A study was carried out to investigate fungi present on grapes grown in Italy. Aspergillus and Penicillium spp. isolates were identified and studied in vitro, and their ability to produce ochratoxi...

Background and Aims: The presence of viable sources and of conditions favourable for conidial production, dispersal and deposition is essential for a high number of Botrytis cinerea conidia to be available at host infection sites. This study investigated the effect of environmental conditions, growing media and grape organs on the sporulation of ten strains of different genotypes and geographical origin. Method and Results: Media of different water activity and similar to berry juice at several maturity stages, grape bunch trash or mature berries were inoculated with B. cinerea and incubated under variable conditions of temperature and relative humidity. Optimal conditions for sporulation were: temperature between 15 and 20°C, relative humidity >65.5%; water activity=0.971; and medium similar to the juice of softening berries. Conidia produced on bunch trash and mature berries were significantly correlated with those on artificial media. Conclusions: Differences among strains did not change the response pattern of sporulation to the environmental conditions. Equations were then developed for describing the effect of temperature and relative humidity on sporulation, and of degree-days on the length of latent period. Significance of the Study: When combined with predictive models for infection, our equations could contribute to the development of an effective disease prediction system for Botrytis bunch rot

The effect of temperature and wetness duration on infection of Vitis vinifera inflorescences (from “inflorescence clearly visible” to “end of flowering” stages) and young berry clusters (at “fruit swelling” and “berries groat-sized” stages) by Botrytis cinerea was investigated. Artificial inoculations were carried out using conidial suspensions of eight B. cinerea strains belonging to the transposon genotypes transposa and vacuma. Infection incidence was significantly affected by strain but not by transposon genotype (transposon genotype accounted for only 6.5% of the variance). Infection incidence was also affected by the interaction between strain and growth stage of the inflorescence or berry cluster (overall accounting for approximately 57% of the experimental variance). Thus, under our experimental conditions, the ability to cause infection was a strain rather than a transposon genotype attribute. Across all strains, infection incidence was lowest when inflorescences were clearly visible or fully developed, highest at flowering (from beginning to end of flowering), and intermediate at the postflowering fruit stages (fruit swelling and berries groat-sized). One transposa strain, however, was highly virulent on all grapevine growth stages tested. The effects of temperature and wetness duration on infection incidence were similar for all fungal strains and grapevine growth stages; infection incidence was highest at 20°C and lowest at 30°C, and was also low at 5°C. Similar results were obtained for mycelial growth and conidial germination. Based on the pooled data for all strains and grapevine growth stages, an equation was developed that accounted for the combined effects of temperature and wetness duration on relative infection incidence. This equation should be useful for developing decision-making systems concerning B. cinerea control at early grapevine growth stages.

Grapevine white rot, caused by Coniella diplodiella, can severely damage berries during ripening. The effects of temperature and wetness duration on the infection severity of C. diplodiella were investigated by artificially inoculating grape berries through via infection pathways (uninjured and injured berries, and through pedicels). The effect of temperature on incubation was also studied, as was that of inoculum dose. Injured berries were affected sooner than uninjured berries, even though 100% of the berries inoculated with C. diplodiella conidia became rotted whether injured or not; infection through pedicels was less severe. On injured berries, the disease increased as the inoculum dose increased. Irrespective of the infection pathway, 1 h of wetness was sufficient to cause infection at any temperature tested (10–35 °C); with the optimal temperature being 23.8 °C. The length of incubation was shorter for injured berries than for uninjured ones, and was shorter at 25–35 °C than at lower temperatures; the shortest incubation period was 14 h for injured berries at 30 °C. Mathematical equations were developed that fit the data, with R² = 0.93 for infection through any infection pathway, and R² = 0.98 for incubation on injured berries, which could be used to predict infection period and, therefore, to schedule fungicide applications.

Botrytis bunch rot (BBR) of grapevine, caused by Botrytis cinerea, is commonly managed by fungicide (FUN) sprays at flowering (A), at prebunch closure (B), at veraison (C), and before harvest. Applications at A, B, and C are recommended to reduce B. cinerea colonization of bunch trash and the production of conidia during berry ripening. The effects of these applications were previously evaluated as reductions in BBR severity at harvest rather than as reductions in bunch trash colonization and sporulation by B. cinerea. This study investigated the effects of FUNs (a commercial mixture of fludioxonil and cyprodonil), biological control agents (BCAs; Aureobasium pullulans and Trichoderma atroviride), and botanicals (BOTs; a commercial mixture of eugenol, geraniol, and thymol) applied at different timings (A, B, C, or ABC) compared with a nontreated control (NT) on B. cinerea bunch trash colonization and sporulation in vineyards. The ability of B. cinerea to colonize the bunch trash (as indicated by B. cinerea DNA content) and sporulate (as indicated by the number of conidia produced under optimal laboratory conditions) was highly variable, and this variability was higher between years (2015 to 2018) than among the three vineyards and three sampling times (i.e., 1 week after applications at A, B, and C). B. cinerea sporulation on bunch trash was significantly lower in plots treated with FUN than in NT in only 3 of 18 cases (3 vineyards × 2 years × 3 sampling times). FUN applications, however, significantly reduced B. cinerea colonization of bunch trash compared with NT; for colonization, BCA efficacy was similar to that of FUN, but BOT efficacy was variable. For all products, colonization reduction was the same with application at A versus ABC, meaning that the effect of an early season application lasted from flowering to 1 week after veraison. These results indicate that the early season control of B. cinerea is important to reduce the saprophytic colonization of bunch trash, especially when the risk of BBR is high.