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The dinoflagellate Karenia brevis is responsible for nearly annual red tides in the Gulf of Mexico that cause extensive marine mortalities and human illness due to the production of brevetoxins. Although the mechanisms regulating its bloom dynamics and toxicity have received considerable attention, investigation into these processes at the cellular and molecular level has only begun in earnest during the past decade. This review provides an overview of the recent advances in our understanding of the cellular and molecular biology on K. brevis. Several molecular resources developed for K. brevis, including cDNA and genomic DNA libraries, DNA microarrays, metagenomic libraries, and probes for population genetics, have revolutionized our ability to investigate fundamental questions about K. brevis biology. Two cellular processes have received particular attention, the vegetative cell cycle and vertical migration behavior, which are of key importance due to their roles in the development of both surface populations that constitute blooms and subsurface cell aggregations that may serve to initiate them. High throughput sequencing of cDNA libraries has provided the first glimpse of the gene repertoire in K. brevis, with approximately 12,000 unique genes identified to date. Phylogenomic analysis of these genes has revealed a high rate of horizontal gene transfer in K. brevis, which has resulted in a chimeric chloroplast through the selective retention of genes of red, green, and haptophyte origin, whose adaptive significance is not yet clear. Gene expression studies using DNA microarrays have demonstrated a prevalence of post-transcriptional gene regulation in K. brevis and led to the discovery of an unusual spliced leader trans-splicing mechanism. Among the trans-spliced gene transcripts are type I polyketide synthases (PKSs), implicated in brevetoxin biosynthesis, which are unique among type I PKSs in that each transcript encodes an individual catalytic domain, suggesting a novel gene structure in this dinoflagellate. Clone libraries of 16S ribosomal DNA sequences developed from bloom waters have unveiled the temporal and spatial complexity of the microbial soup that coexists with K. brevis and its active involvement in both bloom growth and termination processes. Finally, the development and application of population genetic markers has revealed a surprisingly high genetic diversity in K. brevis blooms, long assumed to consist of essentially clonal populations. With these foundations in place, our understanding of K. brevis bloom dynamics is likely to grow exponentially in the next few years.

Macrophages represent a major target and viral reservoir of HIV-1 infection. The susceptibility of macrophages to HIV-1 infection is modulated during monocyte differentiation. IL-27 is an antiviral cytokine which also plays a role in monocyte activation. Here, we present new evidence that IL-27 promotes monocyte differentiation into macrophages that are non-permissive for HIV-1 infection. While IL-27 treatment does not affect expression of macrophage differentiation markers or macrophage biological functions, it confers HIV resistance by down-regulating SPTBN1, a required host factor for HIV-1 infection. IL-27 down-regulates SPTBN1 during monocyte differentiation through a TAK-1-mediated MAPK signaling pathway. Knockdown of SPTBN1 strongly inhibits HIV-1 infection of macrophages; conversely, overexpression of SPTBN1 markedly increases HIV susceptibility of IL-27 treated macrophages. Moreover, we demonstrate that SPTBN1 associates with HIV-1 gag proteins. Collectively, our results underscore the ability of IL-27 to protect macrophages from HIV-1 infection by down-regulating SPTBN1 during monocyte to macrophage differentiation without altering other macrophage biological functions, thus indicating IL-27 as a potential immunotherapeutic reagent to prevent HIV-1 infection.