Resistance to Varroa destructor (Mesostigmata: Varroidae) when mite-resistant queen honey bees (Hymenoptera: Apidae) were free-mated with unselected drones.

This study demonstrated (1) that honey bees, Apis mellifera L, can express a high level of resistance to Varroa destructor Anderson & Trueman when bees were selected for only one resistant trait (suppression of mite reproduction); and (2) that a significant level of mite-resistance was retained when these queens were free-mated with unselected drones. The test compared the growth of mite populations in colonies of bees that each received one of the following queens: (1) resistant--queens selected for suppression of mite reproduction and artificially inseminated in Baton Rouge with drones from similarly selected stocks; (2) resistant x control--resistant queens, as above, produced and free-mated to unselected drones by one of four commercial queen producers; and (3) control--commercial queens chosen by the same four queen producers and free-mated as above. All colonies started the test with approximately 0.9 kg of bees that were naturally infested with approximately 650 mites. Colonies with resistant x control queens ended the 115-d test period with significantly fewer mites than did colonies with control queens. This suggests that beekeepers can derive immediate benefit from mite-resistant queens that have been free-mated to unselected drones. Moreover, the production and distribution of these free-mated queens from many commercial sources may be an effective way to insert beneficial genes into our commercial population of honey bees without losing the genetic diversity and the useful beekeeping characteristics of this population.     

Russian honey bee (Hymenoptera: Apidae) colonies: Acarapis woodi (Acari: Tarsonemidae) infestations and overwintering survival

Honey bee, Apis mellifera L. (Hymenoptera: Apidae), colonies infested by parasitic mites are more prone to suffer from a variety of stresses, including cold temperature. We evaluated the overwintering ability of candidate breeder lines of Russian honey bees, most of which are resistant to both Varroa destructor Anderson & Trueman and Acarapis woodi (Rennie), during 1999-2001. Our results indicate that Russian honey bee colonies (headed by original and supersedure queens) can successfully overwinter in the north, even during adverse weather conditions, owing to their frugal use of food stores and their resistance to tracheal mite infestations. In contrast, colonies of Italian honey bees consumed more food, had more mites, and lost more adult bees than Russian honey bees, even during unusually mild winter conditions.     

The Role of Cuticular Compounds in the Resistance of Honey Bees (Apis Mellifera) to Tracheal Mites (Acarapis Woodi)

This study examined the migration of tracheal mites (Acarapis woodi) into honey bees (Apis mellifera) from different colonies and the relative attraction of mites to hexane extracts from the external body surfaces of young bees. Relative resistance of bees from different colonies initially was assessed with a field bioassay that involved tagging newly emerged bees, pooling them in heavily mite-infested colonies, retrieving them 7 days later, and examining them for tracheal mite prevalence and abundance. For those colonies identified as most resistant and least resistant, cuticular chemicals were extracted in hexane from frozen, newly emerged worker bees. These extracts were presented to individual tracheal mites in pairwise fashion in a laboratory bioassay. The results demonstrated that mites prefer extracts of bees from some colonies more than others, however, no consistent differences were demonstrated. Our inability to predict mite responses to extracts based on our initial assessment of relative resistance indicates that other mechanisms of resistance influence mite success in colonizing new host bees.     

Single and dual parasitic mite infestations on the honey bee, Apis mellifera L.

Summary: The onset of foraging, proportion of pollen collectors, and weight of pollen loads were compared in individual honey bees (Apis mellifera) infested by zero, one (Acarapis woodi, the honey bee tracheal mite, or Varroa jacobsoni,varroa), or both species of parasitic mites. Phoretic varroa host choice also was compared between bees with and without tracheal mites, and tracheal mite infestation of hosts was compared between bees parasitized or not by varroa during development. The proportion of pollen collectors was not significantly different between treatments, but bees parasitized by both mites had significantly smaller pollen loads than uninfested bees. Mean onset of foraging was earliest for bees parasitized by varroa during development, 15.9 days. Bees with tracheal mites began foraging latest, at 20.5 days, and foraging ages were intermediate in bees with no mites and both, 17.6 and 18.0 days respectively. Phoretic varroa were found equally on bees with and without tracheal mite infestations, but bees parasitized by varroa during development were almost twice as likely to have tracheal mite infestations as bees with no varroa parasitism, 63.9 % and 35.5 %, respectively. These results indicate that these two parasites can have a biological interaction at the level of individual bees that is detrimental to their host colonies.     

Influence of resistant honey bee hosts on the life history of the parasite Acarapis woodi

Non-infested, young adult honey bees (Apis mellifera L.) of two stocks were exposed to tracheal mites (Acarapis woodi (Rennie)) in infested colonies to determine how divergent levels of susceptibility in host bees differentially affect components of the mite life history. Test bees were retrieved after exposure and dissected to determine whether resistance is founded on the reduced success of gravid female (foundress) mites to enter the host tracheae, on the suppressed reproduction by foundress mites once established in host tracheae or on both. Cohorts of 30–60 bees from each of ten resistant colonies and eight susceptible colonies were tested in eight trials (three to five colonies per stock per trial) having exposure durations of 4, 9 or 21 days. The principal results were that lower percentages of resistant bees than of susceptible bees routinely became infested by foundress mites, individual infested susceptible bees often had more foundress mites than individual infested resistant bees did and mite fecundity was similar in both host types. The infestation percentage results corresponded well with similar results from a prior field test of these stocks and, thus, suggest that the bioassay is useful for assessing honey bee resistance to A. woodi.     

A sequential sampling scheme for detecting infestation levels of tracheal mites (Heterostigmata: Tarsonemidae) in honey bee (Hymenoptera: Apidae) colonies

The introduction of parasitic honey bee mites, the tracheal mite, Acarapis woodi (Rennie) in 1984 and the Varroa mite, Varroa jacobsoni, in 1987, has dramatically increased the winter mortality of honey bee, Apis mellifera L., colonies in many areas of the United States. Some beekeepers have minimized their losses by routinely treating their colonies with menthol, currently the only Environmental Protection Agency-approved and available chemical for tracheal mite control. Menthol is also expensive and can interfere with honey harvesting. Because of inadequate sampling techniques and a lack of information concerning treatment, this routine treatment strategy has increased the possibility that tracheal mites will develop resistance to menthol. It is important to establish economic thresholds and treat colonies with menthol only when treatment is warranted rather than treating all colonies regardless of infestation level. The use of sequential sampling may reduce the amount of time and effort expended in examining individual colonies and determining if treatment is necessary. Sequential sampling also allows statistically based estimates of the percentage of bees in standard Langstroth hives infested with mites while controlling for the possibility of incorrectly assessing the amount of infestation. On the average, sequential sampling plans require fewer observations (bees) to reach a decision for specified probabilities of type I and type II errors than are required for fixed sampling plans, especially when the proportion of infested bees is either very low or very high. We developed a sequential sampling decision plan to allow the user to choose specific economic injury levels and the probability of making type I and type II errors which can result inconsiderable savings in time, labor and expense.     

Varroa destructor infestation in untreated honey bee (Hymenoptera: Apidae) colonies selected for hygienic behavior

Honey bee (Apis mellifera L.) colonies bred for hygienic behavior were tested in a large field trial to determine if they were able to resist the parasitic mite Varroa destructor better than unselected colonies of"Starline" stock. Colonies bred for hygienic behavior are able to detect, uncap, and remove experimentally infested brood from the nest, although the extent to which the behavior actually reduces the overall mite-load in untreated, naturally infested colonies needed further verification. The results indicate that hygienic colonies with queens mated naturally to unselected drones had significantly fewer mites on adult bees and within worker brood cells than Starline colonies for up to 1 yr without treatment in a commercial, migratory beekeeping operation. Hygienic colonies actively defended themselves against the mites when mite levels were relatively low. At high mite infestations (>15% of worker brood and of adult bees), the majority of hygienic colonies required treatment to prevent collapse. Overall, the hygienic colonies had similar adult populations and brood areas, produced as much honey, and had less brood disease than the Starline colonies. Thus, honey bees bred for hygienic behavior performed as well if not better than other commercial lines of bees and maintained lower mite loads for up to one year without treatment.     

Population growth of Varroa destructor (Acari: Varroidae) in commercial honey bee colonies treated with beta plant acids

Varroa (Varroa destuctor Anderson and Trueman) populations in honey bee (Apis mellifera L.) colonies might be kept at low levels by well-timed miticide applications. HopGuard^® (HG) that contains beta plant acids as the active ingredient was used to reduce mite populations. Schedules for applications of the miticide that could maintain low mite levels were tested in hives started from either package bees or splits of larger colonies. The schedules were developed based on defined parameters for efficacy of the miticide and predictions of varroa population growth generated from a mathematical model of honey bee colony–varroa population dynamics. Colonies started from package bees and treated with HG in the package only or with subsequent HG treatments in the summer had 1.2–2.1 mites per 100 bees in August. Untreated controls averaged significantly more mites than treated colonies (3.3 mites per 100 bees). By October, mite populations ranged from 6.3 to 15.0 mites per 100 bees with the lowest mite numbers in colonies treated with HG in August. HG applications in colonies started from splits in April reduced mite populations to 0.12 mites per 100 bees. In September, the treated colonies had significantly fewer mites than the untreated controls. Subsequent HG applications in September that lasted for 3 weeks reduced mite populations to levels in November that were significantly lower than in colonies that were untreated or had an HG treatment that lasted for 1 week. The model accurately predicted colony population growth and varroa levels until the fall when varroa populations measured in colonies established from package bees or splits were much greater than predicted. Possible explanations for the differences between actual and predicted mite populations are discussed.     

Inheritance of resistance to Acarapis woodi (Acari: Tarsonemidae) in first-generation crosses of honey bees (Hymenoptera: Apidae)

The tendency of honey bees, Apis mellifera L, to become infested with tracheal mites, Acarapis woodi (Rennie), was measured in six different types of F1 colonies. The colonies were produced by mating a stock (Buckfast) known to resist mite infestation to each of five commercially available stocks and to a stock known to be susceptible to mites. Young uninfested bees from progeny and parent colonies were simultaneously exposed to mites in infested colonies, then retrieved and dissected to determine resultant mite infestations. Reduced infestations similar to but numerically greater than those of the resistant parent bees occurred in each of the six crosses made with resistant bees regardless of the relative susceptibility of the other parental stock. Reciprocal crosses between resistant and susceptible queens and drones proved equally effective in improving resistance. Therefore, allowing resistant stock queens to mate naturally with unselected drones, or nonresistant queens to mate with drones produced by pure or outcrossed resistant queens, can be used for improving resistance of production queens.     

Phenotypic variation in susceptibility of honey bees,Apis mellifera,to infestation by tracheal mites,Acarapis woodi

A laboratory bioassay was used to study phenotypic differences in susceptibility of honey bees,Apis mellifera L., to tracheal mites,Acarapis woodi Rennie. Significantly different infestation frequencies were found in bees from 23 colonies containing queens that were instrumentally inseminated with single drones. Queens and drones originated from a closed population composed of commercial stock from various areas of the United States.Mites were randomly distributed with respect to right and left prothoracic tracheae. Tracheae containing mites were no more or less attractive to migrating mites than non-infested tracheae. The same quantity of progeny per female was produced in tracheae containing 1–3 mites. Female mites apparently do not migrate a second time after egg laying begins.The degree of phenotypic variation suggests that selection of honey bees for tracheal mite resistance is feasible.     

Genotypic variability and relationships between mite infestation levels, mite damage, grooming intensity, and removal of Varroa destructor mites in selected strains of worker honey bees (Apis mellifera L.)

The objective of this study was to demonstrate genotypic variability and analyze the relationships between the infestation levels of the parasitic mite Varroa destructor in honey bee (Apis mellifera) colonies, the rate of damage of fallen mites, and the intensity with which bees of different genotypes groom themselves to remove mites from their bodies. Sets of paired genotypes that are presumably susceptible and resistant to the varroa mite were compared at the colony level for number of mites falling on sticky papers and for proportion of damaged mites. They were also compared at the individual level for intensity of grooming and mite removal success. Bees from the "resistant" colonies had lower mite population rates (up to 15 fold) and higher percentages of damaged mites (up to 9 fold) than bees from the "susceptible" genotypes. At the individual level, bees from the "resistant" genotypes performed significantly more instances of intense grooming (up to 4 fold), and a significantly higher number of mites were dislodged from the bees' bodies by intense grooming than by light grooming (up to 7 fold) in all genotypes. The odds of mite removal were high and significant for all "resistant" genotypes when compared with the "susceptible" genotypes. The results of this study strongly suggest that grooming behavior and the intensity with which bees perform it, is an important component in the resistance of some honey bee genotypes to the growth of varroa mite populations. The implications of these results are discussed.     

Brood-cell size does not influence the susceptibility of honey bees (Apis mellifera) to infestation by tracheal mites (Acarapis woodi)

Tracheal mites have been associated with the condition in honey bees that devastated colonies in Britain and Ireland in the early 1900s. The first outbreak of this condition, that became known as the ‘Isle of Wight’ disease, coincided with the period when brood-cell size was increased from about 5.0 mm to about 5.5 mm in width. We undertook an inoculation experiment over a 7-day period to establish if the act of increasing the brood-cell size could have triggered the onset of tracheal mites in honey bees. The standard-sized cells used had a cell width of 5.44 mm and the small-sized cells a width of 5.07 mm. Using callow (newly emerged) bees, from three colonies that had mixed cell sizes, we compared the susceptibility of bees reared in standard-sized cells with that of those raised in small-sized cells. The results indicated similar levels of female mite abundance (0.49 vs. 0.52 mites per bee) and mean fecundity (4.33 vs. 4.22 offspring per female mite), and produced no evidence of any difference in the overall susceptibility between the bees raised in the standard-sized cells versus small-sized brood cells.     

Honey bee colony collapse disorder is possibly caused by a dietary pyrethrum deficiency

Industrialized farming relies on bee keepers transporting hives to the vicinity of large areas of mono-crops for crop pollination. Hives are typically moved multiple times per growing season to satisfy the pollination need. A phenomenon wherein colonies of honey bees collapse in large numbers has been threatening crops in North America. Honey bees are hosts to at least two pathogenic mites; Varroa destructor and Acarapis woodi (a tracheal mite). Pyrethrums are a group of flowering plants which include Chrysanthemum coccineum, Chrysanthemum cinerariifolium, Chrysanthemum marschallii, and related species. These plants produce potent insecticides, also named pyrethrums, which are powerful mite toxins. We believe that a honey bee dietary deficiency of pyrethrums and other micro-nutrients from pyrethrum producing plants allows parasitic mites to either kill the honey bees directly or reduce honey bee resistance to other pathogens. Intermittent feeding of honey bees on pyrethrum producing plants might reverse or prevent colony collapse disorder.     

Comparative performance of two mite-resistant stocks of honey bees (Hymenoptera: Apidae) in Alabama beekeeping operations

The utility of USDA-developed Russian and varroa sensitive hygiene (VSH) honey bees, Apis mellifera L. (Hymenoptera: Apidae), was compared with that of locally produced, commercial Italian bees during 2004-2006 in beekeeping operations in Alabama, USA. Infestations of varroa mites, Varroa destructor Anderson & Truman (Acari: Varroidae), were measured twice each year, and colonies that reached established economic treatment thresholds (one mite per 100 adult bees in late winter; 5-10 mites per 100 adult bees in late summer) were treated with acaricides. Infestations of tracheal mites, Acarapis woodi (Rennie) (Acari: Tarsonemidae), were measured autumn and compared with a treatment threshold of 20% mite prevalence. Honey production was measured in 2005 and 2006 for colonies that retained original test queens. Throughout the three seasons of measurement, resistant stocks required less treatment against parasitic mites than the Italian stock. The total percentages of colonies needing treatment against varroa mites were 12% of VSH, 24% of Russian, and 40% of Italian. The total percentages requiring treatment against tracheal mites were 1% of Russian, 8% of VSH and 12% of Italian. The average honey yield of Russian and VSH colonies was comparable with that of Italian colonies each year. Beekeepers did not report any significant behavioral problems with the resistant stocks. These stocks thus have good potential for use in nonmigratory beekeeping operations in the southeastern United States.     

PCR-based detection of a tracheal mite of the honey bee Acarapis woodi

The effects of the tracheal mite Acarapis woodi on the health of honey bees have been neglected since the prevalence of Varroa mites to Apis mellifera colonies. However, tracheal mite infestation of honey bee colonies still occurs worldwide and could impose negative impact on apiculture. The detection of A. woodi requires the dissection of honey bees followed by microscopic observation of the tracheal sacs. We thus developed PCR methods to detect A. woodi. These methods facilitate rapid and sensitive detection of A. woodi in many honey bee samples for epidemiologic surveys.     

Regular dorsal dimples and damaged mites of <Emphasis Type="Italic">Varroa destructor</Emphasis> in some Iranian honey bees (<Emphasis Type="Italic">Apis mellifera</Emphasis>)

The frequency of damaged Varroa destructor Anderson and Trueman (Mesostigmata: Varroidae) found on the bottom board of hives of the honey bee, Apis mellifera L. (Hymenoptera: Apidae) has been used as an indicator of the degree of tolerance or resistance of honey bee colonies against mites. However, it is not clear that this measure is adequate. These injuries should be separated from regular dorsal dimples that have a developmental origin. To investigate damage to Varroa mites and regular dorsal dimples, 32 honey bee (A. mellifera) colonies were selected from four Iranian provinces: Isfahan, Markazi, Qazvin, and Tehran. These colonies were part of the National Honey bee Breeding Program that resulted in province-specific races. In April, Varroa mites were collected from heavily infested colonies and used to infest the 32 experimental colonies. In August, 20 of these colonies were selected (five colonies from each province). Adult bees from these colonies were placed in cages and after introducing mites, damaged mites were collected from each cage every day. The average percentage of injured mites ranged from 0.6 to 3.0% in four provinces. The results did not show any statistical differences between the colonies within provinces for injuries to mites, but there were some differences among province-specific lines. Two kinds of injuries to the mites were observed: injuries to legs and pedipalps, and injuries to other parts of the body. There were also some regular dorsal dimples on dorsal idiosoma of the mites that were placed in categories separate from mites damaged by bees. This type of classification helps identifying damage to mites and comparing them with developmental origin symptoms, and may provide criteria for selecting bees tolerant or resistant to this mite.     

Host preference of the honey bee tracheal mite (Acarapis woodi (Rennie))

Field and laboratory bioassays were used to test the preference of the honey bee tracheal mite,Acarapis woodi (Rennie), for drones versus workers. Groups of newly-emerged drones and workers were marked and introduced into either heavily infested colonies (field bioassays) or into the cages of infested bees obtained from the field colonies (laboratory bioassays). Seven days later all of the marked bees in each bioassay were removed. The numbers of mites of each life stage in each drone or worker target bee of each experiment were quantified. Mite prevalence values for the two castes were not found to differ significantly for either experiment. However, the caste of the target bee was shown to influence the migration of the adult female mites. Drones contained a greater number of migratory female mites and greater total numbers of all mite stages as compared to workers. These results indicate that migrating female mites preferentially infest drones and suggest that the role of drones in the dissemination and population dynamics of the tracheal mite needs to be examined further.     

Effect of some characters on the population growth of mite Varroa jacobsoni in Apis mellifera L colonies and results of a bi-directional selection

Two lines of honey bees ( Apis mellifera ligustica ) were selectively propagated by instrumental insemination using the population growth of the Varroa mite as a criteria. Different infestation rates are at least partially genetic since selection produced significant bi-directional differences between lines over a period of three subsequent generations. There was no correlation between several behavioural and physiological characteristics which are potentially associated with Varroa resistance (hygienic behaviour, physical damage to mites, infertility of the intruding mites) and the development of the Varroa population after artificial infestation. There was a positive significant correlation between the total mites in the colonies and the amount of reared brood. Colony infestation was also positively correlated with the amount of honey harvested.     

Caste, Sex and Strain of Honey Bees (Apis mellifera) Affect Infestation with Tracheal Mites (Acarapis woodi)*

Worker honey bees from genetic strains selected for being resistant (R) or susceptible (S) to tracheal mites typically show large differences in infestation in field colonies and in bioassays that involve controlled exposure to infested bees. We used bioassays exposing newly emerged individuals to infested workers to compare the propensity for tracheal mites to infest queens, drones and workers from R and S colonies. In tests with queens, newly emerged R and S queens were either simultaneously confined in infested colonies (n = 95 and 87 respectively), or individually caged with groups of 5–20 infested workers (n = 119 and 115 respectively). Mite prevalence (percentage of individuals infested) and abundance (foundress mites per individual) after 4–6 days did not differ between R and S queens. In another test, five newly emerged drones and workers from both an R and an S colony, and a queen of one of the two strains, were caged in each of 38 cages with 20 g of workers infested at 60–96% prevalence. Infestations of the R queens (n = 17) and S queens (n = 19) did not differ significantly, but R workers had half the mite abundance of S workers, while R drones received about a third more migrating mites than S drones. In tests to evaluate possible mechanisms, removal of one mesothoracic leg from R and S workers resulted in 2- to 10-fold increase in mite abundance on the treated side, but excising legs did not affect infestation of the corresponding tracheae in drones. This suggests that differences in infestation between R and S workers, but not drones, are largely determined by their ability to remove mites through autogrooming. If autogrooming is the primary mechanism of colony resistance to tracheal mites, selection for resistance to tracheal mites using infestation of hemizygous drones may be inefficient. *The U.S. Government’s right ot retain a non-exclusive, royalty-free licence in and to any copyright is acknowledged.     

Expression of Varroa sensitive hygiene (VSH) in commercial VSH honey bees (Hymenoptera: Apidae)

We tested six commercial sources of honey bees, Apis mellifera L. (Hymenoptera: Apidae), whose breeding incorporated the trait of Varroa sensitive hygiene (VSH). VSH confers resistance to the parasitic mite Varroa destructor Anderson & Trueman by enhancing the ability of the bees to hygienically remove mite-infested brood. VSH production queens (i.e., queens commercially available for use in beekeepers' production colonies) from the six sources were established in colonies which later were measured for VSH. Their responses were compared with those of colonies with three other types of queens, as follows: VSH queens from the selected closed population maintained by USDA-ARS for research and as a source of breeding germplasm, queens from the cooperating commercial distributor of this germplasm, and queens of a commercial, mite-susceptible source. The reduction of mite infestation in brood combs exposed to test colonies for 1 wk differed significantly between groups. On average, colonies with VSH production queens reduced infestation by 44%. This group average was intermediate between the greater removal by pure ARS VSH (76%) and the cooperators' breeding colonies (64%), and the lesser removal by susceptible colonies (7%). VSH production colonies from the different sources had variable expression of hygiene against mites, with average reduced infestations ranging from 22 to 74%. In addition, infertility was high among mites that remained in infested cells in VSH breeder colonies from ARS and the commercial distributor but was lower and more variable in VSH production colonies and susceptible colonies. Commercial VSH production colonies supply mite resistance that generally seems to be useful for beekeeping. Resistance probably could be improved if more VSH drones sources were supplied when VSH production queens are being mated.