The detection of honey bee (Apis mellifera)-associated viruses in ants.

Interspecies virus transmission involving economically important pollinators, including honey bees (Apis mellifera), has recently sparked research interests regarding pollinator health. Given that ants are common pests within apiaries in the southern U.S., the goals of this study were to (1) survey ants found within or near managed honey bee colonies, (2) document what interactions are occurring between ant pests and managed honey bees, and 3) determine if any of six commonly occurring honey bee-associated viruses were present in ants collected from within or far from apiaries. Ants belonging to 14 genera were observed interacting with managed honey bee colonies in multiple ways, most commonly by robbing sugar resources from within hives. We detected at least one virus in 89% of the ant samples collected from apiary sites (n = 57) and in 15% of ant samples collected at non-apiary sites (n = 20). We found that none of these ant samples tested positive for the replication of Deformed wing virus, Black queen cell virus, or Israeli acute paralysis virus, however. Future studies looking at possible virus transmission between ants and bees could determine whether ants can be considered mechanical vectors of honey bee-associated viruses, making them a potential threat to pollinator health.

Initial Exposure of Wax Foundation to Agrochemicals Causes Negligible Effects on the Growth and Winter Survival of Incipient Honey Bee (Apis mellifera) Colonies.

Widespread use of agrochemicals in the U.S. has led to nearly universal contamination of beeswax in honey bee hives. The most commonly found agrochemicals in wax include beekeeper-applied miticides containing tau-fluvalinate, coumaphos, or amitraz, and field-applied pesticides containing chlorothalonil or chlorpyrifos. Wax contaminated with these pesticides negatively affects the reproductive quality of queens and drones. However, the synergistic effects of these pesticides on the growth and survival of incipient colonies remain understudied. We established new colonies using frames with wax foundation that was pesticide free or contaminated with field-relevant concentrations of amitraz alone, a combination of tau-fluvalinate and coumaphos, or a combination of chlorothalonil and chlorpyrifos. Colony growth was assessed by estimating comb and brood production, food storage, and adult bee population during a colony's first season. We also measured colony overwintering survival. We found no significant differences in colony growth or survivorship between colonies established on pesticide-free vs. pesticide-laden wax foundation. However, colonies that had Varroa destructor levels above 3% in the fall were more likely to die over winter than those with levels below this threshold, indicating that high Varroa infestation in the fall played a more important role than initial pesticide exposure of wax foundation in the winter survival of newly established colonies.

Expression of Separate Proteins in the Same Plant Leaves and Cells Using Two Independent Virus-Based Gene Vectors.

Plant viral vectors enable the expression of proteins at high levels in a relatively short time. For many purposes (e.g., cell biological interaction studies) it may be desirable to express more than one protein in a single cell but that is often not feasible when using a single virus vector. Such a co-expression strategy requires the simultaneous delivery by two compatible and non-competitive viruses that can co-exist to each express a separate protein. Here, we report on the use of two agro-launchable coat-protein gene substitution GFP-expressing virus vector systems based on Tomato bushy stunt virus (TBSV) referred to as TG, and Tobacco mosaic virus (TMV) annotated as TRBO-G. TG expressed GFP in Nicotiana benthamiana, tomato, lettuce and cowpea, whereas expression from TRBO-G was detected only in the first two species. Upon co-infiltration of the two vectors co-expression was monitored by: molecular detection of the two slightly differently sized GFPs, suppressor-complementation assays, and using TG in combination with TRBO-RFP. All the results revealed that in N. benthamiana and tomato the TBSV and TMV vectors accumulated and expressed proteins in the same plants, the same leaves, and in the same cells. Therefore, co-expression by these two vectors provides a platform for fast and high level expression of proteins to study their cell biology or other properties.