1995
DOI: 10.1016/0166-6851(95)00097-k
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Phylogenetic relationships between Old World Leishmania strains revealed by analysis of a repetitive DNA sequence

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Cited by 55 publications
(33 citation statements)
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“…38 Amplification of genomic Leishmania DNA providing an amplification product from a repetitive nucleotide sequence of the parasite with an approximate size of 260 base pair (bp) was performed by using previously described forward (5Ј-CGGCTTCGCACCATGCGGTG-3Ј) and reverse (5Ј-ACATCCCTGCCCACATACGC-3Ј) primers. 27 The PCR for amplification of a 162-bp canine ␣-actin sequence included forward primer ␣-ac1 (5Ј-GAGAC-CACCTACAACAGCATCATG-3Ј) and reverse primer ␣-ac2 (5Ј-CACCTTGATCTTCATGGTGCTGGG-3Ј). 25 Quantitative PCR tests were performed in duplicates and were done with 4 l of 1 : 10 diluted DNA using the Quanti Tect SYBR Green PCR Kit (Qiagen, Basle, Switzerland) in a 10 l standard reaction containing a 0.5 M concentration of forward and reverse primers (Invitrogen, Basle, Switzerland).…”
Section: Histopathologic Evaluationmentioning
confidence: 99%
“…38 Amplification of genomic Leishmania DNA providing an amplification product from a repetitive nucleotide sequence of the parasite with an approximate size of 260 base pair (bp) was performed by using previously described forward (5Ј-CGGCTTCGCACCATGCGGTG-3Ј) and reverse (5Ј-ACATCCCTGCCCACATACGC-3Ј) primers. 27 The PCR for amplification of a 162-bp canine ␣-actin sequence included forward primer ␣-ac1 (5Ј-GAGAC-CACCTACAACAGCATCATG-3Ј) and reverse primer ␣-ac2 (5Ј-CACCTTGATCTTCATGGTGCTGGG-3Ј). 25 Quantitative PCR tests were performed in duplicates and were done with 4 l of 1 : 10 diluted DNA using the Quanti Tect SYBR Green PCR Kit (Qiagen, Basle, Switzerland) in a 10 l standard reaction containing a 0.5 M concentration of forward and reverse primers (Invitrogen, Basle, Switzerland).…”
Section: Histopathologic Evaluationmentioning
confidence: 99%
“…To overcome these problems, DNA-based methods have been widely used for Leishmania spp. identification and/or phylogenetic reconstruction with a variety of targets such as proteincoding genes, non-coding segments, microsatellites, and restriction fragment length polymorphisms (e.g., Piarroux et al 1995;Noyes et al 1997;El Tai et al 2001;Ibrahim and Barker 2001;Kuhls et al 2005;Asato et al 2009;Montalvo et al 2010). Notably, Lukeš et al (2007) went a long way to resolving the issues for the Leishmania donovani complex.…”
Section: Introductionmentioning
confidence: 99%
“…Meanwhile, DNA-based analyses have been widely used for Leishmania spp. identification and phylogenetic inference with various targets such as kDNA genes, introns, and nuclear genes (e.g., Piarroux et al 1995;Noyes et al 1997;El Tai et al 2001;Ibrahim and Barker 2001;Fraga et al 2010). Notably, Lukeš et al (2007) went a long way to resolving the issues for the Leishmania donovani complex.…”
Section: Introductionmentioning
confidence: 99%