Search bioRxiv⌕ Search

bioRxiv · 10.1101/2023.01.28.526042

Examining Horizontal Transmission of Nippostrongylus brasiliensis in Mice to Assess Biosecurity Risks

Abstract

Nippostrongylus brasiliensis (Nb) infected mice are commonly used to study immune responses. There is no consensus regarding the biosecurity measures that should be employed when housing Nb-infected mice and rats. Transmission is reported to not occur when infected mice are co-housed with naive mice. We sought to determine what conditions, if any, favor horizontal transmission. Female NOD.Cg-Prkdcscid Il2rgtm1Wjl/Sz (NSG; n=12) and C57BL/6J (B6; n=12) mice inoculated with 750 Nb L3 larvae were cohoused with naive NSG (n=24) and B6 (n=24) mice at a ratio of 1 infected:2 naive mice per cage for 28 days within static microsiolator (MI) cages changed on a 14-day interval. We also assessed whether larval development to the L3 stage could occur when Nb egg-containing fecal pellets are maintained under 4 different environmental conditions (dry, moist, soiled bedding, and control) and whether infection results when naive NSG mice (n=9) are housed in MI cages with infective L3 larvae-spiked (10,000/cage) soiled bedding. NSG mice (n=3) were also gavaged with Nb eggs to model the potential for infection to occur following coprophagy. Both naive NSG (9 of 24) and B6 (10 of 24) mice cohoused with an infected cagemate passed Nb eggs in feces as early as 1 day and intermittently for varying periods following cohousing, presumably a result of coprophagy as adult worms were not detected at euthanasia. While eggs were able to develop into L3 larvae under 2 environmental conditions (moist and control), none of the NSG mice housed in cages with L3-spiked bedding or gavaged with eggs became infected with Nb. Findings demonstrate that horizontal transmission does not occur when mice are housed with Nb-shedding cagemates in static MI cages with a 14-day cage changing interval. Results from this study can be used to inform biosecurity practices when working with the Nb-infected mouse model.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Floyd, R. J., Ricart Arbona, R. J., Carrasco, S. E., Lipman, N. S.. 2023-01-30. Examining Horizontal Transmission of Nippostrongylus brasiliensis in Mice to Assess Biosecurity Risks. https://doi.org/10.1101/2023.01.28.526042

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

KEEP EXPLORING

Related preprints

De novo design of CR2 binder as vaccine scaffold

Efficient B cell activation during vaccine-induced humoral immunity relies on both B cell receptor (BCR) antigen recognition and synergistic signaling from co-receptors. Complement receptor 2 (CR2), the primary BCR co-receptor on B cells, lowers the activation threshold and amplifies downstream kinase signaling by orders of magnitude when engaged by complement fragment C3d decorated antigens. Targeting CR2 therefore represents a rational vaccine enhancement strategy, yet native C3d suffers from low affinity, poor stability, and manufacturing challenges. Here, we report the de novo design of a highly stable, high-affinity CR2 binder using deep learning driving protein design methods. Biophysical characterization, high-resolution cryoEM structural determination, and functional assays in vitro and in vivo confirm that the designed binder matches computational design models and specifically engages CR2 to boost B cell activation. When fused to antigen as a vaccine scaffold, the trimeric CR2 binder elicits robust humoral immune responses comparable to nanoparticle vaccines, while retaining the simplicity of single-chain protein production. Our work establishes a modular CR2 targeting vaccine scaffold platform with broad translational potential for next-generation protein vaccines.

immunology↗

Chronic opioid-associated immune dysregulation among people living with HIV

Objectives: Persistent immune dysregulation contributes to chronic disease among people living with HIV (PWH), even after viral suppression with antiretroviral therapy (ART). Although chronic opioid exposure is associated with adverse clinical outcomes, its impact on immune homeostasis during ART remains incompletely understood. We investigated whether opioid use disorder (OUD) is associated with persistent systemic and cellular immune dysregulation despite ART-mediated reductions in HIV viral load (VL). Methods: Peripheral blood was collected longitudinally from PWH with OUD (PWH/OUD+) and detectable HIV VL during 6 months of optimized ART (months 0, 3, and 6). A reference cohort of PWH without OUD (PWH/OUD-) and suppressed HIV VL provided a single blood sample. Immune profiling included plasma inflammatory biomarkers, multiplex cytokine analyses, spectral flow cytometry, and assessment of monocyte cytokine responses following lipopolysaccharide (LPS) stimulation. Mixed-effects models adjusted for HIV VL and VL-stratified analyses were performed. Results: PWH/OUD+ exhibited persistent immune dysregulation despite reductions in HIV VL. Plasma sCD163, sCD14, fractalkine, and I-TAC remained elevated, whereas TGF-{beta}1 was reduced. OUD was associated with expansion of CD16 monocytes and altered expression of CCR2, CD38, and CD11b. CD4 and CD8 T cells, NK cells, and B cells also exhibited persistent alterations in markers of activation, metabolism, and trafficking. Monocytes from PWH/OUD+ displayed attenuated cytokine responses following LPS stimulation. Conclusions: OUD is associated with persistent systemic and cellular immune dysfunction in PWH despite ART-mediated viral suppression, supporting opioid exposure as an independent contributor to chronic immune dysregulation that may promote inflammation, immune dysfunction, and long-term HIV-associated comorbidities. Keywords: HIV, Opioid-use disorder, innate immunity, cytokine

immunology↗

The mitochondrial RNA extrusion-induced innate immunity is regulated by N6-methyladenosine machinery

Mitochondrial RNA (mtRNA) released into the cytosol functions as a damage associated molecular pattern that activates pattern-recognition receptor (PRR)-mediated inflammation, yet its release mechanisms and cytoplasmic fate remain poorly understood. Here we report that chemical Abt-373-treatment and Vesicular stomatitis virus (VSV) infection induce mtRNA extrusion through Bax/Bak and VDAC1 channels, accompanied by mtDNA release. Extruded mtRNA in A549 cells activates multiple cytosolic PRRs, including RIG-I, MDA5, TLR3/7/8, and PKR, each contributing differentially to the innate immune signaling. Analysis of GEO datasets and methylated RNA immunoprecipitation (MeRIP) assays further reveals that mtRNA carries methyladenosine (m6A) modification. m6A machinery proteins are involved in the cytoplasmic retention time of mtRNA and its interaction with RIG-I, thereby modulating mtRNA-induced innate immunity. Thus, our work establishes in vitro models of mtRNA extrusion, and highlights m6A-dependent modulation as a potential therapeutic target for mtRNA-driven inflammation.

immunology↗