Resistant cultivars represent the most powerful approach to managing the disease. Within the context of wheat breeding, YrTr1 is a significant stripe rust resistance gene, appearing in the host differential set used to determine the presence of *P. striiformis f. sp*. The United States is a significant site for wheat strain races. In order to map YrTr1, the strain AvSYrTr1NIL was backcrossed against its recurrent parent, Avocet S (AvS). Under controlled environments, BC7F2, BC7F3, and BC8F1 seedlings were subjected to YrTr1-avirulent races. BC7F2 plants' genotypes were determined using simple sequence repeat (SSR) and single nucleotide polymorphism (SNP) markers. Autoimmune kidney disease The short arm of chromosome 1B was determined to harbor YrTr1, as indicated by the analysis of 4 simple sequence repeat (SSR) markers and 7 single nucleotide polymorphism (SNP) markers. IWA2583 was separated from YrTr1 by 18 centimorgans (cM), while IWA7480 was 13 cM away, respectively. Employing DNA amplification with three SSR markers, the chromosome arm location and chromosomal bin region 1BS18(05) assignment of a gene were established in 21 Chinese Spring (CS) nulli-tetrasomic lines and 7 CS 1B deletion lines. Measurements confirmed the gene to be approximately 74 cM from Yr10 in a proximal direction. Analysis of multi-racial responses and chromosomal location revealed that YrTr1 differed from other permanently named stripe rust resistance genes on chromosome arm 1BS and was thus designated Yr85.
Burkholderia gladioli and B. glumae are identified as significant agents for bacterial panicle blight (BPB), a severe rice disease that has become widespread (1). Several types of damage, most notably grain spotting, rot, and panicle blight, are inflicted by this disease, potentially leading to yield losses of 75% or more (13). Recent years have witnessed symptoms of sheath rot, grain spotting, grain rot, and panicle blight in both inbred and hybrid rice varieties. The observed symptoms mirror those characteristic of BPB, resulting in yield reductions that vary depending on the cultivar. (3) similarly documented these same symptoms in instances of BPB. From a farmer's field in Mymensingh, Bangladesh, 21 rice panicles of the Haridhan variety, which displayed typical symptoms of BPB, were collected in mid-October 2021, during the rainy season, to determine the disease's origin. The outbreak's severe consequences were evident in the dark brown color and chaffy nature of the grains produced by the panicles; nearly every rice panicle in that area showed significant infection. To pinpoint the causative pathogen(s) affecting rice, 20 plants exhibiting characteristic BPB symptoms each contributed 1 gram of grain, which was surface-sterilized by initial immersion in 70% ethanol for a few seconds, followed by a 1-minute treatment with a 3% sodium hypochlorite solution. The grains' rinsing with sterilized distilled water was executed in three separate cycles. Employing a mortar and pestle, surface-sterilized grains were ground while 5 milliliters of sterile distilled water was incorporated. The suspension, which had been extracted (20L), was subsequently distributed onto the S-PG selective medium (2), either by spreading or streaking the sample. Purple-hued bacterial colonies cultured on S-PG medium were singled out and purified, deemed as possible pathogens. For molecular characterization, PCR was carried out using species-specific primers targeted at the gyrB gene, producing a 479 base pair amplicon, referenced in 4. Subsequently, 16S rRNA PCR products underwent amplification and partial sequencing, yielding approximately 1400 base pairs of data (1), and five partial sequences were deposited in the NCBI GenBank database (accession numbers OP108276 to OP108280). Sequence analysis using BLAST revealed almost 99% homology between 16S rDNA and Burkholderia gladioli (KU8512481, MZ4254241), and between gyrB and B. gladioli (AB220893, CP033430), respectively. The purified bacterial isolates on King's B medium demonstrated the creation of a diffusible light-yellow pigment, signifying the presence of toxoflavin (3). To confirm the five bacterial isolates identified in the candidate, a 10 mL suspension (108 CFU/mL) was applied to the panicles and sheaths of BRRI Dhan28 plants under net house conditions, as previously described (1). The inoculated leaf sheaths of the rice plants, exposed to bacterial isolates from spotted grains, displayed light brown lesions and spotting on the grains. Bacteria from symptomatic panicles, re-isolated and confirmed as B. gladioli through the analysis of gyrB and 16s rDNA gene sequences, validated the criteria of Koch's postulates. Combining the findings from our analyses, it becomes clear that B. gladioli was responsible for the observed BPB in the collected rice grain samples. As far as we know, this is the inaugural report of BPB caused by B. gladioli in Bangladesh, necessitating further research to establish an efficient disease control method, otherwise rice production will be severely compromised.
Characterized by its aroma, peppermint (Lamiaceae) is a multifaceted herb finding application in the culinary, medicinal, and industrial realms. Four commercial peppermint (Mentha piperita) fields in San Buenaventura Tecalzingo, San Martin Texmelucan, Puebla, Mexico, demonstrated symptoms of foliar rust during June 2022. These locations were geographically pinpointed at 19°14′34″N 98°27′25″W; 19°14′16″N 98°27′21″W; 19°14′37″N 98°27′07″W; and 19°15′06″N 98°26′54″W. The collection at each site included two diseased plants. The disease affected fifty percent of the plants, manifesting in less than seventeen percent of damaged foliar tissue. The initial symptoms included the appearance of small chlorotic spots on the upper surface of the leaves, these spots then merging to create a necrotic area, surrounded by a wide chlorotic ring. Only in locations where reddish-brown pustules densely populated the leaf's underside did necrosis develop; smaller pustules were visible on the upper side. Signs were evident as a multitude of reddish-brown pustules, scattered across the abaxial leaf surfaces. All sampled leaves exhibiting infection displayed subepidermal uredinia, which were erumpent, featuring hyaline, cylindrical paraphyses. Supported individually on pedicels, urediniospores (n=50) were hyaline to light brown, echinulate, and obovoid (165-265 x 115-255 µm, mean ± SD = 22 ± 16 µm and 19 ± 4 µm, and 6 µm wall thickness). Each possessed two germinative pores. The morphological characteristics closely mirrored the description of Puccinia menthae provided by Kabaktepe et al. (2017) and Solano-Baez et al. (2022). Within the Herbarium of the Department of Plant-Insect Interactions at the Biotic Products Development Center of the National Polytechnic Institute, a voucher specimen was registered under its accession number. The item or transaction referenced by IPN 100115 requires attention. Genomic DNA was extracted from a single sample, and subsequent nested PCR amplification focused on the 28S gene segment of rDNA. The initial PCR reaction employed primers Rust2inv (Aime, 2006) and LR6 (Vilgalys and Hester, 1990), followed by a second reaction using Rust28SF (Aime et al., 2018) and LR5 (Vilgalys and Hester, 1990). The obtained sequence, identified by GenBank accession number OQ552847, exhibited a 100% identical sequence (902 out of 1304 base pairs) to the type specimen of P. menthae (DQ354513) from Cunila origanoides, USA, as mentioned in Aime's (2006) publication. A phylogenetic analysis based on Maximum Likelihood, utilizing a previously published 28S dataset encompassing Puccinia species, was conducted. As a result, the isolate IPN 100115 was located within a clade of P. menthae, validated by a 100% bootstrap confidence level. To ascertain pathogenicity, a suspension of urediniospores (1104 spores/ml) from isolate IPN 100115 was applied to a group of six healthy 30-day-old peppermint plants (Mentha piperita). A parallel group of six plants received only sterile distilled water. Plants were retained in a humid chamber, maintaining 28°C and 95% relative humidity, for a period of 48 hours, after which the plastic coverings were removed from each plant. Within 15 days, inoculated plants manifested disease symptoms, whereas control plants continued to be asymptomatic. The pathogenicity assay yielded comparable results on two separate occasions. The morphology of the pathogen isolated from the inoculated plants' pustules was identical to the morphology of the previously collected sample, satisfying the conditions laid out by Koch's postulates. To the best of our knowledge, the present account constitutes the initial documentation of Puccinia menthae as the causative agent of leaf rust on Mentha piperita specimens in Mexico. In Brazil, Canada, Poland, and the USA, previous identifications of this species utilized morphological characteristics, particularly within the Mentha piperita species (Farr and Rossman, 2023). The disease, impacting the leaves of peppermint plants and reducing overall yield, underscores the need for further guidance on disease management procedures.
In the month of February 2023, two specimens of Monstera deliciosa Liebm. were observed. The presence of leaf rust disease, with its characteristic symptoms, was observed on Araceae plants at a grocery store in Oconee County, South Carolina. The leaves displayed chlorotic spots and an abundance of brownish uredinia, concentrated largely on the upper sides of more than fifty percent of the leaves. A greenhouse at a plant nursery in York County, South Carolina, witnessed 11 out of 481 M. deliciosa plants displaying the same disease condition in March 2023. Morphological characterization, molecular identification, and rust fungus pathogenicity confirmation of the plant sample taken in February were conducted. Urediniospores, densely aggregated into a globose form, were colored golden to golden brown, exhibiting sizes ranging from 229 to 279 micrometers on average. selleck inhibitor A 260-meter-diameter cylinder, with a wall thickness ranging from 13 to 26 meters (average), is measured at 11 meters. Trained immunity At 18:03, with n equaling 50, specific conditions prevailed.