Identifying the cellular mechanisms of symbiont-induced epithelial morphogenesis in the squid-Vibrio association

• Published in: The Biological bulletin (Lancaster) Vol. 226; no. 1; p. 56
• Main Authors: Koropatnick, Tanya, Goodson, Michael S, Heath-Heckman, Elizabeth A C, McFall-Ngai, Margaret
• Format: Journal Article
• Language: English
• Published: United States 01.02.2014
• Subjects: Actin Cytoskeleton - metabolism; Aliivibrio fischeri - physiology; Animals; Apoptosis; Decapodiformes - cytology; Decapodiformes - enzymology; Decapodiformes - growth & development; Decapodiformes - microbiology; Epithelial Cells - cytology; Epithelial Cells - enzymology; Host-Pathogen Interactions - physiology; Matrix Metalloproteinases - metabolism; Microscopy, Confocal; Morphogenesis - physiology; Symbiosis
• ISSN: 1939-8697
• DOI: 10.1086/BBLv226n1p56

The symbiotic association between the Hawaiian bobtail squid Euprymna scolopes and the luminous marine bacterium Vibrio fischeri provides a unique opportunity to study epithelial morphogenesis. Shortly after hatching, the squid host harvests bacteria from the seawater using currents created by two elaborate fields of ciliated epithelia on the surface of the juvenile light organ. After light organ colonization, the symbiont population signals the gradual loss of the ciliated epithelia through apoptosis of the cells, which culminates in the complete regression of these tissues. Whereas aspects of this process have been studied at the morphological, biochemical, and molecular levels, no in-depth analysis of the cellular events has been reported. Here we describe the cellular structure of the epithelial field and present evidence that the symbiosis-induced regression occurs in two steps. Using confocal microscopic analyses, we observed an initial epithelial remodeling, which serves to disable the function of the harvesting apparatus, followed by a protracted regression involving actin rearrangements and epithelial cell extrusion. We identified a metal-dependent gelatinolytic activity in the symbiont-induced morphogenic epithelial fields, suggesting the involvement of Zn-dependent matrix metalloproteinase(s) (MMP) in light organ morphogenesis. These data show that the bacterial symbionts not only induce apoptosis of the field, but also change the form, function, and biochemistry of the cells as part of the morphogenic program.