Yr43, YrTr1, and YrTye; low frequencies (<10%) for virulences to Yr10, Yr24, Yr32, and YrSP; and virulences to Yr5 and Yr15 were not detected, indicating that these two genes are still effective against the P. striiformis f. sp. tritici population in the United States. Both positive and negative associations were identified between some of the virulences. In total, 55 races identified from 2010 to 2012 in the United States were clustered into two major virulence groups, and dynamics of predominant races and virulence frequencies for the 3 years were presented and discussed. This information is useful for making decisions when screening wheat germplasm for developing stripe-rust-resistant wheat cultivars and managing the disease by growing cultivars with adequate and durable resistance. The severe epidemics and the occurrence of the large number of races in the 3 years indicate that efforts should be made to use diverse resistance genes, especially to combine effective all-stage resistance genes with genes for high-temperature adult-plant resistance.

scholarly journals First Complete Genome Sequences of Xanthomonas citri pv. vignicola Strains CFBP7111, CFBP7112, and CFBP7113 Obtained Using Long-Read Technology

2017 ◽  
Vol 5 (36) ◽  
Author(s):  
Mylène Ruh ◽  
Martial Briand ◽  
Sophie Bonneau ◽  
Marie-Agnès Jacques ◽  
Nicolas W. G. Chen
Keyword(s):  
Single Molecule ◽  
Bacterial Blight ◽  
Genomic Data ◽  
Transcription Activator ◽  
Xanthomonas Citri ◽  
Genome Sequences ◽  
Content Type ◽  
Legume Crop ◽  
New Information ◽  
Long Read

ABSTRACT Xanthomonas citri pv. vignicola strains cause bacterial blight of the legume crop cowpea. We report whole-genome sequences of three X. citri pv. vignicola strains obtained using PacBio single-molecule real-time sequencing. Such genomic data provide new information on pathogenicity factors, such as transcription activator-like effectors.

scholarly journals A strain of an emerging Indian pathotype of Xanthomonas oryzae pv. oryzae defeats the rice bacterial blight resistance gene xa13 without inducing a clade III SWEET gene and is nearly identical to a recent Thai isolate

2018 ◽  
Author(s):  
Sara C. D. Carpenter ◽  
Prashant Mishra ◽  
Chandrika Ghoshal ◽  
Prasanta Dash ◽  
Li Wang ◽  
...  
Keyword(s):  
Resistance Genes ◽  
Bacterial Blight ◽  
Xanthomonas Oryzae ◽  
Host Susceptibility ◽  
Transcription Activator ◽  
Rice Bacterial Blight ◽  
Indian Strain ◽  
Bacterial Blight Pathogen ◽  
Insight Into ◽  
S Genes

AbstractThe rice bacterial blight pathogen Xanthomonas oryzae pv. oryzae (Xoo) injects transcription activator-like effectors (TALEs) that bind and activate host ‘susceptibility’ (S) genes important for disease. Clade III SWEET genes are major S genes for bacterial blight. The resistance genes xa5, which reduces TALE activity generally, and xa13, a SWEET11 allele not recognized by the cognate TALE, have been effectively deployed. However, strains that defeat both resistance genes individually were recently reported in India and Thailand. To gain insight into the mechanism(s), we completely sequenced the genome of one such strain from each country and examined the encoded TALEs. Strikingly, the two strains are clones, sharing nearly identical TALE repertoires, including a TALE known to activate SWEET11 strongly enough to be effective even when diminished by xa5. We next investigated SWEET gene induction by the Indian strain. The Indian strain induced no clade III SWEET in plants harbouring xa13, indicating a pathogen adaptation that relieves dependence on these genes for susceptibility. The findings open a door to mechanistic understanding of the role SWEET genes play in susceptibility and illustrate the importance of complete genome sequence-based monitoring of Xoo populations in developing varieties with effective disease resistance.

scholarly journals Marker-assisted pyramiding of two major broad-spectrum bacterial blight resistance genes,Xa21andXa33into an elite maintainer line of rice, DRR17B

2018 ◽  
Author(s):  
CH Balachiranjeevi ◽  
S Bhaskar Naik ◽  
V Abhilash Kumar ◽  
G Harika ◽  
H.K Mahadev Swamy ◽  
...  
Keyword(s):  
Resistance Genes ◽  
Bacterial Blight ◽  
Durable Resistance ◽  
Gene Pyramiding ◽  
Resistance Breeding ◽  
Fertility Restorer ◽  
Rice Varieties ◽  
Homozygous Condition ◽  
Specific Pcr ◽  
High Level

AbstractBacterial blight (BB) disease reduces the yield of rice varieties and hybrids considerably in many tropical rice growing countries like India. The present study highlights the development of durable BB resistance into the background of an elite maintainer of rice, DRR17B, by incorporating two major dominant genes,Xa21andXa33through marker-assisted backcross breeding (MABB). Through two sets of backcrosses, the two BB resistance genes were transferred separately to DRR17B. In this process, at each stage of backcrossing, foreground selection was carried out for the target resistance genes and for non-fertility restorer alleles concerning the major fertility restorer genesRf3andRf4, using gene-specific PCR-based markers, while background selection was done using a set of 61 and 64 parental polymorphic SSR markers respectively. Backcross derived lines possessing eitherXa21orXa33along with maximum genome recovery of DRR17B were identified at BC3F1generation and selfed to develop BC3F2s. Plants harboringXa21orXa33in homozygous condition were identified among BC3F2s and were intercrossed with each other to combine both the genes. The intercross F1plants (ICF1) were selfed and the intercross F2(ICF2) plants possessing bothXa21andXa33in homozygous condition were identified with the help of markers. They were then advanced further by selfing until ICF4generation. Selected ICF4lines were evaluated for their resistance against BB with eight virulent isolates and for key agro-morphological traits. Six promising two-gene pyramiding lines of DRR17B with high level of BB resistance and agro-morphological attributes similar or superior to DRR17B with complete maintenance ability have been identified. These lines with elevated level of durable resistance may be handy tool for BB resistance breeding.

Patterns of seed-to-seedling transmission of Xanthomonas citri pv. malvacearum, the causal agent of cotton bacterial blight

2021 ◽  
Author(s):  
Jovana Mijatović ◽  
Paul Severns ◽  
Robert C Kemerait ◽  
Ron Ricardo Walcott ◽  
Brian Kvitko
Keyword(s):  
Bacterial Blight ◽  
Vascular Tissue ◽  
Bacterial Load ◽  
Field Isolate ◽  
The United States ◽  
Xanthomonas Citri ◽  
Systemic Spread ◽  
Colonization Patterns ◽  
Important Disease

Cotton bacterial blight (CBB), caused by Xanthomonas citri pv. malvacearum (Xcm), was a major disease of cotton in the United States in the early part of the 20th century. The recent reemergence of CBB revealed many gaps in our understanding of this important disease. In this study, we employed a wild type (WT) field isolate of Xcm from Georgia USA to generate a non-pathogenic, hrcV mutant lacking a functional type III secretion system (T3SS-). We tagged the WT and T3SS- strains with an auto-bioluminescent Tn7 reporter and compared colonization patterns of susceptible and resistant cotton seedlings using macroscopic image analysis and bacterial load enumeration. Wildtype and T3SS- Xcm strains colonized cotton cotyledons of resistant and susceptible cotton cultivars. However, Xcm populations were significantly higher in susceptible seedlings inoculated with the WT strain. Additionally, WT and T3SS- Xcm strains systemically colonized true leaves, although at different rates. Finally, we observed that seed-to-seedling transmission of Xcm may involve systemic spread through the vascular tissue of cotton plants. These findings yield novel insights into potential Xcm reservoirs for CBB outbreaks.

scholarly journals The immunity of Meiwa kumquat against Xanthomonas citri is associated with a known susceptibility gene induced by a transcription activator-like effector

2020 ◽  
Vol 16 (9) ◽  
pp. e1008886
Author(s):  
Doron Teper ◽  
Jin Xu ◽  
Jinyun Li ◽  
Nian Wang
Keyword(s):  
Susceptibility Gene ◽  
Transcription Activator ◽  
Xanthomonas Citri
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