In-hive variation of the gut microbial composition of honey bee larvae and pupae from the same oviposition time

• Published in: BMC microbiology Vol. 19; no. 1; pp. 110 - 8
• Main Authors: Hroncova, Zuzana, Killer, Jiri, Hakl, Josef, Titera, Dalibor, Havlik, Jaroslav
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 24.05.2019; BioMed Central; BMC
• Subjects: Abundance; Actinobacteria; Agriculture; Animal behavior; Animals; Apis mellifera; Bacteria; Bacteria - classification; Bacteria - genetics; Bacteria - isolation & purification; Bacteroidetes; Bees; Bees - anatomy & histology; Bees - microbiology; Black pupae; Composition; Defecation; European honeybee; Firmicutes; Gammaproteobacteria; Gastrointestinal Microbiome; Genetic aspects; Health; Honey; Honey bee larvae; Insects; Intestinal microflora; Larva - anatomy & histology; Larva - microbiology; Larvae; Microbiomes; Microbiota; Microbiota (Symbiotic organisms); Microorganisms; Oviposition; Phylogeny; Pupa - anatomy & histology; Pupa - microbiology; Pupae; Pupation; RNA, Ribosomal, 16S - genetics; Sequence Analysis, DNA - methods; Studies; Time Factors; United States > US; Black pupae; Gammaproteobacteria; qRT-PCR; Honey bee larvae; Actinobacteria; Bacteroidetes; Firmicutes
• ISSN: 1471-2180; 1471-2180
• DOI: 10.1186/s12866-019-1490-y

Knowledge of microbiota composition, persistence, and transmission as well as the overall function of the bacterial community is important and may be linked to honey bee health. This study aimed to investigate the inter-individual variation in the gut microbiota in honey bee larvae and pupae. Individual larvae differed in the composition of major bacterial groups. In the majority of 5th instar bees, Firmicutes showed predominance (70%); however, after larval defecation and during pupation, the abundance decreased to 40%, in favour of Gammaproteobacteria. The 5th instar larvae hosted significantly more (P < 0.001) Firmicutes than black pupae. Power calculations revealed that 11 and 18 replicate-individuals, respectively, were required for the detection of significant differences (P < 0.05) in the Bacteroidetes and Firmicutes abundance between stages, while higher numbers of replicates were required for Actinobacteria (478 replicates) and Gammaproteobacteria (111 replicates). Although sample processing and extraction protocols may have had a significant influence, sampling is very important for studying the bee microbiome, and the importance of the number of individuals pooled in samples used for microbiome studies should not be underestimated.