Literature DB >> 20869418

Biostable multi-Aib analogs of tachykinin-related peptides demonstrate potent oral aphicidal activity in the pea aphid Acyrthosiphon pisum (Hemiptera: Aphidae).

Ronald J Nachman1, Kamran Mahdian, Dick R Nässel, R Elwyn Isaac, Nan Pryor, Guy Smagghe.   

Abstract

The tachykinin-related peptides (TRPs) are multifunctional neuropeptides found in a variety of arthropod species, including the pea aphid Acyrthosiphon pisum (Hemiptera: Aphidae). Two new biostable TRP analogs containing multiple, sterically hindered Aib residues were synthesized and found to exhibit significantly enhanced resistance to hydrolysis by angiotensin converting enzyme and neprilysin, membrane-bound enzymes that degrade and inactivate natural TRPs. The two biostable analogs were also found to retain significant myostimulatory activity in an isolated cockroach hindgut preparation, the bioassay used to isolate and identify the first members of the TRP family. Indeed one of the analogs (Leuma-TRP-Aib-1) matched the potency and efficacy of the natural, parent TRP peptide in this myotropic bioassay. The two biostable TRP analogs were further fed in solutions of artificial diet to the pea aphid over a period of 3 days and evaluated for antifeedant and aphicidal activity and compared with the effect of treatment with three natural, unmodified TRPs. The two biostable multi-Aib TRP analogs were observed to elicit aphicidal effects within the first 24 h. In contrast natural, unmodified TRPs, including two that are native to the pea aphid, demonstrated little or no activity. The most active analog, double-Aib analog Leuma-TRP-Aib-1 (pEA[Aib]SGFL[Aib]VR-NH(2)), featured aphicidal activity calculated at an LC(50) of 0.0083 nmol/μl (0.0087 μg/μl) and an LT(50) of 1.4 days, matching or exceeding the potency of commercially available aphicides. The mechanism of this activity has yet to be established. The aphicidal activity of the biostable TRP analogs may result from disruption of digestive processes by interfering with gut motility patterns and/or with fluid cycling in the gut; processes shown to be regulated by the TRPs in other insects. These active TRP analogs and/or second generation analogs offer potential as environmentally friendly pest aphid control agents.
Copyright © 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20869418     DOI: 10.1016/j.peptides.2010.09.013

Source DB:  PubMed          Journal:  Peptides        ISSN: 0196-9781            Impact factor:   3.750


  7 in total

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Authors:  Hongbo Jiang; Zhaojun Wei; Ronald J Nachman; Krzysztof Kaczmarek; Janusz Zabrocki; Yoonseong Park
Journal:  Peptides       Date:  2014-11-22       Impact factor: 3.750

Review 2.  Toxins for transgenic resistance to hemipteran pests.

Authors:  Nanasaheb P Chougule; Bryony C Bonning
Journal:  Toxins (Basel)       Date:  2012-06-04       Impact factor: 4.546

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Authors:  Calum T J Ferguson; Areej A Al-Khalaf; R Elwyn Isaac; Olivier J Cayre
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Authors:  Paweł Marciniak; Joanna Pacholska-Bogalska; Lapo Ragionieri
Journal:  J Proteome Res       Date:  2022-09-15       Impact factor: 5.370

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6.  Ligand selectivity in tachykinin and natalisin neuropeptidergic systems of the honey bee parasitic mite Varroa destructor.

Authors:  Hongbo Jiang; Donghun Kim; Sharon Dobesh; Jay D Evans; Ronald J Nachman; Krzysztof Kaczmarek; Janusz Zabrocki; Yoonseong Park
Journal:  Sci Rep       Date:  2016-01-28       Impact factor: 4.379

7.  Function of the natalisin receptor in mating of the oriental fruit fly, Bactrocera dorsalis (Hendel) and testing of peptidomimetics.

Authors:  Shun-Hua Gui; Yu-Xia Pei; Li Xu; Wei-Ping Wang; Hong-Bo Jiang; Ronald J Nachman; Krzysztof Kaczmarek; Janusz Zabrocki; Jin-Jun Wang
Journal:  PLoS One       Date:  2018-02-23       Impact factor: 3.240

  7 in total

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