Improvement of identification methods for honeybee specific Lactic Acid Bacteria; future approaches

Honeybees face many parasites and pathogens and consequently rely on a diverse set of individual and group-level defenses to prevent disease. The crop microbiota of Apis mellifera, composed of 13 Lactic Acid Bacterial (LAB) species within the genera Lactobacillus and Bifidobacterium, form a benefici...

Full description

Saved in:
Bibliographic Details
Published inPloS one Vol. 12; no. 3; p. e0174614
Main Authors Lamei, Sepideh, Hu, Yue O. O., Olofsson, Tobias C., Andersson, Anders F., Forsgren, Eva, Vásquez, Alejandra
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 27.03.2017
Public Library of Science (PLoS)
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Honeybees face many parasites and pathogens and consequently rely on a diverse set of individual and group-level defenses to prevent disease. The crop microbiota of Apis mellifera, composed of 13 Lactic Acid Bacterial (LAB) species within the genera Lactobacillus and Bifidobacterium, form a beneficial symbiotic relationship with each other and the honeybee to protect their niche and their host. Possibly playing a vital role in honeybee health, it is important that these honeybee specific Lactic Acid Bacterial (hbs-LAB) symbionts can be correctly identified, isolated and cultured, to further investigate their health promoting properties. We have previously reported successful identification to the strain level by culture-dependent methods and we recently sequenced and annotated the genomes of the 13 hbs-LAB. However, the hitherto applied techniques are unfortunately very time consuming, expensive and not ideal when analyzing a vast quantity of samples. In addition, other researchers have constantly failed to identify the 13 hbs-LAB from honeybee samples by using inadequate media and/or molecular techniques based on 16S rRNA gene sequencing with insufficient discriminatory power. The aim of this study was to develop better and more suitable methods for the identification and cultivation of hbs-LAB. We compared currently used bacterial cultivation media and could for the first time demonstrate a significant variation in the hbs-LAB basic requirements for optimal growth. We also present a new bacterial identification approach based on amplicon sequencing of a region of the 16S rRNA gene using the Illumina platform and an error correction software that can be used to successfully differentiate and rapidly identify the 13 hbs-LAB to the strain level.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
Competing Interests: I have read the journal's policy and two of the authors of this manuscript have the following competing interests: Alejandra Vásquez and Tobias C. Olofsson hold stocks and are funders of a Lund University spin-off company called ConCellae. They are inventors of one granted patent with number WO 2008/136730 and four patents pending regarding commercial applications of the lactic acid bacteria from honeybees. This company has developed products based on these bacteria. However, ConCellae has not been involved in any of the research activities concerning the present study. These do not alter our adherence to PLOS ONE policies on sharing data and materials.
Conceptualization: SL YOOH TCO AFA EF AV.Formal analysis: SL YOOH TCO AFA EF AV.Investigation: SL YOOH TCO AFA EF AV.Methodology: SL YOOH TCO AFA EF AV.Project administration: SL YOOH TCO AFA EF AV.Resources: SL YOOH TCO AFA EF AV.Software: SL YOOH TCO AFA EF AV.Supervision: AV EF AFA.Validation: SL YOOH TCO AFA EF AV.Visualization: SL YOOH TCO AFA EF AV.Writing – original draft: SL YOOH TCO AFA EF AV.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0174614