2014
DOI: 10.1186/1756-3305-7-1
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Heat treatment prior to testing allows detection of antigen of Dirofilaria immitis in feline serum

Abstract: BackgroundDiagnosis of Dirofilaria immitis infection in cats is complicated by the difficulty associated with reliable detection of antigen in feline blood and serum samples.MethodsTo determine if antigen-antibody complex formation may interfere with detection of antigen in feline samples, we evaluated the performance of four different commercially available heartworm tests using serum samples from six cats experimentally infected with D. immitis and confirmed to harbor a low number of adult worms (mean = 2.0)… Show more

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Cited by 381 publications
(425 citation statements)
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“…If codon usage bias is only caused by mutation pressure, AU or GC should be used equally among the degenerate codon groups in a gene28. Meanwhile, natural selection for codon selection would not necessarily cause proportional use of G and C (A and U)2930. The four-codon amino acids are alanine, glycine, proline, threonine, valine, arginine (CGA, CGU, CGG and CGC), leucine (CUA, CUU, CUG and CUC) and serine (UCA, UCU, UCG and UCC).…”
Section: Resultsmentioning
confidence: 99%
“…If codon usage bias is only caused by mutation pressure, AU or GC should be used equally among the degenerate codon groups in a gene28. Meanwhile, natural selection for codon selection would not necessarily cause proportional use of G and C (A and U)2930. The four-codon amino acids are alanine, glycine, proline, threonine, valine, arginine (CGA, CGU, CGG and CGC), leucine (CUA, CUU, CUG and CUC) and serine (UCA, UCU, UCG and UCC).…”
Section: Resultsmentioning
confidence: 99%
“…Two pairs of primers were designed that were in accordance to GenBank records of nuclear sequences of the 18S rRNA gene (18S-F and 18S-R) and the nuclear ribosomal ITS2 (ITS2-F and ITS2-R) depending on previous publications in consequence to this subject [49,50], with predicted products sizes 780 and 1200-1600 bp, respectively (Table-1). Moreover, three pairs of primers were utilized that were complementary to fragments in three different mitochondrial DNA markers (Table-1).…”
Section: Methodsmentioning
confidence: 99%
“…In recent years, the molecular characterization for taxonomic identification and phylogenetic purposes of ticks has been indispensable by DNA markers, including nuclear (18S rRNA) and mitochondrial (12S rRNA and 16S rRNA, and cytochrome c oxidase subunit-1 [CO1]) genes and nuclear regulatory non-translated stretches (second internal transcribed spacer [ITS2]) [44,47-50]. The 18S rRNA is best used for genera level identification [51] while the 16S rRNA, CO1, and ITS2 are the most useful markers for ticks taxonomy at species level [39,44,47-50,52-56].…”
Section: Introductionmentioning
confidence: 99%
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“…Broad tissue-type sampling can be easily conducted for groups of identically-treated animals, although in practice most animal studies concentrate on a limited set of tissues. Real-time imaging methods have also been developed that allow serial analysis of T. cruzi infections in individual mice [26-29]. These methods employ transgenic parasites expressing luciferases or fluorescent proteins, such that light signals emitted by parasites can be quantified and pinpointed to anatomical locations.…”
Section: Measuring Parasite Loadsmentioning
confidence: 99%