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. 2022 Apr 22;115(6):821–837. doi: 10.1007/s10482-022-01735-7

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© The Author(s) 2022

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 4 — Genotyping of all identified phylotypes isolated from BSFL gut microbiota, based on fingerprint pattern obtained by genomic fingerprinting using primers targeting BOX and (GTG)₅ repetitive elements. (GTG)₅-PCR was employed exclusively with Mammaliicoccus and Enterococcus phylotypes. Cluster analysis was performed in BioNumerics (Applied Maths) using UPGMA clustering, based on a dissimilarity matrices generated by the Pearson correlation. Bold isolates were identified through 16S rRNA gene sequencing. Blue and green dots represent the isolates cultured by direct plating and dilution-to-extinction cultivation. (Color figure online)