This study was conducted to develop a screening method using Colilert-18 and a device for the detection of from agri-food production environments and fresh vegetables. The specificity and sensitivity of Colilert-18 by temperature (37°C and 44°C) were evaluated with 38 and 78 non- strains. The false-positive rate was 3.8% (3/78) and 0% (0/78) at 37°C and 44°C, respectively. The detection limit of at 37°C at<1.0 log CFU/250 ml was lower than that at 44°C. The efficiency of the developed device, which comprised an incubator equipped with a UV lamp to detect in the field, was evaluated by measuring the temperature and UV lamp brightness. The difference between the set temperature and actual temperature of the developed device was about 1.0°C. When applying the developed method and device to various samples, including utensils, gloves, irrigation water, seeds, and vegetables, there were no differences in detection rates of compared with the Korean Food Code method. For sanitary disposal of culture samples after experiments, the sterilization effect of sodium dichloroisocyanurate (NaDCC) tablets was assessed for use as a substitute for an autoclave. The addition of one tablet of NaDCC per 50 ml was sufficient to kill cultured in Colilert-18. These results show that the developed protocol and device can efficiently detect from agri-food production environments and vegetables.

One of the key early season diseases of cotton is Fusarium wilt caused by Fusarium oxysporum f. sp. vasinfectum (Fov). Recent emergence of highly virulent Fov race 4 (Fov4) and its aggressiveness toward Gossypium barbadense (pima) cultivars are raising significant concerns for the US cotton industry. One of the key challenges in studying Fov4 virulence and cotton Fusarium wilt pathogenesis is establishing a disease assay strategy that can help researcher overcome several technical challenges, including efficient infection and highly reproducible and consistent symptom development. Here, we have developed a small-scale, soil-free Fusarium wilt disease assay that can complement conventional assays with faster symptom development and high reproducibility in infected pima cotton seedlings. Our data showed statistically significant differences (p<0.0001) between Fov4-infected and non-infected pima cotton at 4 and 6 days post inoculation (dpi) when compared to control experiments. At 6 dpi, longitudinal observations under magnification showed Fov4 colonization in primary xylem of infected plants, which is a common symptom observed in Fov4 triggered Fusarium wilt in pima cotton. While this is an artificial assay system, this soil-free disease testing strategy can offer another strategy to supplement current assays when studying pathogen-host interaction in soil-borne diseases.

Mediator is a conserved, nucleus-localized, multi-subunit complex highly conserved across eukaryotes. It interacts with RNA polymerase II transcription machinery as well as various transcription factors to regulate gene expression. However, systematic characterization of Mediator complex has not be thoroughly performed in filamentous fungi. In current study, our aim was to investigate key biological functions of Mediator subunits in a mycotoxigentic plant pathogen Fusarium verticillioides. While we recognized some level of divergence in subunits constituent, overall structure remained conserved between Saccharomyces cerevisiae and F. verticillioides. We were able to generate 11 Mediator subunit deletion mutants and characterize serveal important phenotypes associated with fungal development, environmental stress, nutrient utilization, virulence as well as secondary metabolism. While each Mediator subunit deletion mutant showed deficiencies in at least three of the phenotypes tested, it is important to note that different modules or subunits showed unique regulatory role in different cellular processes. Significantly, the deletion of FvMed1 led to increased FB1 production, and we were able to confirm that FvMed1 is transported from the nucleus to the cytoplasm under fumonisin-producing conditions. Taken together, our study characterized the different biological functions of Mediator subunits in plant pathogen F. verticillioides and the possibility of select subunits unique cytoplasmic function independent of the core Mediator.