Baseline susceptibilities of B- and Q-biotype Bemisia tabaci to anthranilic diamides in Arizona
BACKGROUND: Development of pyriproxyfen and neonicotinoid resistance in the B‐biotype whitefly and recent introduction of the Q biotype have the potential to threaten current whitefly management programs in Arizona. The possibility of integrating the novel anthranilic diamides chlorantraniliprole an...
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| Published in: | Pest management science Vol. 68; no. 1; pp. 83 - 91 |
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| Main Authors: | , , , , , , , , |
| Format: | Journal Article |
| Language: | English |
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Chichester, UK
John Wiley & Sons, Ltd
01-01-2012
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| Abstract | BACKGROUND: Development of pyriproxyfen and neonicotinoid resistance in the B‐biotype whitefly and recent introduction of the Q biotype have the potential to threaten current whitefly management programs in Arizona. The possibility of integrating the novel anthranilic diamides chlorantraniliprole and cyantraniliprole into the current program to tackle these threats largely depends on whether these compounds have cross‐resistance with pyriproxyfen and neonicotinoids in whiteflies. To address this question, the authors bioassayed a susceptible B‐biotype strain, a pyriproxyfen‐resistant B‐biotype strain, four multiply resistant Q‐biotype strains and 16 B‐biotype field populations from Arizona with a systemic uptake bioassay developed in the present study.
RESULTS: The magnitude of variations in LC50 and LC99 among the B‐biotype populations or the Q‐biotype strains was less than fivefold and tenfold, respectively, for both chlorantraniliprole and cyantraniliprole. The Q‐biotype strains were relatively more tolerant than the B‐biotype populations. No correlations were observed between the LC50 (or LC99) values of the two diamides against the B‐ and Q‐biotype populations tested and their survival rates at a discriminating dose of pyriproxyfen or imidacloprid.
CONCLUSION: These results indicate the absence of cross‐resistance between the two anthranilic diamides and the currently used neonicotinoids and pyriproxyfen. Future variation in susceptibility of field populations to chlorantraniliprole and cyantraniliprole could be documented according to the baseline susceptibility range of the populations tested in this study. Copyright © 2011 Society of Chemical Industry |
|---|---|
| AbstractList | BACKGROUND:
Development of pyriproxyfen and neonicotinoid resistance in the B‐biotype whitefly and recent introduction of the Q biotype have the potential to threaten current whitefly management programs in Arizona. The possibility of integrating the novel anthranilic diamides chlorantraniliprole and cyantraniliprole into the current program to tackle these threats largely depends on whether these compounds have cross‐resistance with pyriproxyfen and neonicotinoids in whiteflies. To address this question, the authors bioassayed a susceptible B‐biotype strain, a pyriproxyfen‐resistant B‐biotype strain, four multiply resistant Q‐biotype strains and 16 B‐biotype field populations from Arizona with a systemic uptake bioassay developed in the present study.
RESULTS:
The magnitude of variations in LC
50
and LC
99
among the B‐biotype populations or the Q‐biotype strains was less than fivefold and tenfold, respectively, for both chlorantraniliprole and cyantraniliprole. The Q‐biotype strains were relatively more tolerant than the B‐biotype populations. No correlations were observed between the LC
50
(or LC
99
) values of the two diamides against the B‐ and Q‐biotype populations tested and their survival rates at a discriminating dose of pyriproxyfen or imidacloprid.
CONCLUSION:
These results indicate the absence of cross‐resistance between the two anthranilic diamides and the currently used neonicotinoids and pyriproxyfen. Future variation in susceptibility of field populations to chlorantraniliprole and cyantraniliprole could be documented according to the baseline susceptibility range of the populations tested in this study. Copyright © 2011 Society of Chemical Industry BACKGROUNDDevelopment of pyriproxyfen and neonicotinoid resistance in the B-biotype whitefly and recent introduction of the Q biotype have the potential to threaten current whitefly management programs in Arizona. The possibility of integrating the novel anthranilic diamides chlorantraniliprole and cyantraniliprole into the current program to tackle these threats largely depends on whether these compounds have cross-resistance with pyriproxyfen and neonicotinoids in whiteflies. To address this question, the authors bioassayed a susceptible B-biotype strain, a pyriproxyfen-resistant B-biotype strain, four multiply resistant Q-biotype strains and 16 B-biotype field populations from Arizona with a systemic uptake bioassay developed in the present study.RESULTSThe magnitude of variations in LC(50) and LC(99) among the B-biotype populations or the Q-biotype strains was less than fivefold and tenfold, respectively, for both chlorantraniliprole and cyantraniliprole. The Q-biotype strains were relatively more tolerant than the B-biotype populations. No correlations were observed between the LC(50) (or LC(99)) values of the two diamides against the B- and Q-biotype populations tested and their survival rates at a discriminating dose of pyriproxyfen or imidacloprid.CONCLUSIONThese results indicate the absence of cross-resistance between the two anthranilic diamides and the currently used neonicotinoids and pyriproxyfen. Future variation in susceptibility of field populations to chlorantraniliprole and cyantraniliprole could be documented according to the baseline susceptibility range of the populations tested in this study. Development of pyriproxyfen and neonicotinoid resistance in the B-biotype whitefly and recent introduction of the Q biotype have the potential to threaten current whitefly management programs in Arizona. The possibility of integrating the novel anthranilic diamides chlorantraniliprole and cyantraniliprole into the current program to tackle these threats largely depends on whether these compounds have cross-resistance with pyriproxyfen and neonicotinoids in whiteflies. To address this question, the authors bioassayed a susceptible B-biotype strain, a pyriproxyfen-resistant B-biotype strain, four multiply resistant Q-biotype strains and 16 B-biotype field populations from Arizona with a systemic uptake bioassay developed in the present study. The magnitude of variations in LC(50) and LC(99) among the B-biotype populations or the Q-biotype strains was less than fivefold and tenfold, respectively, for both chlorantraniliprole and cyantraniliprole. The Q-biotype strains were relatively more tolerant than the B-biotype populations. No correlations were observed between the LC(50) (or LC(99)) values of the two diamides against the B- and Q-biotype populations tested and their survival rates at a discriminating dose of pyriproxyfen or imidacloprid. These results indicate the absence of cross-resistance between the two anthranilic diamides and the currently used neonicotinoids and pyriproxyfen. Future variation in susceptibility of field populations to chlorantraniliprole and cyantraniliprole could be documented according to the baseline susceptibility range of the populations tested in this study. BACKGROUND: Development of pyriproxyfen and neonicotinoid resistance in the B‐biotype whitefly and recent introduction of the Q biotype have the potential to threaten current whitefly management programs in Arizona. The possibility of integrating the novel anthranilic diamides chlorantraniliprole and cyantraniliprole into the current program to tackle these threats largely depends on whether these compounds have cross‐resistance with pyriproxyfen and neonicotinoids in whiteflies. To address this question, the authors bioassayed a susceptible B‐biotype strain, a pyriproxyfen‐resistant B‐biotype strain, four multiply resistant Q‐biotype strains and 16 B‐biotype field populations from Arizona with a systemic uptake bioassay developed in the present study. RESULTS: The magnitude of variations in LC50 and LC99 among the B‐biotype populations or the Q‐biotype strains was less than fivefold and tenfold, respectively, for both chlorantraniliprole and cyantraniliprole. The Q‐biotype strains were relatively more tolerant than the B‐biotype populations. No correlations were observed between the LC50 (or LC99) values of the two diamides against the B‐ and Q‐biotype populations tested and their survival rates at a discriminating dose of pyriproxyfen or imidacloprid. CONCLUSION: These results indicate the absence of cross‐resistance between the two anthranilic diamides and the currently used neonicotinoids and pyriproxyfen. Future variation in susceptibility of field populations to chlorantraniliprole and cyantraniliprole could be documented according to the baseline susceptibility range of the populations tested in this study. Copyright © 2011 Society of Chemical Industry Development of pyriproxyfen and neonicotinoid resistance in the B-biotype whitefly and recent introduction of the Q biotype have the potential to threaten current whitefly management programs in Arizona. The possibility of integrating the novel anthranilic diamides chlorantraniliprole and cyantraniliprole into the current program to tackle these threats largely depends on whether these compounds have cross-resistance with pyriproxyfen and neonicotinoids in whiteflies. To address this question, the authors bioassayed a susceptible B-biotype strain, a pyriproxyfen-resistant B-biotype strain, four multiply resistant Q-biotype strains and 16 B-biotype field populations from Arizona with a systemic uptake bioassay developed in the present study. The magnitude of variations in LC50 and LC99 among the B-biotype populations or the Q-biotype strains was less than fivefold and tenfold, respectively, for both chlorantraniliprole and cyantraniliprole. The Q-biotype strains were relatively more tolerant than the B-biotype populations. No correlations were observed between the LC50 (or LC99) values of the two diamides against the B- and Q-biotype populations tested and their survival rates at a discriminating dose of pyriproxyfen or imidacloprid. These results indicate the absence of cross-resistance between the two anthranilic diamides and the currently used neonicotinoids and pyriproxyfen. Future variation in susceptibility of field populations to chlorantraniliprole and cyantraniliprole could be documented according to the baseline susceptibility range of the populations tested in this study. |
| Author | Nichols, Robert L Degain, Benjamin A Fournier, Alfred J. Naranjo, Steven E Harpold, Virginia S Palumbo, John C Ellsworth, Peter C Li, Xianchun Marçon, Paula G |
| Author_xml | – sequence: 1 givenname: Xianchun surname: Li fullname: Li, Xianchun email: lxc@email.arizona.edu organization: Department of Entomology and BIO5 institute, University of Arizona, Tucson, AZ, USA – sequence: 2 givenname: Benjamin A surname: Degain fullname: Degain, Benjamin A organization: Department of Entomology and BIO5 institute, University of Arizona, Tucson, AZ, USA – sequence: 3 givenname: Virginia S surname: Harpold fullname: Harpold, Virginia S organization: Department of Entomology and BIO5 institute, University of Arizona, Tucson, AZ, USA – sequence: 4 givenname: Paula G surname: Marçon fullname: Marçon, Paula G organization: DuPont Crop Protection, Stine-Haskell Research Center, Newark, DE, USA – sequence: 5 givenname: Robert L surname: Nichols fullname: Nichols, Robert L organization: Cotton Incorporated, Cary, NC, USA – sequence: 6 givenname: Alfred J. surname: Fournier fullname: Fournier, Alfred J. organization: Department of Entomology and BIO5 institute, University of Arizona, Tucson, AZ, USA – sequence: 7 givenname: Steven E surname: Naranjo fullname: Naranjo, Steven E organization: USDA-ARS, Arid-Land Agricultural Research Center, Maricopa, AZ, USA – sequence: 8 givenname: John C surname: Palumbo fullname: Palumbo, John C organization: Department of Entomology and BIO5 institute, University of Arizona, Tucson, AZ, USA – sequence: 9 givenname: Peter C surname: Ellsworth fullname: Ellsworth, Peter C organization: Department of Entomology and BIO5 institute, University of Arizona, Tucson, AZ, USA |
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| Keywords | cyantraniliprole Insecticide Insecta Pesticides baseline susceptibility Resistance Pest Homoptera chlorantraniliprole Arthropoda Bemisia tabaci resistance management Pyrazole derivatives Biotype Carboxamide Anthranilic acid derivatives Aleyrodidae Invertebrata |
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| SubjectTerms | Animal populations Animals Arizona baseline susceptibility Bemisia tabaci Biological and medical sciences Biological Assay biotype chlorantraniliprole Control cyantraniliprole Diamide - pharmacology Female Fundamental and applied biological sciences. Psychology Hemiptera - classification Hemiptera - drug effects Insecticide Resistance Insecticides Insecticides - pharmacology Insects Male ortho-Aminobenzoates - pharmacology Pest control Phytopathology. Animal pests. Plant and forest protection Protozoa. Invertebrates resistance management Resistance to control |
| Title | Baseline susceptibilities of B- and Q-biotype Bemisia tabaci to anthranilic diamides in Arizona |
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