02621naa a2200301 a 450000100080000000500110000800800410001902400540006010000230011424501280013726000090026552017070027465000390198165300110202065300130203170000190204470000190206370000210208270000210210370000160212470000180214070000160215870000160217470000220219070000160221270000210222877300700224919501912024-02-09       2011    bl uuuu     u00u1 u    #d7 ahttps://doi.org/10.1016/j.vetmic.2011.06.0022DOI1 aDORNELES, E. M. S.  aMolecular characterization of Corynebacterium pseudotuberculosis isolated from goats using ERIC-PCR.h[electronic resource]  c2011  aCaseous lymphadenitis is an infectious sheep and goats disease caused by Corynebacterium pseudotuberculosis and characterized by abscesses in superficial and visceral lymph nodes. C. pseudotuberculosis strains isolated from these hosts have been shown to be very difficult to type by the existing methods. The aim of this study is evaluating the potential of the Enterobacterial Repetitive Intergenic Consensus (ERIC-PCR) as a tool for molecular typing of C. pseudotuberculosis strains isolated in sheep. One hundred and twenty seven isolates of C. pseudotuberculosis were isolated from lesions suspected to have had caseous lymphadenitis collected from sheep at the slaughterhouse. Animals were from 24 flocks in 13 municipalities of the Minas Gerais State, Brazil. Species identification of the isolates was performed by routine biochemical tests and mPCR. Fingerprint was performed by RAPD using ERIC-1R, ERIC-2 and ERIC-1R + ERIC-2 primers. Seventeen different genotypes were generated by ERIC 1-PCR, 21 genotypes by ERIC 2-PCR and 21 genotypes by ERIC 1 + 2-PCR. Hunter-Gaston Discrimination Index (HGDI) found for ERIC 1, ERIC 2, ERIC 1 + 2 PCR were 0.69, 0.87, and 0.84, respectively. For most herds evaluated observed at most three different genotypes among isolates from animals of these property, in all ERIC-PCR assays. However a few flocks observed between four and nine genotypes per flock. The W Kendall value found for correlation among the three techniques of ERIC-PCR was 0.91 (P &lt 5.01 × 10−6). The results show that ERIC-PCR has good discriminatory power and advantages over other DNA-based typing methods, making it a useful tool to discriminate C. pseudotuberculosis isolates.  aCorynebacterium Pseudotuberculosis  aCabras  aERIC-PCR1 aSANTANA, J. A.1 aANDRADE, G. I.1 aSANTOS, E. L. S.1 aGUIMARAES, A. S.1 aMOTA, R. A.1 aSANTOS, A. S.1 aMIYOSHI, A.1 aAZEVEDO, V.1 aGOUVEIA, A. M. G.1 aLAGE, A. P.1 aHEINEMANN, M. B.  tGenetics and Molecular Researchgv. 153, n. 3/4, p. 299-306, 2011