2016
DOI: 10.1653/024.099.0438
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Molecular Diagnostics of the Honey Bee Parasites Lotmaria passim and Crithidia spp. (Trypanosomatidae) Using Multiplex PCR

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Cited by 14 publications
(8 citation statements)
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References 11 publications
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“…Broadly screening and sequencing positive samples may maximize the probability of detecting potential pathogens, for groups that are likely to contain unexpected or undescribed species, such as Crithidia. A similar approach uses species-specific primers coupled with broad-range primers, allowing for the detection of unexpected species (Stevanovic et al 2016;Szalanski et al 2016;.…”
Section: Protozoansmentioning
confidence: 99%
“…Broadly screening and sequencing positive samples may maximize the probability of detecting potential pathogens, for groups that are likely to contain unexpected or undescribed species, such as Crithidia. A similar approach uses species-specific primers coupled with broad-range primers, allowing for the detection of unexpected species (Stevanovic et al 2016;Szalanski et al 2016;.…”
Section: Protozoansmentioning
confidence: 99%
“…Bees were placed on a paper towel for three hours at 22°C to evaporate ethanol preservative from the bees. DNA was extracted using a salting-out protocol with in-house reagents (Sambrook & Russell, 2001) per (Szalanski et al, 2016) and stored at -20°C. Successful DNA extraction was confirmed via PCR amplification of a portion of the honey bee mitochondrial DNA (mtDNA) cytochrome oxidase I and II (COI-COII) region with the use of primers E2 and H2 (Tab.…”
Section: Dna Extractionmentioning
confidence: 99%
“…Samples positive for S. apis yielded a 190 bp amplicon, and samples positive for S. melliferum resulted in a 160 bp amplicon. Trypanosomes Multiplex PCR using primers CBSSU rRNA F2, CBSSU rRNA B4 (Schmid-Hempel & Tognazzo, 2010), and L. passim 18S-F was used to detect trypanosome pathogen species (Szalanski et al, 2016) (Tab. 1).…”
Section: Phorid Flymentioning
confidence: 99%
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“…revealed C. mellificae presence in bee populations with L. passim predominance in A. mellifera worldwide [192]. Building upon this work, a PCR procedure was developed to distinguish between C. mellificae and L. passim in honey bees [193]. A survey of honey bees in different parts of New Zealand revealed high levels of infection with two genotypes of L. passim that remained consistent yearlong with low genetic variation [194].…”
Section: Parasites Pathogens and Pestsmentioning
confidence: 99%