Kathryn Kauffman

Dr. Kathryn Kauffman

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Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

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

Representative Publications

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12 September 2023 in Nature Reviews Microbiology
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Journal Article
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JBJonathon Baker
Jonathon Baker
JWJessica L. Mark Welch
Jessica L. Mark Welch
KKKathryn Kauffman
Kathryn Kauffman
JMJeffrey Scott McLean
Jeffrey Scott McLean
XHXuesong He
Xuesong He

1 May 2019 in Cell Host & Microbe
Verified
Journal Article
Closed access
SZShijie Zhao
Shijie Zhao
TLTami D. Lieberman
Tami D. Lieberman
MPMathilde Poyet
Mathilde Poyet
KKKathryn Kauffman
Kathryn Kauffman
SGSean M. Gibbons
Sean M. Gibbons
EAEric J. Alm
Eric J. Alm

19 August 2010 in Environmental Microbiology Reports
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Journal Article
Open access
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SJSeth G. John
Seth G. John
CMCarolina B. Mendez
Carolina B. Mendez
LDLi Deng
Li Deng
BPBonnie Poulos
Bonnie Poulos
KKKathryn Kauffman
Kathryn Kauffman
MSMatthew B. Sullivan
Matthew B. Sullivan
Summary: Ocean viruses alter ecosystems through host mortality, horizontal gene transfer and by facilitating remineralization of limiting nutrients. However, the study of wild viral populations is limited by inefficient and unreliable concentration techniques. Here, we develop a new technique to recover viruses from natural waters using iron‐based flocculation and large‐pore‐size filtration, followed by resuspension of virus‐containing precipitates in a pH 6 buffer. Recovered viruses are amenable to gene sequencing, and a variable proportion of phages, depending upon the phage, retain their infectivity when recovered. This Fe‐based virus flocculation, filtration and resuspension method (FFR) is efficient (> 90% recovery), reliable, inexpensive and adaptable to many aspects of marine viral ecology and genomics research.

27 June 2022 in Nature Microbiology
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Journal Article
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DPDamien Piel
Damien Piel
MBMaxime Bruto
Maxime Bruto
YLYannick Labreuche
Yannick Labreuche
FBFrançois Blanquart
François Blanquart
DGDavid Goudenège
David Goudenège
FRFrédérique Le Roux
Frédérique Le Roux

24 January 2018 in Nature
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Journal Article
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KKKathryn Kauffman
Kathryn Kauffman
FHFatima A. Hussain
Fatima A. Hussain
JYJoy Yang
Joy Yang
PAPhilip Arevalo
Philip Arevalo
JBJulia M. Brown
Julia M. Brown
MPMartin F. Polz
Martin F. Polz

22 October 2021 in Science
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Journal Article
Closed access
FHFatima Aysha Hussain
Fatima Aysha Hussain
JDJavie Dubert
Javie Dubert
JEJoseph Elsherbini
Joseph Elsherbini
MMMikayla Murphy
Mikayla Murphy
DVDavid VanInsberghe
David VanInsberghe
MPMartin F. Polz
Martin F. Polz
Wild phage evolution: Bacteria possess a diversity of highly specific phage defense mechanisms that evolve rapidly and that account for a large proportion of bacterial genomes. These dynamics must be understood if phage therapy is to be seriously considered for clinical use. Hussain et al . studied a set of nearly clonal wild-caught Vibrio lentus hosts and their phage and found that the hosts segregated into two groups infected by different viruses (see the Perspective by Meaden and Fineran). Puzzlingly, both host groups have the same surface phage receptors. This apparent paradox was resolved by sequencing of the hosts, which revealed distinct suites of endogenous but mobile phage defense elements (PDEs) in the two host phenotypes. Indeed, the PDEs constitute a large fraction of the flexible noncore genome of the bacteria. This means the PDEs can evolve and transfer from cell to cell without interfering with metabolic processes required to synthesize essential cell surface molecules. —CA