Target-Site Resistance to Fenoxaprop-P-ethyl in Keng Stiffgrass (Sclerochloa kengiana) from China

Weed Science ◽  
2017 ◽  
Vol 65 (4) ◽  
pp. 452-460 ◽  
Author(s):  
Haitao Gao ◽  
Jiaxing Yu ◽  
Lang Pan ◽  
Xibao Wu ◽  
Liyao Dong
Keyword(s):  
Eastern China ◽  
Point Mutations ◽  
Amino Acid Position ◽  
Cross Resistance ◽  
Susceptible Population ◽  
Resistant Population ◽  
Sequence Method ◽  
Moderate Resistance ◽  
High Level

Keng stiffgrass is a serious farmland grass weed distributed globally in winter wheat fields and rice–wheat double-cropping areas. The intensive use of acetyl-CoA carboxylase (ACCase)-inhibiting herbicides has led to the evolution of resistance in a growing number of grass weeds. In this study, whole-plant pot bioassay experiments were conducted to establish that a Keng stiffgrass population from eastern China, JYJD-2, has evolved high-level resistance to fenoxaprop-P-ethyl and moderate resistance to quizalofop-P-ethyl and pinoxaden. Using the derived cleaved amplified polymorphic sequence method, a tryptophan-to-cysteine mutation at codon position 1999 (W1999C) was detected in the ACCase gene of the resistant population JYJD-2. Of the 100 JYJD-2 plants tested, we found 47 heterozygous resistant and 53 homozygous sensitive individuals. In vitro ACCase assays revealed that the IC50value of the ACCase activity of the resistant population JYJD-2 was 6.48-fold higher than that of the susceptible population JYJD-1. To the best of our knowledge, this is the first report of the occurrence of W1999C mutation in the ACCase gene of fenoxaprop-P-ethyl–resistant Keng stiffgrass. This study confirmed the resistance of Keng stiffgrass to the ACCase inhibitor fenoxaprop-P-ethyl, cross-resistance to other ACCase inhibitors, and the resistance being conferred by specific ACCase point mutations at amino acid position 1999.

First report of molecular basis of resistance to imazethapyr in common lambsquarters (Chenopodium album)

Weed Science ◽  
2019 ◽  
pp. 1-6
Author(s):  
Zhaofeng Huang ◽  
Xinxin Zhou ◽  
Chaoxian Zhang ◽  
Cuilan Jiang ◽  
Hongjuan Huang ◽  
...  
Keyword(s):  
Herbicide Resistance ◽  
Chenopodium Album ◽  
Acetolactate Synthase ◽  
Amino Acid Position ◽  
Cross Resistance ◽  
Resistance Pattern ◽  
Susceptible Population ◽  
First Report ◽  
Common Lambsquarters

Abstract Common lambsquarters (Chenopodium album L.) is one of the most troublesome weeds in soybean [Glycine max (L.) Merr.] and corn (Zea mays L.) fields in northeast China. In 2017, a C. album population that survived imazethapyr at the recommended field rate was collected from a soybean field in Heilongjiang Province in China. Experiments were conducted to determine the basis of resistance to imazethapyr and investigate the herbicide-resistance pattern in C. album. Dose–response tests showed that the resistant population (R) displayed high resistance to imazethapyr (20-fold) compared with the susceptible population (S). An in vitro acetolactate synthase (ALS) activity assay indicated that the ALS of the R population was resistant to imazethapyr compared with the ALS of the S population. Sequence analysis of the ALS gene revealed that the GCA was replaced by ACA at amino acid position 122, which resulted in an alanine to threonine substitution (Ala-122-Thr) in the R population. The R population displayed cross-resistance to thifensulfuron-methyl and flumetsulam but susceptibility to bispyribac-sodium, flucarbazone, glyphosate, mesotrione, and fomesafen. These results confirmed that the basis of imazethapyr resistance in C. album was conferred by the Ala-122-Thr substitution in the ALS enzyme. This is the first report of the target-site basis of ALS-inhibiting herbicide resistance in C. album.

Molecular Basis for Resistance to Fenoxaprop in Shortawn Foxtail (Alopecurus aequalis) from China

Weed Science ◽  
2015 ◽  
Vol 63 (2) ◽  
pp. 416-424 ◽  
Author(s):  
Wenlei Guo ◽  
Weitang Liu ◽  
Lingxu Li ◽  
Guohui Yuan ◽  
Long Du ◽  
...  
Keyword(s):  
Molecular Basis ◽  
Yellow River ◽  
Amino Acid Position ◽  
Yellow River Basin ◽  
Cross Resistance ◽  
South Central ◽  
First Case ◽  
Resistant Population ◽  
High Level ◽  
Level Resistance

Shortawn foxtail is a competitive annual grass weed widely spread in east, south-central, and southwest China and parts of the Yellow River basin. One shortawn foxtail population (JSQT-1) resistant to fenoxaprop was identified in Jiangyan, Jiangsu province. Whole-plant experiments determined that the resistant population conferred high-level resistance to fenoxaprop (93-fold), clodinafop (21-fold), sethoxydim (107-fold), mesosulfuron (41-fold), and pyroxsulam (12-fold); moderate-level resistance to haloxyfop (8-fold), clethodim (9-fold), and pinoxaden (8-fold), and no resistance to isoproturon. Molecular analyses confirmed that the Ile-1781-Leu mutation was present in the resistant population. A dCAPS marker was used to detect the Ile-1781-Leu mutation. All 97 plants of the resistant population analyzed were homozygous mutants at the 1781 position. Our study established the first case of fenoxaprop resistance in shortawn foxtail, determined cross resistance to other herbicides, and elucidated that the molecular basis of resistance resulted from, at least partly, an Ile to Leu mutation at amino acid position 1781 in the plastid ACCase.

Cross-Resistance of Japanese Foxtail (Alopecurus japonicus) to ACCase Inhibitors in China

2015 ◽  
Vol 29 (3) ◽  
pp. 444-450 ◽  
Author(s):  
Hailan Cui ◽  
Cangyue Wang ◽  
Yujiao Han ◽  
Liang Chen ◽  
Xiangju Li
Keyword(s):  
Cropping Systems ◽  
Resistance Mechanism ◽  
Point Mutations ◽  
Amino Acid Position ◽  
Cross Resistance ◽  
Weed Species ◽  
Susceptible Population ◽  
Two Populations ◽  
Grass Weed ◽  
Clodinafop Propargyl

The increasing use of ACCase-inhibiting herbicides has resulted in evolved resistance in key grass weeds infesting cereal cropping systems worldwide. Japanese foxtail is one of the most important grass weed species in wheat in China. Most populations have evolved resistance to fenoxaprop-p-ethyl, which is one of the most common ACCase-inhibiting herbicides in wheat. The seeds of two Japanese foxtail populations were collected from wheat fields where farmers complained that control could not be effectively obtained with fenoxaprop-p-ethyl. Seeds from one susceptible population were collected from an area along a roadside where ACCase inhibitors had not been used to be used for validating cross-resistance and elucidating the mechanism of resistance. The experimental results showed that the two populations, Aloja-JS10-R1 and Aloja-JS10-R2, expressed high resistance to fenoxaprop-p-ethyl, with resistance indexes (RIs) of 29.2 and 27.9. These populations also expressed high cross-resistance to clodinafop-propargyl with RIs of 12.8 and 14.7, and moderate cross-resistance to clethodim and pinoxaden with RIs ranging from 2.6 to 11.4. Comparison of the ACCase carboxyl-transferase (CT) domain sequences of the susceptible and resistant populations with blackgrass revealed that tryptophan at position 2027 of the ACCase gene was substituted by cysteine in population Aloja-JS10-R1, and isoleucine at position 1781 of the ACCase gene was substituted by leucine in populations Aloja-JS10-R2. The study confirmed Japanese foxtail resistance to the ACCase inhibitor fenoxafop-p-ethyl, cross-resistance to other ACCase inhibitors, and the resistance mechanism being conferred by specific ACCase point mutations at amino acid position 1781 and 2027.

scholarly journals Evidence for Inhibition of Topoisomerase 1A by Gold(III) Macrocycles and Chelates TargetingMycobacterium tuberculosisandMycobacterium abscessus

2018 ◽  
Vol 62 (5) ◽  
Author(s):  
Rashmi Gupta ◽  
Carolina Rodrigues Felix ◽  
Matthew P. Akerman ◽  
Kate J. Akerman ◽  
Cathryn A. Slabber ◽  
...  
Keyword(s):  
Mycobacterium Abscessus ◽  
Cross Resistance ◽  
Human Pathogens ◽  
Intrinsic Resistance ◽  
Content Type ◽  
Starting Point ◽  
Scalable Synthesis ◽  
High Level ◽  
Novel Drug

ABSTRACTMycobacterium tuberculosisand the fast-growing speciesMycobacterium abscessusare two important human pathogens causing persistent pulmonary infections that are difficult to cure and require long treatment times. The emergence of drug-resistantM. tuberculosisstrains and the high level of intrinsic resistance ofM. abscessuscall for novel drug scaffolds that effectively target both pathogens. In this study, we evaluated the activity of bis(pyrrolide-imine) gold(III) macrocycles and chelates, originally designed as DNA intercalators capable of targeting human topoisomerase types I and II (Topo1 and Topo2), againstM. abscessusandM. tuberculosis. We identified a total of 5 noncytotoxic compounds active against both mycobacterial pathogens under replicatingin vitroconditions. We chose one of these hits, compound 14, for detailed analysis due to its potent bactericidal mode of inhibition and scalable synthesis. The clinical relevance of this compound was demonstrated by its ability to inhibit a panel of diverseM. tuberculosisandM. abscessusclinical isolates. Prompted by previous data suggesting that compound 14 may target topoisomerase/gyrase enzymes, we demonstrated that it lacked cross-resistance with fluoroquinolones, which target theM. tuberculosisgyrase.In vitroenzyme assays confirmed the potent activity of compound 14 against bacterial topoisomerase 1A (Topo1) enzymes but not gyrase. Novel scaffolds like compound 14 with potent, selective bactericidal activity againstM. tuberculosisandM. abscessusthat act on validated but underexploited targets like Topo1 represent a promising starting point for the development of novel therapeutics for infections by pathogenic mycobacteria.

scholarly journals Efficacy of Biocides Used in the Modern Food Industry To Control Salmonella enterica, and Links between Biocide Tolerance and Resistance to Clinically Relevant Antimicrobial Compounds

2012 ◽  
Vol 78 (9) ◽  
pp. 3087-3097 ◽  
Author(s):  
Orla Condell ◽  
Carol Iversen ◽  
Shane Cooney ◽  
Karen A. Power ◽  
Ciara Walsh ◽  
...  
Keyword(s):  
Salmonella Enterica ◽  
Food Industry ◽  
Multidrug Resistant ◽  
Cross Resistance ◽  
Antimicrobial Compounds ◽  
Cross Tolerance ◽  
Content Type ◽  
Food Grade ◽  
High Level

ABSTRACTBiocides play an essential role in limiting the spread of infectious disease. The food industry is dependent on these agents, and their increasing use is a matter for concern. Specifically, the emergence of bacteria demonstrating increased tolerance to biocides, coupled with the potential for the development of a phenotype of cross-resistance to clinically important antimicrobial compounds, needs to be assessed. In this study, we investigated the tolerance of a collection of susceptible and multidrug-resistant (MDR)Salmonella entericastrains to a panel of seven commercially available food-grade biocide formulations. We explored their abilities to adapt to these formulations and their active biocidal agents, i.e., triclosan, chlorhexidine, hydrogen peroxide, and benzalkonium chloride, after sequential rounds ofin vitroselection. Finally, cross-tolerance of different categories of biocidal formulations, their active agents, and the potential for coselection of resistance to clinically important antibiotics were investigated. Six of seven food-grade biocide formulations were bactericidal at their recommended working concentrations. All showed a reduced activity against both surface-dried and biofilm cultures. A stable phenotype of tolerance to biocide formulations could not be selected. Upon exposure ofSalmonellastrains to an active biocidal compound, a high-level of tolerance was selected for a number ofSalmonellaserotypes. No cross-tolerance to the different biocidal agents or food-grade biocide formulations was observed. Most tolerant isolates displayed changes in their patterns of susceptibility to antimicrobial compounds. Food industry biocides are effective against planktonicSalmonella. When exposed to sublethal concentrations of individual active biocidal agents, tolerant isolates may emerge. This emergence was associated with changes in antimicrobial susceptibilities.

Resistance to Aryloxyphenoxypropionate and Cyclohexanedione Herbicides in Wild Oat (Avena fatua)

Weed Science ◽  
1993 ◽  
Vol 41 (2) ◽  
pp. 232-238 ◽  
Author(s):  
Ian M. Heap ◽  
Bruce G. Murray ◽  
Heather A. Loeppky ◽  
Ian N. Morrison
Keyword(s):  
Dry Matter ◽  
Cross Resistance ◽  
Western Canada ◽  
Wild Oat ◽  
Recommended Dosage ◽  
Susceptible Population ◽  
South Central ◽  
Repeated Applications ◽  
High Level ◽  
Very High

Resistance to aryloxyphenoxypropionate and cyclohexanedione herbicides was identified in four wild oat populations from western Canada. Populations UM1, UM2, and UM3 originated from northwestern Manitoba and UM33 from south-central Saskatchewan. Field histories indicated that these populations were exposed to repeated applications of diclofop-methyl and sethoxydim over the previous 10 yr. The populations differed in their levels and patterns of cross-resistance to these and five other acetyl-CoA carboxylase inhibitors (ACCase inhibitors). UM1, UM2, and UM3 were resistant to diclofop-methyl, fenoxaprop-p-ethyl, and sethoxydim. In contrast, UM33 was resistant to the aryloxyphenoxy propionate herbicides but not to sethoxydim. The dose of sethoxydim required to reduce growth of UM1 by 50% was 150 times greater than for a susceptible population (UM5) or UM33 based on shoot dry matter reductions 21 d after treatment. This population differed from UM2 and UM3 that had R/S ratios of less than 10. In the field UM1 also exhibited a very high level of resistance to sethoxydim. In contrast to susceptible plants that were killed at the recommended dosage, shoot dry matter of resistant plants treated at eight times the recommended dosage was reduced by only 27%. In growth chamber experiments none of the four populations was cross-resistant to herbicides from five different chemical families.

Resistance to azoxystrobin and thiophanate-methyl is widespread in Colletotrichum spp. isolates from the Mid-Atlantic Strawberry Fields

Plant Disease ◽  
2020 ◽  
Author(s):  
Qiuchen Luo ◽  
Anita Schoeneberg ◽  
Mengjun Hu
Keyword(s):  
Cyt B ◽  
Thiophanate Methyl ◽  
Colletotrichum Species ◽  
Predominant Species ◽  
Strawberry Anthracnose ◽  
Colletotrichum Spp ◽  
Moderate Resistance ◽  
High Level ◽  
Host Tissues

Multiple Colletotrichum species have been found to be responsible for strawberry anthracnose, and prevalence of each species seems to vary by regions and/or host tissues. In this study, a total of 200 Colletotrichum isolates were obtained from different strawberry cultivars displaying anthracnose symptoms in the Mid-Atlantic fields. Analysis of g3pdh, tub2, and/or ITS sequences revealed four Colletotrichum species, including C. nymphaeae, C. fioriniae, C. siamense, and C. lineola. C. nymphaeae was the predominant species, representing 90% of all isolates collected. This species was found from all strawberry organs/tissues examined, whereas C. siamense and C. fioriniae were limited to the crown and fruit, respectively. Further, all Colletotrichum isolates were screened for resistance to azoxystrobin in vitro, and all C. siamense isolates were additionally screened for resistance to thiophanate-methyl. The overall frequency of resistance to azoxystrobin and thiophanate-methyl was 48.0 % and 67.0 %, respectively. G143A in the cytochrome b gene (cyt b) was found in all C. nymphaeae and C. siamense isolates with high level of resistance, with EC50 > 100 µg/ml, while F129L was found in two of the five C. nymphaeae isolates with moderate resistance, with EC50 values ranging from 2.6 to 7.8 µg/ml. All C. fioriniae isolates tested were found to be less sensitive to azoxystrobin, with EC50 values ranging from 9.7 to 14.4 µg/ml, despite no mutations detected in cyt b. Moreover, E198A in tub2 was linked with C. siamense isolates resistant to thiophanate-methyl (EC50 > 100 µg/ml). These results revealed that resistance in Colletotrichum spp. to primary fungicides was widespread in the Mid-Atlantic strawberry fields.

A Rare Ile-2041-Thr Mutation in the ACCase Gene Confers Resistance to ACCase-inhibiting Herbicides in Shortawn Foxtail (Alopecurus aequalis)

Weed Science ◽  
2017 ◽  
Vol 65 (2) ◽  
pp. 239-246 ◽  
Author(s):  
Wenlei Guo ◽  
Lele Zhang ◽  
Hengzhi Wang ◽  
Qi Li ◽  
Weitang Liu ◽  
...  
Keyword(s):  
Herbicide Resistance ◽  
Control Strategies ◽  
Cross Resistance ◽  
Resistance Pattern ◽  
Susceptible Population ◽  
Dcaps Marker ◽  
Heterozygous Plant ◽  
Repeated Use ◽  
Moderate Resistance ◽  
Whole Plants

Understanding the mechanism of herbicide resistance is fundamental for designing sustainable weed control strategies and exploiting herbicides rationally. Shortawn foxtail is a problem grass weed infesting several important crops in China. The repeated use of acetyl-CoA carboxylase (ACCase)-inhibiting herbicides has resulted in herbicide resistance in this weed. The ACCase gene of resistant individuals of a shortawn foxtail population (JSLS-1) has an Ile-2041-Thr mutation. F2 generation seeds, originated from the same heterozygous plant, were harvested, and two homozygous mutant (JSLS-1RR) and wild (JSLS-1SS) populations for the Ile-2041-Thr mutation were obtained. In whole plants, the JSLS-1RR population conferred high resistance to fenoxaprop and clodinafop, moderate resistance to haloxyfop, low resistance to pinoxaden, and no obvious resistance to clethodim and sethoxydim, compared with JSLS-1SS and a proven susceptible population (HNXY-1). A derived cleaved amplified polymorphic sequence (dCAPS) marker was developed to rapidly detect the rare Ile-2041-Thr mutation in the shortawn foxtail population. This is the first report of the cross-resistance pattern of Ile-2041-Thr mutation, and the robust dCAPS marker could quickly detect this mutation in shortawn foxtail.

Multiple Pro197ALS Substitutions Endow Resistance to ALS Inhibitors within and among Mayweed Chamomile Populations

Weed Science ◽  
2011 ◽  
Vol 59 (3) ◽  
pp. 431-437 ◽  
Author(s):  
Suphannika Intanon ◽  
Alejandro Perez-Jones ◽  
Andrew G. Hulting ◽  
Carol A. Mallory-Smith
Keyword(s):  
Pacific Northwest ◽  
Genotypic Variation ◽  
Point Mutations ◽  
Acetolactate Synthase ◽  
Cross Resistance ◽  
Collection Site ◽  
Whole Plant ◽  
The Pacific ◽  
Als Inhibitors

Mayweed chamomile seeds were collected from six different fields across the Pacific Northwest. All populations (each collection site was considered a population) were suspected to have some level of acetolactate synthase (ALS) resistance. Greenhouse and laboratory studies were conducted to determine if these populations were resistant to three different classes of ALS inhibitors: sulfonylureas (SU), imidazolinones (IMI), and triazolopyrimidines (TP). A whole-plant dose–response andin vitroALS activity studies confirmed cross-resistance to thifensulfuron + tribenuron/chlorsulfuron (SU), imazethapyr (IMI), and cloransulam (TP); however, resistance varied by herbicide class and population. TwoALSisoforms of theALSgene (ALS1andALS2) were identified in mayweed chamomile; however, only mutations inALS1were responsible for resistance. No mutations were found inALS2. Sequence analysis of the partialALSgene identified four point mutations at position 197 (Pro197to Leu, Gln, Thr, or Ser) in the resistant populations. This study demonstrates genotypic variation associated with cross-resistance to ALS inhibitors within and between populations.

scholarly journals Contribution of rpoB Mutations to Development of Rifamycin Cross-Resistance in Mycobacterium tuberculosis

1998 ◽  
Vol 42 (7) ◽  
pp. 1853-1857 ◽  
Author(s):  
D. L. Williams ◽  
L. Spring ◽  
L. Collins ◽  
L. P. Miller ◽  
L. B. Heifets ◽  
...  
Keyword(s):  
Mycobacterium Tuberculosis ◽  
Cross Resistance ◽  
In Vitro Mutagenesis ◽  
Missense Mutations ◽  
Resistance Mutations ◽  
Development Of Resistance ◽  
High Level ◽  
The Impact ◽  
Level Resistance

ABSTRACT The contributions of 23 insertion, deletion, or missense mutations within an 81-bp fragment of rpoB, the gene encoding the β-subunit of the DNA-dependent RNA polymerase of Mycobacterium tuberculosis, to the development of resistance to rifamycins (rifampin, rifabutin, rifapentine, and KRM-1648) in 29 rifampin-resistant clinical isolates were defined. Specific mutantrpoB alleles led to the development of cross-resistance to all rifamycins tested, while a subset of mutations were associated with resistance to rifampin and rifapentine but not to KRM-1648 or rifabutin. To further study the impact of specific rpoBmutant alleles on the development of rifamycin resistance, mutations were incorporated into the rpoB gene of M. tuberculosis H37Rv, contained on a mycobacterial shuttle plasmid, by in vitro mutagenesis. Recombinant M. tuberculosis clones containing plasmids with specific mutations in either codon 531 or 526 of rpoB exhibited high-level resistance to all rifamycins tested, whereas clones containing a plasmid with a mutation in codon 516 exhibited high-level resistance to rifampin and rifapentine but were susceptible to both rifabutin and KRM-1648. These results provided additional proof of the association of specificrpoB mutations with the development of rifamycin resistance and corroborate previous reports of the usefulness of rpoB genotyping for predicting rifamycin-resistant phenotypes.

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