Antifungal activity of plant extracts against Colletotrichum gloeosporioides (Penz.) the causative agent of yam anthracnose disease

Yam anthracnose disease is a major constraint to yam production world-wide. The hazardous effects of synthetic fungicides on both humans and the environment have necessitated the use of alternative environmentally friendly fungicides for the control of the disease. This study tested the efficacy of aqueous and ethanol extracts of Azadiratcha indica, Balanites aegyptiaca, Jatropha curcas, and Khaya senegalensis seeds, Icacina oliviformis leaves and Capsicum annuum (Legon 18 variety) fruit against Colletotrichum gloeosporioides (Penz.), the causative agent of yam anthracnose. The antifungal activity of each plant extract was assessed in vitro on potato dextrose agar using the food poison technique. Each extract inhibited significantly (p?≤?.05) the mycelia growth and spore germination of C. gloeosporioides. Qualitative phytochemical tests detected alkaloids, anthraquinones, cardiac glycosides, flavonoids, phlobatinnins, saponins, steroids, tannins and terpenoids. The potential antifungal activity exhibited by these plant material makes them suitable candidates for the control of anthracnose disease of yam.     

The evolutionary origins of pesticide resistance

Durable crop protection is an essential component of current and future food security. However, the effectiveness of pesticides is threatened by the evolution of resistant pathogens, weeds and insect pests. Pesticides are mostly novel synthetic compounds, and yet target species are often able to evolve resistance soon after a new compound is introduced. Therefore, pesticide resistance provides an interesting case of rapid evolution under strong selective pressures, which can be used to address fundamental questions concerning the evolutionary origins of adaptations to novel conditions. We ask: (i) whether this adaptive potential originates mainly from de novo mutations or from standing variation; (ii) which pre‐existing traits could form the basis of resistance adaptations; and (iii) whether recurrence of resistance mechanisms among species results from interbreeding and horizontal gene transfer or from independent parallel evolution. We compare and contrast the three major pesticide groups: insecticides, herbicides and fungicides. Whilst resistance to these three agrochemical classes is to some extent united by the common evolutionary forces at play, there are also important differences. Fungicide resistance appears to evolve, in most cases, by de novo point mutations in the target‐site encoding genes; herbicide resistance often evolves through selection of polygenic metabolic resistance from standing variation; and insecticide resistance evolves through a combination of standing variation and de novo mutations in the target site or major metabolic resistance genes. This has practical implications for resistance risk assessment and management, and lessons learnt from pesticide resistance should be applied in the deployment of novel, non‐chemical pest‐control methods.     

Sequence diversity in the large subunit of RNA polymerase I contributes to Mefenoxam insensitivity in Phytophthora infestans

Phenylamide fungicides have been widely used for the control of oomycete‐incited plant diseases for over 30 years. Insensitivity to this chemical class of fungicide was recorded early in its usage history, but the precise protein(s) conditioning insensitivity has proven difficult to determine. To determine the genetic basis of insensitivity and to inform strategies for the cloning of the gene(s) responsible, genetic crosses were established between Mefenoxam sensitive and intermediate insensitive isolates of Phytophthora infestans, the potato late blight pathogen. F1 progeny showed the expected semi‐dominant phenotypes for Mefenoxam insensitivity and suggested the involvement of multiple loci, complicating the positional cloning of the gene(s) conditioning insensitivity to Mefenoxam. Instead, a candidate gene strategy was used, based on previous observations that the primary effect of phenylamide compounds is to inhibit ribosomal RNA synthesis. The subunits of RNA polymerase I (RNApolI) were sequenced from sensitive and insensitive isolates and F1 progeny. Single nucleotide polymorphisms (SNPs) specific to insensitive field isolates were identified in the gene encoding the large subunit of RNApolI. In a survey of field isolates, SNP T1145A (Y382F) showed an 86% association with Mefenoxam insensitivity. Isolates not showing this association belonged predominantly to one P. infestans genotype. The transfer of the ‘insensitive’ allele of RPA190 to a sensitive isolate yielded transgenic lines that were insensitive to Mefenoxam. These results demonstrate that sequence variation in RPA190 contributes to insensitivity to Mefenoxam in P. infestans.     

新型杀菌剂啶氧菌酯对香蕉叶斑病的防治效果

【目的】香蕉叶斑病是香蕉产业的重要病害,化学防治仍然是当前最为有效的防治手段。于2015—2016年连续2年开展香蕉叶斑病的田间化学防治试验,为生产上推广应用新型杀菌剂啶氧菌酯提供依据。【方法】试验设22.5%啶氧菌酯悬浮剂125、150和187.5 mg·kg~(-1),对照药剂250 g·L-1吡唑醚菌酯乳油125 mg·kg~(-1),以及空白对照共5个处理,3次药后第12或13天调查正常叶数、病叶数及病级,计算平均病指及平均防效。【结果】22.5%啶氧菌酯悬浮剂(有效成分用量125、150和187.5 mg·kg~(-1))2015年的防治效果分别为64.70%、68.16%和71.29%,2016年防治效果分别为68.44%、72.36%和76.29%。此外,在试验期间香蕉嫩叶未见药害现象,叶片生长均正常。【结论】22.5%啶氧菌酯悬浮剂是防治香蕉叶斑病的优良药剂,对香蕉比较安全,值得在香蕉产区推广应用。     

Function of the genetic element ‘Mona’ associated with fungicide resistance in Monilinia fructicola

The genetic element ‘Mona’ has been shown previously to be associated with resistance to demethylation inhibitors (DMIs) in Monilinia fructicola. In this study, the promoter activity of the ‘Mona’ element was demonstrated genetically and the activity was narrowed down to a 20‐bp active region through a series of deletions. ‘Mona’ knockout transformants (ΔMona) were generated from DMI‐resistant isolate Bmpc7, and EC₅₀ values and expression of the MfCYP51 gene were found to be reduced in transformants compared with the parental isolate. When the ‘Mona’ element was inserted into the upstream region of the MfCYP51 gene of the DMI‐sensitive isolate HG3, the EC₅₀ values and expression of the MfCYP51 gene increased in the transformants compared with the parental sensitive isolate. These results indicate that the ‘Mona’ element determines the DMI fungicide resistance through the up‐regulation of the expression of the downstream MfCYP51 gene. No fitness penalty was observed in knockout and insertion transformants, i.e. transformants showed similar mycelial growth rate, sporulation and ability to cause lesions on fruit compared with their parental isolates, suggesting that the ‘Mona’ element does not affect basal life activities.     

Integration of soil solarization with chemical, biological and cultural control for the management of soilborne diseases of vegetables

The long-term effectiveness of soil solarization integrated with (integration of pest management [IPM]) a biological control agent (Trichoderma virens), chemical fungicide (pentachloronitrobenzene [PCNB]), organic amendment (chicken litter) or physical method (black agriplastic mulch) to reduce southern blight (Sclerotium rolfsii) and southern root-knot diseases (Meloidogyne incognita) were evaluated on vegetable production. Results showed that the long-term effectiveness of IPM plus soil solarization reduced soilborne diseases of vegetables more than two years following the termination of solarization. These disease management strategies in 1991 and 1992, following soil solarization in 1990, reduced the numbers of sclerotia in the soil, and the number of plants killed by southern blight and root-knot of tomatoes, compared to nonsolarized bare soil treatment. The integration of a reduced dosage level of PCNB or T. virens in field plots, reduced southern blight of tomatoes by 100% and 71%, respectively, in solarized soil, compared to nonsolarized bare soil two years following soil solarization. PCNB effectively controlled southern blight in nonsolarized bare soil both years. All solarized treatments, except PCNB plus solarized soil increased tomato yields compared to nonsolarized bare soil plots. In the second study (1992) following soil solarization in 1991, the effectiveness of solarized bare soil, and nonsolarized bare soil mulched with black agriplastic film, with or without Reemay spunbounded polyester row cover, were effective in reducing root-knot of tomatoes as indicated by the root-knot gall index. Following a one year fallow period in 1994 three years following soil solarization, the root-knot gall index for severity of tomato roots grown in solarized bare soil, nonsolarized bare soil, black agriplastic mulched bare nonsolarized soil and black agriplastic mulched solarized bare soil, were 1.0, 3.0, 3.0 and 2.0, respectively, on a 0–5 scale, where 0=0% and 5=100% root-knot galled. In the third study 1992 and 1993, different dosage levels of chicken litter were used to amend soil artificially infested with sclerotia of S. rolfsii at different depths following solarization, decreased the number of viable sclerotia by 85–100%. All solarized treatments and nonsolarized bare soil amended with 18.8 MT/ha of chicken litter, were effective in controlling southern root-knot damage, and postharvest storage root rots of sweetpotato storage roots (Fusarium root rot [Fusarium solani] and Java black rot [Diplodia tubericola]). Our study showed that all soil solarization treatments, and soils amended with chicken litter, stimulated a shift in the soil microbial population dynamics. Rhizobacteria of Bacillus spp. and fluorescent pseudomonads increased significantly in the rhizosphere, rhizoplane, and interior root tissues of tomatoes and sweetpoatoes, grown in solarized soil compared to nonsolarized soil. These microorganisms may have contributed to the increased growth response of vegetables and some were probably suppressive to soilborne diseases     

Chitinolytic enzymes from Streptomyces albidoflavus expressed in tomato plants: effects on Trichoplusia ni

Tomato (Lycopersicon esculentum ) cultivars were transformed with genes that encode bacterial chitinolytic enzymes (i.e., endochitinase and chitobiosidase) from Streptomyces albidoflavus. Transgenic tomato plants producing these enzymes were found to have enhanced resistance to cabbage looper, Trichoplusia ni (Hübner) (Lepidoptera: Noctuidae), consistently reducing the growth rates of larvae. Mortality was significantly increased in two of three feeding trials. Ingestion of endochitinase and chitobiosidase not only affected development of larval T. ni from neonate to ultimate instar, but they also caused mortality and decreased insect weight when exposure began during the third instar. The results of this study provide some insight into the mode of action of the chitinolytic enzymes, by supporting the hypothesis that ingested chitinolytic enzymes damage the chitin component of the peritrophic envelope, leading to increased permeability. The size of marker molecules (FITC-dextrans) that permeated the peritrophic envelopes of T. ni feeding on transgenic plants were 50% larger than those permeating the peritrophic envelopes of T. ni feeding on the control plants. Further research is needed to more clearly identify the sites and modes of action of these chitinolytic enzymes, and the potential for synergy between these enzymes and pathogens, allelochemicals, and other environmental factors.     

Using hybrid and backcross larvae of Papilio canadensis and Papilio glaucus to detect induced phytochemical resistance in hybrid poplar trees experimentally defoliated by gypsy moths

Sub-plots of hybrid poplars were experimentally defoliated using 10 million gypsy moth larvae. Half of the defoliated (and undefoliated control) plots were fertilized to see if this would ameliorate the predicted induction of carbon-based phenolic defenses in the regrowth leaves. In order to bioassay the leaves of the four different treatments, we employed a continuum of genotypes (different hybrids and backcrosses of two different species of tiger swallowtail butterflies) with different abilities to detoxify these allelochemicals. Based on our previous studies with phytochemicals from the Salicaceae plant family, Papilio canadensis was likely to consume and process all Populus spp treatments, whereas P. glaucus predicted to either not consume or else quickly die on all Populus treatment leaves. Hybrid and backcross larvae of these two butterfly species are known to have intermediate levels of esterase detoxication enzymes and would therefore be likely to provide a continuum or at least varying degrees of sensitivity in bioassays for even the most subtle induction responses in the regrowth leaves. This presumption was supported in the feeding and growth studies conducted at different times post-defoliation during the 1997 growing season in Michigan.     

The effect of eight fungicides on germination of Conidiobolus obscurus resting spores

Conidiobolus obscurus resting spore germination was greater than 60% after 21 days incubation in 700 ppm concentrations of Rhodiasoufre, Pelt 44, Dithane M-45, Plantvax, and Saprol. No germ tubes were produced under the same treatment with Bavistine, Quin 20, or Benlate at the same dosage. Germination in distilled water was 85%. After only 24 hr contact with Quin 20 (700 ppm) followed by a distilled water wash, germination was not reduced. A higher ability to penetrate the spore wall may account for greater fungicide activity. Resting spores were found to be more resistant to certain fungicides than conidia; however, no general rule could be applied.