Recently, the use of microsatellites as genetic markers has become very popular. While their evolutionary dynamics are not yet fully understood, the emerging picture is that several factors are influencing microsatellite mutation rates. Recent experiments demonstrated a significant effect of repeat motif length on microsatellite mutation rates. Here, we studied the influence of the base composition of the microsatellite. Forty-two microsatellite loci on the second chromosome with the three most abundant dinucleotide repeat motifs (TC/AG, AT/TA, GT/CA) were characterized for six different Drosophila melanogaster populations. Applying ANOVA to the variance in repeat number, we found a significant influence of repeat motif on microsatellite variability. Calculating relative mutation rates, GT/CA appears to have the highest mutation rate, and AT/TA appears to have the lowest. Similar differences in mutation rates were obtained by an alternative method which estimates microsatellite mutation rates from their genomic length distribution.

Cold-water coral ecosystems are more widespread, diverse and productive than previously thought. However, little is known about the interaction of deep-water corals with microorganisms. To understand whether coral species have specific prokaryotic communities, it is necessary to assess the within and between colony variability. This was studied based on 16S rRNA gene and denaturing gradient gel electrophoresis (DGGE) for one of the main cold-water corals Madrepora oculata at Rockall Bank off the coast of Ireland. We successfully applied a rapid, non-toxic and inexpensive method for extracting DNA for 16S rRNA gene fingerprinting of marine prokaryotic communities based on a heat and salt lysis with simultaneous salt extraction (HEATSALT). The within and between colony variability of the community composition of bacteria associated to the mucus and ectodermal tissue of M. oculata was then evaluated using a 16S rRNA gene PCR and DGGE approach. Bacterial community composition (BCC) clearly differed between living coral and reference samples (dead coral and surrounding water; 80% dissimilarity). A large within (35-40% dissimilarity between polyps) and between colony variability (ca. 50% dissimilarity) of BCC was detected. We also found preliminary evidence that BCC differed between M. oculata and Lophelia pertusa. The high intraspecific variability found has consequences for selecting sampling strategies when assessing bacterial diversity and refines the question of controlling mechanisms of bacterial diversity on corals. Sequencing of DGGE bands showed that Spongiobacter type phylotypes (STP) dominated the DGGE bands. STP of M. oculata were grouped together and were different from those detected in other corals and sponges. In addition, the high sequence diversity of STP suggests specific ecological roles and adaptations of this group in M. oculata. KEYWORDS: DNA extraction · Diversity · Spongiobacter · Lophelia pertusa Resale or republication not permitted without written consent of the publisher Contribution to the Theme Section 'Conservation and management of deep-sea corals and coral reefs'OPEN PEN

Spatial increases and temporal shifts in outbreaks of gelatinous plankton have been observed over the past several decades in many estuarine and coastal ecosystems. The effects of these blooms on marine ecosystem functioning and particularly on the dynamics of the heterotrophic bacteria are still unclear. The response of the bacterial community from a Mediterranean coastal lagoon to the addition of dissolved organic matter (DOM) from the jellyfish Aurelia aurita, corresponding to an enrichment of dissolved organic carbon (DOC) by 1.4, was assessed for 22 days in microcosms (8 l). The high bioavailability of this material led to (i) a rapid mineralization of the DOC and dissolved organic nitrogen from the jellyfish and (ii) the accumulation of high concentrations of ammonium and orthophosphate in the water column. DOM from jellyfish greatly stimulated heterotrophic prokaryotic production and respiration rates during the first 2 days; then, these activities showed a continuous decay until reaching those measured in the control microcosms (lagoon water only) at the end of the experiment. Bacterial growth efficiency remained below 20%, indicating that most of the DOM was respired and a minor part was channeled to biomass production. Changes in bacterial diversity were assessed by tag pyrosequencing of partial bacterial 16S rRNA genes, DNA fingerprints, and a cultivation approach. While bacterial diversity in control microcosms showed little changes during the experiment, the addition of DOM from the jellyfish induced a rapid growth of Pseudoalteromonas and Vibrio species that were isolated. After 9 days, the bacterial community was dominated by Bacteroidetes, which appeared more adapted to metabolize high-molecular-weight DOM. At the end of the experiment, the bacterial community shifted toward a higher proportion of Alphaproteobacteria. Resilience of the bacterial community after the addition of DOM from the jellyfish was higher for metabolic functions than diversity, suggesting that jellyfish blooms can induce durable changes in the bacterial community structure in coastal lagoons.