Pub Date : 2025-02-12DOI: 10.1007/s13592-025-01147-2
Giulia Molinatto, Fanny Mondet, Cristina Marzachi, Cedric Alaux, Eleonora Bassi, Virginie Dievart, Massimiliano Gotti, Giovanni Guido, Pascal Jourdan, Guillaume Kairo, Alban Maisonnasse, Lucie Michel, Mathilde Peruzzi, Marco Porporato, Michele Tagliabue, Andre Kretzschmar, Domenico Bosco, Aulo Manino
Viruses occupy a large proportion of the pathogen communities within honey bee colonies, with more than 80 species detected in Apis mellifera. Honey bee viruses are globally distributed and several species have been linked to honey bee diseases that threaten colony health. However, less is known about the ecology and epidemiology of viruses within honey bee colonies, and in particular whether a link exists between virus temporal dynamics and seasonal variations and/or colony dynamics. Using a large-scale longitudinal survey conducted over three years, we report the prevalence and abundance of deformed wing virus, acute bee paralysis virus, black queen cell virus, chronic bee paralysis virus and sacbrood virus (DWV, ABPV complex, BQCV, CBPV and SBV) in more than 300 colonies located in two different environments of southern Europe (Provence in France, Piemonte in Italy), and exhibiting contrasted climatic conditions. Monthly measurements performed throughout the beekeeping seasons indicate distinct seasonal trends in prevalence and abundance of the five virus species: DWV, SBV and ABPV complex displayed marked seasonal variations, that were similar in both environments tested. We also highlight the link between seasonal virus dynamics and colony dynamics for SBV/BQCV, and parasite dynamics for DWV. This study improves our understanding of virus ecology within honey bee colonies.
{"title":"Seasonal variations of the five main honey bee viruses in a three-year longitudinal survey","authors":"Giulia Molinatto, Fanny Mondet, Cristina Marzachi, Cedric Alaux, Eleonora Bassi, Virginie Dievart, Massimiliano Gotti, Giovanni Guido, Pascal Jourdan, Guillaume Kairo, Alban Maisonnasse, Lucie Michel, Mathilde Peruzzi, Marco Porporato, Michele Tagliabue, Andre Kretzschmar, Domenico Bosco, Aulo Manino","doi":"10.1007/s13592-025-01147-2","DOIUrl":"10.1007/s13592-025-01147-2","url":null,"abstract":"<div><p>Viruses occupy a large proportion of the pathogen communities within honey bee colonies, with more than 80 species detected in <i>Apis mellifera</i>. Honey bee viruses are globally distributed and several species have been linked to honey bee diseases that threaten colony health. However, less is known about the ecology and epidemiology of viruses within honey bee colonies, and in particular whether a link exists between virus temporal dynamics and seasonal variations and/or colony dynamics. Using a large-scale longitudinal survey conducted over three years, we report the prevalence and abundance of deformed wing virus, acute bee paralysis virus, black queen cell virus, chronic bee paralysis virus and sacbrood virus (DWV, ABPV complex, BQCV, CBPV and SBV) in more than 300 colonies located in two different environments of southern Europe (Provence in France, Piemonte in Italy), and exhibiting contrasted climatic conditions. Monthly measurements performed throughout the beekeeping seasons indicate distinct seasonal trends in prevalence and abundance of the five virus species: DWV, SBV and ABPV complex displayed marked seasonal variations, that were similar in both environments tested. We also highlight the link between seasonal virus dynamics and colony dynamics for SBV/BQCV, and parasite dynamics for DWV. This study improves our understanding of virus ecology within honey bee colonies.</p></div>","PeriodicalId":8078,"journal":{"name":"Apidologie","volume":"56 1","pages":""},"PeriodicalIF":2.4,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143388747","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-02-11DOI: 10.1007/s13592-025-01154-3
Paloma Quirino Rocha, Lorena Andrade Nunes, Kátia Peres Gramacho, Edilson Divino de Araujo
The analysis of morphology and body asymmetry in organisms can reveal the challenges faced during development. Populations of Varroa destructor exhibit morphological plasticity, but there is a lack of standardization in body structures and measurements used in research. This study aimed to identify, through geometric morphometrics, a body structure that allows for a standardized study of the morphological variations and fluctuating asymmetry of V. destructor in different environmental contexts. To this end, we analyzed the morphology of mites infesting colonies of Africanized honeybees in two contexts: different levels of hygienic behavior in the colonies and distinct environments (Caatinga and Atlantic Forest). Asymmetry is specifically assessed in the context of these environments. In colonies with differentiated hygienic behaviors, the metapodal shield showed a higher classification rate between groups (70%) than the genitoventral shield (64%), and it was the only structure that showed significant size differences between groups (p < 0.001). In mites from different geographic regions, the metapodal shield also exhibited a higher classification rate (78%) than the genitoventral shield (65%), with no significant difference in the size of the shields between the mite populations. Significant differences in fluctuating asymmetry were observed in the shape and size (p < 0.001) of the pair of metapodal shields and the shape of the genitoventral shield (p < 0.001). The results provide important methodological and ecological insights, highlighting the metapodal shield as a reliable structure for assessing shape, size, and fluctuating asymmetry. This standardization can improve consistency across studies and parasite monitoring.
{"title":"Metapodal shields: standardizing the morphometric study of Varroa destructor","authors":"Paloma Quirino Rocha, Lorena Andrade Nunes, Kátia Peres Gramacho, Edilson Divino de Araujo","doi":"10.1007/s13592-025-01154-3","DOIUrl":"10.1007/s13592-025-01154-3","url":null,"abstract":"<div><p>The analysis of morphology and body asymmetry in organisms can reveal the challenges faced during development. Populations of <i>Varroa destructor</i> exhibit morphological plasticity, but there is a lack of standardization in body structures and measurements used in research. This study aimed to identify, through geometric morphometrics, a body structure that allows for a standardized study of the morphological variations and fluctuating asymmetry of <i>V. destructor</i> in different environmental contexts. To this end, we analyzed the morphology of mites infesting colonies of Africanized honeybees in two contexts: different levels of hygienic behavior in the colonies and distinct environments (Caatinga and Atlantic Forest). Asymmetry is specifically assessed in the context of these environments. In colonies with differentiated hygienic behaviors, the metapodal shield showed a higher classification rate between groups (70%) than the genitoventral shield (64%), and it was the only structure that showed significant size differences between groups (<i>p</i> < 0.001). In mites from different geographic regions, the metapodal shield also exhibited a higher classification rate (78%) than the genitoventral shield (65%), with no significant difference in the size of the shields between the mite populations. Significant differences in fluctuating asymmetry were observed in the shape and size (<i>p</i> < 0.001) of the pair of metapodal shields and the shape of the genitoventral shield (<i>p</i> < 0.001). The results provide important methodological and ecological insights, highlighting the metapodal shield as a reliable structure for assessing shape, size, and fluctuating asymmetry. This standardization can improve consistency across studies and parasite monitoring.</p></div>","PeriodicalId":8078,"journal":{"name":"Apidologie","volume":"56 1","pages":""},"PeriodicalIF":2.4,"publicationDate":"2025-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143388683","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}