List of diseases of the honey bee

Last updated

Diseases of the honey bee or abnormal hive conditions include:

Contents

Pests and parasites

Varroa mites

Varroa mite on a honey bee larva Varroa on larvae.jpg
Varroa mite on a honey bee larva

Varroa destructor and V. jacobsoni are parasitic mites that feed on the fat bodies of adult, pupal and larval bees. When the hive is very heavily infested, Varroa mites can be seen with the naked eye as a small red or brown spot on the bee's thorax. Varroa mites are carriers for many viruses that are damaging to bees. For example, bees infected during their development will often have visibly deformed wings.[ citation needed ]

Varroa mites have led to the virtual elimination of feral bee colonies in many areas, and are a major problem for kept bees in apiaries. Some feral populations are now recovering—it appears they have been naturally selected for Varroa resistance.[ citation needed ]

Varroa mites were first discovered in Southeast Asia in about 1904, but are now present on all continents except Australia. They were discovered in the United States in 1987, in New Zealand in 2000, and in Devon, United Kingdom in 1992.[ citation needed ]

To the untrained eye, these mites are generally not a very noticeable problem for a strongly growing hive- as the bees may appear strong in number, and may even be very effective at foraging. However, the mite reproduction cycle occurs inside the capped pupae, and the mite population can surge as a result of colony growth. Careful observation of a colony can help identify signs of disease often spread by mites. When the hive population growth is reduced in preparation for winter or due to poor late summer forage, the mite population growth can overtake that of the bees and can then destroy the hive. It has been observed diseased colonies may slowly die off and be unable to survive through winter even when adequate food stores are present. Often a colony will simply abscond (leave as in a swarm, but leaving no population behind) under such conditions.[ citation needed ]

Varroa in combination with viral vectors and bacteria have been theoretically implicated in colony collapse disorder.[ citation needed ]

It is known that thymol, a compound produced by thyme, naturally occurring in thyme honey, is a treatment for Varroa, though it may cause bee mortality at high concentrations. [1] Provisioning active colonies with crops of thyme may provide the colony with a non-interventional chemical defense against Varroa.[ citation needed ]

Treatment

A variety of chemical and mechanical treatments are used to attempt to control Varroa mites.[ citation needed ]

"Hard" chemicals

"Hard" chemical treatments include amitraz (marketed as "Apivar" [2] ), fluvalinate (marketed as "Apistan"), coumaphos (marketed as CheckMite), flumethrin (marketed as "Bayvarol" and "Polyvar Yellow").

"Soft" chemicals

"Soft" chemical treatments include thymol (marketed as "ApiLife-VAR [3] " and "Apiguard"), sucrose octanoate esters (marketed as "Sucrocide"), oxalic acid (marked as "Api-bioxal [4] ") and formic acid (sold in liquid form or in gel strips as Mite Away Quick Strips and Formic Pro, [5] but also used in other formulations).

According to the U.S. Environmental Protection Agency, when used in beehives as directed, chemical treatments kill a large proportion of the mites while not substantially disrupting bee behavior or life span. Use of chemical controls is generally regulated and varies from country to country. With few exceptions, they are not intended for use during production of marketable honey. [6]

"Mechanical" treatments

Common mechanical controls generally rely on disruption of some aspect of the mites' lifecycle. These controls are generally intended not to eliminate all mites, but merely to maintain the infestation at a level which the colony can tolerate. Examples of mechanical controls include drone brood sacrifice (Varroa mites are preferentially attracted to the drone brood), powdered sugar dusting (which encourages cleaning behavior and dislodges some mites), screened bottom boards (so any dislodged mites fall through the bottom and away from the colony), brood interruption and, perhaps, downsizing of the brood cell size.[ citation needed ]

Acarine (tracheal) mites

Acarapis woodi is a parasitic mite that infests the trachea that lead from the first pair of thoracic spiracles. An unidentified bee illness was first reported on the Isle of Wight in England in 1904, becoming known as the 'Isle of Wight disease' (IoWD), which was initially thought to be caused by Acarapis woodi when it was identified in 1921 by Rennie. The IoWD disease quickly spread to the rest of Great Britain and Ireland, dealing a devastating blow to British and Irish beekeeping, being claimed as having wiped out the indigenous bee population of the British Isles. In 1991 Bailey and Ball stated "The final opinion of Rennie (1923), a co-discoverer of Acarapis woodi, who had much experience with bees said to have the Isle of Wight Disease, was that under the original and now quite properly discarded designation 'Isle of Wight Disease' were included several maladies having analogous superficial symptoms", [7] the authors came to the firm conclusion that the IoWD was not caused by acarine (Acarapis woodi) mites solely, but primarily by chronic bee paralysis virus (CBPV), even though Acarapis woodi was always found to be present within the hive whenever CBPV symptoms were observed. Brother Adam at Buckfast Abbey developed a resistant bee breed known as the Buckfast bee, which is now available worldwide.[ citation needed ]

Diagnosis for tracheal mites generally involves the dissection and microscopic examination of a sample of bees from the hive.[ citation needed ]

Acarapis woodi are believed to have entered the U.S. in 1984, from Mexico.[ citation needed ]

Mature female acarine mites leave the bee's airway and climb out on a hair of the bee, where they wait until they can transfer to a young bee. Once on the new bee, they move into the airways and begin laying eggs.[ citation needed ]

Treatment

Acarine mites are commonly controlled with grease patties (typically made from one part vegetable shortening mixed with three to four parts powdered sugar) placed on the top bars of the hive. The bees come to eat the sugar and pick up traces of shortening, which disrupts the mite's ability to identify a young bee. Some of the mites waiting to transfer to a new host remain on the original host. Others transfer to a random bee—a proportion of which will die of other causes before the mite can reproduce.[ citation needed ]

Menthol, either allowed to vaporize from crystal form or mixed into the grease patties, is also often used to treat acarine mites.[ citation needed ]

Nosema disease

Nosema apis is a microsporidian that invades the intestinal tracts of adult bees and causes Nosema disease, also known as nosemosis. [8] [9] Nosema infection is also associated with black queen cell virus. It spreads via fecal to oral matter to infect bees. [10] [11] [12] It is normally only a problem when the bees cannot leave the hive to eliminate waste (for example, during an extended cold spell in winter or when the hives are enclosed in a wintering barn). When the bees are unable to void (cleansing flights), they can develop dysentery. [13] [14]

Nosema disease is treated by increasing the ventilation through the hive. Some beekeepers treat hives with agents such as fumagillin. [15]

Nosemosis can also be prevented or minimized by removing much of the honey from the beehive, then feeding the bees on sugar water in the late fall. Sugar water made from refined sugar has lower ash content than flower nectar, reducing the risk of dysentery. Refined sugar, however, contains fewer nutrients than natural honey, which causes some controversy among beekeepers.[ citation needed ]

In 1996, a similar type of organism to N. apis was discovered on the Asian honey bee Apis cerana and subsequently named N. ceranae . This parasite apparently also infects the western honey bee. [16]

Exposure to corn pollen containing genes for Bacillus thuringiensis (Bt) production may weaken the bees' defense against Nosema. [17] In relation to feeding a group of bees with Bt corn pollen and a control group with non-Bt corn pollen: "in the first year, the bee colonies happened to be infested with parasites (microsporidia). This infestation led to a reduction in the number of bees and subsequently to reduced broods in the Bt-fed colonies, as well as in the colonies fed on Bt toxin-free pollen. The trial was then discontinued at an early stage. This effect was significantly more marked in the Bt-fed colonies. (The significant differences indicate an interaction of toxin and pathogen on the epithelial cells of the honeybee intestine. The underlying mechanism which causes this effect is unknown.)"[ citation needed ]

This study should be interpreted with caution given that no repetition of the experiment nor any attempt to find confounding factors was made. In addition, Bt toxin and transgenic Bt pollen showed no acute toxicity to any of the life stages of the bees examined, even when the Bt toxin was fed at concentrations 100 times that found in transgenic Bt pollen from maize.[ citation needed ]

Nosema disease is very common when bees get into winter clusters, as they spend an extensive time in their hives as they keep together for warmth and have little to no opportunities to eliminate waste.

Small hive beetle

Comb slimed by hive beetle larvae: Hives infested at this level will drive out bee colonies. Aethina tumida.jpg
Comb slimed by hive beetle larvae: Hives infested at this level will drive out bee colonies.

Aethina tumida is a small, dark-colored beetle that lives in beehives. Originally from Africa, the first discovery of small hive beetles in the Western Hemisphere was made in St. Lucie County, Florida, in 1998. The next year, a specimen that had been collected from Charleston, South Carolina, in 1996 was identified, and is believed to be the index case for the United States. [18] By December 1999, small hive beetles were reported in Iowa, Maine, Massachusetts, Minnesota, New Jersey, Ohio, Pennsylvania, Texas, and Wisconsin, and it was found in California by 2006.[ citation needed ]

The lifecycle of this beetle includes pupation in the ground outside of the hive. Controls to prevent ants from climbing into the hive are believed to also be effective against the hive beetle. Several beekeepers are experimenting with the use of diatomaceous earth around the hive as a way to disrupt the beetle's lifecycle. The diatoms abrade the insects' surfaces, causing them to dehydrate and die.[ citation needed ]

Treatment

Several pesticides are currently used against the small hive beetle. The chemical fipronil (marketed as Combat Roach Gel [19] ) is commonly applied inside the corrugations of a piece of cardboard. Standard corrugations are large enough that a small hive beetle can enter the cardboard through the end, but small enough that honey bees cannot enter (thus are kept away from the pesticide). Alternative controls such as oil-based top-bar traps are also available, but they have had very little commercial success.[ citation needed ]

Wax moths

Wax moth (Aphomia sociella)--more often associated with bumble bees (Bombus sp.) Aphomia sociella 9626.jpg
Wax moth (Aphomia sociella)—more often associated with bumble bees (Bombus sp.)

Galleria mellonella (greater wax moths) do not attack the bees directly, but feed on the shed exoskeletons of bee larvae and pollen that is found in dark brood comb, which was used by the bees to hold the developing bees. Their full development to adults requires access to used brood comb or brood cell cleanings—these contain protein essential for the larval development, in the form of brood cocoons. The destruction of the comb will spill or contaminate stored honey and may kill bee larvae.[ citation needed ]

When honey supers are stored for the winter in a mild climate, or in heated storage, the wax moth larvae can destroy portions of the comb, though they will not fully develop. Damaged comb may be scraped out and replaced by the bees. Wax moth larvae and eggs are killed by freezing, so storage in unheated sheds or barns in higher latitudes is the only control necessary.[ citation needed ]

Because wax moths cannot survive a cold winter, they are usually not a problem for beekeepers in the northern U.S. or Canada, unless they survive winter in heated storage, or are brought from the south by purchase or migration of beekeepers. They thrive and spread most rapidly with temperatures above 30 °C (90 °F), so some areas with only occasional days that are hot rarely have a problem with wax moths, unless the colony is already weak due to stress from other factors.[ citation needed ]

Control and treatment

A strong hive generally needs no treatment to control wax moths; the bees themselves kill and clean out the moth larvae and webs. Wax moth larvae may fully develop in cell cleanings when such cleanings accumulate thickly where they are not accessible to the bees.[ citation needed ]

Wax moth development in comb is generally not a problem with top bar hives, as unused combs are usually left in the hive during the winter. Since this type of hive is not used in severe wintering conditions, the bees are able to patrol and inspect the unused comb.[ citation needed ]

Wax moths can be controlled in stored comb by application of the aizawai variety of B. thuringiensis spores by spraying. It is a very effective biological control and has an excellent safety record.[ citation needed ]

Wax moths can be controlled chemically with paradichlorobenzene (moth crystals or urinal disks). If chemical methods are used, the combs must be well-aired for several days before use. The use of naphthalene (mothballs) is discouraged because it accumulates in the wax, which can kill bees or contaminate honey stores.

Control of wax moths by other means includes the freezing of the comb for a few hours. [20] Langstroth found that placing a spider, such as a daddy-long-legs, with stored combs controlled wax moth and eliminate the need for hash chemicals. [21] This has been confirmed more recently by others, such as Bergqvist. [22]

Tropilaelaps

Tropilaelaps mercedesae and T. clareae are considered serious threats to honeybees. Although they are not currently found outside Asia, these mites have the potential to inflict serious damage to colonies due to their rapid reproduction inside the hive. [23]

Bacterial diseases

Symptoms [24]
Appearance of brood combAge of dead broodColor of dead broodConsistency of dead broodOdor of dead broodScale characteristicsInfectious agent
Sealed brood, discolored, sunken, or punctured cappingsUsually older sealed larvae or young pupae lying lengthwise in cellsDull white, becoming light brown, coffee brown to dark brown, or almost blackSoft, becoming sticky to ropySlightly to pronounced putrid odorLies uniformly flat on lower side of cell, adheres tightly to cell wall, fine, thread-like tongue of dead may be present, head lies flat, black in colorAmerican foulbrood
Unsealed brood, some sealed brood in advanced cases with discolored, sunken or punctured cappingsUsually young unsealed larvae, occasionally older sealed larvae, typically in coiled stageDull white, becoming yellowish white to brown, dark brown, or almost blackWatery, rarely sticky or ropy, granularSlightly to penetrating sourUsually twisted in cell, does not adhere to cell wall, rubbery, black in colorEuropean foulbrood

American foulbrood

American foulbrood (AFB), caused by the spore-forming Paenibacillus larvae [25] (formerly classified as Bacillus larvae, then P. larvae ssp. larvae/pulvifaciens), is the most widespread and destructive of the bee brood diseases. P. larvae is a rod-shaped bacterium. Larvae up to three days old become infected by ingesting spores present in their food. Young larvae less than 24 hours old are most susceptible to infection. Spores germinate in the gut of the larva and the vegetative bacteria begin to grow, taking nourishment from the larva. Spores will not germinate in larvae over three days old. Infected larvae normally die after their cell is sealed. The vegetative form of the bacterium will die, but not before it produces many millions of spores. American foulbrood spores are extremely resistant to desiccation and can remain viable for 80 years in honey and beekeeping equipment. Each dead larva may contain as many as 100 million spores. This disease only affects the bee larvae, but is highly infectious and deadly to bee brood. Infected larvae darken and die.[ citation needed ]

As with European foulbrood, research has been conducted using the "shook swarm" [26] method to control American foulbrood, "the advantage being that chemicals are not used".[ citation needed ]

European foulbrood

European foulbrood (EFB) is caused by the bacterium Melissococcus plutonius that infects the midgut of bee larvae. European foulbrood is considered less serious than American foulbrood. [27] M. plutonius is not a spore-forming bacterium, but bacterial cells can survive for several months on wax foundation. Symptoms include dead and dying larvae which can appear curled upwards, brown or yellow, melted or deflated with tracheal tubes more apparent, or dried out and rubbery. [28] method Scientific research showed that the spread of the disease is density dependent. The higher the density of apiaries, the higher the probability of disease transmission. [29]

European foulbrood is often considered a "stress" disease—dangerous only if the colony is already under stress for other reasons. An otherwise healthy colony can usually survive European foulbrood.

Chemical treatment with oxytetracycline hydrochloride may control an outbreak of the disease, but honey from treated colonies could have chemical residues from the treatment, and prophylactic treatments are not recommended as they may lead to resistant bacteria. [ citation needed ]

The "shook swarm" method [30] of bee husbandry can also effectively control the disease, with the advantage of avoiding the use of chemicals.

The Alexander-House-Miller treatment [31] has also been shown to be effective against the disease. The method requires the hive to be strong and the queen to be prevented from laying for a week or so. A modified version of this method is given by Carr in his article. [32] The queen is placed on frames of foundation below a queen excluder, and all of the brood frames are put above the excluder. Once all of the worker brood has emerged, these frames are removed from the hive and the old comb in them replaced with foundation ready for re-use.

Fungal diseases

Chalkbrood

The entrance to this beehive is littered with chalkbrood mummies that have been expelled from the hive by hygienic worker bees. Ascosphaera apis (Maasen ex Claussen) L.S. Olive & Spiltoir 1324048.jpg
The entrance to this beehive is littered with chalkbrood mummies that have been expelled from the hive by hygienic worker bees.

Ascosphaera apis causes a fungal disease that only affects bee brood, but adult bees can be carriers. [33] It infests the gut of the larvae before the cell is sealed or soon after. [34] The fungus competes with them for food, ultimately causing them to starve. The fungus then goes on to consume the rest of the larval bodies, causing them to appear white, hard, and "chalky". [34] If fungal spores start to develop, the larva can also appear gray or black. [34] One study suggested it could be economically devastating because not only does it weaken the hive, but it can cause honey reductions of 5–37%. [35]

Chalkbrood (ascosphaerosis larvae apium) is most commonly visible during wet springs. [33] Hedtke et al. provided statistical evidence that chalkbrood outbreaks occurred in summer when there was a N. ceranae infection earlier in the spring and there is an ongoing V. destructor infestation. [36] Stress, genetics of the bees, and health can also be contribute to the presence of chalkbrood. [33]

Spores of the fungus can last for up to 15 years, which is why old equipment from a previously infected hive should not be used. [33] These spores can last in pollen, honey, and wax. [33] Even though Hornitzky's literature review of articles on chalkbrood disease concluded that there was no definitive cure or control, there are a variety of prevention mechanisms. [37] Improving genetic stock to be more hygienic, sterilization of old equipment, [33] good ventilation [38] [39] and the replacement of old brood comb [40] [41] are all techniques that can be attempted.

Chalkbrood was first recognized in 1900s in Europe, [33] and then spread to countries such as Argentina, Turkey, Philippines, Mexico, Chile, Central America and Japan. [33] It was first recorded in the United States in the mid-1960s in Utah and spread across the US from there. [33]

Stonebrood

Stonebrood (aspergillosis larvae apium) is a fungal disease caused by Aspergillus fumigatus , A. flavus , and A. niger . It causes mummification of the brood of a honey bee colony. The fungi are common soil inhabitants and are also pathogenic to other insects, birds, and mammals. The disease is difficult to identify in the early stages of infection. The spores of the different species have different colours and can also cause respiratory damage to humans and other animals. When bee larvae take in spores, they may hatch in the gut, growing rapidly to form a collar-like ring near the larval heads. After death, the larvae turn black and become difficult to crush, hence the name stonebrood. Eventually, the fungus erupts from the integument of the larvae and forms a false skin. In this stage, the larvae are covered with powdery fungal spores. Worker bees clean out the infected brood and the hive may recover depending on factors such as the strength of the colony, the level of infection, and hygienic habits of the strain of bees (variation in the trait occurs among different subspecies).[ citation needed ]

Viral diseases

Dicistroviridae

Chronic bee paralysis virus

  • Syndrome 1 result in abnormal trembling of the wings and body. The bees cannot fly, and often crawl on the ground and up plant stems. In some cases, the crawling bees can be found in large numbers (1000+). The bees huddle together on the top of the cluster or on the top bars of the hive. They may have bloated abdomens due to distension of the honey sac. The wings are partially spread or dislocated.[ citation needed ]
  • Syndrome 2-affected bees are able to fly, but are almost hairless. They appear dark or black and look smaller. They have a relatively broad abdomen. They are often nibbled by older bees in the colony and this may be the cause of the hairlessness. They are hindered at the entrance to the hive by the guard bees. A few days after infection, trembling begins. They then become flightless and soon die. [42] [43]

In 2008, the chronic bee paralysis virus was reported for the first time in Formica rufa and another species of ant, Camponotus vagus . [44]

Acute bee paralysis virus

Acute bee paralysis virus [45] is considered to be a common infective agent of bees. It belongs to the family Dicistroviridae , [46] as does the Israel acute paralysis virus, Kashmir bee virus, and the black queen cell virus. It is frequently detected in apparently healthy colonies. This virus seemingly plays a role in cases of sudden collapse of honey bee colonies infested with the parasitic mite V. destructor . [47]

Israeli acute paralysis virus

Described in 2004 the Israeli acute paralysis virus belongs to the family Dicistroviridae , [46] as does the Acute bee paralysis virus. [48] The virus is named after the place where it was first identified – its place of origin is unknown. It has been suggested as a marker associated with colony collapse disorder. [49] [50]

Kashmir bee virus

Kashmir bee virus [51] is related to the preceding viruses. [46] Discovered in 2004, it is currently only positively identifiable by a laboratory test. Little is known about it yet. [52]

Black queen cell virus

Black queen cell virus [53] causes the queen larva to turn black and die. It is thought to be associated with Nosema . [54]

Cloudy wing virus

Cloudy wing virus is a little-studied, small, icosahedral virus commonly found in honey bees, especially in collapsing colonies infested by V. destructor, providing circumstantial evidence that the mite may act as a vector. [55] [56] [57]

Sacbrood virus

A picornavirus-like virus causes sacbrood disease. [58] [59] Affected larvae change from pearly white to gray and finally black. Death occurs when the larvae are upright, just before pupation. Consequently, affected larvae are usually found in capped cells. Head development of diseased larvae is typically retarded. The head region is usually darker than the rest of the body and may lean toward the center of the cell. When affected larvae are carefully removed from their cells, they appear to be a sac filled with water. Typically, the scales are brittle but easy to remove. Sacbrood-diseased larvae have no characteristic odor. [24] [60]

Iflaviridae

Deformed wing virus

Deformed wing virus (DWV) is the causative agent of the wing deformities and other body malformations typically seen in honeybee colonies that are heavily infested with the parasitic mite V. destructor . [61] DWV is part of a complex of closely related virus strains/species that also includes Kakugo virus, V. destructor virus 1 [62] and Egypt bee virus. This deformity can clearly be seen on the honeybee's wings in the image. The deformities are produced almost exclusively due to DWV transmission by V. destructor when it parasitizes pupae. Bees infected as adults remain symptom-free, although they do display behavioral changes and have reduced life expectancy. Deformed bees are rapidly expelled from the colony, leading to a gradual loss of adult bees for colony maintenance. If this loss is excessive and can no longer be compensated by the emergence of healthy bees, the colony rapidly dwindles and dies.[ citation needed ]

Kakugo virus

Kakugo virus is an Iflavirus infecting bees; varroa mites may mediate its prevalence. [63] Kakugo virus appears to be a subtype of Deformed wing virus . [64]

Slow bee paralysis virus

As the name suggests, slow bee paralysis virus induces paralysis to the anterior legs ten to twelve days after infection.

Iridoviridae

Invertebrate iridescent virus type 6 (IIV-6)

Applying proteomics-based pathogen screening tools in 2010, researchers announced they had identified a co-infection of an Iridovirus; [65] specifically invertebrate iridescent virus type 6 (IIV-6) and N. ceranae in all CCD colonies sampled. [66] On the basis of this research, the New York Times reported the colony collapse mystery solved, quoting researcher Bromenshenk, a co-author of the study, "[The virus and fungus] are both present in all these collapsed colonies." [67] [68] Evidence for this association, however, remains minimal [69] and several authors have disputed the original methodology used to associate CCD with IIV-6. [70] [71]

Secoviridae

Tobacco ringspot virus

The RNA virus tobacco ringspot virus, a plant pathogen, was described to infect honeybees through infected pollen, [72] but this unusual claim was soon challenged and remains to be confirmed. [73]

Lake Sinai virus

In 2015, Lake Sinai virus (LSV) genomes were assembled and three main domains were discovered: Orf1, RNA-dependent RNA polymerase and capsid protein sequences. LSV1, LSV2, LSV3, LSV4, LSV5, and LSV6 were described. [74] LSV were detected in bees, mites and pollen. It only actively replicates in honey bees and mason bees (Osmia cornuta) and not in Varroa mites. [75]

Dysentery

Dysentery is a condition resulting from a combination of long periods of inability to make cleansing flights (generally due to cold weather) and food stores that contain a high proportion of indigestible matter. As a bee's gut becomes engorged with feces that cannot be voided in flight as preferred by the bees, the bee voids within the hive. When enough bees do this, the hive population rapidly collapses and death of the colony results. Dark honeys and honeydews have greater quantities of indigestible matter.[ citation needed ]

Occasional warm days in winter are critical for honey bee survival; dysentery problems increase in likelihood during periods of more than two or three weeks with temperatures below 50 °F (10 °C). When cleansing flights are few, bees are often forced out at times when the temperature is barely adequate for their wing muscles to function, and large quantities of bees may be seen dead in the snow around the hives. Colonies found dead in spring from dysentery have feces smeared over the frames and other hive parts.[ citation needed ]

In very cold areas of North America and Europe, where honey bees are kept in ventilated buildings during the coldest part of winter, no cleansing flights are possible; under such circumstances, beekeepers commonly remove all honey from the hives and replace it with sugar water or high-fructose corn syrup, which have nearly no indigestible matter.[ citation needed ]

Chilled brood

Chilled brood is not actually a disease, but can be a result of mistreatment of the bees by the beekeeper. It also can be caused by a pesticide hit that primarily kills off the adult population, or by a sudden drop in temperature during rapid spring build-up. The brood must be kept warm at all times; nurse bees will cluster over the brood to keep it at the right temperature. When a beekeeper opens the hive (to inspect, remove honey, check the queen, or just to look) and prevents the nurse bees from clustering on the frame for too long, the brood can become chilled, deforming or even killing some of the bees.[ citation needed ]

Pesticide losses

Honey bees are susceptible to many of the chemicals used for agricultural spraying of other insects and pests. Many pesticides are known to be toxic to bees. Because the bees forage up to several miles from the hive, they may fly into areas actively being sprayed by farmers or they may collect pollen from contaminated flowers.[ citation needed ]

Carbamate pesticides, such as carbaryl, can be especially pernicious since toxicity can take as long as two days to become evident, allowing infected pollen to be returned and distributed throughout the colony. Organophosphates and other insecticides are also known to kill honey bee clusters in treated areas.[ citation needed ]

Pesticide losses may be relatively easy to identify (large and sudden numbers of dead bees in front of the hive) or quite difficult, especially if the loss results from a gradual accumulation of pesticide brought in by the foraging bees. Quick-acting pesticides may deprive the hive of its foragers, dropping them in the field before they can return home.[ citation needed ]

Insecticides that are toxic to bees have label directions that protect the bees from poisoning as they forage. To comply with the label, applicators must know where and when bees forage in the application area, and the length of residual activity of the pesticide.[ citation needed ]

Some pesticide authorities recommend, and some jurisdictions require, that notice of spraying be sent to all known beekeepers in the area, so they can seal the entrances to their hives and keep the bees inside until the pesticide has had a chance to disperse. This, however, does not solve all problems associated with spraying and the label instructions should be followed regardless of doing this. Sealing honey bees from flight on hot days can kill bees. Beekeeper notification does not offer any protection to bees, if the beekeeper cannot access them, or to wild native or feral honey bees. Thus, beekeeper notification as the sole protection procedure does not really protect all the pollinators of the area, and is, in effect, a circumventing of the label requirements. Pesticide losses are a major factor in pollinator decline.[ citation needed ]

Colony collapse disorder

Colony collapse disorder (CCD) is a poorly understood phenomenon in which worker bees from a beehive or western honey bee colony abruptly disappear. CCD was originally discovered in Florida by David Hackenberg in western honey bee colonies in late 2006. [76]

European beekeepers observed a similar phenomenon in Belgium, France, the Netherlands, Greece, Italy, Portugal, and Spain, [77] and initial reports have also come in from Switzerland and Germany, albeit to a lesser degree. [78] Possible cases of CCD have also been reported in Taiwan since April 2007. [79]

Initial hypotheses were wildly different, including environmental change-related stresses, [80] malnutrition, pathogens (i.e., disease [81] including Israel acute paralysis virus [82] [83] ), mites, or the class of pesticides known as neonicotinoids, which include imidacloprid, clothianidin, and thiamethoxam. Most new research suggests the neonicotinoid hypothesis was incorrect, however, and that pesticides play little role in CCD compared to Varroa and Nosema infestations. [84] Other theories included radiation from cellular phones or other man-made devices [85] and genetically modified crops with pest-control characteristics,. [86] In 2010, U.S. researchers announced they had identified a co-infection of invertebrate iridescent virus type 6 (IIV-6) and N. ceranae in all CCD colonies sampled. [87]

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The Buckfast bee is a breed of honey bee, a cross of many subspecies and their strains, developed by Brother Adam, who was in charge of beekeeping from 1919 at Buckfast Abbey in Devon in the United Kingdom. Breeding of the Buckfast bee is now done by breeders throughout Europe belonging to the Federation of European Buckfast Beekeepers (G.D.E.B.). This organization maintains a pedigree for Buckfast bees, originating from the time of Brother Adam.

<i>European dark bee</i> Subspecies of honey bee

The Apis mellifera mellifera is a subspecies of the western honey bee, evolving in central Asia, with a proposed origin of the Tien Shan Mountains and later migrating into eastern and then northern Europe after the last ice age from 9,000BC onwards. Its original range included the southern Urals in Russia and stretched through northern Europe and down to the Pyrenees. They are one of the two members of the 'M' lineage of Apis mellifera, the other being in western China. Traditionally they were called the Black German Bee, although they are now considered endangered in Germany. However today they are more likely to be called after the geographic / political region in which they live such as the British Black Bee, the Native Irish Honey Bee, the Cornish Black Bee and the Nordic Brown Bee, even though they are all the same subspecies, with the word "native" often inserted by local beekeepers, even in places where the bee is an introduced foreign species. It was domesticated in Europe and hives were brought to North America in the colonial era in 1622 where they were referred to as the English Fly by the Native Americans.

Nosema apis is a microsporidian, a small, unicellular parasite recently reclassified as a fungus that mainly affects honey bees. It causes nosemosis, also called nosema, which is the most common and widespread of adult honey bee diseases. The dormant stage of N. apis is a long-lived spore which is resistant to temperature extremes and dehydration, and cannot be killed by freezing the contaminated comb. Nosemosis is a listed disease with the Office International des Epizooties (OIE).

<i>Varroa destructor</i> Species of mite

Varroa destructor, the Varroa mite, is an external parasitic mite that attacks and feeds on honey bees and is one of the most damaging honey bee pests in the world. A significant mite infestation leads to the death of a honey bee colony, usually in the late autumn through early spring. Without management for Varroa mite, honey bee colonies typically collapse within 2 to 3 years in temperate climates. These mites can infest Apis mellifera, the western honey bee, and Apis cerana, the Asian honey bee. Due to very similar physical characteristics, this species was thought to be the closely related Varroa jacobsoni prior to 2000, but they were found to be two separate species after DNA analysis.

<span class="mw-page-title-main">Russian honey bee</span> Breed of bee

The Russian honeybee refers to honey bees that originate in the Primorsky Krai region of Russia. This strain of bee was imported into the United States in 1997 by the USDA Agricultural Research Service's Honeybee Breeding, Genetics & Physiology Laboratory in Baton Rouge, Louisiana, in response to severe declines in bee populations caused by infestations of parasitic mites, and has been used in breeding programs to improve existing stocks. Many Russian queens openly mate with drones from various stock, creating colonies that are genetically hybrid. Some of these 'uncontrolled' hybrids may exhibit "increased aggressiveness, reduced honey production and a decrease in their ability to withstand mites and detrimental expressions of other traits as well."

<i>Varroa</i> Genus of mites

Varroa is a genus of parasitic mesostigmatan mites associated with honey bees, placed in its own family, Varroidae. The genus was named for Marcus Terentius Varro, a Roman scholar and beekeeper. The condition of a honeybee colony being infested with Varroa mites is called varroosis.

<span class="mw-page-title-main">Small hive beetle</span> Species of beetle

Aethina tumida,commonly known as small hive beetle (SHB), is a beekeeping pest. It is native to sub-Saharan Africa, but has spread to many other regions, including North America, Australia, and the Philippines.

<span class="mw-page-title-main">American foulbrood</span> Bee disease

American foulbrood, caused by the spore-forming bacterium Paenibacillus larvae, is a highly infectious honey bee brood disease. It is the most widespread and destructive of the honey bee brood diseases. It is globally distributed and burning of infected colonies is often considered as the only effective measure to prevent spreading of the disease.

<i>Deformed wing virus</i> Species of virus

Deformed wing virus (DWV) is an RNA virus, one of 22 known viruses affecting honey bees. While most commonly infecting the honey bee, Apis mellifera, it has also been documented in other bee species, like Bombus terrestris, thus, indicating it may have a wider host specificity than previously anticipated. The virus was first isolated from a sample of symptomatic honeybees from Japan in the early 1980s and is currently distributed worldwide. It is found also in pollen baskets and commercially reared bumblebees. Its main vector in A. mellifera is the Varroa mite. It is named after what is usually the most obvious deformity it induces in the development of a honeybee pupa, which is shrunken and deformed wings, but other developmental deformities are often present.

Nosema ceranae is a microsporidian, a small, unicellular parasite that mainly affects Apis cerana, the Asiatic honey bee. Along with Nosema apis, it causes the disease nosemosis, the most widespread of the diseases of adult honey bees. N. ceranae can remain dormant as a long-lived spore which is resistant to temperature extremes and dehydration. This fungus has been shown to act in a synergistic fashion with diverse insecticides such as fipronil or neonicotinoids, by increasing the toxicity of pesticides for bees, leading to higher bee mortality. It may thus play an indirect role in colony collapse disorder. In addition, the interaction between fipronil and N. ceranae induces changes in male physiology leading to sterility.

<span class="mw-page-title-main">Western honey bee</span> European honey bee

The western honey bee or European honey bee is the most common of the 7–12 species of honey bees worldwide. The genus name Apis is Latin for "bee", and mellifera is the Latin for "honey-bearing" or "honey carrying", referring to the species' production of honey.

<span class="mw-page-title-main">Beekeeping in New Zealand</span>

Beekeeping in New Zealand is reported to have commenced in 1839 with the importing of two skep hives by Mary Bumby, a missionary. It has since become an established industry as well a hobby activity.

<span class="mw-page-title-main">Colony collapse disorder</span> Aspect of apiculture

Colony collapse disorder (CCD) is an abnormal phenomenon that occurs when the majority of worker bees in a honey bee colony disappear, leaving behind a queen, plenty of food, and a few nurse bees to care for the remaining immature bees. While such disappearances have occurred sporadically throughout the history of apiculture, and have been known by various names, the syndrome was renamed colony collapse disorder in early 2007 in conjunction with a drastic rise in reports of disappearances of western honey bee colonies in North America. Beekeepers in most European countries had observed a similar phenomenon since 1998, especially in Southern and Western Europe; the Northern Ireland Assembly received reports of a decline greater than 50%. The phenomenon became more global when it affected some Asian and African countries as well. From 1990 to 2021, the United Nation’s FAO calculated that the worldwide number of honeybee colonies increased 47%, reaching 102 million.

<i>Apis cerana</i> Species of insect

Apis cerana, the eastern honey bee, Asiatic honey bee or Asian honey bee, is a species of honey bee native to South, Southeast and East Asia. This species is the sister species of Apis koschevnikovi and both are in the same subgenus as the western (European) honey bee, Apis mellifera. A. cerana is known to live sympatrically along with Apis koschevnikovi within the same geographic location. Apis cerana colonies are known for building nests consisting of multiple combs in cavities containing a small entrance, presumably for defense against invasion by individuals of another nest. The diet of this honey bee species consists mostly of pollen and nectar, or honey. Moreover, Apis cerana is known for its highly social behavior, reflective of its classification as a type of honey bee.

Beekeeping is first recorded in Ireland in the seventh century. It has seen a surge in popularity in modern times, with the membership of beekeeping associations exceeding 4,500. The median average number of hives per beekeeper is three hives, while the average honey output per hive is 11.4 kg. The growth in the practice has occurred despite increased pressures on bees and beekeepers due to parasites, diseases and habitat loss.

<i>Apocephalus borealis</i> Species of fly

Apocephalus borealis is a species of North American parasitoid phorid fly that attacks bumblebees, honey bees, and paper wasps. This parasitoid's genus Apocephalus is best known for the "decapitating flies" that attack a variety of ant species, though A. borealis attacks and alters the behavior of bees and wasps. These flies are colloquially known as zombie flies and the bees they infect are colloquially known as zombees. Association with honey bees has so far only been documented from California, South Dakota, Oregon, Washington, British Columbia, and Vermont.

<span class="mw-page-title-main">Chronic bee paralysis virus</span> Virus which infects bees

Chronic bee paralysis virus (CBPV) commonly affects adult Apis mellifera honey bees and causes a chronic paralysis that can easily spread to other members of a colony. Bees infected with CBPV begin to show symptoms after 5 days and die a few days after. Chronic bee paralysis virus infection is a factor that can contribute to or cause the sudden collapse of honeybee colonies. Since honeybees serve a vital role in ecological resilience, it is important to understand factors and diseases that threaten them.

Honey bee starvation is a problem for bees and beekeepers. Starvation may be caused by unfavorable weather, disease, long distance transportation or depleting food reserve. Over-harvesting of honey is the foremost cause for scarcity as bees are not left with enough of a honey store, though weather, disease, and disturbance can also cause problems. Backyard beekeepers face more colony losses in the winter than in the summer, but for commercial beekeepers there is not much variation in loss by season. Starvation may be avoided by effective monitoring of hives and disease prevention measures. Starvation can amplify the toxic effect of pesticides bees are exposed to.

References

  1. ↑ Natalia Damiani; Liesel B. Gende; Pedro Bailac; Jorge A. Marcangeli & Martín J. Eguaras (2009). "Acaricidal and insecticidal activity of essential oils on Varroa destructor (Acari: Varroidae) and Apis mellifera (Hymenoptera: Apidae)". Parasitology Research . 106 (1): 145–152. doi:10.1007/s00436-009-1639-y. PMID   19795133. S2CID   22756628.
  2. ↑ "Apivar official webpage – Véto-pharma website". apivar.net.
  3. ↑ "Véto-pharma – ApiLife Var". Veto-pharma. Retrieved 23 May 2022.
  4. ↑ "Véto-pharma – Api-Bioxal". Veto-pharma. Retrieved 23 May 2022.
  5. ↑ "NOD Apiary Products Ltd". nodglobal.com.
  6. ↑ Formic Acid (214900) Fact Sheet. Office of Pesticide Programs; US Environmental Protection Agency (Report). 2005.
  7. ↑ Bailey L & Ball BV (January 1991). Honey Bee Pathology. Academic Press. p. 119. ISBN   978-0-12073481-8.
  8. ↑ Garrido, Paula Melisa; Porrini, Martín Pablo; Alberoni, Daniele; Baffoni, Loredana; Scott, Dara; Mifsud, David; Eguaras, Matín Javier; Di Gioia, Diana (13 January 2023). "Beneficial Bacteria and Plant Extracts Promote Honey Bee Health and Reduce Nosema ceranae Infection". Probiotics and Antimicrobial Proteins. 16 (1): 259–274. doi:10.1007/s12602-022-10025-7. hdl: 11585/912269 . ISSN   1867-1314. PMC   10850026 . PMID   36637793. S2CID   255773303.
  9. ↑ Tokarev, Yuri S.; Huang, Wei-Fone; Solter, Leellen F.; Malysh, Julia M.; Becnel, James J.; Vossbrinck, Charles R. (1 January 2020). "A formal redefinition of the genera Nosema and Vairimorpha (Microsporidia: Nosematidae) and reassignment of species based on molecular phylogenetics". Journal of Invertebrate Pathology. 169: 107279. Bibcode:2020JInvP.16907279T. doi: 10.1016/j.jip.2019.107279 . ISSN   0022-2011. PMID   31738888. S2CID   208169117.
  10. ↑ Higes, Mariano; García-Palencia, Pilar; Martín-Hernández, Raquel; Meana, Aránzazu (1 March 2007). "Experimental infection of Apis mellifera honeybees with Nosema ceranae (Microsporidia)". Journal of Invertebrate Pathology. 94 (3): 211–217. Bibcode:2007JInvP..94..211H. doi:10.1016/j.jip.2006.11.001. ISSN   0022-2011. PMID   17217954.
  11. ↑ Goblirsch, Mike (1 February 2018). "Nosema ceranae disease of the honey bee (Apis mellifera)". Apidologie. 49 (1): 131–150. doi: 10.1007/s13592-017-0535-1 . ISSN   1297-9678. S2CID   256204201.
  12. ↑ Blot, Nicolas; Clémencet, Johanna; Jourda, Cyril; Lefeuvre, Pierre; Warrit, Natapot; Esnault, Olivier; Delatte, Hélène (26 July 2023). "Geographic population structure of the honeybee microsporidian parasite Vairimorpha (Nosema) ceranae in the South West Indian Ocean". Scientific Reports. 13 (1): 12122. Bibcode:2023NatSR..1312122B. doi:10.1038/s41598-023-38905-0. ISSN   2045-2322. PMC   10372035 . PMID   37495608.
  13. ↑ Higes, Mariano; Martín-Hernández, Raquel; Meana, Aranzazu (1 May 2010). "Nosema ceranae in Europe: an emergent type C nosemosis". Apidologie. 41 (3): 375–392. doi:10.1051/apido/2010019. ISSN   1297-9678. S2CID   30846922.
  14. ↑ Blot, Nicolas; Clémencet, Johanna; Jourda, Cyril; Lefeuvre, Pierre; Warrit, Natapot; Esnault, Olivier; Delatte, Hélène (26 July 2023). "Geographic population structure of the honeybee microsporidian parasite Vairimorpha (Nosema) ceranae in the South West Indian Ocean". Scientific Reports. 13 (1): 12122. Bibcode:2023NatSR..1312122B. doi:10.1038/s41598-023-38905-0. ISSN   2045-2322. PMC   10372035 . PMID   37495608.
  15. ↑ Braglia, Chiara; Alberoni, Daniele; Porrini, Martin Pablo; Garrido, Paula Melisa; Baffoni, Loredana; Di Gioia, Diana (1 September 2021). "Screening of Dietary Ingredients against the Honey Bee Parasite Nosema ceranae". Pathogens. 10 (9): 1117. doi: 10.3390/pathogens10091117 . ISSN   2076-0817. PMC   8466614 . PMID   34578150.
  16. ↑ Ritter, Wolfgang Nosema ceranae Archived 14 February 2007 at the Wayback Machine Albert Ludwigs University of Freiburg
  17. ↑ "Effects of Bt maize pollen on the honeybee". 12 October 2005. Archived from the original on 26 January 2007. Retrieved 21 March 2007.
  18. ↑ Neumann P, Elzen PJ (2004). "The biology of the small hive beetle (Aethina tumida, Coleoptera: Nitidulidae): Gaps in our knowledge of an invasive species". Apidologie. 35 (3): 229–47. doi: 10.1051/apido:2004010 .
  19. ↑ "Combat Source Kill Max Gel Kills Large and Small Roaches". combatbugs.com. Archived from the original on 28 June 2014. Retrieved 27 February 2014.
  20. ↑ Root, A.I. (1978). ABC and XYZ of Bee Culture. Medina, Ohio: A. I. Root Company. p. 676.
  21. ↑ Root, A.I. (1978). ABC and XYZ of Bee Culture. Medina, Ohio: A. I. Root Company. p. 231.
  22. ↑ Bergqvist, Sanna (2019). Bee wax moth in Embu county, Kenya, the intruder in the hives (Thesis). Uppsala: SLU, Dept of Ecology. pp. 28, 29.
  23. ↑ de Guzman, Lilia; Williams, Geoffrey R.; Khongphinitbunjong, Kitiphong; Chantawannakul, Panuwan (8 March 2017). "Ecology, Life History, and Management of Tropilaelaps Mites". Journal of Economic Entomology . 110 (2): 319–332. doi:10.1093/jee/tow304. PMID   28334185 – via Entomological Society of America.
  24. 1 2 Shimanuki, Hachiro; Knox, David A. Diagnosis of Honey Bee Diseases USDA Archived 9 December 2006 at the Wayback Machine
  25. ↑ Genersch, E; Forsgren, E; Pentikäinen, J; Ashiralieva, A; Rauch, S; Kilwinski, J; Fries, I (March 2006). "Reclassification of Paenibacillus larvae subsp. pulvifaciens and Paenibacillus larvae subsp. larvae as Paenibacillus larvae without subspecies differentiation". International Journal of Systematic and Evolutionary Microbiology. 56 (Pt 3): 501–11. doi: 10.1099/ijs.0.63928-0 . PMID   16514018.
  26. ↑ Controlling American Foulbrood in Honeybees By Shook Swarm Method
  27. ↑ "American and European Foulbrood". Bee Health eXtension. 20 August 2019. Retrieved 9 November 2019.
  28. ↑ "European Foulbrood: A Bacterial Disease Affecting Honey Bee Brood". extension.org. Archived from the original on 24 January 2010. Retrieved 10 November 2009.
  29. ↑ von Büren, Raphael S.; Oehen, Bernadette; Kuhn, Nikolaus J.; Erler, Silvio (31 January 2019). "High-resolution maps of Swiss apiaries and their applicability to study spatial distribution of bacterial honey bee brood diseases". PeerJ. 7: e6393. doi: 10.7717/peerj.6393 . ISSN   2167-8359. PMC   6360077 . PMID   30723636.
  30. ↑ "Shook Swarm and OTC Antibiotics for European Foulbrood Control". extension.org. Archived from the original on 5 February 2013. Retrieved 3 January 2013.
  31. ↑ Root, A.I. (1978). ABC and XYZ of Bee Culture. Medina, Ohio: A. I. Root Company. p. 311.
  32. ↑ Carr, E. G. (February 1917). "Some New and Practical Methods for the Control of European Foulbrood". Journal of Economic Entomology. 10 (1). Entomological Society of America: 200. doi:10.1093/jee/10.1.197.
  33. 1 2 3 4 5 6 7 8 9 Aronstein, K. A.; Murray, K. D. (1 January 2010). "Chalkbrood disease in honey bees". Journal of Invertebrate Pathology. 103: S20–S29. Bibcode:2010JInvP.103S..20A. doi:10.1016/j.jip.2009.06.018. ISSN   0022-2011. PMID   19909969. S2CID   7406384.
  34. 1 2 3 Jones, R., & Sweeney-Lynch, S. (2011). The beekeeper's bible: Bees, honey, recipes & other home uses. Stewart, Tabori & Chang.
  35. ↑ Zaghloul, O. A.; Mourad, A. K.; El Kady, Magda B.; Nemat, F. M.; Morsy, M. E. (2005). "Assessment of losses in honey yield due to the chalkbrood disease, with reference to the determination of its economic injury levels in Egypt". Communications in Agricultural and Applied Biological Sciences. 70 (4): 703–714. ISSN   1379-1176. PMID   16628907.
  36. ↑ Hedtke, Kati; Jensen, Per Moestrup; Jensen, Annette Bruun; Genersch, Elke (1 November 2011). "Evidence for emerging parasites and pathogens influencing outbreaks of stress-related diseases like chalkbrood". Journal of Invertebrate Pathology. 108 (3): 167–173. Bibcode:2011JInvP.108..167H. doi:10.1016/j.jip.2011.08.006. ISSN   0022-2011. PMID   21906600.
  37. ↑ Hornitzky, Michael (November 2001). "Literature review of chalkbrood: a fungal disease of honeybees" (PDF). Rural Industries Research and Development Corporation, NSW Agriculture. pp. 5, 10.
  38. ↑ Southwick, Edward E.; Moritz, R.F.A. (1987). "Social control of air ventilation in colonies of honey bees, Apis mellifera". Journal of Insect Physiology. 33 (9): 623–626. Bibcode:1987JInsP..33..623S. doi:10.1016/0022-1910(87)90130-2.
  39. ↑ Gochnauer, T. A.; Furgala, B.; Shirnamuki, H. "Diseases and enemies of the honey bee". The Hive and the Honey Bee. 1975. AGRIS: 615–622.
  40. ↑ Berry, J. A.; Delaplane, K. S. (2001). "Effect of comb age on honey bee colony growth and brood survivorship". Journal of Apicultural Research. 40 (1). Taylor & Francis: 3–8. Bibcode:2001JApiR..40....3B. doi:10.1080/00218839.2001.11101042. S2CID   15301172.
  41. ↑ Koenig, John P.; Boush, G. Mallory; Erickson Jr., E. H. (1986). "Effect of Type of Brood Comb on Chalk Bee Disease in Honeybee Colonies". Journal of Apicultural Research. 25 (1). Taylor & Francis: 58–62. doi:10.1080/00218839.1986.11100694.
  42. ↑ Ribière M, Faucon J, Pépin M (2000). "Detection of chronic honey bee (Apis mellifera L.) paralysis virus infection: application to a field survey". Apidologie. 31 (5): 567–77. doi: 10.1051/apido:2000147 . Open Access logo PLoS transparent.svg
  43. ↑ "Chronic Bee Paralysis Virus". globalnet.co.uk.
  44. ↑ Celle, O; Blanchard, P; Olivier, V; Schurr, F; Cougoule, N; Faucon, JP; Ribière, M (May 2008). "Detection of Chronic bee paralysis virus (CBPV) genome and its replicative RNA form in various hosts and possible ways of spread" (PDF). Virus Research. 133 (2): 280–4. doi:10.1016/j.virusres.2007.12.011. PMID   18243390. S2CID   16801385. Open Access logo PLoS transparent.svg
  45. ↑ (TaxID 92444)
  46. 1 2 3 "Dicistroviridae".
  47. ↑ Bakonyi T, Grabensteiner E, Kolodziejek J, et al. (December 2002). "Phylogenetic analysis of acute bee paralysis virus strains". Appl. Environ. Microbiol. 68 (12): 6446–50. Bibcode:2002ApEnM..68.6446B. doi:10.1128/AEM.68.12.6446-6450.2002. PMC   134446 . PMID   12450876.
  48. ↑ (TaxID 294365)
  49. ↑ Fox, Maggie (6 September 2007). "New virus may be killing bees". Reuters. Retrieved 6 September 2007.
  50. ↑ Humberto F. Boncristiani; et al. (2013). "In vitro infection of pupae with IAPV suggests disturbance of transcriptional homeostasis in honey bees (Apis mellifera)". PLOS ONE. 8 (9): e73429. doi: 10.1371/journal.pone.0073429 . PMC   3764161 . PMID   24039938.
  51. ↑ (TaxID 68876)
  52. ↑ Kashmir Bee Virus Archived 2 March 2007 at the Wayback Machine Apiculture Factsheet #230, Ministry of Agriculture and Lands, Government of British Columbia, Jul 2004, accessed Jan 2007
  53. ↑ (TaxID 92395)
  54. ↑ "Multiple Virus Infections in the Honey Bee and Genome Divergence of Honey Bee Viruses". usda.gov.
  55. ↑ Carreck, Norman L; Ball, Brenda V; Martin, Stephen J (2010). "The epidemiology of cloudy wing virus infections in honey bee colonies in the UK". Journal of Apicultural Research. 49 (1): 66–71. Bibcode:2010JApiR..49...66C. doi:10.3896/ibra.1.49.1.09. S2CID   84982753. Archived from the original on 22 December 2010.
  56. ↑ Gliński, Z.; Jarosz, J. (2001). "Infection and immunity in the honey bee Apis mellifera". Apiacta. 36 (1): 12–24.
  57. ↑ Cloudy Wing Virus Universal Protein Resource (UniProt); European Bioinformatics Institute (EBI), the Swiss Institute of Bioinformatics (SIB) and the Protein Information Resource (PIR)
  58. ↑ Wu, CY; Lo, CF; Huang, CJ; Yu, HT; Wang, CH (2002). "The complete genome sequence of Perina nuda picorna-like virus, an insect-infecting RNA virus with a genome organization similar to that of the mammalian picornaviruses". Virology. 294 (2): 312–23. doi: 10.1006/viro.2001.1344 . PMID   12009873.
  59. ↑ Grabensteiner, E; Ritter, W; Carter, MJ; Davison, S; Pechhacker, H; Kolodziejek, J; Boecking, O; Derakhshifar, I; Moosbeckhofer, R; Licek, E; Nowotny, N (2001). "Sacbrood Virus of the Honeybee (Apis mellifera): Rapid Identification and Phylogenetic Analysis Using Reverse Transcription-PCR". Clinical and Diagnostic Laboratory Immunology. 8 (1): 93–104. doi:10.1128/CDLI.8.1.93-104.2001. PMC   96016 . PMID   11139201.
  60. ↑ Grabensteiner, Elvira; Ritter, Wolfgang; Carter, Michael J.; Davison, Sean; Pechhacker, Hermann; Kolodziejek, Jolanta; Boecking, Otto; Derakhshifar, Irmgard; Moosbeckhofer, Rudolf; Licek, Elisabeth; Nowotny, Norbert (2001). "Sacbrood Virus of the Honeybee (Apis mellifera): Rapid Identification and Phylogenetic Analysis Using Reverse Transcription-PCR". Clin Diagn Lab Immunol. 8 (1): 93–104. doi:10.1128/CDLI.8.1.93-104.2001. PMC   96016 . PMID   11139201.
  61. ↑ de Miranda, Joachim R.; Genersch, Elke (2010). "Deformed wing virus". Journal of Invertebrate Pathology. 103: S48–S61. Bibcode:2010JInvP.103S..48D. doi:10.1016/j.jip.2009.06.012. PMID   19909976.
  62. ↑ Ongus, Juliette R.; Roode, Els C.; Pleij, Cornelis W. A.; Vlak, Just M.; van Oers, Monique M. (2006). "The 5' non-translated region of Varroa destructor virus 1 (genus Iflavirus): structure prediction and IRES activity in Lymantria dispar cell". J Gen Virol. 87 (Pt 11): 3397–3407. doi: 10.1099/vir.0.82122-0 . PMID   17030876.
  63. ↑ Tomoko Fujiyuki, Seii Ohka, Hideaki Takeuchi, Masato Ono, Akio Nomoto, and Takeo Kubo Prevalence and Phylogeny of Kakugo Virus, a Novel Insect Picorna-Like Virus That Infects the Honeybee (Apis mellifera L.), under Various Colony Conditions Archived 25 July 2011 at the Wayback Machine Journal of Virology, December 2006, pp. 11528–38, Vol. 80, No. 23
  64. ↑ NCBI: Kakugo virus (no rank)
  65. ↑ Williams, Trevor Iridoviridae Instituto de Ecología AC (INECOL)Mexico
  66. ↑ Leal, Walter S.; Bromenshenk, Jerry J.; Henderson, Colin B.; Wick, Charles H.; Stanford, Michael F.; Zulich, Alan W.; Jabbour, Rabih E.; Deshpande, Samir V.; McCubbin, Patrick E. (2010). Leal, Walter S. (ed.). "Iridovirus and Microsporidian Linked to Honey Bee Colony Decline". PLOS ONE. 5 (10): e13181. Bibcode:2010PLoSO...513181B. doi: 10.1371/journal.pone.0013181 . PMC   2950847 . PMID   20949138.
  67. ↑ Kirk Johnson (6 October 2010). "Scientists and Soldiers Solve a Bee Mystery". The New York Times.
  68. ↑ Invertebrate iridescent virus type 6 (IIV-6) Universal Protein Resource (UniProt); European Bioinformatics Institute (EBI), the Swiss Institute of Bioinformatics (SIB) and the Protein Information Resource (PIR).
  69. ↑ Tokarz, Rafal; Cadhla Firth; Craig Street; Diana Cox-Foster; W. Ian Lipkin (2011). "Lack of evidence for an Association between Iridovirus and Colony Collapse Disorder". PLOS ONE. 6 (6): e21844. Bibcode:2011PLoSO...621844T. doi: 10.1371/journal.pone.0021844 . PMC   3128115 . PMID   21738798.
  70. ↑ Foster, Leonard (2011). "Interpretation of data underlying the link between colony collapse disorder (CCD) and an invertebrate iridescent virus". Molecular & Cellular Proteomics. 10 (3): M110.006387. doi: 10.1074/mcp.m110.006387 . PMC   3047166 . PMID   21364086.
  71. ↑ Knudsen, Giselle; Robert Chalkley (2011). "The Effect of Using an Inappropriate Protein Database for Proteomic Data Analysis". PLOS ONE. 6 (6): e20873. Bibcode:2011PLoSO...620873K. doi: 10.1371/journal.pone.0020873 . PMC   3114852 . PMID   21695130.
  72. ↑ Li, J. L.; Cornman, R. S.; Evans, J. D.; Pettis, J. S.; Zhao, Y.; Murphy, C.; Peng, W. J.; Wu, J.; Hamilton, M.; Boncristiani, H. F.; Zhou, L.; Hammond, J.; Chen, Y. P. (21 January 2014). "Systemic Spread and Propagation of a Plant-Pathogenic Virus in European Honeybees, Apis mellifera". mBio. 5 (1): e00898–13. doi:10.1128/mBio.00898-13. PMC   3903276 . PMID   24449751.
  73. ↑ Miller, W. Allen; Carrillo-Tripp, Jimena; Bonning, Bryony C.; Dolezal, Adam G.; Toth, Amy L. (27 May 2014). "Conclusive Evidence of Replication of a Plant Virus in Honeybees Is Lacking". mBio. 5 (3): e00985-14. doi:10.1128/mBio.00985-14. ISSN   2150-7511. PMC   4045069 . PMID   24865552.
  74. ↑ Daughenbaugh, Katie F.; et al. (2015). "Honey Bee Infecting Lake Sinai Viruses". Viruses. 7 (6): 3285–3309. doi: 10.3390/v7062772 . PMC   4488739 . PMID   26110586.
  75. ↑ Ravoet, Jorgen; et al. (2015). "Genome sequence heterogeneity of Lake Sinai Virus found in honey bees and Orf1/RdRP-based polymorphisms in a single host". Virus Research. 201: 67–72. doi:10.1016/j.virusres.2015.02.019. PMID   25725149.
  76. ↑ "Honey Bee Die-Off Alarms Beekeepers, Crop Growers and Researchers". Penn State University College of Agricultural Sciences. 29 January 2007.
  77. ↑ Gaëlle Dupont, Les abeilles malades de l'homme, Le Monde , 29 August 2007. Retrieved 10 July 2020. (in French)
  78. ↑ Petra Steinberger (12 March 2007). "Das spurlose Sterben" (in German). sueddeutsche.de. Archived from the original on 6 April 2008.
  79. ↑ Paul Molga, La mort des abeilles met la planète en danger, Les Echos , 20 August 2007 (in French)
  80. ↑ Amy Sahba (29 March 2007). "The mysterious deaths of the honeybees". CNN Money . Retrieved 4 April 2007.
  81. ↑ "Colony Collapse Disorder Working Group".
  82. ↑ JR Minkel (7 September 2007). "Mysterious Honeybee Disappearance Linked to Rare Virus". Science News. Scientific American. Archived from the original on 26 September 2007. Retrieved 7 September 2007.
  83. ↑ Andrew C. Refkin (7 September 2007). "Virus Is Seen as Suspect in Death of Honeybees". The New York Times . Retrieved 7 September 2007.
  84. ↑ Jon Entine (12 October 2018). "'Gold standard' assessing neonicotinoids: Field bee hive studies find pesticides not major source of health issues". Genetic Literacy Project. Retrieved 15 December 2018.
  85. ↑ Geoffrey Lean & Harriet Shawcross (15 April 2007). "Are mobile phones wiping out our bees?". The Independent . Archived from the original on 29 November 2007. Retrieved 10 December 2007.
  86. ↑ "GE and bee Colony Collapse Disorder – science needed!". 21 March 2005. Archived from the original on 27 April 2007. Retrieved 23 March 2007.
  87. ↑ Leal, Walter S.; Bromenshenk, Jerry J.; Henderson, Colin B.; Wick, Charles H.; Stanford, Michael F.; Zulich, Alan W.; Jabbour, Rabih E.; Deshpande, Samir V.; McCubbin, Patrick E. (2010). Leal, Walter S. (ed.). "Iridovirus and Microsporidian Linked to Honey Bee Colony Decline". PLOS ONE. 5 (10): e13181. Bibcode:2010PLoSO...513181B. doi: 10.1371/journal.pone.0013181 . PMC   2950847 . PMID   20949138.

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