2011
DOI: 10.1016/j.jip.2011.02.003
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Prevalence and infection intensity of Nosema in honey bee (Apis mellifera L.) colonies in Virginia

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Cited by 88 publications
(113 citation statements)
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“…N. apis causes nosemosis (type A), the clinical outbreak which is characterized mainly by dysentery, whereas, N. ceranae causes death of individuals and colonies without any visible symptoms (Higes et al, 2008). However, Traver, and Fell (2011) found no significant correlation between Nosema infection and colony strength even the infection prevalence of N. ceranae was 69.3%. Thus, Nosema has not been found responsible for loss of honey bees in all the cases.…”
Section: ) European Foulbroodmentioning
confidence: 92%
“…N. apis causes nosemosis (type A), the clinical outbreak which is characterized mainly by dysentery, whereas, N. ceranae causes death of individuals and colonies without any visible symptoms (Higes et al, 2008). However, Traver, and Fell (2011) found no significant correlation between Nosema infection and colony strength even the infection prevalence of N. ceranae was 69.3%. Thus, Nosema has not been found responsible for loss of honey bees in all the cases.…”
Section: ) European Foulbroodmentioning
confidence: 92%
“…Studies from central Spain suggest much less variation in infection prevalence over the season for N. ceranae compared to what has been described for N. apis (Higes et al, 2008a). However, a clear seasonal effect on disease prevalence, with higher prevalence and infection levels in the early season has been documented in eastern USA (Traver and Fell, 2011;Traver et al, 2012) and in untreated colonies in maritime Canada (Williams et al, 2010;. There is an urgent need for long-term studies of the temporal dynamics of N. ceranae infections under different climatic conditions.…”
Section: Colony Level Infection Dynamicsmentioning
confidence: 99%
“…A qPCR was subsequently performed following the protocols described by Traver and Fell (2011a). Briefly, Nosema species-specific TaqMan Gene Expression assays (Applied Biosystems, Foster City, CA, USA) were used to quantify infection levels and to identify the Nosema species present in each colony sampled.…”
Section: Genomic Dna Extraction and Quantitative Real-time Pcrmentioning
confidence: 99%
“…Genomic DNA was extracted from individual abdomens of ten workers from each cavity sampled per year as described previously (Traver et al 2009;Traver and Fell 2011a). Briefly, a Bender buffer lysis followed by a proteinase K digestion and phenol/chloroform extraction was performed.…”
Section: Genomic Dna Extraction and Quantitative Real-time Pcrmentioning
confidence: 99%
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