01982naa a2200373 a 450000100080000000500110000800800410001902400340006010000230009424501200011726000090023752009200024665000130116665000290117965000160120865000150122465000140123965000170125365000110127065300160128165300080129765300370130565300230134270000180136570000220138370000230140570000240142870000160145270000200146870000190148870000230150770000230153077300550155321139652019-11-06       2019    bl uuuu     u00u1 u    #d7 a10.22456/1679-9216.908622DOI1 aFERREIRA, M. R. A.  aProtection efficacy of the rLTB-R1 chimera against experimental swine mycoplasmal pneumonia.h[electronic resource]  c2019  aAbstract: Mycoplasma hyopneumoniae is the etiological agent of the Swine Mycoplasmal Pneumonia (SMP), one of the most economically significant diseases in the swine industry worldwide. Commonly used vaccines for SMP control consist of inactivated whole cells (bacterins). These vaccines are efficacious against M. hyopneumoniae challenge, but do not prevent colonization by the pathogen or completely eliminate pneumonia. P97 adhesin is conserved in the M. pneumoniae virulent strains, therefore it is an attractive target to be used in recombinant vaccines against M. hyopneumoniae. The aim of the present study was to evaluate protection afforded by rLTB-R1, a recombinant chimera composed by LTB fused with the R1 repeat region of P97 adhesin of M. hyopneumoniae, in specific-pathogen-free (SPF) piglets vaccinated by intranasal or intramuscular route and challenged with a pathogenic strain of M. hyopneumoniae.  aAdhesins  aMycoplasma hyopneumoniae  aVaccination  aMicoplasma  aPneumonia  aSuinocultura  aVacina  aAdesina P97  aLTB  aPneumonia micoplasmática suína  aVacinação mucosa1 aFINGER, P. F.1 aMAGALHÃES, C. G.1 aCUNHA, C. E. P. da1 aMOREIRA JÚNIOR, C.1 aKICH, J. D.1 aMORES, M. A. Z.1 aMOREIRA, A. N.1 aDELLAGOSTIN, O. A.1 aCONCEIÇÃO, F. R.  tActa Scientiae Veterináriagv. 47, n. 1660, 2019.