ArticleFrontiers in microbiology2015
The Membrane Proteins Involved in Virulence of Cronobacter sakazakii Virulent G362 and Attenuated L3101 Isolates.
Article in Frontiers in microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
What it found
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Who cites it
12 citing papers in PubMed.
- DecipheringMicroorganisms · 2026Review
- Recurring food source-basedHealth science reports · 2024Article
- Comprehensive Genomic Characterization ofMicroorganisms · 2023Article
- Membrane Proteins and Proteomics of Cronobacter sakazakii Cells: Reliable Method for Identification and Subcellular Localization.Applied and environmental microbiology · 2022Article
- The Secretion of Toxins and Other Exoproteins ofMicroorganisms · 2020Review
- Protective Effect of Recombinant Proteins ofFrontiers in cellular and infection microbiology · 2020Article
- Chaperone OsmY facilitates the biogenesis of a major family of autotransporters.Molecular microbiology · 2019Article
- The Involvement of theFrontiers in cellular and infection microbiology · 2018Article
- Temperature-Dependent Gene Expression inFrontiers in microbiology · 2018Article
- Caco-2 Invasion byFrontiers in microbiology · 2017Article
- Comparative Outer Membrane Protein Analysis of High and Low-Invasive Strains ofFrontiers in microbiology · 2017Article
- Analysis and Characterization of Proteins Associated with Outer Membrane Vesicles Secreted byFrontiers in microbiology · 2017Article
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Cronobacter sakazakii is an opportunistic foodborne pathogen and the virulence differences were previously documented. However, information about membranous proteins involved in virulence differences was not available. In this study, virulent characterization such as biofilm formation and flagella motility between virulent C. sakazakii isolate G362 and attenuated L3101 were determined. Then, two-dimensional gel electrophoresis (2-DE) technology was used to preliminarily reveal differential expression of membranous proteins between G362 and L3101. On the mass spectrometry (MS) analysis and MASCOT research results, fourteen proteins with differential expression were successfully identified. At the threshold of twofold changes, five out of eight membranous proteins were up-regulated in G362. Using RT-PCR, the expression abundance of the protein (enzV, ompX, lptE, pstB, and OsmY) genes at mRNA levels was consistent with the results by 2-DE method. The findings presented here provided novel information and valuable knowledge for revealing pathogenic mechanism of C. sakazakii.
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