9 research outputs found

    A communal catalogue reveals Earth's multiscale microbial diversity

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    Our growing awareness of the microbial world's importance and diversity contrasts starkly with our limited understanding of its fundamental structure. Despite recent advances in DNA sequencing, a lack of standardized protocols and common analytical frameworks impedes comparisons among studies, hindering the development of global inferences about microbial life on Earth. Here we present a meta-analysis of microbial community samples collected by hundreds of researchers for the Earth Microbiome Project. Coordinated protocols and new analytical methods, particularly the use of exact sequences instead of clustered operational taxonomic units, enable bacterial and archaeal ribosomal RNA gene sequences to be followed across multiple studies and allow us to explore patterns of diversity at an unprecedented scale. The result is both a reference database giving global context to DNA sequence data and a framework for incorporating data from future studies, fostering increasingly complete characterization of Earth's microbial diversity.Peer reviewe

    A communal catalogue reveals Earth’s multiscale microbial diversity

    Get PDF
    Our growing awareness of the microbial world’s importance and diversity contrasts starkly with our limited understanding of its fundamental structure. Despite recent advances in DNA sequencing, a lack of standardized protocols and common analytical frameworks impedes comparisons among studies, hindering the development of global inferences about microbial life on Earth. Here we present a meta-analysis of microbial community samples collected by hundreds of researchers for the Earth Microbiome Project. Coordinated protocols and new analytical methods, particularly the use of exact sequences instead of clustered operational taxonomic units, enable bacterial and archaeal ribosomal RNA gene sequences to be followed across multiple studies and allow us to explore patterns of diversity at an unprecedented scale. The result is both a reference database giving global context to DNA sequence data and a framework for incorporating data from future studies, fostering increasingly complete characterization of Earth’s microbial diversity

    Data supporting the PhD Thesis 'Socio-economic responses to Late Holocene climate variability and environmental change in the Peruvian Andes'

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    Primary data included within the Handley 2022 PhD Thesis 'Socio-economic responses to Late Holocene climate variability and environmental change in the Peruvian Andes'. Data consists of pollen, phytolith, micro-XRF, and organic matter content records for three infilled basins in the Peruvian Andes (Huarca, CallejĂłn de Huaylas, Ancash Region; Antaycocha, ChillĂłn Valley, Lima Region; Ayapampa, Chicha-Soras Valley, ApurĂ­mac Region). The three sites provide a transect across the Andes to better understand regional differences in social responses to, and variations in, environmental change over the past 2500 years. The three basins span from full-Holocene (Huarca ~11,500 yrs) sequences to Late Holocene timescales (Antaycocha ~3000 yrs; Ayapampa ~4000 yrs). However the focus for most of the analysis for this thesis has focused on the last 2500 years as this is the period of greatest cultural and agricultural development in the Peruvian Andes. Pollen data was obtained by standard procedures following Faegri and Irersen (1989) and Moore, Web and Collinson (1991) and involving the sieving, heavy liquid density separation and acetolysis of pollen samples. Phytolith analysis was carried out using the dry-ashing method outlined in Parr et al., 2001, with the addition of a sonication step (Lombardo et al., 2016). Both phytolith and pollen analysis was carried out using a high-powered stereo microscope and the raw counts obtained from these analyses is included within this dataset. Micro-XRF data was obtained using a ITRAX core scanner housed at the British Ocean Sediment Core Research Facility, National Oceanography Centre, Southampton (BOSCORF). XRF exposure time was 15 seconds per sampling point, using a Mo tube and run at a voltage of 30KV and a current of 30mA. Data presented in this dataset are in counts per second as obtained via the ITRAX scanner. Organic Matter Content (OMC) was obtained via Loss on Ignition, with material being heated to 550oC (following Bengtsson and Enell, 1986)

    Mitogen-Activated Protein Kinase-Dependent Interleukin-1α Intracrine Signaling Is Modulated by YopP during Yersinia enterocolitica Infection

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    Yersinia enterocolitica is a food-borne pathogen that preferentially infects the Peyer's patches and mesenteric lymph nodes, causing an acute inflammatory reaction. Even though Y. enterocolitica induces a robust inflammatory response during infection, the bacterium has evolved a number of virulence factors to limit the extent of this response. We previously demonstrated that interleukin-1α (IL-1α) was critical for the induction of gut inflammation characteristic of Y. enterocolitica infection. More recently, the known actions of IL-1α are becoming more complex because IL-1α can function both as a proinflammatory cytokine and as a nuclear factor. In this study, we tested the ability of Y. enterocolitica to modulate intracellular IL-1α-dependent IL-8 production in epithelial cells. Nuclear translocation of pre-IL-1α protein and IL-1α-dependent secretion of IL-8 into the culture supernatant were increased during infection with a strain lacking the 70-kDa virulence plasmid compared to the case during infection with the wild type, suggesting that Yersinia outer proteins (Yops) might be involved in modulating intracellular IL-1α signaling. Infection of HeLa cells with a strain lacking the yopP gene resulted in increased nuclear translocation of pre-IL-1α and IL-1α-dependent secretion of IL-8 similar to what is observed with bacteria lacking the virulence plasmid. YopP is a protein acetylase that inhibits mitogen-activated protein kinase (MAP kinase)- and NF-ÎșB-dependent signal transduction pathways. Nuclear translocation of pre-IL-1α and IL-1α-dependent secretion of IL-8 in response to Yersinia enterocolitica infection were dependent on extracellular signal-regulated kinase (ERK) and p38 MAP kinase signaling but independent of NF-ÎșB. These data suggest that Y. enterocolitica inhibits intracellular pre-IL-1α signaling and subsequent proinflammatory responses through inhibition of MAP kinase pathways
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