Evidence map›Paper›PMID 39774432›Full record

ArticlePloS one2024

Designing of immunodiagnostic assay using polyclonal antibodies for detection of Enteropathogenic Escherichia coli strains.

Aliyi Hassen Jarso, Biniam Moges Eskeziyaw, Degisew Yinur Mengistu, Tesfaye Sisay Tessema

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Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Aliyi Hassen JarsoCenter for Innovative for Drug Development and Therapeutic Trials for Africa (CDT-Africa), Addis Ababa University, Addis Ababa, Ethiopia.
Biniam Moges EskeziyawDepartment of Biotechnology, Debre Berhan University, Debre Berhan, Ethiopia.
Degisew Yinur MengistuInstitute of Biotechnology, University of Gondar, Gondar, Ethiopia.ORCID 0000-0001-9086-132X
Tesfaye Sisay TessemaInstitute of Biotechnology, Addis Ababa University, Addis Ababa, Ethiopia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Enteropathogenic Escherichia coli (EPEC) is a significant bacterial pathogen that causes infantile diarrhea, particularly in low- and middle-income countries. The lack of a reliable diagnostic method greatly contributes to the increased occurrence and severity of the disease. This study aimed at developing of a cost-effective, rapid, and efficient immunodiagnostic assay for detecting EPEC infection. Lipopolysaccharide (LPS) was extracted from overnight EPEC cultures and combined with alum adjuvant, and then injected into mice for three rounds of immunizations. Subsequently, sera were collected after each immunization and utilized in agglutination assays conducted on glass slides. Both the LPS and colonies of the EPEC isolate used for LPS preparation were employed in these agglutination assays. To evaluate the assay's performance, a total of 34 bacteria, which comprise pathogenic, non-diarrheic E. coli and non-E. coli pathogenic bacteria were used. The developed assay detected EPEC, which yielded positive reactions within 6 minutes on average for both purified LPS and bacterial isolates. The assay exhibited 100% sensitivity and a 95.83% specificity for the detection of EPEC local isolates. Moreover, the assay also detected a low number of bacteria forming units (104X 104 CFU/ml) in spiked fecal samples. This study conclusively confirms that the developed immunodiagnostic assay possesses multiple favorable characteristics, including user-friendliness, high sensitivity, high specificity, cost-effectiveness, and time-efficiency. Hence, this assay can be used as ideal diagnostic assay, which is highly suitable for the detection and screening of EPEC infection in both humans and cattle in one health perspective of resource-limited laboratories.

Indexed as

Antibodies, BacterialEnteropathogenic Escherichia coliEscherichia coli InfectionsLipopolysaccharidesAnimalsFecesHumansImmunologic TestsMiceSensitivity and SpecificityAntibodies, BacterialLipopolysaccharides

Identifiers

PMID39774432
PMCPMC11684673

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.