Evidence map›Paper›PMID 37549892›Full record

ArticleThe American journal of tropical medicine and hygiene2023

Molecular Epidemiology and Assemblage Typing of Giardia duodenalis in School-Age Children Situated along the Southern Shoreline of Lake Malawi, Malawi.

John Archer, Lucas J Cunningham, Alexandra Juhàsz, Sam Jones, Ffion Doull, James E LaCourse, Bright Mainga, Peter Makaula, Sekeleghe A Kayuni, Janelisa Musaya and 1 more

Abstract read
In one paragraph

Article in The American journal of tropical medicine and hygiene, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

John ArcherDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Lucas J CunninghamDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Alexandra JuhàszDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Sam JonesDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Ffion DoullDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
James E LaCourseDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Bright MaingaLaboratory Department, Mangochi District Hospital, Mangochi, Malawi.
Peter MakaulaMalawi Liverpool Wellcome Trust Programme of Clinical Tropical Research, Queen Elizabeth Central Hospital, Blantyre, Malawi.
Sekeleghe A KayuniDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Janelisa MusayaMalawi Liverpool Wellcome Trust Programme of Clinical Tropical Research, Queen Elizabeth Central Hospital, Blantyre, Malawi.
J Russell StothardDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Almost all human giardiasis infections are caused by Giardia duodenalis assemblages A and B. Differentiation between human infections with these assemblages, as well as between single-assemblage (A or B) and mixed-assemblage (A and B) infections, is therefore needed to better understand the pathological impact of infection with either, or both, assemblages. We assessed the prevalence of G. duodenalis assemblages A and B using 305 fecal samples provided by school-age children situated along the southern shoreline of Lake Malawi. Concurrently, intestinal pathology data were also collected to test for association(s) between assemblage infection status and intestinal health. Prevalence of G. duodenalis infection was 39.3% by real-time polymerase chain reaction. Of all identified infections, 32% were single G. duodenalis assemblage A and 32% were single G. duodenalis assemblage B, whereas 33% were mixed-assemblage infections. Fifteen unique G. duodenalis assemblage A and 13 unique G. duodenalis assemblage B β-giardin haplotypes were identified. There was a positive association between single infection with G. duodenalis assemblage B and both self-reporting of abdominal pain (odds ratio [OR]: 3.05, P = 0.004) and self-reporting of diarrhea (OR: 3.1, P = 0.003). No association between single infection with assemblage A and any form of intestinal pathology was found. Additionally, there was a positive association between mixed-assemblage infections and self-reporting of abdominal pain (OR: 3.1, P = 0.002). Our study highlights the importance G. duodenalis assemblage typing and reaffirms the need for improved access to water, sanitation and hygiene infrastructure in rural areas of low- and middle-income countries.

Indexed as

Giardia lambliaGiardiasisChildCytoskeletal ProteinsFecesGenotyping TechniquesHaplotypesHumansLakesMalawiMolecular Diagnostic TechniquesMolecular EpidemiologyPrevalenceProtozoan ProteinsRapid Diagnostic TestsCytoskeletal Proteinsgiardin protein, Giardia lambliaProtozoan Proteins

Identifiers

PMID37549892
PMCPMC10484258

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LicenceCC BY
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Registered trials

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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.