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| Ryan Schwarz, Renata Borba, Patricia Wolf-Veiga (left to right). |
July 12, 2016
Visiting with the National Bee Diagnostic Centre of Canada
April 28, 2016
Five Small Hive Beetle adults detected in sentinel hives: Italy, April 2016
Passing on recent info. sent out by Prof. Dr. Peter Neumann.
A link to the Italian Health Authority report is here.
June 29, 2015
European Foulbrood: Microscopy and Diagnostics
Brief background
Melissococcus plutonius is the bacteria that causes a disease of honey bee larvae known as "European foulbrood" (EFB). Bee keepers who suspect EFB by clinical signs in the colony ('scales', spotty brood pattern, smell) may want confirmation to help them decide how to best manage and control a potential outbreak in their apiary. Diagnostic confirmation of EFB has traditionally required laboratory microscopy, but more recent techniques can be faster or more informative.
Microscopy
Confirmation of this disease can be made with staining and light microscopy examination. Figure 1A shows what M. plutonius looks like during light microscopy examination. Sometimes, however, the infection with M. plutonius may be largely cleared by the time examination is performed, and replaced with the secondary pathogens (Brevibacillus laterosporus (Figure 1B) and Paenibacillus alvei (Figure 1C). What this means is, even if M. plutonius is not observed during examination, observation of B. laterosporus and/or P. alvei are pretty good indicators that M. plutonius was there, or is still there but in smaller numbers, and are indicative of EFB disease.
Diagnostics
Other diagnostic measures can be performed to confirm EFB (M. plutonius) infection without microscopy and can be very sensitive detection options. This includes detection of M. plutonius DNA using the molecular biology technique polymerase chain reaction (PCR). This approach requires expensive equipment and reagents and is most useful for research purposes, offering the possibility of identifying genetic differences in EFB isolates (strains). Alternatively, a 'snap test' is now available as a fast and easy alternative for simple presence / absence confirmation (Figure 2).
These 'snap tests' are commonly used in veterinary medicine for parasite and pathogen diagnostics. Briefly, the scale of interest (dead larva) is picked out of the comb cell, dropped into a lysis buffer, homogenized with metal beads, then a few drops are applied to the test membrane and you wait patiently for a few minutes. A positive reference reaction will appear in the "Control" area on the membrane as a blue stripe, so you know the test is working properly (Figure 3). If M. plutonius bacteria is present in your sample, a similar blue stripe will appear in the "Test" area of the membrane.
If there is no M. plutonius present, no color change will occur in this area of the membrane. Simple as that! If you want the ability to quickly confirm the presence/absence of EFB for management decisions, these snap test kits may be just what you're looking for.
Melissococcus plutonius is the bacteria that causes a disease of honey bee larvae known as "European foulbrood" (EFB). Bee keepers who suspect EFB by clinical signs in the colony ('scales', spotty brood pattern, smell) may want confirmation to help them decide how to best manage and control a potential outbreak in their apiary. Diagnostic confirmation of EFB has traditionally required laboratory microscopy, but more recent techniques can be faster or more informative.
Microscopy
Confirmation of this disease can be made with staining and light microscopy examination. Figure 1A shows what M. plutonius looks like during light microscopy examination. Sometimes, however, the infection with M. plutonius may be largely cleared by the time examination is performed, and replaced with the secondary pathogens (Brevibacillus laterosporus (Figure 1B) and Paenibacillus alvei (Figure 1C). What this means is, even if M. plutonius is not observed during examination, observation of B. laterosporus and/or P. alvei are pretty good indicators that M. plutonius was there, or is still there but in smaller numbers, and are indicative of EFB disease.
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| (1A) |
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| (1B) |
(1C)
Figure 1. Light microscopy examination of A. mellifera brood "scales". A) Melissococcus plutonius. B) Brevibacillus laterosporus spores (the large, football-like shapes abundant throughout the image). C) Paenibacillus alvei (clustered in the central region of the image). Specimen preparation by Sam Abban of the USDA Beltsville Bee Diagnostics Lab. Photo credits: R. Schwarz @Bee Bugs.
Diagnostics
Other diagnostic measures can be performed to confirm EFB (M. plutonius) infection without microscopy and can be very sensitive detection options. This includes detection of M. plutonius DNA using the molecular biology technique polymerase chain reaction (PCR). This approach requires expensive equipment and reagents and is most useful for research purposes, offering the possibility of identifying genetic differences in EFB isolates (strains). Alternatively, a 'snap test' is now available as a fast and easy alternative for simple presence / absence confirmation (Figure 2).
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| Figure 2. European Foulbrood 'snap test'. Photo credit: R. Schwarz Bee Bugs. |
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| Figure 3. Close-up of the European Foulbrood 'snap test' membrane. "Control" area is on the right and the "Test" area is on the left. This sample was positive for M. plutonius, confirming the microscopy examination shown above. |
If there is no M. plutonius present, no color change will occur in this area of the membrane. Simple as that! If you want the ability to quickly confirm the presence/absence of EFB for management decisions, these snap test kits may be just what you're looking for.
May 6, 2015
Bee parasite movie: Lotmaria passim strain 'BRL' by R. Schwarz
This is a short microscopy movie of parasites from the honey bee (Apis mellifera) known as Lotmaria passim. These cells look so nice and clean because they are from a pure cell culture I grow. Note the flagella which they use for motility, as it whips about and pulls the parasite through the media. These guys are kind of squished on the slide, so they are having a bit of trouble moving (this way I could get a good, clear image of them). Normally, they can move about quite quickly.
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