# Association of Escherichia coli pathotypes with fecal markers of enteropathy and nutritional status among underweight adults in Bangladesh

**Authors:** Rahvia Alam Sthity, Md. Zahidul Islam, Md. Ehsanul Kabir Sagar, Md. Amran Gazi, Jafrin Ferdous, Md. Mamun Kabir, Mustafa Mahfuz, Tahmeed Ahmed, Ishita Mostafa

PMC · DOI: 10.3389/fcimb.2025.1553688 · 2025-04-10

## TL;DR

This study explores how different types of Escherichia coli are linked to gut inflammation and other infections in underweight adults in Bangladesh.

## Contribution

The study identifies specific E. coli pathotypes associated with intestinal biomarkers in malnourished adults, revealing their role in gut inflammation and co-infections.

## Key findings

- Atypical EPEC is significantly associated with higher Myeloperoxidase levels, indicating intestinal inflammation.
- STEC infection correlates with increased alpha-1-antitrypsin levels, suggesting gut permeability changes.
- Coinfections with E. coli pathotypes and other pathogens like Giardia and Salmonella are common in malnourished adults.

## Abstract

Environmental enteric dysfunction (EED), a subclinical intestinal disorder, is characterized by chronic fecal-oral exposure to entero-pathogens and could be diagnosed by measuring non-invasive biomarkers. Escherichia coli is the one of the key bacterial enteric pathogens that drives EED, but there is a lack of information on the E. coli pathotypes in relation to the biomarkers of EED in malnourished adults. Here, we intended to measure the possible association of these pathotypes with EED biomarkers and nutritional status of adults residing in a slum in Bangladesh.

Fecal samples were collected from 524 malnourished adults (BMI ≤18.5 kg/m2) living in a slum-setting in Dhaka from March 2016 to September 2019 and analyzed by TaqMan Array Card assays to evaluate the presence of E. coli pathotypes and other entero-pathogens. The multivariable linear regression model was used to assess the association.

In these malnourished adults, the most prevalent pathotype of E. coli was EAEC (61.7%) and the least prevalent was STEC (6.7%). The prevalence of atypical EPEC, ETEC and Shigella/EIEC were 52%, 48.9% and 45.1% respectively. The infection with atypical EPEC had significant positive association with levels of Myeloperoxidase (b = 0.38; 95% CI = 0.11, 0.65; p-value = 0.006). Similarly, a significantly higher concentration of alpha-1-antitrypsin (b = 0.13; 95% CI = 0.03, 0.22; p-value = 0.011) was found in the STEC-infected adults. However, no notable association was found between the E. coli pathotypes and nutritional status of these adult participants. Moreover, Plesiomonas infected adults were more likely to be infected with EAEC (p-value = 0.017), ETEC (p-value <0.001) and STEC (pvalue = 0.002). Significant coinfection was also detected among the pathotypes and other entero-pathogens such as Giardia, Ascaris, Campylobacter, Salmonella, Enterocytozoon bieneusi, and Adenovirus.

The study results imply that there is an influence of particular E. coli pathotypes (EPEC and STEC) on intestinal inflammation and gut permeability of the malnourished Bangladeshi adults, but no association with nutritional status is found. Potential pathogenicity of the E. coli pathotypes is also observed when co-infection with other pathogens exists in these adults.

## Linked entities

- **Proteins:** SPIA5 (serpin family A member 1)
- **Species:** Escherichia coli (taxon 562), Plesiomonas (taxon 702)

## Full-text entities

- **Diseases:** EED (MESH:D004751), infected (MESH:D007239), intestinal inflammation (MESH:D007249), intestinal disorder (MESH:D007410), malnourished (MESH:D044342), enteropathy (MESH:C538273), underweight (MESH:D013851)
- **Species:** Campylobacter (genus) [taxon 194], Escherichia coli (E. coli, species) [taxon 562], Giardia (genus) [taxon 5740], Shigella (genus) [taxon 620], Enterocytozoon bieneusi (species) [taxon 31281], Ascaris (genus) [taxon 6251], Salmonella (genus) [taxon 590], Adenoviridae (family) [taxon 10508]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12018316/full.md

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Source: https://tomesphere.com/paper/PMC12018316