Herbicide resistance within key driver weeds, such as common waterhemp [Amaranthus tuberculatus (Moq.) Sauer var. rudis (Sauer) Costea and Tardif ], constrains available management options for crop production. Routine surveillance for herbicide resistance provides a mechanism to monitor the development and spread of resistant populations over time. Furthermore, the identification and quantification of resistance mechanisms at the population level can provide information that helps growers develop effective management plans. Populations of Amaranthus spp., including A. tuberculatus, redroot pigweed (Amaranthus retroflexus L.), and Palmer amaranth (Amaranthus palmeri S. Watson), were collected from 51 fields in Ohio during the 2016 growing season. Twenty-four A. tuberculatus populations were screened for resistance to the herbicides lactofen, atrazine, and glyphosate. Phenotypically resistant plants were further investigated to determine the frequency of known resistance mechanisms. Resistance to lactofen was infrequently observed throughout the populations, with 8 of 22 populations exhibiting resistant plants. Within those eight resistant populations, the ΔG210 resistance mechanism was observed in 17 of 30 phenotypically resistant plants, and the remainder lacked all known resistance mechanisms. Resistance to atrazine was observed in 12 of 15 populations; however, a target-site resistance mechanism was not observed in these populations. Resistance to glyphosate was observed in all populations. Gene amplification was the predominant glyphosate-resistance mechanism (147 of 322 plants) in the evaluated populations. The Pro-106-Ser mutation was identified in 24 plants, half of which also possessed gene amplification. In this study, molecular screening generally underestimated the phenotypically observed resistance. Continued mechanism discovery and marker development is required for improved detection of herbicide resistance through molecular assays.

At least 57 weed species, including both dicots and monocots, have been reported to have biotypes selected for resistance to the triazine herbicides. In addition, at least 47 species have been reported to have biotypes resistant to one or more of 14 other herbicides or herbicide families. These herbicides include the aryloxyphenoxypropionics, bipyridiliums, dinitroanilines, phenoxys, substituted areas, and sulfonylureas, with two or more resistant biotypes each, as well as several other herbicides in which resistance is less well documented. Although evolved resistance presents a serious problem for chemical weed control, it has also offered new potential for transferring herbicide resistance to crop species. Mechanisms of resistance that are due to single or a few genes have become the focus of biotechnology, as the probability of their successful transfer to crop species is high.

In Europe, 18 weedy grass species had been confirmed to have biotypes with resistance to herbicides. The most frequent is that of atrazine resistance, with nine resistant biotypes found. These biotypes are mainly resistant because of changes in the D1 protein of photosystem II. All atrazine-resistant biotypes, except that of bristly foxtail, show cross-resistance to s-triazine and as-triazines. From an agriculture point of view, the most important cases of resistance are those found in blackgrass, wild oat, Italian ryegrass, rigid ryegrass, and barnyardgrass. In these species, cross- and multiple resistances were observed due to metabolism or changes in the target protein by genetic mutations or both. These biotypes are extremely difficult to control with alternative herbicides.

Overreliance on tribenuron has resulted in resistance evolution in water starwort. This study investigates the resistance mechanisms to tribenuron in water starwort populations from China. The cytochrome P450 monooxygenase (P450) inhibitor malathion increased tribenuron sensitivity in all populations. The decrease in the amount of herbicide dose that causes 50% growth reduction (GR50) for the sensitive (S) population JS24 and the resistant (R) populations JS16 and JS17 were 2.3-, 2.5-, and 4.1-fold, respectively. However, the GR50 values for the R populations were still much higher than those of the S population. This observation indicates that P450-mediated enhanced metabolism is one mechanism for resistance in water starwort. The glutathione-S-transferase (GST) activity could be induced by tribenuron for all tested populations. In particular, the GST activity of JS16 is inherently greater and is more rapidly induced than that of JS17 or JS24. Resistance attributed to mutant acetolactate synthase (ALS) alleles was identified by sequence analysis for each population. Pro197Ser substitution was detected in JS16 and JS17. Molecular markers were also developed to rapidly identify resistance as well as individuals carrying the specific Pro197Ser mutation in water starwort populations. The resistance patterns experiment revealed that the R populations exhibited different levels of resistance to pyrithiobac sodium salt, florasulam, pyroxsulam, and flucarbazone-Na; however, R populations were sensitive to imazethapyr, fluroxypyr-meptyl, 2,4-D butylate, isoproturon, and diflufenican. This study establishes that either one or at least two resistance mechanisms are involved in herbicide resistance in water starwort. Moreover, these mechanisms might contribute to the different levels of resistance to tribenuron among water starwort populations.

A waterhemp population (MCR) previously characterized as resistant to 4-hydroxyphenylpyruvate dioxygenase and photosystem II inhibitors demonstrated both moderate and high levels of resistance to acetolactate synthase (ALS) inhibitors. Plants from the MCR population exhibiting high resistance to ALS inhibitors contained the commonly found Trp574Leu ALS amino acid substitution, whereas plants with only moderate resistance did not have this substitution. A subpopulation (JG11) was derived from the MCR population in which the moderate-resistance trait was isolated from the Trp574Leu mutation. Results from DNA sequencing and ALS enzyme assays demonstrated that resistance to ALS inhibitors in the JG11 population was not due to an altered site of action. This nontarget-site ALS-inhibitor resistance was characterized with whole-plant dose–response experiments using herbicides from each of the five commercialized families of ALS-inhibiting herbicides. Resistance ratios ranging from 3 to 90 were obtained from the seven herbicides evaluated. Nontarget-site resistance to ALS has been rarely documented in eudicot weeds, and adds to the growing list of resistance traits evolved in waterhemp.

The free living nematode, C. elegans is understood at a level of detail equalled by few other organisms, and much of the cell biology and sequence information is proving of considerable utility in the study of parasitic nematodes. Already, C. elegans provides a convenient vehicle for investigating anthelmintic drug action and resistance mechanisms. Among the ionotropic receptors, with their important roles in the behaviour and development of the organism, are targets for anthelmintics. The subunits of nicotinic acetylcholine receptors of C. elegans form a large and diverse multigene family. Members of this family are among the 11 genes associated with resistance to the anthelmintic drug levamisole.

The legume pod borer (Helicoverpa armigera (Hubner)) is one of the most important pests of pigeonpea. The levels of resistance to H. armigera in the cultivated germplasm are quite low, and therefore there is a need to introgress resistance genes from wild relatives into the cultigen. We evaluated a diverse array of wild relatives of pigeonpea for oviposition non-preference and antibiosis components of resistance to H. armigera. The accessions ICPW 1 (Cajanus acutifolius), ICPW 13 and 14 (C. albicans), ICPW 159 and 160 (C. sericeus), ICPW 68 (C. platycarpus), ICPW 83, 90, 94, 125, 137, 141 and 280 (C. scarabaeoides), ICPW 207 (Paracalyx scariosa) and ICPW 210 (Rhynchosia aurea) showed high levels of antixenosis for oviposition under no-choice, dual-choice and multi-choice conditions. High levels of antibiosis were observed when the larvae were reared on leaves and/or pods of C. acutifolius (ICPW 1), C. cajanifolius (ICPW 29), C. sericeus (ICPW 160), P. scariosa (ICPW 207), C. scarabaeoides and C. albicans. Lyophilized leaf or pod powder incorporated into the artificial diet can be used to assess antibiosis to H. armigera, and high levels of antibiosis to H. armigera were observed in diets with leaf and/or pod powder of some of the accessions of C. acutifolius, C. lineatus, C. sericeus, C. scarabaeoides, C. platycarpus, P. scariosa and R. aurea. Post-embryonic development period was prolonged in insects reared on leaves and pods of wild relatives of pigeonpea. The accessions showing high levels of antixenosis and antibiosis can be used to increase the levels and diversify the bases of resistance to H. armigera in pigeonpea.

Triclabendazole (TCBZ) is a halogenated benzimidazole compound that possesses high activity against immature and adult stages of the liver fluke, Fasciola hepatica. The intensive use of TCBZ in endemic areas of fascioliasis has resulted in the development of liver flukes resistant to this compound. TCBZ sulphoxide (TCBZSO) and TCBZ sulphone (TCBZSO2) are the main molecules recovered in the bloodstream of TCBZ-treated animals. In order to gain some insight into the possible mechanisms of resistance to TCBZ, the goals of the work described here were: to compare the ex vivo transtegumental diffusion of TCBZ parent drug and its sulpho-metabolites (TCBZSO and TCBZSO2) into TCBZ-susceptible and -resistant liver flukes; and to assess the comparative pattern of TCBZ biotransformation by TCBZ-susceptible and -resistant F. hepatica. For the tegumental diffusion studies, TCBZ-susceptible (Cullompton) and -resistant (Sligo) adult flukes collected from untreated infected sheep were incubated (15–180 min) in KRT buffer containing either TCBZ, TCBZSO or TCBZSO2 (5 nmol.ml−1). For the metabolism studies, microsomal fractions obtained from TCBZ-susceptible and -resistant flukes were incubated for 60 min with TCBZ (40 μM), and the amount of the formed metabolic product (TCBZSO) was measured. Drug/metabolite concentrations were quantified by HPLC. All the assayed TCBZ-related molecules penetrated through the tegument of both TCBZ-susceptible and -resistant flukes. However, significantly lower (approximately 50%) concentrations of TCBZ and TCBZSO were recovered within the TCBZ-resistant flukes compared to the TCBZ-susceptible ones over the 180 min incubation period. The rate of TCBZ sulphoxidative metabolism into TCBZSO was significantly higher (39%) in TCBZ-resistant flukes. The flavin-monooxigenase (FMO) enzyme system appears to be the main metabolic pathway involved in the formation of TCBZSO in both TCBZ-susceptible and -resistant flukes. The altered drug influx/efflux and enhanced metabolic capacity identified in TCBZ-resistant liver flukes may account for the development of resistance to TCBZ.

Glasshouse studies were conducted to determine mechanisms of resistance of five genotypes of lentil Lens culinaris (Medikus) previously identified as resistant and moderately resistant to the pea aphid Acyrthosiphon pisum (Harris). A susceptible standard, ILL 8127, was also included. French Indigo had high levels of antibiosis, demonstrated by reduced reproductive period, fecundity and longevity, while Spanish Brown had high levels of antixenotic and tolerance components of resistance. Based on overall resistance, French Indigo was the most resistant genotype followed by Spanish Brown. These genotypes could be a source for resistance to A. pisum. All five genotypes had varying levels of antibiosis, antixenosis and tolerance components of resistance compared with ILL 8127.

Host-plant resistance plays an important role in the insect-pest management either alone or in combination with other control methods. A number of sorghum genotypes showing varying levels of resistance to spotted stem borer, Chilo partellus Swinhoe have been identified using natural and artificial infestations. Major resistance mechanisms are antibiosis and tolerance, though some genotypes exhibit ovipositional non-preferences. There have been a number of factors involved in spotted stem borer resistance; a resistant genotype possesses either one or a combination of these traits. Progress has been made in developing borer resistant breeding lines with moderate yield and acceptable grain quality. Borer resistance is a quantitatively inherited trait governed by additive and non-additive genes. Epistatic gene effects are more pronounced under artificial borer infestation. Cytoplasmic effects appear to be present.

Laboratory and field methodologies for screening for resistance against Chilo partellus on sorghum and maize are reviewed in relation to the insect biology, plant phenology and insect-plant interaction. The value of field and laboratory techniques in achieving the goal to produce resistance varieties and hybrids is discussed. Recommendations for future work are made.

Plant resistance research requires many entomological and plant breeding techniques and methodologies of which some are critical to the success of the programme. The entomologist has the responsibility of developing techniques for: providing sufficient numbers of insects for screening and other plant resistance studies; creating uniform and controlled populations of the test insect for identifying and developing resistant germplasm; measuring resistance; and determining mechanisms and bases of resistance. A thorough knowledge of the insect-host plant relationship is essential for developing efficient techniques. Some of the considerations involved in developing these techniques are discussed with selected examples to illustrate various techniques employed in plant resistance to insects research.