<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(1)</volume><submitter>Kabiri K</submitter><pubmed_abstract>&lt;h4>Background and objectives&lt;/h4>Interrogation of the genomic relations between Iranian &lt;i>Mycoplasma agalactiae&lt;/i> vaccine strains of Taliqan, Lorestan and Shiraz.&lt;h4>Materials and methods&lt;/h4>Two MLVA (covering VNTR loci of 5, 9, 17 and 19) and MLST (comprising &lt;i>dnaA, gltX, gyrB,&lt;/i> C, &lt;i>tufA&lt;/i> genes) genotyping systems plus nucleotide structure analysis of P80 gene, was conducted.&lt;h4>Results&lt;/h4>The shared MLVA pattern represented by the three strains differed to that of the &lt;i>Mag&lt;/i> PG2 laboratory strain, only at locus VNTR19 where the PG2 genome hold a 3 bp longer stretch. In MLST analysis, at &lt;i>dnaA, gltX, gyrB, metS&lt;/i> and &lt;i>tufA&lt;/i> loci, the three strains displayed alleles 1, 21, 2, 2 and 1, respectively. At, &lt;i>gltX&lt;/i> locus a new allele (21) was detected where a ne</pubmed_abstract><journal>Iranian journal of microbiology</journal><pagination>48-54</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6462265</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Homogeneity of &lt;i>Mycoplasma agalctiae&lt;/i> vaccine strains in an agalaxy- high-burden environment.</pubmed_title><pmcid>PMC6462265</pmcid><pubmed_authors>Tadayon K</pubmed_authors><pubmed_authors>Kabiri K</pubmed_authors><pubmed_authors>Norouzi J</pubmed_authors><pubmed_authors>Sekhavati M</pubmed_authors><pubmed_authors>Pourbakhsh SA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Homogeneity of &lt;i>Mycoplasma agalctiae&lt;/i> vaccine strains in an agalaxy- high-burden environment.</name><description>&lt;h4>Background and objectives&lt;/h4>Interrogation of the genomic relations between Iranian &lt;i>Mycoplasma agalactiae&lt;/i> vaccine strains of Taliqan, Lorestan and Shiraz.&lt;h4>Materials and methods&lt;/h4>Two MLVA (covering VNTR loci of 5, 9, 17 and 19) and MLST (comprising &lt;i>dnaA, gltX, gyrB,&lt;/i> C, &lt;i>tufA&lt;/i> genes) genotyping systems plus nucleotide structure analysis of P80 gene, was conducted.&lt;h4>Results&lt;/h4>The shared MLVA pattern represented by the three strains differed to that of the &lt;i>Mag&lt;/i> PG2 laboratory strain, only at locus VNTR19 where the PG2 genome hold a 3 bp longer stretch. In MLST analysis, at &lt;i>dnaA, gltX, gyrB, metS&lt;/i> and &lt;i>tufA&lt;/i> loci, the three strains displayed alleles 1, 21, 2, 2 and 1, respectively. At, &lt;i>gltX&lt;/i> locus a new allele (21) was detected where a ne</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Feb</publication><modification>2025-04-22T10:24:22.002Z</modification><creation>2019-06-06T21:10:48Z</creation></dates><accession>S-EPMC6462265</accession><cross_references><pubmed>30996831</pubmed></cross_references></HashMap>