Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Commonality of Virulence-Promoting Function in Rhodococcus equi Virulence Associated Proteins (Vaps)
by
Hogg, Karen
, Baumann, Christoph G.
, Ganderton, Timothy R.
, Pryor, Paul R.
, Ghete, Daniel
, Park, Graeme J.
, Wilkinson, Anthony J.
in
Acidity
/ Antibiotics
/ Antibodies
/ Commonality
/ Drug development
/ Drug therapy
/ Genes
/ Infections
/ Intracellular
/ Kinases
/ Laboratories
/ Macrophages
/ Medical research
/ Mode of action
/ Molecular modelling
/ Plasmids
/ Proteins
/ Rhodococcus equi
/ Survival
/ Virulence
2023
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Commonality of Virulence-Promoting Function in Rhodococcus equi Virulence Associated Proteins (Vaps)
by
Hogg, Karen
, Baumann, Christoph G.
, Ganderton, Timothy R.
, Pryor, Paul R.
, Ghete, Daniel
, Park, Graeme J.
, Wilkinson, Anthony J.
in
Acidity
/ Antibiotics
/ Antibodies
/ Commonality
/ Drug development
/ Drug therapy
/ Genes
/ Infections
/ Intracellular
/ Kinases
/ Laboratories
/ Macrophages
/ Medical research
/ Mode of action
/ Molecular modelling
/ Plasmids
/ Proteins
/ Rhodococcus equi
/ Survival
/ Virulence
2023
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Commonality of Virulence-Promoting Function in Rhodococcus equi Virulence Associated Proteins (Vaps)
by
Hogg, Karen
, Baumann, Christoph G.
, Ganderton, Timothy R.
, Pryor, Paul R.
, Ghete, Daniel
, Park, Graeme J.
, Wilkinson, Anthony J.
in
Acidity
/ Antibiotics
/ Antibodies
/ Commonality
/ Drug development
/ Drug therapy
/ Genes
/ Infections
/ Intracellular
/ Kinases
/ Laboratories
/ Macrophages
/ Medical research
/ Mode of action
/ Molecular modelling
/ Plasmids
/ Proteins
/ Rhodococcus equi
/ Survival
/ Virulence
2023
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Commonality of Virulence-Promoting Function in Rhodococcus equi Virulence Associated Proteins (Vaps)
Journal Article
Commonality of Virulence-Promoting Function in Rhodococcus equi Virulence Associated Proteins (Vaps)
2023
Request Book From Autostore
and Choose the Collection Method
Overview
Rhodococcus equi is a Gram-positive facultative intracellular pathogen associated with life-threatening bronchopneumonial disease in foals. Key to R. equi’s intracellular survival in host macrophages is the production of virulence associated proteins (Vaps). Numerous vap genes are found on virulence plasmids isolated from different species, and the Vaps share a high degree of sequence identity. VapA has been extensively studied, and although vapK and vapN genes from other R. equi virulence plasmids have been shown to be essential for R. equi intracellular survival, their mode of action is less characterised. We, therefore, examined whether VapK and VapN worked mechanistically in the same way as VapA. Indeed, like VapA, VapK and VapN neutralised lysosomal pH and reduced lysosomal hydrolase activity. A loss of VapA and R. equi virulence could be regained by the presence of either VapK or VapN. The acid-neutralisation activity was also observed to a lesser extent with VapB. There was a differential activity across these virulence-promoting Vaps with the most “acid-neutralising” activity found with VapN, then VapA and K, and finally VapB. These data suggest that VapA production, which is often found in equine infections, can be substituted by VapK and B (produced by plasmids often found in porcine species) or VapN (produced by plasmids often isolated in bovine and human samples). These data imply that the molecular mechanism(s) that VapA uses to neutralise lysosomal acidity should also be seen in VapN and K which will help guide researchers in identifying their precise mode of action and aid the future development of targeted therapeutics.
MBRLCatalogueRelatedBooks
Related Items
Related Items
This website uses cookies to ensure you get the best experience on our website.