Biochemical characterization of digestive membrane-associated alkaline phosphatase from the velvet bean caterpillar Anticarsia gemmatalis

Arch Insect Biochem Physiol. 2019 Sep;102(1):e21591. doi: 10.1002/arch.21591. Epub 2019 Jul 1.

Abstract

In Brazil, the use of transgenic plants expressing the insect-toxic Bacillus thuringiensis endotoxin has been successfully used as pest control management since 2013 in transgenic soybean lineages against pest caterpillars such as Helicoverpa armigera. These toxins, endogenously expressed by the plants or sprayed over the crops, are ingested by the insect and bind to receptors in the midgut of these animals, resulting in disruption of digestion and lower insect survival rates. Here, we identified and characterized a membrane-associated alkaline phosphatase (ALP) in the midgut of Anticarsia gemmatalis, the main soybean defoliator pest in Brazil, and data suggested that it binds to Cry1Ac toxin in vitro. Our data showed a peak of ALP activity in homogenate samples of the midgut dissected from the 4th and 5th instars larvae. The brush border membrane vesicles obtained from the midgut of these larvae were used to purify a 60 kDa ALP, as detected by in-gel activity and in vitro biochemical characterization using pharmacological inhibitors and mass spectrometry. When Cry1Ac toxin was supplied to the diet, it was efficient in decreasing larval weight gain and survival. Indeed, in vitro incubation of Cry1Ac toxin with the purified ALP resulted in a 43% decrease in ALP specific activity and enzyme-linked immunosorbent assay showed that ALP interacts with Cry1Ac toxin in vitro, thus suggesting that ALP could function as a Cry toxin ligand. This is a first report characterizing an ALP in A. gemmatalis.

Keywords: Anticarsia gemmatalis; Cry1Ac; alkaline phosphatase; biological control; pest insect.

MeSH terms

  • Alkaline Phosphatase / antagonists & inhibitors
  • Alkaline Phosphatase / isolation & purification
  • Alkaline Phosphatase / metabolism*
  • Animals
  • Bacillus thuringiensis Toxins
  • Bacterial Proteins / metabolism*
  • Bacterial Proteins / toxicity
  • Endotoxins / metabolism*
  • Endotoxins / toxicity
  • Gastrointestinal Tract / enzymology
  • Gastrointestinal Tract / ultrastructure
  • Hemolysin Proteins / metabolism*
  • Hemolysin Proteins / toxicity
  • Larva / enzymology*
  • Microvilli / enzymology
  • Moths / enzymology*

Substances

  • Bacillus thuringiensis Toxins
  • Bacterial Proteins
  • Endotoxins
  • Hemolysin Proteins
  • insecticidal crystal protein, Bacillus Thuringiensis
  • Alkaline Phosphatase