[Otitis media due to Vibrio cholerae non-O1/O139: A case report and short review]. [PDF]
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Differential endopeptidase requirements during adaptation to changing growth conditions in <i>Vibrio cholerae</i>. [PDF]
Rosch K +5 more
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Draft genome sequences of three non-O1/non-O139 <i>Vibrio cholerae</i> isolates from Lake Wonderwood near Seminole Beach, Florida. [PDF]
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Conformations and sequence determinants in the lipid binding of an adhesive peptide derived from Vibrio cholerae biofilms. [PDF]
Huang X +12 more
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A colorimetric method for detecting virulent bacteriophage to Vibrio cholerae in fecal and environmental samples. [PDF]
Luo W +8 more
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Fusobacterium nucleatum Enhances Intestinal Adaptation of Vibrio cholerae via Interspecies Biofilm Formation. [PDF]
Chen G, Chen J, Wang X, Guo D, Liu Z.
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Vibrio cholerae: Cholera toxin
The International Journal of Biochemistry & Cell Biology, 2007The bacterial protein toxin of Vibrio cholerae, cholera toxin, is a major agent involved in severe diarrhoeal disease. Cholera toxin is a member of the AB toxin family and is composed of a catalytically active heterodimeric A-subunit linked with a homopentameric B-subunit.
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Biofilms are communities of bacteria immersed in an extracellular matrix. Biofilms are considered a defensive strategy that protects bacteria from a hostile environment, including our immune system. Vidakovic et al. recently reported that Vibrio cholerae can build biofilms around immune cells and kill them, discovering an aggressive role for biofilms.
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Metabolomics of Vibrio cholerae
2018Metabolomics is an "omics" approach to quantitatively measure a large set of metabolites. In this chapter, we describe an example method for performing liquid chromatography coupled to mass spectrometry (LC-MS)-based untargeted metabolomics on a cell extract from Vibrio cholerae.
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Several approaches to the development of a safe and effective vaccine against Vibrio cholerae are currently being pursued. These candidate vaccines include (1) live V. cholerae strains attenuated by recombinant DNA techniques; (2) killed whole V. cholerae organisms plus purified cholera enterotoxin B subunit; and (3) cloned V.
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