2008
DOI: 10.1016/j.vetpar.2007.12.013
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Assessment of primers designed for the subspecies-specific discrimination among Babesia canis canis, Babesia canis vogeli and Babesia canis rossi by PCR assay

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Cited by 53 publications
(44 citation statements)
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“…Similarities of between 99.4 and 100% were reported on the basis of B. canis vogeli 18S rRNA gene analyses on isolates from five dogs in the states of Minas Gerais and São Paulo (PASSOS et al, 2005). B. canis vogeli has also been identified in samples from Rio de Janeiro by means of RFLP-PCR (DE SÁ et al, 2006) and from Goiás by means of a novel subspecies-specific PCR assay (DUARTE et al, 2008a Morphological examination of blood smears revealed small piroplasms similar to B. gibsoni in one dog in southern Brazil (BRACCINI et al, 1992) but this finding was not confirmed by means of any molecular technique. Based on sequence analysis on a partial fragment of the 18S rRNA gene, B. gibsoni genotype Asia 1 was characterized from four dogs in southern Brazil (TRAPP et al, 2006).…”
Section: Discussionmentioning
confidence: 57%
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“…Similarities of between 99.4 and 100% were reported on the basis of B. canis vogeli 18S rRNA gene analyses on isolates from five dogs in the states of Minas Gerais and São Paulo (PASSOS et al, 2005). B. canis vogeli has also been identified in samples from Rio de Janeiro by means of RFLP-PCR (DE SÁ et al, 2006) and from Goiás by means of a novel subspecies-specific PCR assay (DUARTE et al, 2008a Morphological examination of blood smears revealed small piroplasms similar to B. gibsoni in one dog in southern Brazil (BRACCINI et al, 1992) but this finding was not confirmed by means of any molecular technique. Based on sequence analysis on a partial fragment of the 18S rRNA gene, B. gibsoni genotype Asia 1 was characterized from four dogs in southern Brazil (TRAPP et al, 2006).…”
Section: Discussionmentioning
confidence: 57%
“…The PCR mix was prepared for a final volume of 50 µL, as described by Duarte et al (2008a), as follows: 1× PCR buffer (Invitrogen, Carlsbad, USA); 2.0 mM magnesium chloride (Invitrogen); 0.2 mM dNTP (GE Healthcare, Buckinghamshire, England); 10 pM forward primer Bab7; 10 pM reverse primer Bab9; 1.25 U of Taq DNA polymerase (Invitrogen) and 5 µL of DNA sample. Amplification was performed in a thermocycler (Eppdendorf Mastercycler Personal, Hamburg, Germany), programmed for 35 cycles of denaturation at 94 °C for 30 seconds, annealing at 56 °C for 30 seconds and extension at 72 °C, preceded by an initial denaturation for 2 minutes and followed by a final elongation at 72 °C.…”
Section: Pcr Assaymentioning
confidence: 99%
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“…DNA samples were tested by means of the polymerase chain reaction (PCR) using the sets of primers described in Table 1. For Babesia spp., a single PCR was used (DUARTE et al, 2008); for Ehrlichia canis, a nested PCR was performed, with the second reaction specific for E. canis (DAWSON et al, 1996;MURPHY et al, 1998). Reactions were performed in a final volume of 25 µl, containing 10 mM of Tris-HCl (pH 8.3), 50 µM of KCl, 1.5 mM of MgCl 2 , 0.2 mM of each deoxynucleoside triphosphate, 1.5 U of Taq DNA polymerase (Invitrogen), 11 pmol of each primer and approximately 100 ηg of canine genomic DNA.…”
Section: Methodsmentioning
confidence: 99%
“…Olguda inguinal bölgede 3 adet keneye rastlanırken, hastanın çevreye karşı ilgisinin azaldığı, mukozalarında hafif ikterusla birlikte solgunluk ve yüksek ateşi (40.6ºC) olduğu belirlendi. Hematolojik muayenede RBC, Hb, HCT değerlerinde hafif [15] …”
Section: Olgu IIIunclassified