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1.
Dev Comp Immunol ; 22(4): 387-99, 1998.
Article in English | MEDLINE | ID: mdl-9699484

ABSTRACT

A bacteria inducible antibacterial protein, P2, was isolated from the old world bollworm Helicoverpa armigera. Fifth-instar larvae were injected with live Escherichia coli NCTC 8196. P2 was isolated by HPLC using reversed-phase and size-exclusion columns. In addition, P2 was isolated by an alternative method of sequential cation-exchange and reversed-phase HPLC. The structure of P2 was determined by N-terminal Edman degradation and mass spectrometry. P2 had similar mass (14.1 kDa) structure and activity to gloverin, an inducible glycine-rich antibacterial protein isolated from Hyalophora gloveri [Axén, A.; Carlsson, A.; Engström, A.; Bennich, H. Eur. J. Biochem. 247:614-619; 1997]. At the N-terminus P2 had approximately 60% identity with gloverin. P2 is basic, heat stable, and displayed rapid antibacterial action. P2 was active against the Gram-negative bacteria tested and was inactive against the Gram-positive bacteria, Candida albicans, a bovine turbinate cell line, and pestivirus.


Subject(s)
Anti-Infective Agents/metabolism , Escherichia coli/physiology , Lepidoptera/microbiology , Protein Biosynthesis , Amino Acid Sequence , Animals , Anti-Bacterial Agents , Anti-Infective Agents/isolation & purification , Anti-Infective Agents/pharmacology , Candida albicans/drug effects , Cell Line/drug effects , Chromatography, High Pressure Liquid , Gram-Negative Bacteria/drug effects , Gram-Positive Bacteria/drug effects , Hemolymph/chemistry , Intercellular Signaling Peptides and Proteins , Lepidoptera/metabolism , Molecular Sequence Data , Molecular Weight , Pestivirus/drug effects , Proteins/isolation & purification , Proteins/pharmacology , Sequence Homology, Amino Acid
2.
Can J Microbiol ; 41(2): 136-44, 1995 Feb.
Article in English | MEDLINE | ID: mdl-7720011

ABSTRACT

Secretions from exocrine metapleural glands of Myrmecia gulosa (Australian bull ant) exhibit broad-spectrum antimicrobial activity. Treatment of the yeast Candida albicans with metapleural secretion resulted in the rapid and total leakage of K+ ions from cells within 10 min. Ultrastructural analysis of the bacteria Bacillus cereus, Escherichia coli, and Pseudomonas aeruginosa, and cells and protoplasts of Candida albicans demonstrated gross damage of the cell membrane and aggregation of the cytoplasmic matrix of treated cells. Degradation of membrane-bound organelles was also observed in Candida albicans. The antimicrobially active components of metapleural secretions were nonpolar and interacted with the phospholipid bilayer, causing damage to the structural integrity of liposomes and the release of carboxyfluorescein. The data suggest that the antimicrobial agents in metapleural secretion act primarily by disrupting the structure and function of the phospholipid bilayer of the cytoplasmic membrane.


Subject(s)
Anti-Infective Agents/pharmacology , Bacillus cereus/drug effects , Candida albicans/drug effects , Escherichia coli/drug effects , Insecta/chemistry , Pseudomonas aeruginosa/drug effects , Animals , Anti-Bacterial Agents , Anti-Infective Agents/isolation & purification , Bacillus cereus/ultrastructure , Candida albicans/ultrastructure , Cell Membrane/drug effects , Cell Membrane/ultrastructure , Escherichia coli/ultrastructure , Insecta/microbiology , Liposomes , Microscopy, Electron , Potassium , Pseudomonas aeruginosa/ultrastructure
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