Fusarium wilt of Luffa, caused by Fusarium oxysporum f. sp. luffae, causes great losses in Luffa plants worldwide. In this study, 45 accessions of Luffa germplasm were used to determine their resistance to F. oxysporum f. sp. luffae isolates (FOLUST, FOLUSC, Fomh16, and Fol114) in two independent trials. In the first trial, only FOLUST was used to preliminarily identify resistant accessions. Nine accessions of Luffa acutangula and five of L. aegyptiaca were resistant to the FOLUST isolate. In the second trial, the other three isolates were then used to reevaluate the 14 resistant accessions. The results indicated that the 14 accessions were resistant to FOLUSC but exhibited variable resistance to the Fomh16 and Fol114 isolates. Eight accessions of L. acutangula and one accession of L. aegyptiaca were resistant to Fol114. Seven accessions of L. acutangula and one accession of L. aegyptiaca were resistant to Fomh16. Despite the lack of any symptoms, the F. oxysporum f. sp. luffae isolates were recovered from the hypocotyls of all resistant accessions at 28 days postinoculation, except for isolates FOLUSC and FOLUST on one accession (LA140). A high percentage (87.5%) of accessions collected from Bangladesh were identified as resistant, highlighting the effect of local adaptation on resistance. These results provide potentially valuable genetic resources for breeding programs to develop new varieties or rootstocks that could be beneficial for controlling soilborne diseases in different cucurbit crops and further investigating the mechanisms of resistance to F. oxysporum f. sp. luffae in Luffa plants.

Fusarium oxysporum f. sp. luffae (Folu) is a severe plant pathogen that causes vascular wilt and root rot in Luffa plants worldwide. A green fluorescent protein (GFP)-tagged isolate of Folu (Fomh16-GFP) was utilized to investigate the infection progress and colonization of Fomh16-GFP in resistant (LA140) and susceptible (LA100) Luffa genotypes. Seven days post-inoculation (dpi), it was observed that Fomh16-GFP had successfully invaded and colonized the vascular bundle of all LA100 parts, including the roots, hypocotyl, and stem. Pathogen colonization continued to increase over time, leading to the complete wilting of plants by 14–17 dpi. In LA140, the Fomh16-GFP isolate colonized the roots and hypocotyl vascular system at 7 dpi. Nevertheless, this colonization was restricted in the hypocotyl and decreased significantly, and no fungal growth was detected in the vascular system at 21 dpi. Thus, the resistant genotype might trigger a robust defense mechanism. In addition, while the pathogen was present in LA140, the inoculated plants did not exhibit any symptoms until 28 dpi. Quantitative PCR was utilized to measure the Fomh16-GFP biomass in various parts of LA100 and LA140 at different time points. The findings indicated a positive correlation between the quantity of Fomh16-GFP DNA and disease development in LA100. Alternatively, a high amount of Fomh16-GFP DNA was identified in the roots of LA140. Nonetheless, no significant correlations were found between DNA amount and disease progression in LA140. Aqueous extracts from LA140 significantly reduced Fomh16-GFP spore germination, while no significant reduction was detected using LA100 extracts. IMPORTANCE: Fusarium wilt of Luffa , caused by Fusarium oxysporum f. sp. luffae (Folu), causes great losses in Luffa plants worldwide. This study used a green fluorescent protein (GFP)-tagged isolate of Folu (Fomh16-GFP) to investigate the infection progress and colonization dynamics of Fomh16-GFP in the resistant and susceptible Luffa genotypes, which could be important in understanding the resistance mechanism of Folu in Luffa plants. In addition, our work highlights the correlations between DNA amount and disease progression in resistant plants using real-time PCR. We observed a positive correlation between the quantity of Fomh16-GFP DNA and disease progression in LA100, while no significant correlation was found in LA140. These results could be valuable to further investigate the resistance mechanism of Luffa genotypes against Folu. Gaining a better understanding of the interaction between Folu and Luffa plants is crucial for effectively managing Fusarium wilt and enhancing resistance in Luffa rootstock and its varieties.

Fusarium solani species complex (FSSC) is a causal agent of collar rot and fruit rot in passion fruit worldwide. This study investigated the diversity and characteristics of FSSC isolates causing collar rot and fruit rot in Taiwanese passion fruit. Thirty-five FSSC isolates were harvested from collar rot and fruit rot samples of passion fruit from various cultivars and different geographical locations in Taiwan. The majority of these FSSC isolates caused collar rot and fruit rot disease of varying virulence in the stems and fruits of the purple and yellow cultivars of passion fruit. FSSC isolates were categorized into four groups: F. solani-melongenae (FSSC 21; n = 29), F. solani (FSSC 5; n = 1), F. liriodendri (FSSC 24; n = 1), and an unknown group (n = 4) based on the phylogenetic analysis of internal transcribed sequence (ITS), translation elongation factor 1 alpha (TEF-1α), and RNA polymerase II subunit 2 (RPB2) sequences. In Taiwan, F. solani-melongenae was the dominant species causing collar rot and fruit rot in passion fruit. F. solani-melongenae was a homothallic fungus that produced perithecia in diseased tissues. However, F. solani and F. liriodendri did not produce perithecia. The unknown FSSC group showed morphological characteristics similar to F. solani-melongenae and produced perithecia. Phylogenetic analysis based on the ITS and TEF-1α sequences demonstrated that the Taiwanese FSSC isolates were distinct from the Brazilian and Chinese FSSC isolates. In summary, FSSC isolates causing collar rot and fruit rot of Taiwanese passion fruit showed high diversity, potentially associated with the geographical locations.

Fusarium wilt in bitter gourd caused by Fusarium oxysporum f. sp. momordicae (Fomo) is a severe plant disease that affects the world’s bitter gourd (Momordica charantia L.) cultivation. This study evaluated nine luffa hybrids for their performance as rootstocks with bitter gourd to control Fusarium oxysporum f. sp. luffae (Folu) isolate Fomh16 and Fomo isolate Fomo33. In the first evaluation, five hybrids (LF1, LF2, LF3, LF15, and LF16) exhibited resistance to the Fomh16 isolate and showed no symptoms. One hybrid, LF10, was resistant with a mean disease rating (MDR) of 0.9 at 28 days post-inoculation (dpi). Seven luff hybrids that displayed resistant and moderate resistance in the first evaluation were used as rootstocks with susceptible bitter gourd cultivars. Five rootstocks exhibited high resistance to Fomh16 and Fomo33 isolates, with their MDR ranging from 0.0 to 0.7. In addition, the findings revealed that both isolates could colonize the vascular bundle of all resistant luffa rootstocks at 28 dpi. However, the Fomo33 isolate could extend and colonize the vascular bundle of bitter gourd scion when grafted only with rootstock LF5 and LF11. The quantitative PCR results indicated that there were significant differences in the amount of the Fomo33 DNA between the bitter gourd grafted onto LF15 and LF16 rootstocks and the self-grafted plants; however, the pathogen cannot be detected in the bitter gourd scions grafted with resistant rootstocks. These findings provide valuable resistant sources that can be used as rootstocks to manage Fusarium wilt disease in bitter gourd.

The Fusarium incarnatum-equiseti species complex (FIESC) is a harmful plant pathogen responsible for diseases, such as root rot, fruit rot, leaf blight, and wilt, in various crops. Recently, it has been increasingly associated with both superficial and invasive infections in humans and animals. Additionally, this pathogen produces mycotoxins, posing significant risks to public health. This study aims to characterize the molecular and morphological characteristics of FIESC isolates obtained from various sources, including human, veterinary, and plant samples. Molecular identification was performed using multilocus sequence typing (MLST), targeting the internal transcribed spacer (ITS) rDNA, the second-largest subunit of the RNA polymerase gene (RPB2), and translation elongation factor 1 alpha (TEF-1α). Based on MLST analysis, all FIESC isolates were found to belong to the Incarnatum clade and were classified into two species: F. irregulare and F. pernambucanum . Furthermore, these isolates demonstrated the ability to penetrate and colonize human nails, porcine skin, and muskmelon fruits. In this study, we report members of FIESC as a newly identified pathogens in Taiwan capable of cross-infection among humans, animals, and plants. These findings highlight the dual significance of Fusarium : it poses a serious threat to agriculture by compromising plant health and crop yields while also representing a public health risk due to its ability to infect humans and animals. IMPORTANCE: The Fusarium incarnatum-equiseti species complex (FIESC) is a significant plant pathogen affecting a wide range of crops, leading to substantial agricultural losses worldwide. In this study, we report that Fusarium isolates belonging to F. pernambucanum and F . irregulare obtained from various sources, including respiratory specimens from human, cat, rabbit, and turtle, along with plant samples from muskmelon fruits, represent newly identified pathogens in Taiwan. Our findings suggest that these isolates possess the potential for cross-infection among plants, animals, and humans, underscoring their importance in both agricultural and medical contexts. Notably, the plant isolates PLMF1 and BDMF7 demonstrate the ability to transition from plant pathogens to zoonotic pathogens, highlighting a concerning adaptability.

Bacterial wilt (BW), caused by soil-borne bacteria of the Ralstonia solanacearum species complex (RSSC), is a serious disease affecting eggplant (Solanum melongena) in tropical and subtropical regions. Resistance to BW in eggplant has been identified in several accessions and wild relatives, but no source has shown broad and stable resistance across diverse strains and environmental conditions. In the first screening trial, six eggplant genotypes, including five previously identified as resistant to RSSC, were evaluated along with two tomato checks against eight BW strains representing two phylotypes (I and II) and three biovars (2, 3, and 4). In the second screening trial, 26 hybrids developed from seven parental eggplant genotypes (including the six evaluated genotypes in the first screening plus an additional one) were evaluated, together with the parents, against three BW strains (Pss97, Pss2016, and Pss4). The results showed that the parental line EG048 was highly susceptible, whereas EG44 was resistant to the three strains, with a disease index (DI) of ≤20%. Furthermore, fourteen hybrids were classified as resistant or moderately resistant to the three strains. Among them, hybrid EG27 was categorized as highly resistant to all three strains with a disease index of 5.6–7.3%. In addition, three hybrids (EG8, EG20, and EG29) were highly resistant or resistant to all three strains, with a disease index of 3.8–15.8%. A strong positive correlation was observed between wilting percentage and disease index in the eggplant hybrids across the tested strains. Our results provide valuable support for eggplant breeding programs aimed at developing hybrid rootstocks with broader and potentially broad-spectrum resistance to RSSC in tomato and eggplant.