The tomato is one of the most important vegetable crops grown worldwide. Tomato brown rugose fruit virus (ToBRFV), a seed-borne tobamovirus, poses a serious threat to tomato production due to its ability to break the resistant genes (Tm-1, Tm-2, Tm-2²) in tomatoes. The objective of this work was to identify new resistant source(s) of tomato germplasm against ToBRFV. To achieve this aim, a total of 476 accessions from 12 Solanum species were tested with the ToBRFV US isolate for their resistance and susceptibility. As a result, a total of 44 asymptomatic accessions were identified as resistant/tolerant, including thirty-one accessions of S. pimpinellifolium, one accession of S. corneliomulleri, four accessions of S. habrochaites, three accessions of S. peruvianum, and five accessions of S. subsection lycopersicon hybrid. Further analyses using serological tests identified four highly resistant S. pimpinellifolium lines, PI 390713, PI 390714, PI 390716, and PI 390717. The inheritance of resistance in the selected lines was verified in the next generation and confirmed using RT-qPCR. To our knowledge, this is a first report of high resistance to ToBRFV in S. pimpinellifolium. These new genetic resources will expand the genetic pool available for breeders to develop new resistant cultivars of tomato against ToBRFV.

Tomato is one of the most important vegetable crops grown worldwide. Tomato brown rugose fruit virus (ToBRFV), a seed-borne tobamovirus, poses a serious threat to tomato productions due to its ability to break the resistant genes (Tm-1, Tm-2, Tm-22) in tomato. The objective of this work was to identify new resistance source(s) of tomato germplasm against ToBRFV. To achieve this aim, a total of 476 accessions from 12 Solanum species were tested with the ToBRFV US isolate for their resistance and susceptibility. As a result, a total of 44 asymptomatic accessions were identified as resistance/tolerance, including 31 accessions of S. pimpinellifolium, one accession of S. corneliomulleri, four accessions of S. habrochaites, three accessions of S. peruvianum and five accessions of S. subsection lycopersicon hybrid. Further analysis using serological tests identified four highly resistant S. pimpinellifolium lines, PI 390713, PI 390714, PI 390716 and PI 390717. The inheritance of resistance in the selected lines was verified in next generation and confirmed by RT-qPCR. To our knowledge, this is a first report of high resistance to ToBRFV in S. pimpinellifolium. These new genetic resources will expand the genetic pool available for breeders to develop new resistant cultivars of tomato against ToBRFV.

Tomato (Solanum lycopersicum L.), one of the most widely grown vegetables in the world, has been seriously impacted in the past decade by the emerging tomato brown rugose fruit virus (ToBRFV). ToBRFV is a seed-borne tobamovirus, with ability to overcome the commonly used Tm-2² resistance gene in tomato. The objective of this study was to conduct quantitative trait locus (QTL) mapping and identify single-nucleotide polymorphism (SNP) markers associated with ToBRFV resistance in tomato. Two F₂ populations were used for QTL mapping: One derived from a cross between S. pimpinellifolium USVL333 (PI 390718) × USVL332 (PI 390717) and another from ‘Moneymaker’ × USVL332 (PI 390717), with population sizes of 195 and 79 plants, respectively. The resistance trait was derived from the S. pimpinellifolium accession USVL332 (PI 390717). A major QTL for ToBRFV resistance was identified on chromosome 11 (SL4.0ch11), with the peak located at approximately 46.84 Mbp. This QTL spans a 22-kb interval between 46,825,788 bp and 46,847,421 bp, as determined through both genome-wide association study (GWAS) and QTL linkage mapping. Three SNP markers, SL4.0ch11_46825788, SL4.0ch11_46847421, and SL4.0ch11_46850215, demonstrated the most significant association with high LOD values (LOD = 13 in the Blink model) in GWAS analysis. In this genomic region, two disease resistance gene analogs, Solyc11g062150 (TIR-NBS-LRR resistance protein, Toll-Interleukin receptor) and Solyc11g062180 (disease resistance protein, leucine-rich repeat), were identified, which may serve as candidates for ToBRFV resistance. The QTL identified in this study could be valuable for plant breeders in facilitating tomato breeding with ToBRFV resistance.

Watermelon (Citrullus lanatus) is an important vegetable fruit crop, widely grown in many countries in the tropical and subtropical regions around the world. The narrow genetic base of cultivated watermelon makes it susceptible to many pests and diseases, especially viruses. However, genetic sources of resistance are available in wild relatives that could potentially be used to incorporate the resistance genes into watermelon cultivars. Ribosome-inactivating proteins (RIPs) are prevalent in many plant species and are known to have an important role in defense against bacteria, fungi, and viruses. The objective of this study was to identify RIP-like sequences in the watermelon genome and to conduct comparative measurement of RIP gene expression between the potyvirus-resistant Citrullus amarus ‘PI 244019ʹ versus the susceptible watermelon (C. lanatus) ‘Charleston Gray’ in response to infection by papaya ringspot virus (PRSV). Taking advantage of the recently available genome sequences of ‘PI 244019ʹ and ‘Charleston Gray’, in this study we mined out watermelon RIP genes and conducted comparative sequence and expression analyses of RIP-I and RIP-II between the genotypes. The RIP gene expression analysis revealed elevated RIP gene expression in resistant PI 244019 plants, but not in susceptible ‘Charleston Gray’ plants, in response to inoculation with PRSV, indicating a potential association of RIP gene expression and resistance to potyviruses in watermelon. This elevated expression of RIP genes in association with potyvirus resistance opens a new avenue to investigate the underlying mechanism of potyvirus resistance in watermelon.

Powdery mildew, caused by Podosphaera xanthii, poses a significant threat to watermelon (Citrullus lanatus) cultivation. Development of resistant cultivars is one of the best strategies to manage powdery mildew. To elucidate the genetic basis of resistance, bulked segregant analysis (BSA) was conducted on an F ₂ population derived from a cross between resistant (USVL608-PMR) and susceptible (USVL677-PMS) genotypes. A 570-kb region on chromosome 2 was identified using QTLseq, containing 99 single-nucleotide polymorphisms (SNP) and eight putative genes. A tightly linked kompetitive allele specific PCR (KASP) marker was developed and validated across three F ₂ populations (USVL608-PMR × USVL677-PMS, USVL608-PMR × ‘Sugar Baby,’ USVL608-PMR × ‘Dixie Lee’), showing a 3:1 segregation ratio and very strong linkage to resistance. Marker-disease resistance linkage was further validated in the F ₃ generation of all three populations. RNAseq analysis revealed the upregulation of lipoxygenase (LOX), jasmonic acid (JA), and reactive oxygen species (ROS) pathways after inoculation, suggesting their role in powdery mildew resistance in watermelon. The development of tightly linked KASP markers in three different backgrounds for powdery mildew resistance and a molecular understanding of disease resistance will be useful for breeding and selecting new disease-resistant watermelon cultivars.

Bottle gourd (Lagenaria siceraria L.) belongs to the cucurbit family and has a long history of cultivation in tropical and subtropical regions worldwide, both for food and medicine. Popularized by its unique fruit shapes, gourds are used to make ornaments and musical instruments. However, there is limited information on volatile organic compounds (VOCs) in the bottle gourd fruit. In the present study, we conducted a comparative analysis of VOCs profiled in two accessions (USVL5 and USVL10) with distinct fruit shapes: bottle and cylinder. While USVL5 only produced long cylinder fruits, USVL10 produced two fruit types, cylinder (USVL10CYN) and bottle (USVL10A and USVL10B). VOCs in each line were analyzed using headspace solid-phase microextraction–gas chromatography/mass spectrometry (HS-SPME-GC/MS). Aliphatic aldehydes and alcohols were the most abundant compounds found in these bottle gourd accessions. Based on the functional profile of the identified VOCs, our results reveal the suitability of our tested line (USVL10), enriched in functionally important VOCs such as hexanal (abundance = 381.07), nonanal (abundance = 9.85), 2-methoxy-2-methylpropane (abundance = 21.26) and D-limonene (abundance = 31.48). The VOCs profiling and functional analyses support the notion that the bottle gourd accession USVL10 can be a good candidate for its use in agriculture, the health care industry and domestic uses.