2012
DOI: 10.1007/978-1-4614-3561-7_17
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Field and Clinical Applications of Advanced Bacteriophage-Based Detection of Yersinia pestis

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Cited by 7 publications
(5 citation statements)
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“…Carrillo et al demonstrated Campylobacter isolates which significantly reduced the ability to colonize the broiler intestine compared with the original susceptible strain [54]. Further, Filippov et al proved that the phage-resistant Yersinia pestis was less virulent because of modifications in lipopolisacharides (LPS), and Lin et al showed similar effects in Klebsiella pneumoniae when the K1 capsule, being a phage receptor, was modified [55,56]. Moreover, there was a study in which a phage-resistant V. anguillarum strain lost its virulence, which was notified by the reduced mortality of cod [57].…”
Section: Bacterial Resistance and Other Safety Aspectsmentioning
confidence: 99%
“…Carrillo et al demonstrated Campylobacter isolates which significantly reduced the ability to colonize the broiler intestine compared with the original susceptible strain [54]. Further, Filippov et al proved that the phage-resistant Yersinia pestis was less virulent because of modifications in lipopolisacharides (LPS), and Lin et al showed similar effects in Klebsiella pneumoniae when the K1 capsule, being a phage receptor, was modified [55,56]. Moreover, there was a study in which a phage-resistant V. anguillarum strain lost its virulence, which was notified by the reduced mortality of cod [57].…”
Section: Bacterial Resistance and Other Safety Aspectsmentioning
confidence: 99%
“…ϕA1122 is able to infect most Y. pestis strains tested and will only infect the near neighbor Y. pseudotuberculosis under certain temperature constraints [24,55,63]. Two other phages are used for plague diagnosis, the Pokrovskaya phage and the L-413C phage [25,26].…”
Section: Plaguementioning
confidence: 99%
“…developed a quantitative real-time PCR (real time-qPCR) assay for ϕA1122 and L-413C that could be used to detect replicating phage DNA in live Y. pestis with a sensitivity of 10 3 cfu/mL to 10 5 cfu/mL or one bacterium to 100 cfu per qPCR sample, respectively [25]. This assay proved to be suitable for both lab-based (LightCycler 2.0) and field-deployable (JBAIDS) real time-qPCR systems [26]. The assay was sensitive in simulated blood specimens, serum, and organ samples.…”
Section: Plaguementioning
confidence: 99%
“…As mentioned, due to the limitations of traditional antibodies, a number of alternative amino acid-based recognition elements have been explored that remove the immunoglobulin scaffold. One such alternative with growing interest is phage display where recent efforts have been focused on transitioning to clinical detection. , Phage display offers an alternative backbone by using the bacteriophage particle for selection while providing a variable region for binding similar to that of antibodies. Phage have an immense sequence pool, and are estimated to be the most abundant organism on the planet numbering roughly 10 31 ! Use of this format also provides the ability to potentially differentiate between live and dead cells with bacteriophage replication assays, which require a viable host bacteria for growth; this is a unique diagnostic tool not achievable using DNA hybridization assays .…”
Section: Biochemical Sensorsmentioning
confidence: 99%
“…One such alternative with growing interest is phage display where recent efforts have been focused on transitioning to clinical detection. 331,332 Phage display offers an alternative backbone by using the bacteriophage particle for selection while providing a variable region for binding similar to that of antibodies. Phage have an immense sequence pool, and are estimated to be the most abundant organism on the planet numbering roughly 10 31 !…”
Section: ■ Biochemical Sensorsmentioning
confidence: 99%