In this study, dual culture, poison agar, and direct methods were used to assess the ability of Trichoderma virens IMI-392430, T. pseudokoningii IMI-392431, T. harzianum IMI-392432, T. harzianum IMI-392433, and T. harzianum IMI-392434 to control Ceratocystis paradoxa, which causes the pineapple disease of sugarcane. The highest percentage inhibition of radial growth (PIRG) values were observed with T. harzianum IMI-392432 using two dual culture methods, 63.80% in Method I and 80.82% in Method II. The minimum colony overgrowth time was observed with T. harzianum IMI-392432 and the maximum was observed with T. pseudokoningii IMI-392431. Different concentrations of different day-old metabolites of Trichoderma isolates were tested against mycelial growth of C. paradoxa. The highest PIRG (84.685%) exhibited at 80% concentration of 30-day-old metabolites of T. harzianum IMI-392432 using the modified bilayer poison agar method. In the direct assay method the maximum mycelial growth weight (PIGW) was observed at the same concentration and the same day-old metabolites of T. harzianum IMI-392432. This study showed that Trichoderma isolates have a good antagonistic effect on C. paradoxa mycelial growth and T. harzianum IMI-392432 has the most potential to control the pineapple disease pathogen.

The soybean is prone to be attacked by Colletotrichum truncatum at seed and seedling stages, resulting in pre-and post-emergence damping-off. The efficacy of bio-priming for the control of damping-off of soybean caused by C. truncatum and the final seedling stand using two fungal biocontrol agents (BCAs) Trichoderma harzianum and T. virens and one bacterial BCA Pseudomonas aeruginosa was evaluated under field conditions. Treatments consisted of chemo-primed with Benlate® as a positive control; bio-primed with P. aeruginosa; bioprimed with T. harzianum; bio-primed with T. virens; bio-primed with the mixture of T. virens and T. harzianum and the controls as hydro-primed and non-primed seeds. Trichoderma isolates used singly or as a mixture established on the seed surface with germinating hyphae, whereas the strain P. aeruginosa colonized profusely as determined by increased colony forming units (CFU) from 1.2 × 109 to 5.1 × 109 seed−1 after 12 h of biopriming. All bio-priming treatments significantly reduced pre-and post-emergence dampingoff relative to hydro-and non-primed seed controls. In general, bio-priming with P. aeruginosa was the most effective treatment for controlling pre and post-emergence dampingoff, with reductions in disease incidence with increases ranging from 48.6% to 51.9% and 65.0% to 97.2%, respectively. Moreover, P. aeruginosa resulted in enhancement of seed germination and healthy seedling stand ranging from 32.4% to 60.0% and 56.0% to 73.9%, respectively. Bio-priming with T. harzianum reduced pre-and post-emergence damping-off by 42.8-46.8% and 35.0-85.1%, respectively. However, P. aeruginosa was generally comparable to T. harzianum and the fungicide Benlate®. The combination treatment of T. harzianum and T. virens produced compareable results to T. harzianum alone, and T. virens was the least effective of the bio-primed treatments. Bio-priming with P. aeruginosa or T. harzianum offered an effective biological seed treatment system and an alternative to the fungicide Benlate® for control of damping-off of soybean caused by C. truncatum of soybean.

Trichoderma strains were evaluated under field conditions to assay their efficacy in suppressing Alternaria fruit rot disease and promoting chili plant growth. The experiment was conducted at the Botanical Garden, Rajshahi University, Bangladesh from July 2006 to March 2007. Application of Trichoderma harzianum IMI 392432 significantly (p = 0.05) suppressed the disease compared to Alternaria tenuis (T2) treatment and improved both growth and yield. The treatment T4 (T. harzianum IMI-392432 + A. tenuis) was most effective in reducing disease percentage (72.27%) compared to A. tenuis (T1) treatment. The highest seed germination rate (85.56%) and the highest growth and yield (12.5 g/plant) was also recorded in the same treatment (T4), followed by T5 (T. harzianum IMI-392433 000000 + A. tenuis), T6 (T. harzianum IMI-392434 +A. tenuis), T2 (T. virens IMI-392430 + A. tenuis), and T3 (T. pseudokoningii IMI-392431 +A. tenuis) treatment, while single treatment with A. tenuis significantly decreased these values.

Dengue fever is a mosquito-borne viral disease caused by the dengue virus of the Flaviviridae family and is responsible for colossal health and economic burden worldwide. This study aimed to investigate the effect of environmental, seasonal, and spatial variations on the spread of dengue fever in Sri Lanka. The study used secondary data of monthly dengue infection and the monthly average of environmental parameters of 26 Sri Lankan regions from January 2015 to December 2019. Besides the descriptive measurements, Kendall's tau_b, Spearman's rho, and Kruskal-Wallis H test have been performed as bivariate analyses. The multivariate generalized linear negative binomial regression model was applied to determine the impacts of meteorological factors on dengue transmission. The aggregate negative binomial regression model disclosed that precipitation (odds ratio: 0.97, p < 0.05), humidity (odds ratio: 1.05, p < 0.01), and air pressure (odds ratio: 1.46, p < 0.01) were significantly influenced the spread of dengue fever in Sri Lanka. The bioclimatic zone is the vital factor that substantially affects the dengue infection, and the wet zone (odds ratio: 6.41, p < 0.05) was more at-risk than the dry zone. The climate season significantly influenced dengue fever transmission, and a higher infection rate was found (odds ratio: 1.46, p < 0.01) in the northeast monsoon season. The findings of this study facilitate policymakers to improve the existing dengue control strategies focusing on the meteorological condition in the local as well as global perspectives.

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