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<titleInfo><title>Dynamic persistence of antibiotic-stressed mycobacteria</title></titleInfo>


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<name type="personal">
  <namePart type="given">Yurichi</namePart>
  <namePart type="family">Wakamoto</namePart>
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  <namePart type="given">Neraaj</namePart>
  <namePart type="family">Dhar</namePart>
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  <namePart type="given">Remy P</namePart>
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  <namePart type="given">Katrin</namePart>
  <namePart type="family">Schneider</namePart>
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  <namePart type="given">François</namePart>
  <namePart type="family">Signorino Gelo</namePart>
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  <namePart type="given">Stanislas</namePart>
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  <namePart type="given">John</namePart>
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<abstract lang="eng">Exposure of an isogenic bacterial population to a cidal antibiotic typically fails to eliminate a small fraction of refractory cells. Historically, fractional killing has been attributed to infrequently dividing or nondividing &amp;quot;persisters.&amp;quot; Using microfluidic cultures and time-lapse microscopy, we found that Mycobacterium smegmatis persists by dividing in the presence of the drug isoniazid (INH). Although persistence in these studies was characterized by stable numbers of cells, this apparent stability was actually a dynamic state of balanced division and death. Single cells expressed catalase-peroxidase (KatG), which activates INH, in stochastic pulses that were negatively correlated with cell survival. These behaviors may reflect epigenetic effects, because KatG pulsing and death were correlated between sibling cells. Selection of lineages characterized by infrequent KatG pulsing could allow nonresponsive adaptation during prolonged drug exposure.</abstract>

<originInfo><publisher>American Association for the Advancement of Science</publisher><dateIssued encoding="w3cdtf">2013</dateIssued>
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<language><languageTerm authority="iso639-2b" type="code">eng</languageTerm>
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<relatedItem type="host"><titleInfo><title>Science</title></titleInfo>
  <identifier type="ISI">000312985800059</identifier><identifier type="doi">10.1126/science.1229858</identifier>
<part><detail type="volume"><number>339</number></detail><detail type="issue"><number>6115</number></detail><extent unit="pages">91 - 95</extent>
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<apa>Wakamoto, Y., Dhar, N., Chait, R. P., Schneider, K., Signorino Gelo, F., Leibler, S., &amp;#38; Mckinney, J. (2013). Dynamic persistence of antibiotic-stressed mycobacteria. &lt;i&gt;Science&lt;/i&gt;. American Association for the Advancement of Science. &lt;a href=&quot;https://doi.org/10.1126/science.1229858&quot;&gt;https://doi.org/10.1126/science.1229858&lt;/a&gt;</apa>
<ieee>Y. Wakamoto &lt;i&gt;et al.&lt;/i&gt;, “Dynamic persistence of antibiotic-stressed mycobacteria,” &lt;i&gt;Science&lt;/i&gt;, vol. 339, no. 6115. American Association for the Advancement of Science, pp. 91–95, 2013.</ieee>
<ama>Wakamoto Y, Dhar N, Chait RP, et al. Dynamic persistence of antibiotic-stressed mycobacteria. &lt;i&gt;Science&lt;/i&gt;. 2013;339(6115):91-95. doi:&lt;a href=&quot;https://doi.org/10.1126/science.1229858&quot;&gt;10.1126/science.1229858&lt;/a&gt;</ama>
<mla>Wakamoto, Yurichi, et al. “Dynamic Persistence of Antibiotic-Stressed Mycobacteria.” &lt;i&gt;Science&lt;/i&gt;, vol. 339, no. 6115, American Association for the Advancement of Science, 2013, pp. 91–95, doi:&lt;a href=&quot;https://doi.org/10.1126/science.1229858&quot;&gt;10.1126/science.1229858&lt;/a&gt;.</mla>
<chicago>Wakamoto, Yurichi, Neraaj Dhar, Remy P Chait, Katrin Schneider, François Signorino Gelo, Stanislas Leibler, and John Mckinney. “Dynamic Persistence of Antibiotic-Stressed Mycobacteria.” &lt;i&gt;Science&lt;/i&gt;. American Association for the Advancement of Science, 2013. &lt;a href=&quot;https://doi.org/10.1126/science.1229858&quot;&gt;https://doi.org/10.1126/science.1229858&lt;/a&gt;.</chicago>
<ista>Wakamoto Y, Dhar N, Chait RP, Schneider K, Signorino Gelo F, Leibler S, Mckinney J. 2013. Dynamic persistence of antibiotic-stressed mycobacteria. Science. 339(6115), 91–95.</ista>
<short>Y. Wakamoto, N. Dhar, R.P. Chait, K. Schneider, F. Signorino Gelo, S. Leibler, J. Mckinney, Science 339 (2013) 91–95.</short>
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