Bacterial lipoproteins and other factors released by Francisella tularensis modulate human neutrophil lifespan: Effects of a TLR1 SNP on apoptosis inhibition

Francisella tularensis infects several cell types including neutrophils, and aberrant neutrophil accumulation contributes to tissue destruction during tularaemia. We demonstrated previously that F. tularensis strains Schu S4 and live vaccine strain markedly delay human neutrophil apoptosis and thereby prolong cell lifespan, but the bacterial factors that mediate this aspect of virulence are undefined. Herein, we demonstrate that bacterial conditioned medium (CM) can delay apoptosis in the absence of direct infection. Biochemical analyses show that CM contained F. tularensis surface factors as well as outer membrane components. Our previous studies excluded roles for lipopolysaccharide and capsule in apoptosis inhibition, and current studies of [¹⁴C] acetate‐labelled bacteria argue against a role for other bacterial lipids in this process. At the same time, studies of isogenic mutants indicate that TolC and virulence factors whose expression requires FevR or MglA were also dispensable, demonstrating that apoptosis inhibition does not require Type I or Type VI secretion. Instead, we identified bacterial lipoproteins (BLPs) as active factors in CM. Additional studies of isolated BLPs demonstrated dose‐dependent neutrophil apoptosis inhibition via a TLR2‐dependent mechanism that is significantly influenced by a common polymorphism, rs5743618, in human TLR1. These data provide fundamental new insight into pathogen manipulation of neutrophil lifespan and BLP function.     

The Role of Ceramide Synthases in the Pathogenicity of Cryptococcus neoformans

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Extracellular Neutrophil Proteases Are Efficient Regulators of IL-1, IL-33, and IL-36 Cytokine Activity but Poor Effectors of Microbial Killing

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Primary Cilium-Mediated Retinal Pigment Epithelium Maturation Is Disrupted in Ciliopathy Patient Cells

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Aggregating fields of annual crops to form larger-scale monocultures can suppress dispersal-limited herbivores

An important part of landscape ecology is determining how the arrangement (aggregation or fragmentation) of patches in space influences the population dynamics of foraging organisms. One hypothesis in agricultural ecology is that fine-grain spatial heterogeneity in cropping (many small agricultural fields) should provide better pest control than coarse-grain heterogeneity (few large agricultural fields); this hypothesis has been proposed as an explanation for the increased pest abundance associated with agricultural intensification. However, empirical studies have found mixed support for this hypothesis, and some, surprisingly, demonstrate a strong decrease in pest abundance with increased crop aggregation. We developed a spatially explicit simulation model of pest movement across an agricultural landscape to uncover basic processes that could reduce pest abundance in landscapes with fewer, larger fields. This model focuses on herbivore movement and does not include predation effects or other biological interactions. We found that field aggregation in the model led to severely reduced pest densities and further discovered that this relationship was due to an increased distance between fields and a decreased “target area” in more aggregated landscapes. The features that create a negative relationship between aggregation and pest densities rely on crop rotation and limited dispersal capabilities of the pests. These findings help to explain seemingly counter-intuitive empirical studies and provide an expectation for when field aggregation may reduce pest populations in agro-ecosystems.     

The human MAPT locus generates circular RNAs

The microtubule-associated protein Tau, generated by the MAPT gene is involved in dozens of neurodegenerative conditions (“tauopathies”), including Alzheimer's disease (AD) and frontotemporal lobar degeneration/frontotemporal dementia (FTLD/FTD). The pre-mRNA of MAPT is well studied and its aberrant pre-mRNA splicing is associated with frontotemporal dementia. Using a PCR screen of RNA from human brain tissues, we found that the MAPT locus generates circular RNAs through a backsplicing mechanism from exon 12 to either exon 10 or 7. MAPT circular RNAs are localized in the cytosol and contain open reading frames encoding Tau protein fragments. The MAPT exon 10 is alternatively spliced and proteins involved in its regulation, such as CLK2, SRSF7/9G8, PP1 (protein phosphatase 1) and NIPP1 (nuclear inhibitor of PP1) reduce the abundance of the circular MAPT exon 12?→?10 backsplice RNA after being transfected into cultured HEK293 cells. In summary, we report the identification of new bona fide human brain RNAs produced from the MAPT locus. These may be a component of normal human brain Tau regulation and, since the circular RNAs could generate high molecular weight proteins with multiple microtubule binding sites, they could contribute to taupathies.     

Impact of host cell line choice on glycan profile

Protein glycosylation is post-translational modification (PTM) which is important for pharmacokinetics and immunogenicity of recombinant glycoprotein therapeutics. As a result of variations in monosaccharide composition, glycosidic linkages and glycan branching, glycosylation introduces considerable complexity and heterogeneity to therapeutics. The host cell line used to produce the glycoprotein has a strong influence on the glycosylation because different host systems may express varying repertoire of glycosylation enzymes and transporters that contributes to specificity and heterogeneity in glycosylation profiles. In this review, we discuss the types of host cell lines currently used for recombinant therapeutic production, their glycosylation potential and the resultant impact on glycoprotein properties. In addition, we compare the reported glycosylation profiles of four recombinant glycoproteins: immunoglobulin G (IgG), coagulation factor VII (FVII), erythropoietin (EPO) and alpha-1 antitrypsin (A1AT) produced in different mammalian cells to establish the influence of mammalian host cell lines on glycosylation.     

Social-trap or mimicry? An empirical evaluation of the Hypoplectrus unicolor–Chaetodon capistratus association in Bocas del Toro,Panama

Coral Reefs - Associations between resembling species have been noted long ago by naturalists and have been traditionally interpreted in terms of mimicry, whereby a mimetic species is naturally...     

Non-cultivable microorganisms from symbiotic associations of insects and other hosts

Many symbiotic associations involve microorganisms which cannot be cultivated on laboratory media. These organisms remained little known until the recent advent of methods of recombinant DNA analysis and molecular phylogenetics. Applications of these methods to endosymbionts have resulted in substantial new insights concerning the genetics and evolution of these organisms. This communication provides a listing of recently studied associations involving non-cultivable symbionts. The associations involve a diverse set of host taxa and a wide range of effects, both favorable and deleterious, on host biology. Among beneficial endosymbionts, a variety of nutritional interactions have been documented. One type of association has been demonstrated for a number of animal hosts, namely endosymbioses that result from a single infection of an ancestral host by a prokaryote. In these associations, endosymbionts are transmitted maternally and are not exchanged between host lineages, resulting in a long-term pattern of codiversification of hosts and endosymbionts. The association between aphids and non-cultivable prokaryotic endosymbionts is a well studied example of such a symbiosis.     

Trichloroethylene biodegradation by mesophilic and psychrophilic ammonia oxidizers and methanotrophs in groundwater microcosms.

This study investigated the efficiency of methane and ammonium for stimulating trichloroethylene (TCE) biodegradation in groundwater microcosms (flasks and batch exchange columns) at a psychrophilic temperature (12 degrees C) typical of shallow aquifers in the northern United States or a mesophilic temperature (24 degrees C) representative of most laboratory experiments. After 140 days, TCE biodegradation rates by ammonia oxidizers and methanotrophs in mesophilic flask microcosms were similar (8 to 10 nmol day-1), but [14C]TCE mineralization (biodegradation to 14CO2) by ammonia oxidizers was significantly greater than that by methanotrophs (63 versus 53%). Under psychrophilic conditions, [14C]TCE mineralization in flask systems by ammonia oxidizers and methanotrophs was reduced to 12 and 5%, respectively. In mesophilic batch exchange columns, average TCE biodegradation rates for methanotrophs (900 nmol liter-1 day-1) were not significantly different from those of ammonia oxidizers (775 nmol liter-1 day-1). Psychrophilic TCE biodegradation rates in the columns were similar with both biostimulants and averaged 145 nmol liter-1 day-1. Methanotroph biostimulation was most adversely affected by low temperatures. At 12 degrees C, the biodegradation efficiencies (TCE degradation normalized to microbial activity) of methanotrophs and ammonia oxidizers decreased by factors of 2.6 and 1.6, respectively, relative to their biodegradation efficiencies at 24 degrees C. Collectively, these experiments demonstrated that in situ bioremediation of TCE is feasible at the psychrophilic temperatures common in surficial aquifers in the northern United States and that for such applications biostimulation of ammonia oxidizers could be more effective than has been previously reported.