<?xml version='1.0' encoding='utf-8'?>
<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:contributor>Joseph Bisesi</dc:contributor>
  <dc:contributor>Jason Tyler Magnuson</dc:contributor>
  <dc:contributor>Daniel Schlenk</dc:contributor>
  <dc:contributor>Carlos Zarza</dc:contributor>
  <dc:contributor>David Peggs</dc:contributor>
  <dc:contributor>Daniela Pampanin</dc:contributor>
  <dc:creator>Giovanna Monticelli</dc:creator>
  <dc:date>2024</dc:date>
  <dc:description>&lt;p id="sp0030"&gt;&lt;span&gt;Although concerns about the impacts of antibiotics in aquatic organisms are reported worldwide, the potential adverse effects on fish gut&amp;nbsp;microbial communities&amp;nbsp;and fish health are still not well known. In this study, we investigated the effects of&amp;nbsp;florfenicol&amp;nbsp;(FFC) on the gut&amp;nbsp;microbiome&amp;nbsp;and gastrointestinal (GIT) gene expression in juvenile Atlantic&amp;nbsp;salmon&amp;nbsp;(&lt;/span&gt;&lt;i&gt;Salmo salar&lt;/i&gt;&lt;span&gt;). Three doses of FFC were used to coat experimental feed at 10, 20 and 30&amp;nbsp;mg/kg/ fish body weight (bw). The feed was administered for 18&amp;nbsp;days, followed by a 10-day recovery period. The metatranscriptome analysis revealed that 10 and 30&amp;nbsp;mg/kg bw of FFC led to the downregulation of genes involved in the transcription of NADH-ubiquinone oxidoreductase chain-1, suggesting that the antibiotic targets bacterial respiratory metabolism. The 30&amp;nbsp;mg/kg bw FFC treatment upregulated genes that encode glycolytic enzymes, such as&amp;nbsp;phosphoglycerate kinase, indicating a disruption of energy metabolism in the microbiome. Analysis of the fish host&amp;nbsp;transcriptome&amp;nbsp;showed that the FFC treatment affected cellular processes in the&amp;nbsp;GIT system&amp;nbsp;of fish, including pathways related to apoptosis and DNA metabolism. The 30&amp;nbsp;mg/kg bw FFC treatment specifically activated pathways related to cellular regulation, including LXR/RXR activation, FXR/RXR activation, and protein&amp;nbsp;ubiquitination. At the end of the recovery phase, the 30&amp;nbsp;mg/kg bw FFC treated group altered pathways related to EIF2 signaling and lysine degradation.&lt;/span&gt;&lt;/p&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1016/j.aquaculture.2023.740310</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>Elsevier</dc:publisher>
  <dc:title>Effect of florfenicol administered through feed on Atlantic salmon (Salmo salar) gut and its microbiome</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>