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. 2020 Oct 30;11:577481. doi: 10.3389/fmicb.2020.577481

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Copyright © 2020 Cano, Ryder, Webb, Jones, Brosnahan, Carrasco, Bodinier, Furones, Pretto, Carella, Chollet, Arzul, Cheslett, Collins, Lohrmann, Valdivia, Ward, Carballal, Villalba, Marigómez, Mortensen, Christison, Kevin, Bustos, Christie, Green and Feist.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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In situ hybridization analysis of intracellular microcolonies of bacteria (IMC) and extracellular bacterial aggregates in mollusks using a 16S rRNA gene probe generated with a 527 bp fragment of the king scallop Endozoicomonas-like organism (KX780138). Specific dark blue labeling (arrows) observed either in digestive gland (A,C,D) or gill section (B,E,F) of (A) Peruvian scallop Argopecten purpuratus, Chile; (B) common cockle Cerastoderma edulis, United Kingdom; (C) smooth clam Callista chione, Italy; (D) Mediterranean limpet Patella caerulea, Italy; (E) Chilean mussel Mytilus chilensis Chile; and (F) king scallop Pecten maximus, United Kingdom.