# Rigorous Process for Isolation of Gut-Derived Extracellular Vesicles (EVs) and the Effect on Latent HIV

**Authors:** Nneoma C. J. Anyanwu, Lakmini S. Premadasa, Wasifa Naushad, Bryson C. Okeoma, Mahesh Mohan, Chioma M. Okeoma

PMC · DOI: 10.3390/cells14080568 · Cells · 2025-04-09

## TL;DR

A new method isolates gut-derived extracellular vesicles, which can activate HIV and may help study gut-related diseases.

## Contribution

A novel protocol using PPLC and PVPP for purifying gut-derived EVs that are functional and non-toxic.

## Key findings

- ColEVs isolated with PVPP are pure, non-toxic, and can activate the HIV LTR promoter.
- ColEVs contain reductases that can reduce MTT in the absence of living cells.
- ColEVs are composed of both bacterial and host-derived particles.

## Abstract

The human gastrointestinal (GI) track host trillions of microorganisms that secrete molecules, including extracellular vesicles (EVs) and extracellular condensates (ECs) that may affect physiological and patho-physiological activities in the host. However, efficient protocols for the isolation of pure and functional GI-derived EVs|ECs is lacking. Here, we describe the use of high-resolution particle purification liquid chromatography (PPLC) gradient-bead-column integrated with polyvinylpolypyrrolidone (PVPP)-mediated extraction of impurities to isolate EVs from colonic content (ColEVs). PVPP facilitates the isolation of pure, non-toxic, and functionally active ColEVs that were internalized by cells and functionally activate HIV LTR promoter. ColEVs isolated without PVPP have a reductive effect on MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) without living cells, suggesting that ColEVs contain reductases capable of catalyzing the reduction of MTT to formazan. The assessment of the origin of ColEVs reveals that they are composed of both bacteria and host particles. This protocol requires ~12 h (5 h preprocessing, 7 h isolation) to complete and should be used to purify EVs from sources contaminated with microbial agents to improve rigor. This protocol provides a robust tool for researchers and clinicians investigating GI-derived EVs and the translational use of GI-derived EVs for diagnostic and therapeutic use. Additionally, GI-derived EVs may serve as a window into the pathogenesis of diseases.

## Linked entities

- **Chemicals:** 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (PubChem CID 64965), formazan (PubChem CID 9567750)

## Full-text entities

- **Species:** Human immunodeficiency virus 1 (no rank) [taxon 11676], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12025545/full.md

## References

77 references — full list in the complete paper: https://tomesphere.com/paper/PMC12025545/full.md

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Source: https://tomesphere.com/paper/PMC12025545