2009
DOI: 10.1556/avet.57.2009.3.4
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First detection and dominance of Nosema ceranae in Hungarian honeybee colonies

Abstract: Microsporidiosis (nosema disease) of the European honeybee (Apis mellifera L.) is present in bee colonies worldwide. Until recently, Nosema apis had been regarded as the causative agent of the disease, which may have many negative effects on the colony and cause heavy economic losses in apicultures. Another microsporidium species, Nosema ceranae, was reported to infest the Asian honeybee (Apis ceranae), but both honeybee species are susceptible to both microsporidia. In the European honeybee N. ceranae was fir… Show more

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Cited by 51 publications
(41 citation statements)
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“…In contrast, N. ceranae is persistent. Tapaszti et al (2009) showed that N. ceranae was dominant in the summer season, and data from the current study prove that it is dominant throughout the year.…”
Section: Discussionsupporting
confidence: 67%
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“…In contrast, N. ceranae is persistent. Tapaszti et al (2009) showed that N. ceranae was dominant in the summer season, and data from the current study prove that it is dominant throughout the year.…”
Section: Discussionsupporting
confidence: 67%
“…The first purpose of present study was to detect the presence of N. ceranae in Hungarian honey bee colonies prior to the 2007 samples collected by Tapaszti et al (2009). The second purpose was to propose investigation of the distribution of the two different Nosema spp.…”
mentioning
confidence: 99%
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“…In the group of 38 analyzed samples, Nosema apis spores were found in only one sample, while the remaining 37 samples showed the presence of Nosema ceranae. The above authors have concluded that Nosema ceranae has become the predominant pathogenic species affecting Hungarian bee colonies (Tapaszti et al 2009). Chen et al (2008) investigated bee specimens infected with Nosema spp., collected in 1995-2007 in 12 states of the USA.…”
Section: Discussionmentioning
confidence: 99%
“…Both classical (microscopic examination of the spores) and molecular methods are applied. For the identification and differentiation of the two nosema species, and also for their quantitative determination are used PCR, PCR-RFLP, Real-time PCR and multiplex PCR method [31,32].…”
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confidence: 99%