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

Nachman, Ronald J. (author)
Mahdian, Kamran (author)
Nässel, Dick R. (author)
Stockholms universitet,Avdelningen för funktionell zoomorfologi
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Isaac, R. Elwyn (author)
Pryor, Nan (author)
Smagghe, Guy (author)
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 (creator_code:org_t)
Elsevier BV, 2011
2011
English.
In: Peptides. - : Elsevier BV. - 0196-9781 .- 1873-5169. ; 32:3, s. 587-594
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • 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 24h. 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 0.0083nmol/μl (0.0087μg/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.

Subject headings

NATURVETENSKAP  -- Biologi -- Zoologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Zoology (hsv//eng)

Keyword

Aphicide
Hindgut myotropic
Diuresis
Peptidase resistant

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Nachman, Ronald ...
Mahdian, Kamran
Nässel, Dick R.
Isaac, R. Elwyn
Pryor, Nan
Smagghe, Guy
About the subject
NATURAL SCIENCES
NATURAL SCIENCES
and Biological Scien ...
and Zoology
Articles in the publication
Peptides
By the university
Stockholm University

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