Thailand is the leading producer and exporter of durians worldwide. Serious diseases in durians include root rot, stem rot, and fruit rot, which are caused by Phytophthora palmivora, P. nicotianae, and Pythium cucurbitacearum, respectively. Thai farmers have applied fungicides for more than 20 years to control rot, but it remains difficult to control. Thus, the monitoring of fungicide-resistance development in pathogens is important for disease management. Pathogens were isolated from naturally infected durians between 2016 and 2017 in southern Thailand. The sequences of the internal transcribed spacer (ITS) and 5.8S regions of rDNA were used for the identification of their species. Seventeen out of twenty isolates were confirmed to be P. palmivora. All the isolates were tested for mycelium-growth sensitivity to metalaxyl, azoxystrobin, and dimethomorph. The results showed that nine isolates were resistant to metalaxyl with the 50% effective concentration (EC₅₀) higher than 100 mg L⁻¹. By contrast, all the isolates were sensitive to both azoxystrobin and dimethomorph, with EC₅₀ < 1 mg L⁻¹. Metalaxyl-resistant isolates were not controlled (−25.6% to 22.2%) by the treatment of the detached leaves of ‘Monthong’ durian with 100 mg L⁻¹ metalaxyl prior to inoculation, but all the metalaxyl-sensitive and moderately metalaxyl-resistant isolates were better controlled (33.0% to 62.6%). These results clearly indicate that metalaxyl-resistant strains are present in the populations of P. palmivora in Thailand.

Scab, caused by Venturia nashicola, is among the most serious diseases of Asian pears and control of this disease largely relies on sterol demethylation inhibitor (DMI) fungicides. However, pear growers have complained about field performance of DMIs since the mid-2000s. In this study, to evaluate pathogen sensitivity, mycelial growth tests and inoculation tests were conducted using DMI-amended culture medium and fungicide-sprayed potted pear trees, respectively. Results confirmed distribution of isolates resistant to fenarimol, hexaconazole, and difenoconazole in the field populations. Importantly, results from tests in culture did not fully correlate with those from tests in planta. Due to phenotypic instability of resistance and poor sporulation of this pathogen in culture, resistance is generally assessed by laborious and time-consuming inoculation with conidia collected from a field. To improve the result interpretation from in vitro tests, the isolates were genotyped: the CYP51 gene which encodes the target sterol 14α-demethylase was sequenced and various mutations have been detected in the coding sequence of DMI-resistant isolates. In addition to the detected single nucleotide polymorphisms, alternative mechanisms, not based on changes in the structure of the target protein, may also increase DMI resistance. Development of molecular methods for the diagnosis of DMI resistance seems to be challenging in V. nashicola.