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Dive into the research topics where Kathleen M. Morrow is active.

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Featured researches published by Kathleen M. Morrow.


Annual Review of Microbiology | 2016

Insights into the Coral Microbiome: Underpinning the Health and Resilience of Reef Ecosystems

David G. Bourne; Kathleen M. Morrow; Nicole S. Webster

Corals are fundamental ecosystem engineers, creating large, intricate reefs that support diverse and abundant marine life. At the core of a healthy coral animal is a dynamic relationship with microorganisms, including a mutually beneficial symbiosis with photosynthetic dinoflagellates (Symbiodinium spp.) and enduring partnerships with an array of bacterial, archaeal, fungal, protistan, and viral associates, collectively termed the coral holobiont. The combined genomes of this coral holobiont form a coral hologenome, and genomic interactions within the hologenome ultimately define the coral phenotype. Here we integrate contemporary scientific knowledge regarding the ecological, host-specific, and environmental forces shaping the diversity, specificity, and distribution of microbial symbionts within the coral holobiont, explore physiological pathways that contribute to holobiont fitness, and describe potential mechanisms for holobiont homeostasis. Understanding the role of the microbiome in coral resilience, acclimation, and environmental adaptation is a new frontier in reef science that will require large-scale collaborative research efforts.


The ISME Journal | 2015

Natural volcanic CO2 seeps reveal future trajectories for host-microbial associations in corals and sponges

Kathleen M. Morrow; David G. Bourne; Craig Humphrey; Emmanuelle S. Botté; Patrick W. Laffy; Jesse Zaneveld; Sven Uthicke; Katharina E. Fabricius; Nicole S. Webster

Atmospheric carbon dioxide (CO2) levels are rapidly rising causing an increase in the partial pressure of CO2 (pCO2) in the ocean and a reduction in pH known as ocean acidification (OA). Natural volcanic seeps in Papua New Guinea expel 99% pure CO2 and thereby offer a unique opportunity to explore the effects of OA in situ. The corals Acropora millepora and Porites cylindrica were less abundant and hosted significantly different microbial communities at the CO2 seep than at nearby control sites <500 m away. A primary driver of microbial differences in A. millepora was a 50% reduction of symbiotic Endozoicomonas. This loss of symbiotic taxa from corals at the CO2 seep highlights a potential hurdle for corals to overcome if they are to adapt to and survive OA. In contrast, the two sponges Coelocarteria singaporensis and Cinachyra sp. were ∼40-fold more abundant at the seep and hosted a significantly higher relative abundance of Synechococcus than sponges at control sites. The increase in photosynthetic microbes at the seep potentially provides these species with a nutritional benefit and enhanced scope for growth under future climate scenarios (thus, flexibility in symbiosis may lead to a larger niche breadth). The microbial community in the apparently pCO2-sensitive sponge species S. massa was not significantly different between sites. These data show that responses to elevated pCO2 are species-specific and that the stability and flexibility of microbial partnerships may have an important role in shaping and contributing to the fitness and success of some hosts.


Frontiers in Marine Science | 2015

The ReFuGe 2020 Consortium—using “omics” approaches to explore the adaptability and resilience of coral holobionts to environmental change

Christian R. Voolstra; David J. Miller; Mark A. Ragan; Ary A. Hoffmann; Ove Hoegh-Guldberg; David G. Bourne; Eldon E. Ball; Hua Ying; Sylvain Forêt; Shunichi Takahashi; Karen D. Weynberg; Madeleine J. H. van Oppen; Kathleen M. Morrow; Cheong Xin Chan; Nedeljka N. Rosic; William Leggat; Susanne Sprungala; Michael Imelfort; Gene W. Tyson; Karin S. Kassahn; Petra Lundgren; Roger Beeden; Timothy Ravasi; Michael L. Berumen; Eva Abal; Theresa Fyffe

Human-induced environmental changes have been linked directly with loss of biodiversity. Coral reefs, which have been severely impacted by anthropogenic activities over the last few decades, exemplify this global problem and provide an opportunity to develop research addressing key knowledge gaps through ‘omics’-based approaches. While many stressors, e.g. global warming, ocean acidification, overfishing and coastal development have been identified, there is an urgent need to understand how corals function at a basic level in order to conceive strategies for mitigating future reef loss. In this regard, availability of fully sequenced genomes has been immensely valuable in providing answers to questions of organismal biology. Given that corals are metaorganisms comprised of the coral animal host, its intracellular photosynthetic algae, and associated microbiota (i.e. bacteria, archaea, fungi, viruses), these efforts must focus on entire coral holobionts. The Reef Future Genomics 2020 (ReFuGe 2020) consortium has formed to sequence hologenomes of ten coral species representing different physiological or functional groups to provide foundation data for coral reef adaptation research that is freely available to the research community.


Environmental Microbiology | 2016

Environmental drivers of microbial community shifts in the giant barrel sponge, Xestospongia muta, over a shallow to mesophotic depth gradient

Kathleen M. Morrow; Cara L. Fiore; Michael P. Lesser

The giant barrel sponge, Xestospongia muta, is a high microbial abundance sponge found on Caribbean coral reefs along shallow to mesophotic depth gradients where multiple abiotic factors change with depth. Sponges were collected along a depth gradient at Little Cayman (LC) and Lee Stocking Island (LSI), and the microbiome of these samples was analysed using 16S rRNA amplicon sequencing. Statistically significant shifts in community structure and dissimilarity (∼ 40%) were detected from 10 to 90 m in LC sponges, but a similar shift was not identified in sponges from 10 to 60 m at LSI (only 17% dissimilar). Additionally, inorganic nutrient levels steadily increased with depth at LSI but not at LC. Based on bulk stable isotopic variability, sponges collected from LC were generally more enriched in (15) N and less enriched in (13) C as depth increased, suggesting a transition from dependency on photoautotrophy to heterotrophy as depth increased. Patterns of stable isotopic enrichment were largely invariant at LSI, which is also reflected in the more stable microbial community along the depth gradient. It appears that environmental factors that change with depth may contribute to differences in X. muta microbial assemblages, demonstrating the importance of contemporaneous environmental sampling in studies of the microbiome of sponges.


Frontiers in Marine Science | 2016

Implications of Ocean Acidification for Marine Microorganisms from the Free-Living to the Host-Associated

Paul A. O'Brien; Kathleen M. Morrow; Bette L. Willis; David G. Bourne

Anthropogenic CO2 emissions are causing oceans to become more acidic, with consequences for all marine life including microorganisms. Studies reveal that from the microbes that occupy the open ocean to those intimately associated with their invertebrate hosts, changing ocean chemistry will alter the critical functions of these important organisms. Our current understanding indicates that bacterial communities associated with their host will shift as pH drops by another 0.2-0.4 units over the next 100 years. It is unclear what impacts this will have for host health, however increased vulnerability to disease seems likely for those associated with reef corals. Natural CO2 seeps have provided a unique setting for the study of microbial communities under OA in situ, where shifts in the bacterial communities associated with corals at the seep are correlated with a decline in abundance of the associated coral species. Changes to global biogeochemical cycles also appear likely as photosynthesis and nitrogen fixation by pelagic microbes becomes enhanced under low pH conditions. However, recent long-term studies have shown that pelagic microbes are also capable of evolutionary adaptation, with some physiological responses to a decline in pH restored after hundreds of generations at high pCO2 levels. The impacts of ocean acidification (OA) also will not work in isolation, thus synergistic interactions with other potential stressors, such as rising seawater temperatures, will likely exacerbate the microbial response to OA. This review discusses our existing understanding of the impacts of OA on both pelagic and host-associated marine microbial communities, whilst highlighting the importance of controlled laboratory studies and in situ experiments, to fill the current gaps in our knowledge.


The ISME Journal | 2018

Diazotroph diversity and nitrogen fixation in the coral Stylophora pistillata from the Great Barrier Reef

Michael P. Lesser; Kathleen M. Morrow; Sabrina M. Pankey; Sam H. C. Noonan

Diazotrophs, both Bacteria and Archaea, capable of fixing nitrogen (N2), are present in the tissues and mucous, of corals and can supplement the coral holobiont nitrogen budget with fixed nitrogen (N) in the form of ammonia (NH3). Stylophora pistillata from Heron Island on the Great Barrier Reef collected at 5 and 15 m, and experimentally manipulated in the laboratory, showed that the rates of net photosynthesis, steady state quantum yields of photosystem II (PSII) fluorescence (∆Fv/Fm′) and calcification varied based on irradiance as expected. Rates of N2 fixation were, however, invariant across treatments while the amount of fixed N contributing to Symbiodinium spp. N demand is irradiance dependent. Additionally, both the Symbiodinium and diazotrophic communities are significantly different based on depth, and novel Cluster V nifH gene phylotypes, which are not known to fix nitrogen, were recovered. A functional analysis using PICRUSt also showed that shallow corals were enriched in genes involved in nitrogen metabolism, and N2 fixation specifically. Corals have evolved a number of strategies to derive nitrogen from organic (e.g., heterotrophic feeding) and inorganic sources (e.g., N2 fixation) to maintain critical pathways such as protein synthesis to succeed ecologically in nitrogen-limited habitats.


FEMS Microbiology Ecology | 2018

A member of the Roseobacter clade, Octadecabacter sp., is the dominant symbiont in the brittle star Amphipholis squamata

Kathleen M. Morrow; Abbey Rose Tedford; M. Sabrina Pankey; Michael P. Lesser

Abstract Symbiotic associations with subcuticular bacteria (SCB) have been identified and studied in many echinoderms, including the SCB of the brooding brittle star, Amphipholis squamata. Previous studies on the SCB of A. squamata placed the isolated bacterium, designated as AS1, in the genus Vibrio (Gammaproteobacteria), but subsequent studies suggested that the SCB of echinoderms belong to the Alphaproteobacteria. This study examines the taxonomic composition of SCB associated with A. squamata from the Northwest Atlantic using the 16S rRNA gene and next generation sequencing. Results show the presence of a single dominant bacterial type, within the Roseobacter clade, family Rhodobacteraceae, which composes 70%‐80% of the A. squamata microbiome. These Rhodobacteraceae sequences were identified as members of the genus Octadecabacter. Additionally, the original isolate, AS1, from the brittle star A. squamata also belongs in the genus Octadecabacter based on Sanger sequencing of cloned 16S rRNA gene sequences. By comparison, adjacent seawater and sediment porewater communities were significantly more diverse, hosting bacteria in the phyla Proteobacteria, Bacteroidetes, Cyanobacteria, Verrucomicrobia and Actinobacteria. Thus, a distinct SCB community is present in A. squamata that is dominated by a member of the genus Octadecabacter and is identical to the original isolate, AS1, from this brittle star. Figure. No Caption available.


Molecular Ecology | 2017

Diversity and stability of coral endolithic microbial communities at a naturally high p CO2 reef

Vanessa R. Marcelino; Kathleen M. Morrow; Madeleine J. H. van Oppen; David G. Bourne; Heroen Verbruggen

The health and functioning of reef‐building corals is dependent on a balanced association with prokaryotic and eukaryotic microbes. The coral skeleton harbours numerous endolithic microbes, but their diversity, ecological roles and responses to environmental stress, including ocean acidification (OA), are not well characterized. This study tests whether pH affects the diversity and structure of prokaryotic and eukaryotic algal communities associated with skeletons of Porites spp. using targeted amplicon (16S rRNA gene, UPA and tufA) sequencing. We found that the composition of endolithic communities in the massive coral Porites spp. inhabiting a naturally high pCO2 reef (avg. pCO2 811 μatm) is not significantly different from corals inhabiting reference sites (avg. pCO2 357 μatm), suggesting that these microbiomes are less disturbed by OA than previously thought. Possible explanations may be that the endolithic microhabitat is highly homeostatic or that the endolithic micro‐organisms are well adapted to a wide pH range. Some of the microbial taxa identified include nitrogen‐fixing bacteria (Rhizobiales and cyanobacteria), algicidal bacteria in the phylum Bacteroidetes, symbiotic bacteria in the family Endozoicomoniaceae, and endolithic green algae, considered the major microbial agent of reef bioerosion. Additionally, we test whether host species has an effect on the endolithic community structure. We show that the endolithic community of massive Porites spp. is substantially different and more diverse than that found in skeletons of the branching species Seriatopora hystrix and Pocillopora damicornis. This study reveals highly diverse and structured microbial communities in Porites spp. skeletons that are possibly resilient to OA.


European Journal of Phycology | 2015

Genome Analysis of Two Symbiodinium Isolates

Cheong Xin Chan; Timothy G. Stephens; Edmund Y. S. Ling; Sylvain Forêt; Kathleen M. Morrow; David G. Bourne; Christian R. Voolstra; William Leggat; David J. Miller; Mark A. Ragan

Station Biologique de Roscoff, Sorbonne Universités, Université Pierre et Marie Curie, CNRS, Roscoff 29688, France; Institut de Systématique, Evolution, Biodiversité, UMR 7205CNRS-EPHE-MNHN-UPMC, Muséum National d’Histoire Naturelle, Paris 75231, France; Station Biologique de Roscoff, CNRS, Sorbonne Universités, Université Pierre et Marie Curie, Roscoff 29688, France and Station Biologique de Roscoff, CNRS, Sorbonne Universités, Université Pierre et Marie Curie, Roscoff 29688, FranceEarly life-stage of the bladderwrack Fucus vesiculosus is highly influenced by the climate change factors temperature, CO2 and eutrophication. Intraspecific genetic diversity of Baltic Fucus vesiculosus populations is low, compared to e.g. Atlantic populations, which may limit their potential for adaptation. To assess the role of intraspecific genetic diversity on the tolerance towards environmental change we manipulated their diversity: Plots with full-sibling Keynote and Oral Papers 106 Downloaded by [University of Kiel] at 02:13 22 September 2015 groups of Fucus germlings each originating from one parental pair represents the low diversity level, whereas plots with sibling groups from multiple parental pairs represent the high diversity level. Climate change was simulated according to the year 2100 in the near-natural scenario Kiel Benthocosms by maintaining the environmental fluctuations of the Baltic Sea and adding 5°C warming, 600 μatm pCO2 and doubling the nutrient concentrations. Germlings responded to warming with higher mortality and enhanced growth rates. High pCO2 concentrations increased growth due to a fertilisation effect. Nonphotochemical quenching was lower under warmed than ambient temperatures. A positive co-tolerance among sibling groups towards warming and acidification indicates the possible attenuation in presence of the multiple factors. Considerable differences among sibling group performance indicate a higher adaptive potential for genetically diverse populations. The high diversity levels also showed higher survival, indicating possible facilitation processes among genotypes. Microsatellite genotyping is in progress for revealing whether and how selection processes took place in high diversity levels. We conclude that impacts on early life-stage bladderwrack depend on the combination of stressors and season and that genetic variation is crucial for local adaptation to climate change stress


Scientific Reports | 2017

Comparative Genomics of Color Morphs In the Coral Montastraea cavernosa

Jessica Jarett; Matthew D. MacManes; Kathleen M. Morrow; M. Sabrina Pankey; Michael P. Lesser

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Michael P. Lesser

University of New Hampshire

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David G. Bourne

Australian Institute of Marine Science

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Abbey Rose Tedford

University of New Hampshire

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Mark A. Ragan

University of Queensland

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