bioRxiv ScienceSearch

bioRxiv · 10.1101/380345

A survey of influenza subtypes in olive baboons in selected areas in Kenya

Abstract

3.BackgroundWorldwide infections with influenza A viruses are associated with substantial illness and death among mammals and birds, in humans it accounts for 250,000-500,000 deaths per year its continuous mutation in different hosts poses a threat that can result in the emergence of a novel virus with an ability to cause a widespread pandemic. Surveillance of Influenza A viral genome from diverse hosts and subtyping is critical in understanding of the antigenic shift and drift of the influenza virus especially in hosts that are closely related to human beings like the Non-Human Primates (NHPs),pigs and birds. This study therefore identified the influenza subtypes circulating in Papio anubis (Olive baboons) at the interface of human and NHPs in Kenya.\n\nMethodsFifty nasal swabs samples were collected from baboons from the colony at the Institute of Primate Research (IPR), these animals were originally collected from Olorbototo, Yatta, Aberdares, Movoloni and Laikipia. The nasal swabs were collected in viral transport media using sterile dacron swabs and stored at -80{degrees}C. In this study, samples were screened initially using real time RT-PCR-CDC protocol for influenza A virus detection that targets the matrix gene and twenty five were found to be positive.\n\nResultsThe proportion positive were as follows, Olorbototo (75%), Ngurumani (44%) Aberdares (43%), Mavoloni (37.5%), Yatta (14%), and Laikipia (9%). These samples were taken through conventional PCR to amplify the haemagglutinin, neuraminidase and the matrix genes and eight samples were successfully amplified and later sequenced through 24-capillaries ABI 3500 XL Genetic Analyzer.Upon BLAST of these sequences, influenza subtypes H1N1 and H3N2 were detected. It was observed that the subtypes in baboons were as follows Olorbototo H1N1,Yatta H3N2, Aberdares H3N2, Mavoloni H1N1, Ngurumani H1N1 and Laikipia H1N1.Upon further analysis, the influenza positive Olive baboons were found to have been reared in the colony at at IPR colony for between 1-2 years and were in close contact with personnel.\n\nCoclusionGiven the presence of H1N1 and H3N2 subtypes in baboons suggests that baboons can be naturally infected with seasonal endemic human influenza viruses, avian emerging pandemic or pandemic swine flu origin.

Explore related subjects

Keep this discovery

BibTeXRIS

Bunuma, E., Ochola, L., Nyerere, A.. 2018-08-07. A survey of influenza subtypes in olive baboons in selected areas in Kenya. https://doi.org/10.1101/380345

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Trans-branching of polyubiquitin chains orchestrates the DNA replication stress response

Polyubiquitin chain geometry dictates functional consequences of ubiquitylation. Although branched polyubiquitin chains are abundant in cells, little is known about their functions. Here we show that branching on the DNA replication factor PCNA, mediated by the ubiquitin-conjugating enzyme UBE2K and involving lysines 63 and 48 of ubiquitin, orchestrates the sequence of events in response to replication stress. By inducing VCP-dependent extraction of PCNA from chromatin, branching promotes re-priming of stalled forks and necessitates a BRCA1-dependent pathway of daughter-strand gap repair. Our study identifies hyper-accumulation of daughter-strand gaps as the mechanistic basis underlying the toxicity of inhibitors of the PCNA-specific isopeptidase, USP1, in BRCA1-deficient cells. Moreover, an unexpected preference of UBE2K to operate in trans suggests a general timing mechanism to organize hierarchies amongst ubiquitin signals.

molecular biology

Impaired proteostasis is an early feature of the diabetic heart in humans and mice

Diabetes and obesity increase cardiac lipid levels leading to cardiomyopathy and heart failure. We hypothesized that intermittent fasting would reduce cardiac lipid levels. Surprisingly, intermittent fasting increased myocardial triglyceride content, but rescued mortality and attenuated cardiomyopathy in mice overexpressing cardiomyocyte acyl-CoA synthetase 1 (MHC-ACSL1). Lipid overload caused cardiomyocyte accumulation of polyubiquitinated protein aggregates containing desmin, a scaffolding intermediate filament protein, which intermittent fasting prevented. Furthermore, intermittent fasting reversed elevated myocardial C16:0 ceramide content, and knockdown of ceramide synthase CerS5 and CerS6 reduced palmitate-induced protein aggregation, highlighting a role for C16:0 ceramides in this pathology. Conversely, impairing aggrephagy with cardiomyocyte-specific p62 ablation induced heart failure in mice fed a high-fat diet, with paradoxically reduced cardiac lipid content. Crucially, non-failing diabetic human hearts also exhibited protein aggregate pathology. Taken together, these results demonstrate that impaired proteostasis characterizes cardiomyopathy from cardiac lipid overload and identify a promising new therapeutic target for this condition.

molecular biology

Spatial profiling and neurovascular communication in the developing and adolescent cortex following prenatal alcohol exposure

Fetal alcohol spectrum disorders (FASD) constitute a wide range of developmental, cognitive, and behavioral impairments caused by prenatal alcohol exposure (PAE). Although neuronal and vascular consequences of PAE have been studied, how alcohol affects the cerebrovasculature within the framework of the neurovascular unit (NVU) across development remains poorly understood. At minimum, the NVU comprises neurons, astrocyte endfeet, and endothelial cells (ECs), which coordinate to maintain brain homeostasis. Here, we used the NanoString Digital Spatial Profiling platform to characterize spatial transcriptomic data from neurons, astrocytes, and ECs from PAE and saccharin (SAC) control cortices at embryonic day 18 (E18) and postnatal day 28 (P28). Differentially expressed genes were then used for Ingenuity Pathway Analysis (IPA) to identify altered biological pathways and perform comparison analyses across developmental time points, while CellChat was used to infer cell cell communication networks. We uncovered thousands of differentially expressed genes and numerous altered pathways and biological processes in PAE cortices across development. Both IPA and CellChat analyses implicated dysregulation of vascular and extracellular matrix (ECM) remodeling, cell adhesion, and neuroinflammatory signaling. CellChat further predicted the loss of several key bidirectional relationships and altered ligand-receptor interactions among neurovascular cell types at E18 and P28. Overall, these findings identify PAE associated alterations in neurovascular gene expression and intercellular signaling across development, providing potential mechanisms by which PAE may disrupt neurodevelopment.

molecular biology