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Clinical case: Impact of Varroa on bee colony performance

Table of contents

Varroosis, caused by Varroa destructor, is a major challenge to honey bee colonies (Apis mellifera). Even with the development and successful implementation of various management strategies to control this parasite, concerns persist about the long-term effects of initial infestations on colony health and productivity. 

In the Pays de la Loire region of France, the 2023-2024 beekeeping season was characterized by unfavorable climatic conditions, resulting in a poor spring harvest and necessitating additional feeding. This case study examines the persistence of varroosis signs in bee colonies despite effective management of Varroa infestation. Fourteen colonies were monitored from mid-August 2023 to spring 2024, using treatments such as Apivar®, Formicpro®, and Oxybee®. Results indicated that four colonies exhibited delayed development and persistent brood anomalies, while nine colonies progressed normally. Virological analyses revealed significant levels of DWV-B, BQCV, and SBV, and European foulbrood was confirmed in one colony. Despite reduced infestation levels, the negative long-term impacts on colony health, likely due to persistent viral infections and other factors such as queen age and nutritional deficiencies, underscored the need for proactive and continuous Varroa management throughout the season to ensure colony health and productivity. 

In colonies heavily infested the previous fall and successfully managed, how does Varroa continue its negative effects? 

Apiary History

The colonies are part of a multi-active beekeeper’s stock (about sixty colonies), with 14 of them being particularly monitored for Varroa counts on the bottom board from August 15th, 2023, to spring 2024. These colonies followed a “standard” production path in 2023 (rapeseed, all spring and summer flowers) without special parasite management during the season. The queens are from 2022 or 2023, with at least 35 kg of honey produced per hive.  

One of the monitoring objectives was to verify Varroa infestation levels in colonies managed “standardly” in the french region: production colonies with no biotechnical measures during the year and summer management after the harvest. Therefore, hive monitoring was deliberately initiated from August 15th. 

 

In 2022, the colonies received Apivar® management in summer and Oxybee® in winter (2022/2023). For summer 2023, management was adapted based on the parasitic loads observed during pre-counts from August 15th  to 26th  (bottom board method with bee vs, Apisfero scanner) or during clinical examination (signs of varroosis present or not). 

 

Treatments implemented: 

  • Apivar on August 26 for 10 weeks on less infested colonies (less than 10 Varroa per day during pre-counting) and without apparent clinical signs of varroosis, 
  • A Formicpro application on August 26 to quickly reduce an estimated high infestation (more than 10 Varroa per day or clinical signs present), followed by Apivar application for 9 weeks (same removal date for the strips in both groups). 
  • An oxalic acid-based treatment (Oxybee®) was applied on December 20, with fall monitoring for 15 days after application. 

 

Winter exit assessment (April 23, 2024) noted one colony dead (with signs of varroosis and an infestation of over 8000 Varroa during the counting period). Four colonies showed delayed development, with some exhibiting persistent brood anomalies despite “low” parasitic loads. One colony showed high Varroa falls (and persistent nymph mortality since the previous summer). These prompted the consultation. The other nine colonies continued their path normally without notable Varroa-related anomalies, with varying count results.  

A poor spring harvest was observed due to unfavorable climatic conditions in the region, requiring feeding for some colonies. 

Clinical examination and laboratory analysis

The raw results of cumulative falls during pre-counting are illustrated in Table 1 below (15 days before treatment), during treatment, up to 10 days after removal, 15 days after oxalic acid application, and in spring during the rapeseed honey flow. 

Table 1: Cumulative falls at different monitoring phases, in yellow, colonies receiving Formicpro for 7 days before Apivar® application.

During the August 2023 visits, anomalies in capped brood were identified in colonies 1, 2, 3, 4, 7, 8, 10, 11, and 12: nymph mortality at various developmental stages (pink to black eyes), with these anomalies limited in number (a few dozen cells scattered across brood frames), except for colony 10, which was more impacted and died in winter. A Varroa impact is probable given the signs and loads observed. Autumn visits showed persistence of these signs at lower frequencies. The spring visit (April 23) identified four lagging colonies still showing the same signs, while the other nine continued their path.

 

June 2, 2024 Visit:

Focused on four colonies: colonies 3, 4, 12, and 14. These showed persistent brood anomalies over time or delayed restarts in the spring visit (April 23rd). Except for colony 4, which always showed high counts, falls and counts on bees were within the season’s accepted norms. Nonetheless, varroosis or associated viral signs were observed: compact brood but with sacbrood-like larvae or dead nymphs at various stages, signs limited but persistent since the previous autumn. No signs on adult bees.

 

Details by colony:

Colony 3:

  • Delayed development since early spring visit: slowed laying associated with slow adult bee core growth, reduced capped brood frame expansion, the hive was on 4 frames on April 23rd, barely 5 frames on June 2nd, reserves were moderate (no deficiency) to strong at each visit.
  • The queen was from 2022, a supersedure attempt was observed on June 2nd (laying absent, old queen disappeared), identified as queen age-related and its consequences. Adult bee depopulation will prevent colony restart.

 

Colony 4: This colony was monitored for observed signs and consistently high parasite counts above the season’s accepted norm.

  • Development: the queen was on 7 frames on April 23rd with strong reserves and a strong population, multiple swarms occurred without queen replacement observed (no laying) on that day. Reduced adult bee population and significant brood reduction (only closed). That day, a lack of reserve buildup was observed with moderate to low honey and pollen quantities. Dozens of dead nymphs were noted with a high Varroa count possibly related to laying cessation and brood reduction.
  • The queen was from 2023.
  • An unsuccessful requeening led to depopulation in a colony showing persistent varroosis signs and high counts.

 

Colonies 12 and 14:

  • Successful requeening after swarming in each colony (over a month ago). These colonies showed moderate populations during the spring visit (April 23) with some dead nymphs and discrete Sacbrood Bee Virus (SBV) signs as well as larval damage possibly indicating European foulbrood in colony 14 (a few dozen cells on one frame). Queen replacement was planned but delayed, and the colonies swarmed in the meantime.
Image 1: Pupa in an alveolus being de-operculated, tongue stretched, abdomen shortened. This type of dead nymph can be found at various stages of development, with the same signs and sometimes atrophied wings in more advanced stages.

Colony 12:

  • No harvest and an empty super. Requeened. On 7 frames, low honey, moderate pollen. Population covers only half the surfaces of the 7 frames. Brood still spread across 6 frames, mostly closed, tight laying but hundreds of depressed or de-capping cells, dead nymphs at all stages, some larvae with SBV appearance.
  • Alcohol Varroa count 0.6/100 bees. Bottom board count: (June 2-11th: 6 Varroa).
Image 2: Brood observed in colony 12, with collapsed cells in the process of uncapping (sac-like larvae and dead pupae).
Images 3: Uncapped cells suspect of SBV (larvae will emerge with the typical appearance of sacciform brood, accumulation of liquid in a small sac).
Images 3: Uncapped cells suspect of SBV (larvae will emerge with the typical appearance of sacciform brood, accumulation of liquid in a small sac).

Samples taken for virus detection related to Varroa:

  • Results on asymptomatic live interior bees: Genomes of Deformed Wing Virus (DWV-B 2.2 x 10^8), Black Queen Cell Virus (BQCV 2.3 x 10^9), and Sacbrood Bee Virus (SBV 8.5 x 10^9) detected.
  • On the queen: Genome of Deformed Wing Virus (DWV-B > 1E+10 copies > limit of quantification), Black Queen Cell Virus (BQCV 3.2 x 107), and Sacbrood Bee Virus (SBV 1.0 x 106) detected.
  • On the brood: Genomes of Deformed Wing Virus (DWV-A < 2.5 x 103 and DWV-B < 1E+05) and Black Queen Cell Virus (BQCV 2.2 x 103) detected.

 

Note that all samples are virus carriers, but according to current standards, bees and the queen show the most significant viral infestations.

 

Colony 14:

  • Spring Harvest: Little harvest (2 or 3 frames of honey). One super three-quarters filled with honey, strong pollen quantity in the hive body.
  • Requeened: On 8 frames, 6 occupied by open and closed brood, two new waxes extended, tight laying but many sunken cells or abnormal larval colorations in open brood resembling European foulbrood.
  • Dead Nymphs: Found in sunken cells (various stages), mainly larvae with SBV appearance in closed brood and suspected European foulbrood in open brood.
  • Population: Strong, 8 frames covered both sides and overflow the partition, the supers (especially the first) are filled with bees.
  • Varroa Alcohol Count: 0.5 per hundred bees. Bottom board count (June 2-11th): 6 Varroa.

 

Virus and European Foulbrood Detection Samples:

  • On bees: Genomes of Deformed Wing Virus (DWV-B < 1E+05), Black Queen Cell Virus (BQCV 5.3 x 106), and Sacbrood Virus (SBV 1.9 x 107) detected.
  • On the queen: Genomes of Deformed Wing Virus (DWV-B 4.9 x 105), Black Queen Cell Virus (BQCV 3.8 x 106), and Sacbrood Virus (SBV 7.2 x 105) detected.
  • On the brood: Genomes of Deformed Wing Virus (DWV-A < 2.5 x 103 and DWV-B < 1E+05), Black Queen Cell Virus (BQCV 1.3 x 104), and Sacbrood Virus (SBV 1.2 x 105) detected.
  • Bacteria: Melissococcus plutonius (European foulbrood) detected in sick larvae.

 

Analyses confirm the presence of European foulbrood, all apiary matrices carry viruses at varying levels, including the recently born queen.

Discussion of Results

During the colony examination, and when interpretable, phoretic Varroa counts and natural mortality on bottom boards were within acceptable seasonal norms. However, persistently high mite falls on the bottom board of colony 4 raised concerns.

 

Testing for common viral agents yielded positive results with highly variable rates. While these results do not necessarily indicate a declared infection, they confirm the presence of viruses, even in newly born and laying queens from natural requeening.

 

Clinical signs observed could be attributed to DWV-B and SBV viruses, with European foulbrood confirmed in colony 14. It is also relevant to consider queen contamination. Although not unusual, in this case, queens were born less than two months ago, raising questions about vertical virus transmission.

Follow-up and discussion

At the end of wintering (2023/2024), 9 out of 14 colonies survived as healthy colonies ready to produce the following spring. The other 5 colonies were more severely affected:

  • One colony died due to varroosis.
  • Four colonies did not meet the criteria of a healthy colony (without signs of disease) and/or were not capable of production. Planned sanitary or zootechnical actions on these colonies were not carried out due to climatic factors and swarming.

 

It is crucial to emphasize that late treatment is always detrimental to colonies, impacting them in the long-term, ashighlighted here. By late summer 2023, most colonies had already reached a high parasitic threshold, posing a colony risk. Although management adaptation helped recover 2/3 of the colonies, the persistent damage initiated by Varroa and associated viruses remains evident.

 

It is also interesting to verify that once parasitic infestation is controlled, the colony may have experienced imbalances leading to super-organism disorganization, particularly from an immunological standpoint.

 

In this case, the 4 colonies showed variable evolutions:

  • Linked to viruses transmitted by Varroa and brood diseases resulting from these viruses.
  • Linked to persistent viral carriage within the colony (potentially all colonies) and vertical transmission in some (colonies 13, 14).
  • Linked to other diseases appearing (European foulbrood) in colonies already identified with brood anomalies (colony 14).
  • Linked to queen age (colony 3), requeening failures (colonies 3 and 4), and nutritional deficiencies, whether climate-related or not (colony 4).

These factors lead us to consider the overall immunity of the colony and the risks impacting it, with Varroa management being the cornerstone the previous summer.

 

In combating the parasite, proactive counting and visits have been shown to provide good predictions of colony health evolution. However, once colony´s equilibrium is too severely impacted, can the beekeeper still implement effective corrective measures?

 

Thus, this case study concludes with the need for anticipated parasite management throughout the season to keep parasitic loads below a critical threshold, protecting production, bee health, and colony health.

Acknowledgements

We would like to express our gratitude and thank Jean Luc DENECHERE for monitoring and contributing to the realization of this clinical case.

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