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WAMP-2

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WAMP-2 is an antibacterial peptide isolated from Triticum kiharae.

Category
Functional Peptides
Catalog number
BAT-011055
Synonyms
Cys-Gly-Asp-Gln-Ala-Arg-Gly-Ala-Lys-Cys-Pro-Asn-Cys-Leu-Cys-Cys-Gly-Lys-Tyr-Gly-Phe-Cys-Gly-Ser-Gly-Asp-Ala-Tyr-Cys-Gly-Lys-Gly-Ser-Cys-Gln-Ser-Gln-Cys-Arg
Sequence
CGDQARGAKCPNCLCCGKYGFCGSGDAYCGKGSCQSQCR
1. [Genes encoding hevein-like antimicrobial peptides WAMPs: Expression in response to phytohormones and environmental factors]
E A Istomina, T V Korostyleva, N A Rozhnova, E A Rogozhin, V A Pukhalskiy, T I Odintsova Genetika. 2016 Nov;52(11):1300-10.
We investigated the role of genes of hevein-like antimicrobial peptides of the WAMP family in the protection of wheat plants against biotic and abiotic stress. The semiquantitative RT-PCR method was used to examine the expression of wamp genes in wheat seedlings in response to infection by pathogens and exposure to phytohormones and ions of a heavy metal ion-cadmium. We discovered that wheat germ contamination by harmful fungi significantly increases expression of genes of the wamp family, and the primary transcript is wamp-2. We determined that salicylic acid, rather than methyl jasmonate, induces expression of genes of the wamp family. We showed that abiotic stress induced by cadmium ions inhibits expression of wamp genes in the roots with no effect on their expression in shoots. The results support the protective role of wamp genes in the response of wheat plants to infections by pathogens. In turn, the resistance to abiotic stress induced by cadmium ions does not appear to be associated with expression of genes of the wamp family.
2. Fragments of a Wheat Hevein-Like Antimicrobial Peptide Augment the Inhibitory Effect of a Triazole Fungicide on Spore Germination of Fusarium oxysporum and Alternaria solani
Larisa Shcherbakova, Tatyana Odintsova, Tatyana Pasechnik, Lenara Arslanova, Tatyana Smetanina, Maxim Kartashov, Marina Slezina, Vitaly Dzhavakhiya Antibiotics (Basel). 2020 Dec 4;9(12):870. doi: 10.3390/antibiotics9120870.
There are increasing environmental risks associated with extensive use of fungicides for crop protection. Hence, the use of new approaches using natural plant defense mechanisms, including application of plant antimicrobial peptides (AMPs), is of great interest. Recently, we studied the structural-function relationships between antifungal activity and five hevein-like AMPs from the WAMP (wheat AMP) family of Triticum kiharae Dorof. et Migush. We first discovered that short peptides derived from the central, N-, and C-terminal regions of one of the WAMPs (WAMP-2) were able to augment the inhibitory effect of Folicur® EC 250, a triazole fungicide, on spore germination of the wheat pathogenic fungi, including Fusarium spp. and Alternaria alternata. In this research, we explored the ability of chemically synthesized WAMP-2-derived peptides for enhancing the sensitivity of two other Fusarium and Alternaria species, F. oxysporum and A. solani, causing wilt and early blight of tomato, respectively, to Folicur®. The synthesized WAMP-2-derived peptides synergistically interacted with the fungicide and significantly increased its efficacy, inhibiting conidial germination at much lower Folicur® concentrations than required for the same efficiency using the fungicide alone. The experiments on co-applications of some of WAMP-2-fragments and the fungicide on tomato leaves and seedlings, which confirmed the results obtained in vitro, are described.
3. Novel mode of action of plant defense peptides - hevein-like antimicrobial peptides from wheat inhibit fungal metalloproteases
Anna A Slavokhotova, Todd A Naumann, Neil P J Price, Eugene A Rogozhin, Yaroslav A Andreev, Alexander A Vassilevski, Tatyana I Odintsova FEBS J. 2014 Oct;281(20):4754-64. doi: 10.1111/febs.13015. Epub 2014 Sep 24.
The multilayered plant immune system relies on rapid recognition of pathogen-associated molecular patterns followed by activation of defense-related genes, resulting in the reinforcement of plant cell walls and the production of antimicrobial compounds. To suppress plant defense, fungi secrete effectors, including a recently discovered Zn-metalloproteinase from Fusarium verticillioides, named fungalysin Fv-cmp. This proteinase cleaves class IV chitinases, which are plant defense proteins that bind and degrade chitin of fungal cell walls. In this study, we investigated plant responses to such pathogen invasion, and discovered novel inhibitors of fungalysin. We produced several recombinant hevein-like antimicrobial peptides named wheat antimicrobial peptides (WAMPs) containing different amino acids (Ala, Lys, Glu, and Asn) at the nonconserved position 34. An additional Ser at the site of fungalysin proteolysis makes the peptides resistant to the protease. Moreover, an equal molar concentration of WAMP-1b or WAMP-2 to chitinase was sufficient to block the fungalysin activity, keeping the chitinase intact. Thus, WAMPs represent novel protease inhibitors that are active against fungal metalloproteases. According to in vitro antifungal assays WAMPs directly inhibited hyphal elongation, suggesting that fungalysin plays an important role in fungal development. A novel molecular mechanism of dynamic interplay between host defense molecules and fungal virulence factors is suggested.
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