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    <responseDate>2026-10-12T11:33:30Z</responseDate>
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    <identifier>10.57760/sciencedb.23561</identifier>
    <datestamp>2025-04-17T09:24:25Z</datestamp>
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  <dc:date>2025-04-17</dc:date>
  <dc:title>Effects of different housing density treatment and fecal microbiota transplantation on the gut microbiota of male microtus brandi</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.23561</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Fecal microbiota of donor male Brandt's voles were collected at week 8 after low-density (LD group) or high-density (HD group) treatment (Experiment 1). Fecal microbiota of recipient male Brandt's voles under low-density conditions were collected at week 8 after sliane (S-LV group), &amp;quot;LD-microbiota&amp;quot; (L-LV group), and &amp;quot;HD-microbiota&amp;quot; (H-LV group) transplantation (Experiment 2). Fecal microbiota of recipient male Brandt's voles under high-density conditions were collected at week 8 after saline (S-HV), &amp;quot;LD-exposed microbiota&amp;quot; (L-HV), and &amp;quot;HD-exposed microbiota&amp;quot; (H-HV) transplantation (Experiment 3). PCR amplification was performed using primers (341F: 5&amp;prime;-CCTAYGGGRBGCASCAG-3&amp;prime;; 806R: 5&amp;prime;-GGACTACNNGGGTATCTAAT-3&amp;prime;) to target the V3-V4 regions of 16S rDNA gene of fecal microbiota.</dc:description>
  <dc:subject>density-dependency; gut microbiota; Brandt's voles; 16s amplicon</dc:subject>
  <dc:creator>Hanyi Zhu</dc:creator>
  <dc:creator>Zhibin Zhang</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by-nc-sa/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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