11th ICRS Abstract book - Nova Southeastern University
11th ICRS Abstract book - Nova Southeastern University
11th ICRS Abstract book - Nova Southeastern University
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8.238<br />
Coral Mucus As A Source Of Bacteria With Antimicrobial Activity<br />
Maya SHNIT-ORLAND* 1 , Ariel KUSHMARO 2<br />
1 Environmental engineering, Ben Gurion <strong>University</strong> of the Negev, Beer-Sheva, Israel,<br />
2 Biotechnology engineering, Ben Gurion <strong>University</strong> of the Negev, Beer-Sheva, Israel<br />
In the oligotrophic marine environment there are ecological niches rich in nutrients and<br />
diverse in bacterial populations. One such niche is the coral surface mucus layer.<br />
Interactions amongst microorganisms found in coral mucus may be symbiotic or<br />
competitive; competing over space and food. It has been hypothesized that the microbial<br />
communities found on the coral surface may play a role in the coral defense, possibly<br />
through the production of antimicrobial substances. To find potentially active compounds<br />
produced by coral-mucus bacteria, over 200 selected microorganisms isolated from<br />
mucus layer of a number of scleractinian coral species were grown using agar plating<br />
technique. Screening for antimicrobial substances was performed using overlay and drop<br />
techniques, and antibacterial activity was tested against indicator microorganisms.<br />
Results indicated that approximately 25% of the mucus-associated bacteria demonstrated<br />
bioactivity. Isolates related to the genus Vibrio and Pseudoalteromonas demonstrated<br />
high activity against both gram positive and gram negative bacteria. Isolates related to the<br />
genus Shewanella demonstrated activity against gram positive bacteria. Gram positive<br />
bacteria (Bacillus, Planomicrobium) demonstrated lower activity, primarily against gram<br />
positive bacteria. These results demonstrate the existence of microorganisms with<br />
antimicrobial activity on the coral surface, indicating that they may play a role in<br />
protecting the coral host against pathogens. Further isolation and characterization of these<br />
active substances may lead to novel substances for use in medical and biotechnological<br />
applications.<br />
8.239<br />
Changes in Coral-Surface Bacterial Communities Following Bleaching Induced<br />
Coral Mortality And Their Implications For Ecosystem Function.<br />
Ron JOHNSTONE* 1 , Mark DAVEY 1 , Anna EDLUND 2 , Sara SJÖLING 2<br />
1 Centre for Marine Studies, <strong>University</strong> of Queensland, St Lucia, Australia, 2 School of<br />
Life Sciences, Södertörn <strong>University</strong> College, Huddinge, Sweden<br />
The processing and remineralisation of carbon and nutrients by prokaryotes is critical to<br />
the development and sustainability of coral reef ecosystems - underpinning productivity<br />
at all trophic levels. Both the structure and function of coral associated bacterial<br />
communities can alter following a disturbance. This study investigated the differences in<br />
the primary colonization and early succession of bacteria on coral skeletons over time<br />
after coral mortality. Bacterial populations were characterised using denaturing gradient<br />
gel electrophoresis (DGGE) and terminal-restriction fragment length polymorphism (T-<br />
RFLP) analysis of the 16S rRNA gene. This determined there were significant<br />
differences in surface bacterial populations between live and dead coral and a clear<br />
succession of bacteria on dead coral surfaces over a period of 6 months after coral<br />
mortality. Sequencing of DNA fragments from DGGE additionally allowed identification<br />
of specific individuals. By assessing these changes in light of concurrent community<br />
metabolism studies there is clear indication that the changes observed in bacterial<br />
populations from living to dead coral may have significant consequences for<br />
biogeochemical process.<br />
Poster Mini-Symposium 8: Coral Microbial Interactions<br />
8.240<br />
Phenotypic characterization of a coral white pox pathogen, Serratia marcescens<br />
Cory KREDIET* 1 , Kim RITCHIE 2 , Erin LIPP 3 , Max TEPLITSKI 4<br />
1 School of Natural Resources and Environment, <strong>University</strong> of Florida, Gainesville, FL, 2 Marine<br />
Microbiology, Mote Marine Laboratory, Sarasota, FL, 3 Environmental Health Science,<br />
<strong>University</strong> of Georgia, Athens, GA, 4 Soil and Water Science, <strong>University</strong> of Florida, Gainesville,<br />
FL<br />
The surface mucopolysaccharide layer (SML) secreted by corals is a rich environment where<br />
bacteria proliferate, with population levels often being several orders of magnitude higher than<br />
in the surrounding waters. Colonization of coral SML and bacterial growth on coral mucus<br />
most likely requires specific regulatory genes and catabolic enzymes. However, the activities<br />
that are required for SML colonization by bacterial pathogens and commensals are not yet<br />
known. Serratia marcescens is an opportunistic pathogen that causes white pox disease of the<br />
elkhorn coral, Acropora palmata. To characterize mechanisms of SML colonization by the S.<br />
marcescens White Pox pathogen, its ability for carbohydrate catabolism was characterized. A<br />
complement of enzymatic activities induced by growth on coral mucus was identified using<br />
defined chromogenic (p-Nitrophenyl) substrates. N-Acetyl-B-D-Galactosaminadase, a-Dgalactopyranosidase,<br />
a-D-glucopyranosidase, B-D-glucopyranosidase and a-L-fucopyranosidase<br />
were induced after two hours of S. marcescens incubation with coral mucus, while B-Dgalactopyranosidase,<br />
a-L-arabinopyranosidase and B-D-fucopyranosidase were induced after<br />
eighteen hours of incubation. The characterization of glycosidases induced by growth on coral<br />
mucus demonstrates that Serratia marcescens relies on specific catabolic genes for its<br />
colonization of Acroporid SML. Induction of these specific enzymes also provides insight into<br />
the types of bonds found in coral mucus. A Biolog EcoPlate was used to characterize the ability<br />
of several isolates of S. marcescens to catabolize model carbon sources. The ability to utilize<br />
fourteen substrates was common to the isolates of S. marcescens isolated from humans, plant<br />
soft rots, channel water, and a White Pox lesion. The coral pathogenic S. marcescens was able<br />
to utilize no additional substrates while the known pathogenic isolates were capable of<br />
metabolizing 13 additional carbon sources. The repertoire of carbohydrate degrading enzymes<br />
in the coral pathogen is likely to be distinct from that of the human and plant pathogenic<br />
isolates.<br />
8.241<br />
Free living Symbiodinium sp. existence in the rocky reef of the Pacific Coast of<br />
Colombia<br />
Pedro CASTRO* 1 , Juan A. SANCHEZ 2<br />
1 Ciencias Biologicas, Universidad de los Andes, Bogota, Colombia, 2 Laboratorio de Biologia<br />
Molecular Marina, Departamento de Ciencias Biologicas, Universidad de los Andes, Bogota,<br />
Colombia<br />
The major climate changes occurring in the Colombian pacific coast are producing dramatic<br />
transformations in the coral reef ecosystems. The free living dynoflagellate Symbiodinium sp.<br />
is a great biological indicator of the resilience of the reef. The hypothesis of the adaptive<br />
bleaching explains how the coral expels the less convenient symbionts and up-takes, from the<br />
water column, the better adapted ones to the actual conditions of the reef. Some studies have<br />
proven the actual existence of this free-living symbionts in the Indopacific ocean, the<br />
Caribbean sea, the Chinese sea and in the Australian great barrier.<br />
The Gorgona Island is a continental-oceanic land mass located at 56 km of the Colombian<br />
Pacific coast. It possesses a perfect environment for the coral reef development. The coral reefs<br />
in Gorgona have been highly affected by the negative action of commercial fisheries and<br />
natives, plus the climatic phenomena such as the ENSO. These harmful environmental and<br />
human-induced factors almost resulted in the total loss of the coral ecosystem. Today a no-take<br />
Marine Protected Area has been established by the government to help to protect the marine<br />
Island Biodiversity. The main goal of this study was to isolate free-living zooxanthella from the<br />
water column taken from the surroundings of the Gorgona Island. The samples were cultured in<br />
a specific-Symbiodinium F/2 media, and subsequently analyzed using a number of molecular<br />
tools. Here we present ecological and molecular evidence demonstrating the existence of<br />
demersal free-living Symbiodinium populations in Pacific reefs. Different cultures were<br />
identified according to the nuclear internal transcribed spacer (ITS2) and posterior banding<br />
pattern (fingerprinting) with the Denaturing Gradient Gel Electrophoresis, DGGE. It is<br />
suggestive that predictions on coral-zooxanthellae symbiosis aclimatation/adaptation and reef<br />
resilience could significantly improve by including the occurrence of free-living zooxanthellae<br />
and their potential dispersers as part of the reef ecosystem<br />
323