Inheritance and activity of some esterases associated with organophosphate resistance in mosquitoes of the complex of Culex pipiens L. (Diptera: Cnlicidae)

1983 ◽  
Vol 73 (1) ◽  
pp. 153-170 ◽  
Author(s):  
F. Villani ◽  
G. B. White ◽  
C. F. Curtis ◽  
S. J. Miles
Keyword(s):  
Sri Lanka ◽  
High Intensity ◽  
Culex Pipiens ◽  
Resistance Mechanisms ◽  
Enzyme Assays ◽  
Resistance Level ◽  
Organophosphate Resistance ◽  
Esterase Pattern ◽  
Resistant Strains ◽  
Low Activity

AbstractEighteen strains of the complex of Culex pipiens L. from Africa, Asia and Europe were bioassayed for resistance to chlorpyrifos and electro-phoresed and stained for esterases. Susceptible strains showed only low activity esterase bands. The resistant strains of C. quinquefasciatus Say from hot countries (Liberia, Nigeria, Sri Lanka, Tanzania, Thailand) all showed the same two high intensity esterase bands (Rm 0·60 + 0·82). Different patterns of high esterase were found in resistant C. pipiens strains from cooler localities in Nairobi, Kenya (Rm 100), and Mont-pellier, France (Rm 0–50). Selection experiments on strains originally polymorphic for resistance and esterase pattern showed, without exception, that high esterase remained associated with resistance, and it is concluded that the association is almost certainly causal and not merely due to genetic linkage. The high intensity esterase bands were probably due to alleles of the loci Est-l, Est-2 and Est-3, separated by crossover distances of approximately 2·4 and 5·5 units, respectively. Strains monomorphic for what appeared to be the same high esterase pattern varied markedly in resistance level. Enzyme assays showed a direct relationship between levels of enzyme activity and resistance. Bioassays with fenthion and chlorpyrifos revealed differences in the relative resistance of C. quinquefasciatus from Colombo (Sri Lanka) and Dar-es-Salaam (Tanzania). Despite these differential degrees of cross-effectiveness, it is concluded that high intensity esterases are reliable indicators of organophosphate resistance in mosquitoes of the C. pipiens complex, although the possibility of other resistance mechanisms means that the lack of abnormally active esterases does not necessarily indicate the absence of resistance.

Carbamate and organophosphate resistance in Culex pipiens L. (Diptera: Culicidae) in southern France and the significance of Est-3A

1984 ◽  
Vol 74 (4) ◽  
pp. 677-687 ◽  
Author(s):  
R. J. Wood ◽  
N. Pasteur ◽  
G. Sinégre
Keyword(s):  
Culex Pipiens ◽  
Larval Instar ◽  
Piperonyl Butoxide ◽  
Southern France ◽  
Organophosphate Resistance ◽  
Metabolic Component ◽  
Carbamate Insecticides ◽  
Fourth Larval Instar ◽  
Resistant Strains ◽  
Tributyl Phosphorotrithioate

AbstractThree French strains of Culex pipiens L. were compared at the fourth larval instar for tolerance to organophosphate and carbamate insecticides, with and without the addition of synergists (the oxidase inhibitors piperonyl butoxide and CGA 84708) (a propynyl compound) and the carboxylesterase inhibitors triphenyl phosphate (TPP) and S,S,S-tributyl phosphorotrithioate (TBPT). The S54 strain was resistant to all the organophosphates tested (chlorpyrifos, malathion, monocrotophos and profenofos) compared to the susceptible LA VIS strain but only slightly tolerant to the two carbamates (carbaryl and naphthyl phenylcarbamate). The MAURIN strain was resistant to all the insecticides, including the carbamates, at a higher level. The action of chlorpyrifos and malathion on S54 was very strongly synergised by TBPT, less strongly by TPP and not at all by piperonyl butoxide. In fact, resistance was enhanced by piperonyl butoxide, as was resistance to monocrotophos and profenofos by CGA 84708. No synergist had much effect on the MAURIN strain, although TPP slightly increased the toxicity of malathion, and piperonyl butoxide and CGA 84708 slightly increased the toxicity of carbaryl. The toxic effect of carbaryl was also increased by the addition of extra acetone. Electrophoretic studies showed that the carboxylesterase enzyme coded by gene Est-20.64 (which is in linkage disequilibrium withEst-3A and acts as a marker for it) was absent from LA VIS but present in the resistant strains; but, whereas S54 was monomorphic for the gene, MAURIN was polymorphic (frequency 0·5). It is concluded that organophosphate resistance in S54 was due to detoxification by carboxylesterase wherease organophosphate and carbamate resistance in MAURIN had a strong non-metabolic component, possibly an insensitive acetylcholinesterase.

Organophosphate resistance in vector Populations of the complex of Culex Pipiens L. (Diptera: Culicidae)

1981 ◽  
Vol 71 (1) ◽  
pp. 153-161 ◽  
Author(s):  
C. F. Curtis ◽  
N. Pasteur
Keyword(s):  
Sri Lanka ◽  
High Activity ◽  
Culex Quinquefasciatus ◽  
Urban Areas ◽  
Culex Pipiens ◽  
Single Gene ◽  
Field Studies ◽  
Susceptible Strain ◽  
Organophosphate Resistance ◽  
Closely Linked Group

AbstractResistance to chlorpyrifos and other commonly used organophosphate larvicides was found in Culex quinquefasciatus Say from several urban areas in Tanzania. Lower levels of resistance were found in laboratory strains of the complex of C. pipiens L. collected in Sri Lanka, Egypt, Liberia and Brazil. Crosses of the Tanzanian strains to a more susceptible strain gave results consistent with causation of the resistance by a single gene or closely linked group of genes. Electrophoresis of one of the Tanzanian stocks indicated two esterase bands of high activity. The resistance in Tanzania did not prevent larval killing by freshly sprayed chlorpyrifos, but it is suggested that a spraying would probably no longer remain effective for three months as reported in earlier field studies.

Cross-resistance in DDT-resistant strains of various mosquitoes (Diptera, Culicidae)

1975 ◽  
Vol 65 (3) ◽  
pp. 459-471 ◽  
Author(s):  
Y. Rongsriyam ◽  
J. R. Busvine
Keyword(s):  
Culex Pipiens ◽  
Large Degree ◽  
Resistance Mechanisms ◽  
Cross Resistance ◽  
Normal Strain ◽  
Anopheles Quadrimaculatus ◽  
Culex Pipiens Fatigans ◽  
Resistant Strains ◽  
Ddt Resistance ◽  
Oxidation System

AbstractLarvicide tests were conducted on five species of mosquitoes, each of which had one or more DDT-resistant strains. The high potencies of DDT and, to a large degree, of DDD were completely lost by resistance. Other compounds were affected in different degrees according to the resistance mechanisms present, as indicated by resistance spectra and the effects of synergists. DDT-resistant strains of Culex pipiens fatigans Wied., Anopheles quadrimaculatus Say and A. stephensi List, showed highly specific resistance to DDT, probably dependent on a dehydrochlorination mechanism. DDT-resistance in Aedes aegypti (L.) and A. gambiae was also high, but there was definite evidence of cross-resistance to biodegradable DDT-analogues (about ×4 and ×10, respectively). This low-level, but definite, cross-resistance extended to a number of other compounds, notably pyrethroids, insect development inhibitors, amines, etc. The presence of synergistic action by piperonyl butoxide suggested that this depended on a microsomal oxidation system.Isotopically labelled (14C) DDT and malathion were used to study pick-up and penetration of these insecticides by larvae of normal and resistant Ae. aegypti. Both the actual and the percentage penetration of DDT were greater in the resistant than in the normal strain. Whatever the reason for this, it disposes of the possibility of reduced pick-up and penetration as a factor in DDT-resistance. With malathion, the percentage penetration was always higher in the susceptible strain than in the resistant one, though in some cases the actual amount was less.

Synergism Effects of Ursolic Acid Supplementation on the Levels of Irisin, C-reactive Protein, IL-6, and TNF-α During High-intensity Resistance Training in Low Activity Men

2020 ◽  
Vol 20 (2) ◽  
pp. 138-144 ◽  
Author(s):  
Ehsan Asghari ◽  
Amir Rashidlamir ◽  
Seyyed R.A. Hosseini ◽  
Mahtab Moazzami ◽  
Saeed Samarghandian ◽  
...  
Keyword(s):  
Resistance Training ◽  
Ursolic Acid ◽  
High Intensity ◽  
Plasma Levels ◽  
Group Versus ◽  
Current Data ◽  
C Reactive Protein ◽  
Reactive Protein ◽  
Tnf Α ◽  
Low Activity

Background:: Ursolic Acid (UA) is a pentacyclic triterpenoid carboxylic acid which is extracted from plants. UA may enhance the effect of Resistance Training (RT) in human. Objective: Current research was designed to show the effect of High-Intensity Resistance Training (HIRT) in the presence or absence of UA on the serum levels of irisin, CRP, IL-6 and TNF-α in the low activity men. Method:: The study included twenty-two healthy male HIRT with placebo, supplementation, and HIRT in the presence of UA supplementation. The two groups received eight-week intervention including 2 sets of 8 exercises, with 8~10 repetitions at 70~75% of 1 repetition maximum and a 2 min rest interval between sets, performed 3 times/week. Placebo or UA orally was evaluated as 1 capsule 3 times/day during 8 weeks. The subsequent factors were measured post- and preintervention: C-Reactive Protein (CRP), Irisin, Tumor Necrotic Factor (TNF-α) and Interleukin-6 (IL-6). Results:: UA supplementation significantly increased the plasma levels of irisin in the HIRT+UA group versus the HIRT+P group (p<0.05). UA treatment also dramatically decreased the plasma levels of CRP, IL-6, and TNF-α in the HIRT+UA group versus the HIRT+P group (p<0.05). Conclusion:: The current data showed that UA-induced an increase in serum irisin and reduction of CRP, IL-6, and TNF-α may have beneficial effects as a chemical for increasing of the effects of HIRT in low activity men.

scholarly journals 1280. In-Vitro Activity of Cefiderocol, Imipenem/Relebactam, & Ceftazidime/Avibactam in Ceftolozane/Tazobactam Resistant Strains of Multidrug Resistant Pseudomonas aeruginosa

2020 ◽  
Vol 7 (Supplement_1) ◽  
pp. S655-S655
Author(s):  
Daniel Navas ◽  
Angela Charles ◽  
Amy Carr ◽  
Jose Alexander
Keyword(s):  
Multidrug Resistant ◽  
Resistance Mechanisms ◽  
Vitro Activity ◽  
Clinical Isolates ◽  
Resistance Testing ◽  
Clinical Samples ◽  
In Vitro Activity ◽  
Carbapenemase Gene ◽  
Resistant Strains

Abstract Background The activity of imipenem/relebactam (I/R), ceftazidime/avibactam (CZA) and cefiderocol (FDC) were evaluated against clinical isolates of multidrug resistant (MDR) strains of P. aeruginosa which was resistant to ceftolozane/tazobactam (C/T). The recent increase of MDR P. aeruginosa strains isolated from clinical samples has prompted research and development of new antimicrobials that can withstand its multiple resistance mechanisms. C/T is an effective option for treatment of MDR P. aeruginosa in our facility with only 10% of resistance in MDR strains, but the emergence of resistance may occur due to the presence of a carbapenemase gene or an ampC mutation. Methods Antimicrobial susceptibility testing for C/T Etest® (bioMérieux, Inc.) were performed on all MDR strains initially screened by the VITEK2® (bioMérieux, Inc.). 10% (n=20) of all MDR isolates were resistant to C/T by the CLSI 2019 breakpoints. These resistant isolates were tested for presence of a carbapenemase gene using the GeneXpert CARBA-R (Cepheid®) PCR and against CZA Etest® (bioMérieux, Inc.) I/R gradient strips (Liofilchem®) and FDC broth microdilution (Thermo Scientific™ Sensititre™). Results A total of 20 clinical isolates of MDR P. aeruginosa resistant to C/T were tested following standardized CLSI protocols and techniques. All 20 isolates were screened for the presence of a carbapenemase gene (blaVIM, blaNDM, blaKPC, blaOXA-48, blaIMP). A blaVIM gene was detected in 6 (30%) out of 20 isolates. FDC demonstrated the greatest activity with 85% (n=17) of susceptible isolates (CLSI MIC &lt;4µg/dL). CZA (CLSI MIC &lt;8µg/dL) and I/R (FDA MIC &lt;2µg/dL) showed 15% (n=3) and 10% (n=2) of susceptible isolates respectively. FDC was active against all 6 blaVIM isolates, where all 6 strains were resistant to CZA and I/R as expected. 3 isolates tested non-susceptible against FDC; additional characterization was not performed at this time. Conclusion Based on these results, FDC demonstrated the greatest in-vitro activity against C/T resistant strains of MDR P. aeruginosa. FDC also demonstrated activity against all 6 MDR P. aeruginosa carrying blaVIM gene. FDC is a strong option to consider on MDR P. aeruginosa strains based on a resistance testing algorithm and a cost/effective protocol. Disclosures All Authors: No reported disclosures

scholarly journals Emergence of Resistance Mutations in Salmonella enterica Serovar Typhi Against Fluoroquinolones

2017 ◽  
Vol 4 (4) ◽  
Author(s):  
Takashi Matono ◽  
Masatomo Morita ◽  
Koji Yahara ◽  
Ken-ichi Lee ◽  
Hidemasa Izumiya ◽  
...  
Keyword(s):  
Salmonella Enterica ◽  
Evolutionary Process ◽  
Resistance Mechanisms ◽  
Single Mutation ◽  
Nucleotide Polymorphisms ◽  
Resistance Mutations ◽  
Single Nucleotide ◽  
Salmonella Enterica Serovar Typhi ◽  
Resistant Strains ◽  
Emergence Of Resistance

Abstract Background Little is known about the evolutionary process and emergence time of resistance mutations to fluoroquinolone in Salmonella enterica serovar Typhi. Methods We analyzed S. Typhi isolates collected from returned travelers between 2001 and 2016. Based on ciprofloxacin susceptibility, isolates were categorized as highly resistant (minimum inhibitory concentration [MIC] ≥ 4 μg/mL [CIPHR]), resistant (MIC = 1–2 μg/mL [CIPR]), intermediate susceptible (MIC = 0.12–0.5 μg/mL [CIPI]), and susceptible (MIC ≤ 0.06 μg/mL [CIPS]). Results A total of 107 isolates (33 CIPHR, 14 CIPR, 30 CIPI, and 30 CIPS) were analyzed by whole-genome sequencing; 2461 single nucleotide polymorphisms (SNPs) were identified. CIPS had no mutations in the gyrA or parC genes, while each CIPI had 1 of 3 single mutations in gyrA (encoding Ser83Phe [63.3%], Ser83Tyr [33.3%], or Asp87Asn [3.3%]). CIPHR had the same 3 mutations: 2 SNPs in gyrA (encoding Ser83Phe and Asp87Asn) and a third in parC (encoding Ser80Ile). CIPHR shared a common ancestor with CIPR and CIPI isolates harboring a single mutation in gyrA encoding Ser83Phe, suggesting that CIPHR emerged 16 to 23 years ago. Conclusions Three SNPs—2 in gyrA and 1 in parC—are present in S. Typhi strains highly resistant to fluoroquinolone, which were found to have evolved in 1993–2000, approximately 10 years after the beginning of the ciprofloxacin era. Highly resistant strains with survival advantages arose from strains harboring a single mutation in gyrA encoding Ser83Phe. Judicious use of fluoroquinolones is warranted to prevent acceleration of such resistance mechanisms in the future.

scholarly journals Computational Analysis of Molecular Interaction Networks Underlying Change of HIV-1 Resistance to Selected Reverse Transcriptase Inhibitors

2010 ◽  
Vol 4 ◽  
pp. BBI.S6247 ◽  
Author(s):  
Marcin Kierczak ◽  
Michał Dramiński ◽  
Jacek Koronacki ◽  
Jan Komorowski
Keyword(s):  
Drug Resistance ◽  
Reverse Transcriptase ◽  
Molecular Interaction ◽  
3D Structure ◽  
Resistance Mechanisms ◽  
Interaction Networks ◽  
Resistance Level ◽  
Molecular Interaction Networks ◽  
Monte Carlo Feature Selection ◽  
Hiv 1

Motivation Despite more than two decades of research, HIV resistance to drugs remains a serious obstacle in developing efficient AIDS treatments. Several computational methods have been developed to predict resistance level from the sequence of viral proteins such as reverse transcriptase (RT) or protease. These methods, while powerful and accurate, give very little insight into the molecular interactions that underly acquisition of drug resistance/hypersusceptibility. Here, we attempt at filling this gap by using our Monte Carlo feature selection and interdependency discovery method (MCFS-ID) to elucidate molecular interaction networks that characterize viral strains with altered drug resistance levels. Results We analyzed a number of HIV-1 RT sequences annotated with drug resistance level using the MCFS-ID method. This let us expound interdependency networks that characterize change of drug resistance to six selected RT inhibitors: Abacavir, Lamivudine, Stavudine, Zidovudine, Tenofovir and Nevirapine. The networks consider interdependencies at the level of physicochemical properties of mutating amino acids, eg,: polarity. We mapped each network on the 3D structure of RT in attempt to understand the molecular meaning of interacting pairs. The discovered interactions describe several known drug resistance mechanisms and, importantly, some previously unidentified ones. Our approach can be easily applied to a whole range of problems from the domain of protein engineering. Availability A portable Java implementation of our MCFS-ID method is freely available for academic users and can be obtained at: http://www.ipipan.eu/staff/m.draminski/software.htm .

scholarly journals Taking nature into lab: biomineralization by heavy metal resistant streptomycetes in soil

2013 ◽  
Vol 10 (2) ◽  
pp. 2345-2375 ◽  
Author(s):  
E. Schütze ◽  
A. Weist ◽  
M. Klose ◽  
T. Wach ◽  
M. Schumann ◽  
...  
Keyword(s):  
Heavy Metal ◽  
Resistance Mechanisms ◽  
Metal Resistance ◽  
Control Soil ◽  
Natural Conditions ◽  
Laboratory Methods ◽  
Dominant Property ◽  
Resistant Strains ◽  
Heavy Metal Resistant ◽  
And Control

Abstract. Biomineralization by heavy metal resistant streptomycetes was tested to evaluate the potential influence on metal mobilities in soil. Thus, we designed an experiment adopting conditions from classical laboratory methods to natural conditions prevailing in metal-rich soils with media spiked with heavy metals, soil agar, and nutrient enriched or unamended soil incubated with the bacteria. As a result, all strains were able to form struvite minerals on tryptic soy broth (TSB) media supplemented with AlCl2, MnCl2 and CuSO4, as well as on soil agar. Some strains additionally formed struvite on nutrient enriched contaminated and control soil, as well as on metal contaminated soil without addition of media components. In contrast, switzerite was exclusively formed on minimal media spiked with MnCl2 by four heavy metal resistant strains, and on nutrient enriched control soil by one strain. Hydrated nickel hydrogen phosphate was only crystallized on complex media supplemented with NiSO4 by most strains. Thus, mineralization is a~dominant property of streptomycetes, with different processes likely to occur under laboratory conditions and sub-natural to natural conditions. This new understanding may be transferred to formation of minerals in rock and sediment evolution, to ore deposit formation, and also might have implications for our understanding of biological metal resistance mechanisms. We assume that biogeochemical cycles, nutrient storage and metal resistance might be affected by formation and re-solubilization of minerals like struvite in soil at microscale.

Relative Fitness of Three Organophosphate-Resistant Strains of Culex pipiens pattens (Diptera: Culicidae)

1998 ◽  
Vol 35 (5) ◽  
pp. 716-719 ◽  
Author(s):  
Wang Jinfu ◽  
Lu Shaohong ◽  
Chen Rui ◽  
Wang Lingling
Keyword(s):  
Culex Pipiens ◽  
Relative Fitness ◽  
Resistant Strains
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