scholarly journals Live and dead qPCR detection demonstrates that feeding of Nosema ceranae results in infection in the honey bee but not the bumble bee

Author(s):  
Jozef J. M. van der Steen ◽  
Marc J. A. Hendriks ◽  
Anne D. van Diepeningen ◽  
Marga P. E. van Gent-Pelzer ◽  
Theo A. J. van der Lee
Keyword(s):  
2021 ◽  
Vol 217 ◽  
pp. 112258
Author(s):  
Hanine Almasri ◽  
Daiana Antonia Tavares ◽  
Marie Diogon ◽  
Maryline Pioz ◽  
Maryam Alamil ◽  
...  

Apidologie ◽  
2011 ◽  
Vol 42 (5) ◽  
pp. 650-658 ◽  
Author(s):  
Wenjun Peng ◽  
Jilian Li ◽  
Humberto Boncristiani ◽  
James P. Strange ◽  
Michele Hamilton ◽  
...  

2012 ◽  
Vol 109 (2) ◽  
pp. 187-193 ◽  
Author(s):  
Brenna E. Traver ◽  
Matthew R. Williams ◽  
Richard D. Fell

2020 ◽  
Vol 59 (4) ◽  
pp. 468-471
Author(s):  
Anais Rodríguez Luis ◽  
Carlos Ariel Yadró García ◽  
Ciro Invernizzi ◽  
Belén Branchiccela ◽  
Adolfo Mauricio Pérez Piñeiro ◽  
...  
Keyword(s):  

2020 ◽  
Vol 113 (3) ◽  
pp. 1055-1061 ◽  
Author(s):  
Laura Šimenc ◽  
Urška Kuhar ◽  
Urška Jamnikar-Ciglenečki ◽  
Ivan Toplak

Abstract The complete genome of Lake Sinai virus 3 (LSV3) was sequenced by the Ion Torrent next-generation sequencing (NGS) technology from an archive sample of honey bees collected in 2010. This strain M92/2010 is the first complete genome sequence of LSV lineage 3. From October 2016 to December 2017, 56 honey bee samples from 32 different locations and 41 bumble bee samples from five different locations were collected. These samples were tested using a specific reverse transcriptase-polymerase chain reaction (RT-PCR) method; 75.92% of honey bee samples and 17.07% of bumble bee samples were LSV-positive with the RT-PCR method. Phylogenetic comparison of 557-base pair-long RNA-dependent RNA polymerase (RdRp) genome region of selected 23 positive samples of honey bees and three positive bumble bee samples identified three different LSV lineages: LSV1, LSV2, and LSV3. The LSV3 lineage was confirmed for the first time in Slovenia in 2010, and the same strain was later detected in several locations within the country. The LSV strains detected in bumble bees are from 98.6 to 99.4% identical to LSV strains detected among honey bees in the same territory.


1987 ◽  
Vol 65 (9) ◽  
pp. 2168-2176 ◽  
Author(s):  
K. W. Richards

Diversity, density, efficiency, and effectiveness of pollinators of cicer milkvetch, Astragalus cicer L., grown at two locations in southern Alberta were studied from 1978 to 1983. Twenty-seven species of bees were identified as pollinators. At Lethbridge, honey bees (Apis mellifera) comprised 74% of the observations, bumble bees 16%, and leafcutter bees 10%, while at Spring Coulee, the proportions were honey bees 14%, bumble bees 69%, and leafcutter bees 17%. The rate of foraging by pollinator species from flower to flower varied; bumble bee species, especially Bombus nevadensis Cress., foraged consistently more efficiently than honey bees or alfalfa leafcutter bees, Megachile rotundata (F.). A theoretical approach used to predict the bee populations required to pollinate varying flower densities shows that the population of B. nevadensis required is about half those of Bombus huntii Greene and M. rotundata and less than one-quarter that of the honey bee. Pollination by B. nevadensis consistently resulted in more seeds per pod than with any other bumble bee species, the honey bee, or M. rotundata. Of the nine species of bumble bee that established colonies in artificial domiciles near the field, B. nevadensis established the most colonies each year. The number of workers and sexuals produced per colony varied considerably among bumble bee species with only 55% of the colony establishments producing workers and 31% producing sexuals. The propagation rate and quality of alfalfa leafcutter bees produced on cicer milkvetch was excellent.


Insects ◽  
2020 ◽  
Vol 11 (2) ◽  
pp. 124 ◽  
Author(s):  
Alessandra Mura ◽  
Michelina Pusceddu ◽  
Panagiotis Theodorou ◽  
Alberto Angioni ◽  
Ignazio Floris ◽  
...  

Nosema ceranae is a widespread obligate intracellular parasite of the ventriculus of many species of honey bee (Apis), including the Western honey bee Apis mellifera, in which it may lead to colony death. It can be controlled in A. mellifera by feeding the antibiotic fumagillin to a colony, though this product is toxic to humans and its use has now been banned in many countries, so in beekeeping, there exists a need for alternative and safe products effective against N. ceranae. Honeybees produce propolis from resinous substances collected from plants and use it to protect their nest from parasites and pathogens; propolis is thought to decrease the microbial load of the hive. We hypothesized that propolis might also reduce N. ceranae infection of individual bees and that they might consume propolis as a form of self-medication. To test these hypotheses, we evaluated the effects of an ethanolic extract of propolis administered orally on the longevity and spore load of experimentally N. ceranae-infected worker bees and also tested whether infected bees were more attracted to, and consumed a greater proportion of, a diet containing propolis in comparison to uninfected bees. Propolis extracts and ethanol (solvent control) increased the lifespan of N. ceranae-infected bees, but only propolis extract significantly reduced spore load. Our propolis extract primarily contained derivatives of caffeic acid, ferulic acid, ellagic acid and quercetin. Choice, scan sampling and food consumption tests did not reveal any preference of N. ceranae-infected bees for commercial candy containing propolis. Our research supports the hypothesis that propolis represents an effective and safe product to control N. ceranae but worker bees seem not to use it to self-medicate when infected with this pathogen.


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