Coral recruitment is a key process in the maintenance and recovery of coral reef ecosystems. While intense competition between coral and algae is often assumed on reefs that have undergone phase shifts from coral to algal dominance, data examining the competitive interactions involved, particularly during the larval and immediate post-settlement stage, are scarce. Using a series of field and outdoor seawater table experiments, we tested the hypothesis that common species of macroalgae and cyanobacteria inhibit coral recruitment. We examined the effects of Lyngbya spp., Dictyota spp., Lobophora variegata (J. V. Lamouroux) Womersley, and Chondrophycus poiteaui (J. V. Lamouroux) Nam (formerly Laurencia poiteaui) on the recruitment success of Porites astreoides larvae. All species but C. poiteaui caused either recruitment inhibition or avoidance behavior in P. astreoides larvae, while L. confervoides and D. menstrualis significantly increased mortality rates of P. astreoides recruits. We also tested the effect of some of these macrophytes on larvae of the gorgonian octocoral Briareum asbestinum. Exposure to Lyngbya majuscula reduced survival and recruitment in the octocoral larvae. Our results provide evidence that algae and cyanobacteria use tactics beyond space occupation to inhibit coral recruitment. On reefs experiencing phase shifts or temporary algal blooms, the restocking of adult coral populations may be slowed due to recruitment inhibition, thereby perpetuating reduced coral cover and limiting coral community recovery.
The identification of new pharmacophores is of paramount biomedical importance and natural products have recently been regaining attention for this endeavor. 1 This renaissance is closely tied to the successful exploitation of the marine environment which harbors unmatched biodiversity that is presumably concomitant with chemical diversity. 2 In particular, marine cyanobacteria are prolific producers of bioactive secondary metabolites, 3 many of which are modified peptides or peptide-polyketide hybrids with promising antitumor activities, such as dolastatin 10, 4 curacin A, 5 and apratoxin A. 6 As a result of our ongoing investigations to identify new drug leads from cyanobacteria in Florida, we report here the structure determination and preliminary biological characterization of a marine cyanobacterial metabolite with novel chemical scaffold and nanomolar antiproliferative activity from a cyanobacterium of the genus Symploca. Symploca species have scarcely been investigated compared to the more prevalent Lyngbya spp., yet a Palauan Symploca sp. previously yielded the clinical trial compound dolastatin 10, 4 prompting us to target this genus.A sample of Symploca sp. was collected from Key Largo, Florida Keys, and extracted with organic solvents. The resulting cytotoxic crude extract was subjected to bioassay-guided fractionation by solvent partition, silica gel chromatography, and reversed-phase HPLC to yield largazole (1) as a colorless, amorphous solid {[R] 20 D +22 (c 0.1, MeOH)}.
An outbreak of stony coral tissue loss disease (SCTLD), emerged on reefs off the coast of southeast Florida in 2014 and continues to spread throughout Florida's Reef Tract. SCTLD is causing extensive mortality of multiple coral species and disease signs vary among affected coral species with differences in rates of tissue loss (acute and subacute), lesion morphology (adjacent bleached zone or not) and lesion occurrence (focal and multi-focal). We examined the virulence, transmission dynamics and response to antibiotic treatment of coral species exhibiting different types of tissue loss lesions from two regions in Florida. Montastraea cavernosa with subacute tissue loss lesions in the southeast Florida region near Fort Lauderdale was compared to corals (multiple species) with acute tissue loss lesions in the Middle Keys. Corals from both regions showed progressive tissue loss but the in situ rate of mortality was significantly higher in tagged colonies in the Keys. Aquaria studies showed disease transmission occurred through direct contact and through the water column for corals from both regions. However, transmission success was higher for corals with acute vs. subacute lesions. There was 100% transmission for both test species, M. cavernosa and Meandrina meandrites, touching acute lesions. Among the three species touching subacute lesions, the disease transmitted readily to Orbicella faveolata (100%) followed by M. cavernosa (30%) with no transmission occurring with Porites astreoides. Diseased fragments of all species tested responded to antibiotic treatment with a cessation or slowing of the disease lesions suggesting that bacteria are involved in disease progression. Mortality was higher for in situ corals with acute lesions and transmission was higher in M. cavernosa exposed to acute lesions compared to subacute lesions, suggesting that different microbes may be involved with the two lesion types. However, since in situ mortality of M. cavernosa was not measured in the Middle Keys, we cannot completely rule out that a common pathogen is involved but is less virulent within M. cavernosa.
Bacterial quorum sensing (QS) is a cell-cell communication and gene regulatory mechanism that allows bacteria to coordinate swarming, biofilm formation, stress resistance, and production of toxins and secondary metabolites in response to threshold concentrations of QS signals that accumulate within a diffusion-limited environment. This review focuses on the role of QS signaling and QS inhibition in marine bacteria by compounds derived from marine organisms. Since the formation of a biofilm is considered to be an initial step in the development of fouling, direct and indirect effects of QS signals and inhibitors on the process of marine biofouling are discussed. Directions for future investigations and QS-related biotechnological applications are highlighted.
The potent antitumor agent dolastatin 10 (1) was originally isolated from the sea hare Dolabella auricularia, and we now report its isolation from the marine cyanobacterium Symploca sp. VP642 from Palau. The chemically related analogue symplostatin 1 (2) has been reisolated from Guamanian and Hawaiian varieties of S. hydnoides and its total stereochemistry completed by determining the N,N-dimethylisoleucine unit to be L. Symplostatin 1 (2), like dolastatin 10 (1), is a potent microtubule inhibitor. The antitumor activity of 2 was assessed in vivo against several murine tumors. Symplostatin 1 (2) was effective against a drug-insensitive mammary tumor and a drug-insensitive colon tumor; however, it was only slightly effective against two MDR tumors.
The susceptibility of 82 species of tropical seaweeds to grazing by herbivorous fishes was assessed on 8 different coral reefs in the Florida Keys, USA. Most species were simultaneously assayed for the presence or absence of unusual secondary rnetabolites and recorded as having either calcified or uncalcified thalli. Both production of secondary rnetabolites and of a calcified thallus were associated with low susceptibility to herbivory. However, the relative importance of calcification versus chemical deterrents cannot be assessed for the calcified species since almost all these also contained secondary metabolites. Eighty-five % of calcified species, but only 39 % of uncalcified species, produced secondary metabohtes. Secondary metabolites were produced by 71 % of the species least suscephble to herbivory ( t 2 5 % eaten) but by only 20 O/ O of the species most susceptible to herbivory (>75 % eaten). Calcified thalh were produced by 50 % of the lowest preference species but by only 9 O/O of the highest preference species. Thus, several common reef seaweeds appear to resist herbivory by relying primarily on chemical deterrents (genera Dictyota, Dilophus, Stypopodium, Lobophora, Avrainvrllea, and some Caulerpa species) but many appear to combine both chemical and morphological defenses (genera Penicillus, Halimeda, Rhipocephalus, Udotea, Amphiroa, and Galaxaura). We suggest that multiple defenses will be common among seaweeds on coral reefs since herbivore diversity is high and it is unlikely that any single defense will be effective against the many types of herbivores that encounter these plants. Thls may account, in part, for the diversity of secondary metabolites produced by some tropical seaweeds.
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