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Contribution of S-Layer Proteins to the Mosquitocidal Activity of Lysinibacillus sphaericus

Lysinibacillus sphaericus strains belonging the antigenic group H5a5b produce spores with larvicidal activity against larvae of Culex mosquitoes. C7, a new isolated strain, which presents similar biochemical characteristics and Bin toxins in their spores as the reference strain 2362, was, however, m...

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Autores principales: Allievi, Mariana Claudia, Palomino, María Mercedes, Prado Acosta, Mariano, Lanati, Leonardo, Ruzal, Sandra Mónica, Sánchez-Rivas, Carmen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213006/
https://www.ncbi.nlm.nih.gov/pubmed/25354162
http://dx.doi.org/10.1371/journal.pone.0111114
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author Allievi, Mariana Claudia
Palomino, María Mercedes
Prado Acosta, Mariano
Lanati, Leonardo
Ruzal, Sandra Mónica
Sánchez-Rivas, Carmen
author_facet Allievi, Mariana Claudia
Palomino, María Mercedes
Prado Acosta, Mariano
Lanati, Leonardo
Ruzal, Sandra Mónica
Sánchez-Rivas, Carmen
author_sort Allievi, Mariana Claudia
collection PubMed
description Lysinibacillus sphaericus strains belonging the antigenic group H5a5b produce spores with larvicidal activity against larvae of Culex mosquitoes. C7, a new isolated strain, which presents similar biochemical characteristics and Bin toxins in their spores as the reference strain 2362, was, however, more active against larvae of Culex mosquitoes. The contribution of the surface layer protein (S-layer) to this behaviour was envisaged since this envelope protein has been implicated in the pathogenicity of several bacilli, and we had previously reported its association to spores. Microscopic observation by immunofluorescence detection with anti S-layer antibody in the spores confirms their attachment. S-layers and BinA and BinB toxins formed high molecular weight multimers in spores as shown by SDS-PAGE and western blot detection. Purified S-layer from both L. sphaericus C7 and 2362 strain cultures was by itself toxic against Culex sp larvae, however, that from C7 strain was also toxic against Aedes aegypti. Synergistic effect between purified S-layer and spore-crystal preparations was observed against Culex sp. and Aedes aegypti larvae. This effect was more evident with the C7 strain. In silico analyses of the S-layer sequence suggest the presence of chitin-binding and hemolytic domains. Both biochemical characteristics were detected for both S-layers strains that must justify their contribution to pathogenicity.
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spelling pubmed-42130062014-11-05 Contribution of S-Layer Proteins to the Mosquitocidal Activity of Lysinibacillus sphaericus Allievi, Mariana Claudia Palomino, María Mercedes Prado Acosta, Mariano Lanati, Leonardo Ruzal, Sandra Mónica Sánchez-Rivas, Carmen PLoS One Research Article Lysinibacillus sphaericus strains belonging the antigenic group H5a5b produce spores with larvicidal activity against larvae of Culex mosquitoes. C7, a new isolated strain, which presents similar biochemical characteristics and Bin toxins in their spores as the reference strain 2362, was, however, more active against larvae of Culex mosquitoes. The contribution of the surface layer protein (S-layer) to this behaviour was envisaged since this envelope protein has been implicated in the pathogenicity of several bacilli, and we had previously reported its association to spores. Microscopic observation by immunofluorescence detection with anti S-layer antibody in the spores confirms their attachment. S-layers and BinA and BinB toxins formed high molecular weight multimers in spores as shown by SDS-PAGE and western blot detection. Purified S-layer from both L. sphaericus C7 and 2362 strain cultures was by itself toxic against Culex sp larvae, however, that from C7 strain was also toxic against Aedes aegypti. Synergistic effect between purified S-layer and spore-crystal preparations was observed against Culex sp. and Aedes aegypti larvae. This effect was more evident with the C7 strain. In silico analyses of the S-layer sequence suggest the presence of chitin-binding and hemolytic domains. Both biochemical characteristics were detected for both S-layers strains that must justify their contribution to pathogenicity. Public Library of Science 2014-10-29 /pmc/articles/PMC4213006/ /pubmed/25354162 http://dx.doi.org/10.1371/journal.pone.0111114 Text en © 2014 Allievi et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Allievi, Mariana Claudia
Palomino, María Mercedes
Prado Acosta, Mariano
Lanati, Leonardo
Ruzal, Sandra Mónica
Sánchez-Rivas, Carmen
Contribution of S-Layer Proteins to the Mosquitocidal Activity of Lysinibacillus sphaericus
title Contribution of S-Layer Proteins to the Mosquitocidal Activity of Lysinibacillus sphaericus
title_full Contribution of S-Layer Proteins to the Mosquitocidal Activity of Lysinibacillus sphaericus
title_fullStr Contribution of S-Layer Proteins to the Mosquitocidal Activity of Lysinibacillus sphaericus
title_full_unstemmed Contribution of S-Layer Proteins to the Mosquitocidal Activity of Lysinibacillus sphaericus
title_short Contribution of S-Layer Proteins to the Mosquitocidal Activity of Lysinibacillus sphaericus
title_sort contribution of s-layer proteins to the mosquitocidal activity of lysinibacillus sphaericus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213006/
https://www.ncbi.nlm.nih.gov/pubmed/25354162
http://dx.doi.org/10.1371/journal.pone.0111114
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