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Evidence That a Laminin-Like Insect Protein Mediates Early Events in the Interaction of a Phytoparasite with Its Vector's Salivary Gland

Overview of attention for article published in PLOS ONE, October 2012
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Title
Evidence That a Laminin-Like Insect Protein Mediates Early Events in the Interaction of a Phytoparasite with Its Vector's Salivary Gland
Published in
PLOS ONE, October 2012
DOI 10.1371/journal.pone.0048170
Pubmed ID
Authors

Felipe de Almeida Dias, Andre Luis Souza dos Santos, Letícia Miranda Santos Lery, Thiago Luiz Alves e Silva, Mauricio Martins Oliveira, Paulo Mascarello Bisch, Elvira Maria Saraiva, Thaïs Cristina Souto-Padrón, Angela Hampshire Lopes

Abstract

Phytomonas species are plant parasites of the family Trypanosomatidae, which are transmitted by phytophagous insects. Some Phytomonas species cause major agricultural damages. The hemipteran Oncopeltus fasciatus is natural and experimental host for several species of trypanosomatids, including Phytomonas spp. The invasion of the insect vectors' salivary glands is one of the most important events for the life cycle of Phytomonas species. In the present study, we show the binding of Phytomonas serpens at the external face of O. fasciatus salivary glands by means of scanning electron microscopy and the in vitro interaction of living parasites with total proteins from the salivary glands in ligand blotting assays. This binding occurs primarily through an interaction with a 130 kDa salivary gland protein. The mass spectrometry of the trypsin-digest of this protein matched 23% of human laminin-5 β3 chain precursor sequence by 16 digested peptides. A protein sequence search through the transcriptome of O. fasciatus embryo showed a partial sequence with 51% similarity to human laminin β3 subunit. Anti-human laminin-5 β3 chain polyclonal antibodies recognized the 130 kDa protein by immunoblotting. The association of parasites with the salivary glands was strongly inhibited by human laminin-5, by the purified 130 kDa insect protein, and by polyclonal antibodies raised against the human laminin-5 β3 chain. This is the first report demonstrating that a laminin-like molecule from the salivary gland of O. fasciatus acts as a receptor for Phytomonas binding. The results presented in this investigation are important findings that will support further studies that aim at developing new approaches to prevent the transmission of Phytomonas species from insects to plants and vice-versa.

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Geographical breakdown

Country Count As %
Unknown 21 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 6 29%
Researcher 5 24%
Student > Bachelor 2 10%
Student > Ph. D. Student 2 10%
Professor 1 5%
Other 3 14%
Unknown 2 10%
Readers by discipline Count As %
Agricultural and Biological Sciences 14 67%
Biochemistry, Genetics and Molecular Biology 1 5%
Immunology and Microbiology 1 5%
Medicine and Dentistry 1 5%
Unknown 4 19%