Abstract

In obligate symbioses, the host’s survival relies on the successful acquisition and maintenance of symbionts. Symbionts can either be transferred from parent to offspring via direct inheritance (vertical transmission) or acquired anew each generation from the environment (horizontal transmission). With vertical symbiont transmission, progeny benefit by not having to search for their obligate symbionts, and, with symbiont inheritance, a mechanism exists for perpetuating advantageous symbionts. But, if the progeny encounter an environment that differs from that of their parent, they may be disadvantaged if the inherited symbionts prove suboptimal. Conversely, while in horizontal symbiont acquisition host survival hinges on an unpredictable symbiont source, an individual host may acquire genetically diverse symbionts well suited to any given environment. In horizontal acquisition, however, a potentially advantageous symbiont will not be transmitted to subsequent generations. Adaptation in obligate symbioses may require mechanisms for both novel symbiont acquisition and symbiont inheritance. Using denaturing-gradient gel electrophoresis and real-time PCR, we identified the dinoflagellate symbionts (genus Symbiodinium) hosted by the Red Sea coral Stylophora pistillata throughout its ontogenesis and over depth. We present evidence that S. pistillata juvenile colonies may utilize both vertical and horizontal symbiont acquisition strategies. By releasing progeny with maternally derived symbionts, that are also capable of subsequent horizontal symbiont acquisition, coral colonies may acquire physiologically advantageous novel symbionts that are then perpetuated via vertical transmission to subsequent generations. With symbiont inheritance, natural selection can act upon the symbiotic variability, providing a mechanism for coral adaptation.

Highlights

  • Obligate mutualistic symbioses are ubiquitous on earth and play pivotal roles in many ecosystems [1,2]

  • The Symbiodinium types present in S. pistillata samples collected from shallow (2–6 m) and deep (24–26 m) water habitats were identified using denaturing gradient gel electrophoresis (DGGE) (Figure 1)

  • Subsequent sequencing of the dominant bands confirmed that all shallow-water adults and their planulae (N = 266) contained Symbiodinium type A1

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Summary

Introduction

Obligate mutualistic symbioses are ubiquitous on earth and play pivotal roles in many ecosystems [1,2]. In obligate mutualisms, the host must possess symbionts in order to survive. If a host releases aposymbiotic progeny that must acquire symbionts from the environment (horizontal transmission), progeny may acquire symbionts that are beneficial in a new environment [4]. As partner fidelity is not absolute in horizontal transmission, strong partner choice and symbiont sexual recombination can allow mutualisms to persist and evolve in systems with horizontal transmission [2,5,6]. Since subsequent offspring do not inherit the symbionts, advantageous symbionts may or may not be acquired again, leaving each generation to potentially gamble with the continuation of a beneficial symbiosis

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