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INTRODUCTION
Invertebrates employ non-adaptive, germline-encoded immunity that
efficiently identifies allogeneic and xenogeneic attributes through
the expression of a multiplicity of cellular and morphological
phenomena (Rinkevich, 1999). The literature provides ample
evidence for the crucial role of invertebrates’ innate immunity in
manifesting these highly specified arrays of effector mechanisms
(Loker et al., 2004) and the importance of high polymorphism for
their efficient maintenance and expression (Rinkevich, 2004;
Cadavid et al., 2004). While allorecognition is one of the major
characteristics of invertebrate immunity, its qualities and the events
expressed morphologically by the effector arms vary fundamentally
between different taxa, although all share the hallmark nature of
precise discriminatory capability between ‘self’ and ‘non-self’, even
between closely related conspecifics (Grosberg, 1988; Leddy and
Green, 1991; Rinkevich, 1996; Rinkevich, 1999; Schwarz et al.,
2007). Historecognition of ‘self’ versus ‘non-self’, however, may
represent two separate avenues for immunity, either by detecting
the presence or absence of attributes that define self or by detecting
the presence or absence of non-self attributes (Neigel, 1988).
As in other invertebrates, it is above dispute that self/non-self
recognition is hallmark to cnidarian immunity (Neigel, 1988; Leddy
and Green, 1991; Rinkevich, 1996; Rinkevich, 1999), albeit without
being able to distinguish between the two different immunological
routes. Literature on cnidarian immunity documents that
allorecognition and xenorecognition are naturally expressed
phenomena that result in either fusion between contacting allogeneic
partners in a wide array of histoincompatible outcomes or
culminating in various ‘rejection’ phenomena (Rinkevich and Loya,
1983; Hidaka, 1985; Chadwick-Furman and Rinkevich, 1994;
Rinkevich, 1996; Rinkevich, 1999; Frank et al., 1997; Hidaka et
al., 1997; Amar et al., 2008). All cnidarian’s immune characteristics
implicate innate immunity parameters as no true adaptive
components have been identified in these innate systems (Rinkevich,
1999; Loker et al., 2004; Dunn, 2009), although elements suggesting
memory and specificity were documented in several cases
(Rinkevich, 1996; Rinkevich, 1999). However, as in other
invertebrate taxa (Magor et al., 1999), the major obstacle for finding
a true evolutionary relationship is that homologous molecules
operating in non-identical systems may have different constraints
on structural conservation and, therefore, may display distinct
patterns of activities.
Working on hard and soft corals’ immunity, definitive studies
(Hidaka, 1985; Frank et al., 1997; Hidaka et al., 1997; Barki et al.,
2002) showed that high proportions of allogeneic interactions between
young partners culminated in fusions, an outcome not documented
when branches of adult colonies were paired. This is of special interest
because allorecognition is thought to reduce costly tissue fusion with
individuals other than self (Rinkevich, 1999). Fusion between
conspecifics is not restricted to corals and is commonly found even
in hydrozoans (Frank and Rinkevich, 1994; Cadavid et al., 2004).
Fusion between juveniles of scleractinian corals (the formation of
chimeric entities) were first detailed by Hidaka (Hidaka, 1985) in
Pocillopora damicornis and then in other pocilloporid corals like
Stylophora pistillata (Frank et al., 1997), Seriatopora caliendrum and
Seriatopora hystrix (Nozawa and Loya, 2005). Histocompatible
The Journal of Experimental Biology 213, 535-540
© 2010. Published by The Company of Biologists Ltd
doi:10.1242/jeb.039529
Mounting of erratic histoincompatible responses in hermatypic corals: a multi-year
interval comparison
K.-O. Amar* and B. Rinkevich
Israel Oceanographic and Limnological Research, National Institute of Oceanography,Tel-Shikmona, PO Box 8030, Haifa 31080,
Israel
*Author for correspondence (sunshine@ocean.org.il)
Accepted 29 October 2009
SUMMARY
Studies on allorecognition in the phylum Cnidaria have disclosed complex arrays of effector mechanisms, specificity and
competency to distinguish precisely between self and non-self attributes, and have revealed the existence of allogeneic maturity.
Here we studied allo-responses between young Stylophora pistillata colonies by following 517 allogeneic interactions between
naturally settled kin aggregates and by establishing 417 forced allogeneic and autogeneic assays made of solitarily settled spat
that were cut into two similar size subclones, of which one had been challenged allogeneically. Fused assays were exposed to a
second allorecognition challenge, made of three allogeneic types. Whereas about half of the kin allogeneic interactions led to
tissue fusions and chimera formations, none of the 83 non-sibling pair combinations were histocompatible. In contrast to
previous results we recorded rejections between siblings at the age of less than two months. More challenging, we documented
cases of fusions between interacting siblings at ages older than one-year-old partners, all differing from a previous study made
on the same coral population more than a decade ago. Similar erratic histoincompatible responses were recorded in other
pocilloporid species. We suggest that these results reflect reduced genetic heterogeneity caused by chronic anthropogenic
impacts on shallow water coral populations where planulae originating from the same mother colony or from different mother
colonies that are genetically related share increasing parts of their genomes. Offspring born to related parents may also reveal an
increase in genomic homozygosity, and altogether impose erratic alloimmunity.
Key words: allorecognition, corals, histocompatibility, fusion, rejection.
THE JOURNAL OF EXPERIMENTAL BIOLOGY