Kevin Tyler

Dr. Kevin Tyler

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Research Focus & Metrics

Academic Career Length

33Years (1994-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2013 in Clinical Microbiology Reviews
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Journal Article
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MBMaha Bouzid
Maha Bouzid
PHPaul Hunter
Paul Hunter
RCRachel M. Chalmers
Rachel M. Chalmers
KTKevin Tyler
Kevin Tyler
SUMMARY: Cryptosporidiumis a protozoan parasite of medical and veterinary importance that causes gastroenteritis in a variety of vertebrate hosts. Several studies have reported different degrees of pathogenicity and virulence amongCryptosporidiumspecies and isolates of the same species as well as evidence of variation in host susceptibility to infection. The identification and validation ofCryptosporidiumvirulence factors have been hindered by the renowned difficulties pertaining to thein vitroculture and genetic manipulation of this parasite. Nevertheless, substantial progress has been made in identifying putative virulence factors forCryptosporidium. This progress has been accelerated since the publication of theCryptosporidium parvumandC. hominisgenomes, with the characterization of over 25 putative virulence factors identified by using a variety of immunological and molecular techniques and which are proposed to be involved in aspects of host-pathogen interactions from adhesion and locomotion to invasion and proliferation. Progress has also been made in the contribution of host factors that are associated with variations in both the severity and risk of infection. Here we provide a review comprised of the current state of knowledge onCryptosporidiuminfectivity, pathogenesis, and transmissibility in light of our contemporary understanding of microbial virulence.

1 May 2001 in International Journal for Parasitology
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Journal Article
Closed access
KTKevin Tyler
Kevin Tyler
DED.M. Engman
D.M. Engman

18 August 2010 in PLOS ONE
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RRRobert A. Robinson
Robert A. Robinson
BLBecki Lawson
Becki Lawson
MTMike P. Toms
Mike P. Toms
KPKirsi M. Peck
Kirsi M. Peck
JKJames K. Kirkwood
James K. Kirkwood
ACAndrew A. Cunningham
Andrew A. Cunningham
Emerging infectious diseases are increasingly cited as threats to wildlife, livestock and humans alike. They can threaten geographically isolated or critically endangered wildlife populations; however, relatively few studies have clearly demonstrated the extent to which emerging diseases can impact populations of common wildlife species. Here, we report the impact of an emerging protozoal disease on British populations of greenfinch Carduelis chloris and chaffinch Fringilla coelebs, two of the most common birds in Britain. Morphological and molecular analyses showed this to be due to Trichomonas gallinae. Trichomonosis emerged as a novel fatal disease of finches in Britain in 2005 and rapidly became epidemic within greenfinch, and to a lesser extent chaffinch, populations in 2006. By 2007, breeding populations of greenfinches and chaffinches in the geographic region of highest disease incidence had decreased by 35% and 21% respectively, representing mortality in excess of half a million birds. In contrast, declines were less pronounced or absent in these species in regions where the disease was found in intermediate or low incidence. Also, populations of dunnock Prunella modularis, which similarly feeds in gardens, but in which T. gallinae was rarely recorded, did not decline. This is the first trichomonosis epidemic reported in the scientific literature to negatively impact populations of free-ranging non-columbiform species, and such levels of mortality and decline due to an emerging infectious disease are unprecedented in British wild bird populations. This disease emergence event demonstrates the potential for a protozoan parasite to jump avian host taxonomic groups with dramatic effect over a short time period.

25 January 2021 in Virulence
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Journal Article
Open access
Cock Van OosterhoutCock Van Oosterhout
Cock Van Oosterhout
NHNeil Hall
Neil Hall
Hinh LyHinh Ly
Hinh Ly
KTKevin Tyler
Kevin Tyler
In recent weeks, several new strains of SARS-CoV-2, the causative agent of COVID-19, have emerged. These variants have evolved an increased transmission rate compared to the original strains, which...

4 March 2019 in Nature Microbiology
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JNJohanna L. Nader
Johanna L. Nader
TMThomas C. Mathers
Thomas C. Mathers
BWBen J. Ward
Ben J. Ward
JPJustin A Pachebat
Justin A Pachebat
MSMartin T. Swain
Martin T. Swain
KTKevin Tyler
Kevin Tyler

15 March 2009 in Journal of Cell Science
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Journal Article
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KTKevin Tyler
Kevin Tyler
AFAlina Fridberg
Alina Fridberg
KTKrista M. Toriello
Krista M. Toriello
COCheryl L. Olson
Cheryl L. Olson
JCJohn A. Cieslak
John A. Cieslak
DEDavid M. Engman
David M. Engman
The eukaryotic flagellar membrane has a distinct composition from other domains of the plasmalemma. Our work shows that the specialized composition of the trypanosome flagellar membrane reflects increased concentrations of sterols and saturated fatty acids, correlating with direct observation of high liquid order by laurdan fluorescence microscopy. These findings indicate that the trypanosome flagellar membrane possesses high concentrations of lipid rafts: discrete regions of lateral heterogeneity in plasma membranes that serve to sequester and organize specialized protein complexes. Consistent with this, a dually acylated Ca2+ sensor that is concentrated in the flagellum is found in detergent-resistant membranes and mislocalizes if the lipid rafts are disrupted. Detergent-extracted cells have discrete membrane patches localized on the surface of the flagellar axoneme, suggestive of intraflagellar transport particles. Together, these results provide biophysical and biochemical evidence to indicate that lipid rafts are enriched in the trypanosome flagellar membrane, providing a unique mechanism for flagellar protein localization and illustrating a novel means by which specialized cellular functions may be partitioned to discrete membrane domains.