Stephen C. Hardies

Dr. Stephen C. Hardies


Research Focus & Metrics

Academic Career Length

40Years (1987-Present)

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

Representative Publications

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1 January 2007 in Virology Journal
Verified
Journal Article
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Philip SerwerPhilip Serwer
Philip Serwer
SHShirley J Hayes
Shirley J Hayes
Julie ThomasJulie Thomas
Julie Thomas
SHStephen C. Hardies
Stephen C. Hardies
The number of successful propagations/isolations of soil-borne bacteriophages is small in comparison to the number of bacteriophages observed by microscopy (great plaque count anomaly). As one resolution of the great plaque count anomaly, we use propagation in ultra-dilute agarose gels to isolate a Bacillus thuringiensis bacteriophage with a large head (95 nm in diameter), tail (486 × 26 nm), corkscrew-like tail fibers (187 × 10 nm) and genome (221 Kb) that cannot be detected by the usual procedures of microbiology. This new bacteriophage, called 0305φ8-36 (first number is month/year of isolation; remaining two numbers identify the host and bacteriophage), has a high dependence of plaque size on the concentration of a supporting agarose gel. Bacteriophage 0305φ8-36 does not propagate in the traditional gels used for bacteriophage plaque formation and also does not produce visible lysis of liquid cultures. Bacteriophage 0305φ8-36 aggregates and, during de novo isolation from the environment, is likely to be invisible to procedures of physical detection that use either filtration or centrifugal pelleting to remove bacteria. Bacteriophage 0305φ8-36 is in a new genomic class, based on genes for both structural components and DNA packaging ATPase. Thus, knowledge of environmental virus diversity is expanded with prospect of greater future expansion.

1 July 2008 in Virology
Verified
Journal Article
Closed access
Julie ThomasJulie Thomas
Julie Thomas
MRMandy R. Rolando
Mandy R. Rolando
CCChristopher A. Carroll
Christopher A. Carroll
PSPeter S. Shen
Peter S. Shen
DBDavid M. Belnap
David M. Belnap
SHStephen C. Hardies
Stephen C. Hardies

1 November 2007 in Virology
Verified
Journal Article
Closed access
Julie ThomasJulie Thomas
Julie Thomas
SHStephen C. Hardies
Stephen C. Hardies
MRMandy Rolando
Mandy Rolando
SHShirley J. Hayes
Shirley J. Hayes
KLKaren Lieman
Karen Lieman
PSPhilip Serwer
Philip Serwer


6 May 2012 in Applied Microbiology and Biotechnology
Verified
Journal Article
Closed access
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NKNatia Karumidze
Natia Karumidze
Julie ThomasJulie Thomas
Julie Thomas
NKNino Kvatadze
Nino Kvatadze
MGMarina Goderdzishvili
Marina Goderdzishvili
KHKevin W. Hakala
Kevin W. Hakala
SHStephen C. Hardies
Stephen C. Hardies

1 April 2000 in Molecular Biology and Evolution
Verified
Journal Article
Open access
PDF file
SHStephen C. Hardies
Stephen C. Hardies
LWLiping Wang
Liping Wang
LZLanxin Zhou
Lanxin Zhou
YZYingping Zhao
Yingping Zhao
NCN. Carol Casavant
N. Carol Casavant
SHShijun Huang
Shijun Huang
Recently, a rapidly amplifying family of mouse LINE-1 (L1) has been identified and named TF. The evolutionary context surrounding the derivation of the TF family was examined through phylogenetic analysis of sequences in the 3′ portion of the repeat. The Mus musculus domesticus TF family was found to be the terminal subfamily of the previously identified L1Md4 lineage. The L1Md4 lineage joins the other prototypical mouse LINE-1 lineage (the L1MdA2 lineage) approximately 1 MYA at about the time of the common ancestor of M. m. domesticus, Mus spicilegus, and Mus spretus. However, the TF family from M. m. domesticus was found to join to the previously reported M. spretus Ms475 and Ms7024 LINE-1 families at just 0.5 MYA, indicating horizontal transfer. The TF family from M. m. domesticus was then found to be even more recently related to LINE-1's from another species, M. spicilegus. A separate spretus A2 lineage was found through a directed search of a PCR library. This lineage, in contrast to the spretus TF lineage, does join domesticus at about 1 MYA, as would be expected in the absence of horizontal transfer. A third major family was also found that splits off from the L1Md4 lineage shortly after its departure from the L1MdA2 lineage. The new family, named the Z family, was found to contain the de novo LINE-1 inserts causing the beige and med mutations. Whether the split with the Z family was before or after the recombination that introduced the F-type promoters and defined the inception of TF as a lineage is unclear. In enumerating copies of the various LINE-1 families, we found that TF 3′ ends were not much more numerous than the reported number of 5′ ends, suggesting that TF may not be subjected to the 90% truncation pattern typical of LINE-1 as a whole.