Protoporphyrinogen oxidase (PPO)-inhibiting herbicides remain an important and useful chemistry 60 yr after their first introduction. In this review, based on topics introduced at the Weed Science Society of America 2021 symposium titled “A History, Overview, and Plan of Action on PPO Inhibiting Herbicides,” we discuss the current state of PPO-inhibiting herbicides. Renewed interest in the PPO-inhibiting herbicides in recent years, due to increased use and increased cases of resistance, has led to refinements in knowledge regarding the mechanism of action of PPO inhibitors. Herein we discuss the importance of the two isoforms of PPO in plants, compile a current knowledge of target-site resistance mechanisms, examine non–target site resistance cases, and review crop selectivity mechanisms. Consistent and reproducible greenhouse screening and target-site mutation assays are necessary to effectively study and compare PPO-inhibitor resistance cases. To this end, we cover best practices in screening to accurately identify resistance ratios and properly interpret common screens for point mutations. The future of effective and sustainable PPO-inhibitor use relies on development of new chemistries that maintain activity on resistant biotypes and the promotion of responsible stewardship of PPO inhibitors both new and old. We present the biorational design of the new PPO inhibitor trifludimoxazin to highlight the future of PPO-inhibitor development and discuss the elements of sustainable weed control programs using PPO inhibitors, as well as how responsible stewardship can be incentivized. The sustained use of PPO inhibitors in future agriculture relies on the effective and timely communication from mode of action and resistance research to agronomists, Extension workers, and farmers.

Two aphid-transmitted RNA viruses, broad bean wilt virus 2 (BBWV2) and cucumber mosaic virus (CMV), are the most prevalent viruses in Korean pepper fields and cause chronic damage in pepper production. In this study, we employed a screening system for pathotype-specific resistance of pepper germplasm to BBWV2 and CMV by utilizing infectious cDNA clones of different pathotypes of the viruses (two BBWV2 strains and three CMV strains). We first examined pathogenic characteristics of the BBWV2 and CMV strains in various plant species and their phylogenetic positions in the virus population structures. We then screened 34 commercial pepper cultivars and seven accessions for resistance. While 21 pepper cultivars were resistant to CMV Fny strain, only two cultivars were resistant to CMV P1 strain. We also found only one cultivar partially resistant to BBWV2 RP1 strain. However, all tested commercial pepper cultivars were susceptible to the resistance-breaking CMV strain GTN (CMV-GTN) and BBWV2 severe strain PAP1 (BBWV2-PAP1), suggesting that breeding new cultivars resistant to these virus strains is necessary. Fortunately, we identified several pepper accessions that were resistant or partially resistant to CMV-GTN and one symptomless accession despite systemic infection with BBWV2-PAP1. These genetic resources will be useful in pepper breeding programs to deploy resistance to BBWV2 and CMV.

The sugarcane aphid Melanaphis sacchari (Zehnt.) has become a serious pest of sorghum, particularly during the post-rainy season in India and East and Southern Africa. Therefore, we tested a number of techniques to screen sorghum genotypes for their resistance to M. sacchari. Infesting the plants with aphid-infested leaf cuttings and covering with a nylon net was effective in screening sorghum genotypes for their resistance to M. sacchari. Sprinkling the plants with aphids (filled in an 0.5 ml eppendorf tube) in the greenhouse was also used to confirm whether the resistance of genotypes selected is less susceptible to the aphids under natural infestation. Nine genotypes (Line 61510, ICSV 12001, ICSV 12002, ICSV 12003, ICSV 12004, ICSV 12005, SLR 41, PU 10-1 and DJ 6514) exhibited moderate levels of resistance to M. sacchari. These genotypes also exhibited a lower rate of aphid multiplication in the clip cage and leaf disc assays. The rates of aphid multiplication were lower on the genotypes IS 21807, IS 40615, IS 40616 and IS 40618 than on the susceptible check, Swarna in the clip cage assay under the field conditions. Also, lower rates of aphid increase were also recorded on IS 21807 and IS 40615 in the leaf disc assay under laboratory conditions. Some of the genotypes that exhibited resistance to aphid damage under field conditions showed comparatively higher rates of aphid increase than the susceptible check, Swarna in the clip cage assay, indicating that antixenosis could be one of the components of resistance to M. sacchari in these genotypes. Therefore, the clip cage assay could be used to gain further understanding of the mechanisms of resistance to M. sacchari. There is a need to assess the role of antixenosis and colonization in genotypic reaction against M. sacchari to identify the lines with different mechanisms of resistance to this pest. The results suggested that the nylon net technique could be used to screen sorghum genotypes for resistance to M. sacchari. The genotypes exhibiting resistance to M. sacchari can be used to develop aphid-resistant sorghums for sustainable crop production.

Two hundred seventy-three lines of the cultivated African rice species Oryza glaberrima Steud were screened in a paddy screenhouse at the National Cereals Research Institute, near Bida, Niger State, Nigeria for resistance to the African rice gall midge, Orseolia oryzivora Harris and Gagné, an increasingly important pest of lowland rice in Nigeria. Twenty entries which showed no galls in the screenhouse evaluation were retested under natural infestation in a gall midge-endemic field location near Abakaliki, Ebonyi State. Whereas the susceptible check variety, FARO 37, had 39.6 % of tillers infested 60 days after transplanting, damage in the test entries ranged from 0 to 3.7 %, an indication that they were all highly to moderately resistant to the pest. Greater host plant resistance is a central requirement for more effective management of O. oryzivora. Using resistance genes from O. glaberrima is a promising approach to achieving this.

Sorghum head bug, Calocoris angustatus Leth. (Hemiptera: Miridae) is an important insect pest of sorghum in the semi-arid tropics. A technique to screen for resistance to head bugs under field conditions was tested. Planting infester rows of susceptible cultivars (CSH 1 or CSH 5), 20 days before the test material or planting early (40–45 days) flowering lines (IS 802, IS 13429 and IS 24439) along with the test material, split planting of test material at 15-day intervals, grouping test material according to maturity, and use of sprinkler irrigation to maintain high humidity, were found effective in increasing the efficiency of screening and selecting for resistance to head bugs.

A headcage technique to screen for resistance under no-choice conditions has also been developed. Panicles infested with 10 pairs of bugs at pre- and half-anthesis, result in maximum population build-up and grain damage under headcage. This technique is useful for confirming the resistance observed under field conditions.

Under natural infestation, five genotypes harboured relatively lower head bug numbers than the susceptible checks, but only three (IS 17610, IS 17618 and IS 17645) maintained their level of resistance under the headcage. Seed germination was > 70% in these genotypes compared to < 10% in CSH 1 and CSH 5.

A headcage technique to screen for resistance to sorghum head bug, Eurystylus immaculatus Odh. (Hemiptera: Miridae) was standardized for use in West Africa. Panicles infested at the half-anthesis to complete-anthesis stage had greater population build-up and suffered maximum grain damage, loss in grain mass, grain hardness and seed germination. Panicles with higher grain damage also showed greater severity of grain mould incidence. Maximum population build-up and grain damage was recorded in panicles infested with 20 pairs of adults. Panicles infested with 30–40 pairs of bugs generally showed a decrease in population build-up, possibly because of crowding. Head bug numbers decreased with a decrease in panicle size, while the extent of grain damage increased. To screen for resistance to head bugs, data should be recorded both on head bug numbers and grain damage. Fifty nymphs (third to fourth instar) or 40 bugs collected at random can also be used in the headcage to screen for resistance to head bugs.

Several species of Chilo are serious pests of cereal crops. The important species attacking cereals are Chilo agamemnon, C. orichalcociliellus and C. partellus on maize and sorghum; C. auricilius and C. zacconius on sugar-cane, and rice; C. suppressalis on rice; and C. sacchariphagus indicus on sugar-cane. Insects are reared in the laboratory on natural and artificial diets for various purposes, namely for insecticide testing, hormone and pheromone manipulation, biological control, host-plant resistance, etc. Rearing of an insect in the laboratory requires rearing facilities, colony establishment, research and development of rearing techniques, resources, and maintenance of insect quality. All these aspects for rearing major Chilo spp. have been discussed. However, detailed information is available only for C. partellus and C. suppressalis. Techniques used for resistance screening and damage evaluation against spotted stem borer, C. partellus using naturally occurring population and artificial infestation are described.

In the tropics, insect pests cause considerable damage to soybean, Glycine max and mungbean, Vigna radiata from germination until harvest and even in storage. Agromyzid flies in the seedling stage, lepidopterous and coleopterous defoliators in the vegetative and early reproductive stages, pentatomid and coreid bugs and lepidopterous pod-borers in the reproductive stage, and bruchids in storage all cause significant damage. Sources of resistance to agromyzids in mungbean (AVRDC accession V 4281), defoliators (PI 171451, PI 227687, PI 229358) and stink bugs (PI 227687 and PI 171444) in soybean, and bruchids in mungbean (V 2164) are available. In most cases, antibiosis appears to be the major mechanism of resistance. These sources are being exploited in the development of agromyzid-resistant mungbean, defoliator- and stink bug-resistant soybean, and bruchid-resistant mungbean at the Asian Vegetable Research and Development Center (AVRDC). Diversity in insect species within a pest complex and, in certain cases, biotypes of single pest at different locations as well as pest ecology are likely to influence the resistance reaction and, in practical terms, the utilization of pest resistance as a tool in the management of insect pests of soybean and mungbean. Greater efforts are required at local level to fully utilize insect pest resistant germplasm.

Available pieces of information on Cicadulina sp. leafhopper biology, with specific references to the suitability of various species for mass rearing and resistance screening for maize streak virus (MSV) are critically reviewed. The following are summarized: (a) effect of distribution pattern and species composition on the efficiency of collection of live specimens for establishing a colony for mass rearing; (b) species biology and fecundity as affected by temperature and humidity; (c) species specificity in MSV transmission; (d) host plant preference and adaptation to mass rearing conditions. All these parameters affect the suitability of various Cicadulina species used as vectors in maize resistance screening and breeding to MSV disease.