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Ceja-Navarro, J. A.

Publications and source records attributed to Ceja-Navarro, J. A..

3 recordsLinked to original sources

Rapid Changes in Transcription During a Feast-Famine Event

AbstractSoil microbes have sophisticated mechanisms to detect and respond to short pulses of C inputs, often involving changes in gene-expression. We studied gene transcription in a soil microbial community before, and 8, 24, and 48h after glucose addition (0.7 mg C g-1 dry soil) to understand how microbes react to periods of substrate excess and subsequent starvation. The relative transcript abundance of genes associated with energy metabolism and biosynthesis of amino acids, lipids, nucleotides, and cell wall components increased 8h after glucose addition. By 24 and 48h, the abundances of these transcripts reversed. Transcript abundance for genes associated with degradation of lipids, nucleotides, and (hetero)cyclic hydrocarbons decreased at 8h, but increased 24 and 48h after glucose addition. Simultaneously with a rise in transcripts for energy production and biosynthesis at 8h, transcription of regulatory genes for the exponential growth phase and ribosome assembly and maturation increased. In contrast, at 24 and 48h, transcript abundance for genes associated with ribosomal hibernation, sporulation, and regulation of the stationary phase increased, while transcripts for regulators for the exponential phase, and ribosome activation decreased. Based on changes in transcript abundance of phosphoenolpyruvate carboxylase and pyruvate carboxylase, it appeared that 8h after glucose addition glycolytic activity was high, however, gluconeogenesis returned at 24 and 48h. High levels of transcripts for nrtC-ntrB indicated N limitation 8 and 24h after glucose addition. Transcripts associated with Type VI Secretion Systems increased 24 and 48h after start of the experiment, suggesting a short lag between primary consumers and predatory bacteria. These results illustrate how metatranscriptome analysis can be used to study the ecophysiology of soil microbes providing details on the timing of exponential and stationary phase processes, coordination between anabolism and catabolism, and emerging nutrient limitations in natural soil communities. Research HighlightsO_LIWe studied gene transcription of a soil microbial community after glucose addition C_LIO_LITranscript abundances for biosynthesis and energy production initially increased, while those for degradation decreased C_LIO_LITranscripts of regulators and sporulation genes indicated start of stationary phase at 24h C_LIO_LINitrogen limitation induced transcription of nitrogen stress genes C_LI

ecology↗

The PAAR5 Protein of a Polarly-Localized Type VI Secretion System (T6SS-5) is Required for the Formation of Multinucleated Cells (MNCs) and Virulence by Burkholderia pseudomallei.

The Burkholderia pseudomallei complex (Bpc) includes B. pseudomallei, B. mallei and B. thailandensis. These species share conserved virulence determinants that facilitate survival in mammalian cells and can spread from cell to cell by a unique mechanism involving fusion of plasma membranes. The activity of a contractile type VI secretion system, T6SS-5, is a central requirement. Using fluorescence confocal microscopy, we found localization and dynamic turnover of fluorescently-labeled T6SS-5 components at the forward pole of Burkholderia residing at the ends of actin protrusions. We identified the proline-alanine-alanine-arginine repeat protein of T6SS-5 (PAAR5), which forms the heteromeric tip of the T6SS-5 apparatus along with VgrG5. Mutational analysis revealed a unique N-terminal extension (NTE) of PAAR5 that is indispensable for cell fusion. Deletion of paar5 allowed us to uncouple fusogenic activity from the functionality of T6SS-5 for exploring the role of cell fusion in pathogenesis. B. pseudomallei {Delta}paar5 deletion mutants retained a functional T6SS-5 apparatus and the ability to secrete the Hcp5 protein. In cellular and animal infection models, {Delta}paar5 mutants mirrored the phenotype of a T6SS-5-defective {Delta}vgrG5 strain, being defective for cell fusion and avirulent in hamsters. These results demonstrate concordance between the fusogenic and in vivo virulence phenotypes, suggesting that T6SS-5-mediated cell fusion may be a central feature of B. pseudomallei pathogenesis and not an in vitro artifact.

microbiology↗

Enhancement of antimicrobial diversity in situ through relaxed symbiont specificity in an insect/actinomycete partnership

Some insects form symbioses in which actinomycetes provide defense against pathogens by making antimicrobials. The range of chemical strategies employed across these associations, and how these strategies relate to insect lifestyle, remains underexplored. We assessed subsocial passalid beetles of the species Odontotaenius disjunctus, and their frass (fecal material) which is an important food resource within their galleries, as a model insect/actinomycete system. Through chemical and phylogenetic analyses, we found that O. disjunctus frass collected across eastern North America harbored multiple lineages of Streptomyces and diverse antimicrobials. Metabolites detected in frass displayed synergistic and antagonistic inhibition of a fungal entomopathogen, Metarhizium anisopliae, and multiple streptomycete isolates inhibited this pathogen when co-cultivated directly in frass. These findings support a model in which the lifestyle of O. disjunctus accommodates multiple Streptomyces lineages in their frass, resulting in a rich repertoire of antimicrobials that likely insulates their galleries against pathogenic invasion.

microbiology↗