The capacities of the begomoviruses Bean dwarf mosaic virus (BDMV) and Bean golden yellow mosaic virus (BGYMV) to differentially infect certain common bean (Phaseolus vulgaris) cultivars were used to identify viral determinants of the hypersensitive response (HR) and avirulence (avr) in BDMV. A series of hybrid DNA-B components, containing BDMV and BGYMV sequences, was constructed and coinoculated with BDMV DNA-A (BDMV-A) or BDMVA-green florescent protein into seedlings of cv. Topcrop (susceptible to BDMV and BGYMV) and the BDMV-resistant cvs. Othello and Black Turtle Soup T-39 (BTS). The BDMV avr determinant, in bean hypocotyl tissue, was mapped to the BDMV BV1 open reading frame and, most likely, to the BV1 protein. The BV1 also was identified as the determinant of the HR in Othello. However, the HR was not required for resistance in Othello nor was it associated with BDMV resistance in BTS. BDMV BV1, a nuclear shuttle protein that mediates viral DNA export from the nucleus, represents a new class of viral avr determinant. These results are discussed in terms of the relationship between the HR and resistance.

The BV1 gene of the bipartite Begomovirus genome encodes a nuclear shuttle protein (NSP) that is also an avirulence determinant in common bean. The function of the NSP of two common bean-infecting bipartite begomoviruses, Bean dwarf mosaic virus (BDMV) and Bean golden yellow mosaic virus (BGYMV), was investigated using a series of hybrid DNA-B components expressing chimeric BDMV and BGYMV NSP, and genotypes of the two major common bean gene pools: Andean (cv. Topcrop) and Middle American (cvs. Alpine and UI 114). BDMV DNA-A coinoculated with HBDBG4 (BDMV DNA-B expressing the BGYMV NSP) and HBDBG9 (BDMV DNA-B expressing a chimeric NSP with the N-terminal 1 to 42 amino acids from BGYMV) overcame the BDMV resistance of UI 114. This established that the BDMV NSP is an avirulence determinant in UI 114, and mapped the domain involved in this response to the N-terminus, which is a variable surface-exposed region. BDMV DNA-A coinoculated with HBDBG10, expressing a chimeric NSP with amino acids 43 to 92 from BGYMV, was not infectious, revealing an essential virus-specific domain. In the BGYMV background, the BDMV NSP was a virulence factor in the Andean cv. Topcrop, whereas it was an avirulence factor in the Middle American cultivars, particularly in the absence of the BGYMV NSP. The capsid protein (CP) also played a gene pool–specific role in viral infectivity; it was dispensable for infectivity in the Andean cv. Topcrop, but was required for infectivity of BDMV, BGYMV, and certain hybrid viruses in the Middle American cultivars. Redundancy of the CP and NSP, which are nuclear proteins involved directly or indirectly in viral movement, provides a masking effect that may allow the virus to avoid host defense responses.

The essential oils of plants of the genus Piper have secondary metabolites that have antimicrobial activity related to their chemical composition. The objective of our work was to determine the chemical composition and evaluate the antifungal activity of the aerial part essential oil of P. auritum obtained by hydrodistillation on Fusarium oxysporum and Fusarium equiseti isolated from Capsicum chinense. The antifungal activity was evaluated by direct contact and poisoned food tests, and the minimum inhibitory concentration (MIC₅₀) and maximum radial growth inhibition (MGI) were determined. The identification of oil metabolites was carried out by direct analysis in real time mass spectrometry (DART-MS). By direct contact, the essential oil reached an inhibition of over 40% on Fusarium spp. The 8.4 mg/mL concentration showed the highest inhibition on F. oxysporum (40–60%) and F. equiseti (>50%). The MIC₅₀ was 6 mg/mL for F. oxysporum FCHA-T7 and 9 mg/mL for F. oxysporum FCHJ-T6 and F. equiseti FCHE-T8. DART-MS chemical analysis of the essential oil showed [2M-H]⁻ and [M-H]⁻ adducts of high relative intensity that were mainly attributed to eugenol and thymol/p-cimen-8-ol. The findings found in this study show a fungistatic effect of the essential oil of P. auritum on Fusarium spp.

Black Sigatoka is the main constraint to banana production worldwide, and epidemic outbreaks are continuously causing huge losses. Successful management of diseases requires a profound knowledge of the epidemiological factors that influence disease dynamics. Information regarding alternative hosts of Pseudocercospora fijiensis, the causal agent, is still very scarce. To date, only Heliconia psittacorum has been reported as an alternative plant host, and we hypothesized that other plants can house P. fijiensis. In the present report, ten plant species with suspicious leaf spots were collected inside and around commercial banana crops in Mexico. Diagnostic PCR gave positive amplification for six of these plant species, and DNA sequencing confirmed the presence of the pathogen in four. This is the first report of the presence of P. fijiensis in unrelated plants and it represents a breakthrough in the current knowledge of black Sigatoka. This finding is very important given the polycyclic nature of this disease whose successful management requires the control of initial inoculum to minimize epidemic outbreaks. The results presented herein can be used to introduce innovations in integrated black Sigatoka management programs to reduce initial inoculum, and help the international initiative to reduce the use of fungicides in banana production.

Mango anthracnose in mango in the tropical and subtropical regions of Mexico is a disease that induces serious economic losses, caused by Colletotrichum gloesporioides. The objective of this research was to determine the efficiency of integrated management for anthracnose control and to identify the critical moment for disease management. The work was carried out on cv. ‘Ataúlfo’, in Guerrero, Mexico, in three production cycles. The identification of the pathogen was confirmed and during a period of 11 months the abundance of spores in the canopy of the trees was examined. Three treatments were evaluated: integrated management with severe pruning (MIM-Pruning), integrated management without severe pruning (MIM) and Control treatment. The climate was conducive to the development of the disease (>80% incidence). The greatest increase in spores, with 65.9 to 84.1 spores/week, was observed during summer vegetative growth, in the phase of flowering and fruit set on the rachis, with its subsequent decrease in fruit growth. The MIM-Pruning and MIM treatment showed consistent results of less area under the disease curve progress (AUDCP), in foliage and flowering, causing a greater definitive fruit set per inflorescence and marketable fruits per tree with respect to the Control (P ≤0.05). Field pathogen population management should begin with the spraying of fungicide products in the summer vegetative growth phase and before the full flowering stage. Pruning is a practice that should be included in anthracnose management.