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      <ref-type name="Journal Article">17</ref-type>
      <contributors>
        <authors>
          <author>A. Rasool</author>
          <author>A. A. Anjum</author>
          <author>M. Rabbani</author>
          <author>M. Lateef</author>
          <author>F. Akhter</author>
          <author>H. Afroz</author>
          <author>J. Muhammad</author>
          <author>M. Nawaz</author>
        </authors>
      </contributors>
      <titles>
        <title>MOLECULAR CHARACTERIZATION AND PHYLOGENETIC ANALYSIS OF MYCOPLASMA SYNOVIAE ISOLATED FROM CHICKEN</title>
        <secondary-title>Journal of Animal and Plant Sciences</secondary-title>
        <alt-title>JAPS</alt-title>
      </titles>
      <dates><year>2018</year><pub-dates><date>2018/04/01</date></pub-dates></dates>
      <volume>28</volume>
      <number>2</number>
      <pages>491-497</pages>
      <isbn>1018-7081</isbn>
      <electronic-resource-num>NA</electronic-resource-num>
      <abstract>&lt;p&gt;&lt;em&gt;Mycoplasma synoviae&lt;/em&gt;&amp;nbsp;is one of the paramount causes of economic losses for poultry industry. Present study was carried out with the aim to isolate, identify and characterize&amp;nbsp;&lt;em&gt;M. synoviae&lt;/em&gt;&amp;nbsp;from suspected chicken. Tracheal and cloacal swabs samples (n=500), collected from suspected chicken, were cultured on Modified Frey, s medium for isolation of&amp;nbsp;&lt;em&gt;Mycoplasma&lt;/em&gt;. Preliminary identification of&amp;nbsp;&lt;em&gt;Mycoplasma&lt;/em&gt;&amp;nbsp;was done by culturing and biochemical characterization. Partial 16 S r RNA was amplified and sequenced for confirmation and molecular identification of&amp;nbsp;&lt;em&gt;M. synoviae&lt;/em&gt;. For strain identification and phylogenetic analysis, partial amplification and sequence of vlhA gene was performed. Out of 500 samples,&amp;nbsp;&lt;em&gt;Mycoplasma&amp;nbsp;&lt;/em&gt;was successfully isolated from 40 samples. Out of 40 mycoplasma isolates, 20 were identified as&amp;nbsp;&lt;em&gt;M. synoviae&amp;nbsp;&lt;/em&gt;by specie specific 16S ribosomal RNA gene, partial amplification (~213 bp). The vlhA gene was also successfully partially amplified (~375 bp) and sequenced from five isolates. GenBank accession numbers of reported local isolates in this study are KJ130523-KJ130542.and KP316017-KP316021 respectively.&lt;/p&gt;</abstract>
      <keywords><keyword>Mycoplasma, fried egg colonies, 16S rRNA, vlhA gene</keyword></keywords>
      <publisher>Pakistan Agricultural Scientists Forum</publisher>
      <urls><related-urls><url>https://thejaps.org.pk/AbstractView.aspx?mid=2018-JAPS-216</url></related-urls></urls>
    </record>
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