<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:creator>Josi, Christoph</dc:creator>
  <dc:creator>Bürki, Sibylle</dc:creator>
  <dc:creator>Vidal, Sara</dc:creator>
  <dc:creator>Dordet-Frisoni, Emilie</dc:creator>
  <dc:creator>Citti, Christine</dc:creator>
  <dc:creator>Falquet, Laurent</dc:creator>
  <dc:creator>Pilo, Paola</dc:creator>
  <dc:date>2019-09-13</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Mycoplasma bovis is an important pathogen of cattle causing bovine mycoplasmosis.  Clinical manifestations are numerous, but pneumonia, mastitis, and arthritis cases are  mainly reported. Currently, no efficient vaccine is available and antibiotic treatments  are not always satisfactory. The design of new, efficient prophylactic and therapeutic  approaches requires a better understanding of the molecular mechanisms responsible  for M. bovis pathogenicity. Random transposon mutagenesis has been widely used in  Mycoplasma species to identify potential gene functions. Such an approach can also  be used to screen genomes and search for essential and non-essential genes for  growth. Here, we generated a random transposon mutant library of M. bovis strain  JF4278 containing approximately 4000 independent insertion sites. We then coupled  high-throughput screening of this mutant library to transposon sequencing and  bioinformatic analysis to identify M. bovis non-essential, adhesion- and virulence- related genes. Three hundred and fifty-two genes of M. bovis were assigned as  essential for growth in rich medium. Among the remaining non-essential genes,  putative virulence-related factors were subsequently identified. The complete mutant  library was screened for adhesion using primary bovine mammary gland epithelial  cells. Data from this assay resulted in a list of conditional-essential genes with  putative adhesion-related functions by identifying non-essential genes for growth that  are essential for host cell-adhesion. By individually assessing the adhesion capacity of  six selected mutants, two previously unknown factors and the adhesin TrmFO were  associated with a reduced adhesion phenotype. Overall, our study (i) uncovers new,  putative virulence-related genes; (ii) offers a list of putative adhesion-related factors;  and (iii) provides valuable information for vaccine design and for exploring M. bovis  biology, pathogenesis, and host-interaction.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/308332</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/308332/files/fal_lsa.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.3389/fmicb.2019.02085</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Frontiers in Microbiology. - 2019, vol. 10, p. 2085</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Large-scale analysis of the mycoplasma bovis genome identified non-essential, adhesion- and virulence-related genes</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
