Evidence map›Paper›PMID 24069499›Full record

ArticlePLoS neglected tropical diseases2013

Non-invasive sampling of schistosomes from humans requires correcting for family structure.

Michelle L Steinauer, Mark R Christie, Michael S Blouin, Lelo E Agola, Ibrahim N Mwangi, Geoffrey M Maina, Martin W Mutuku, Joseph M Kinuthia, Gerald M Mkoji, Eric S Loker

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Direct measurement ofbioRxiv : the preprint server for biology · 2026
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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

10 authors.

Michelle L SteinauerCollege of Osteopathic Medicine of the Pacific Northwest, Western University of Health Sciences, Lebanon, Oregon, United States of America.
Mark R Christie
Michael S Blouin
Lelo E Agola
Ibrahim N Mwangi
Geoffrey M Maina
Martin W Mutuku
Joseph M Kinuthia
Gerald M Mkoji
Eric S Loker

Funding

UNM COBRE: THEORETICAL STUDY OF SPECIFICITY OF RNA SILENCING MECHANISMP20RR018754 · NCRR · UNIVERSITY OF NEW MEXICO · PI LOKER, ERIC SAMUEL · 2003 to 2011
$16.7M
Determinants of resistance in human schistosomiasisR01AI053695 · NIAID · UNIVERSITY OF GEORGIA (UGA) · PI COLLEY, DANIEL G · 2003 to 2014
$5.2M
EVOLUTION OF SCHISTOSOMA MANSONI AND ITS SNAIL HOSTSR01AI044913 · NIAID · UNIVERSITY OF NEW MEXICO · PI LOKER, ERIC SAMUEL · 1999 to 2008
$2.2M
Snail-Related Studies of Transmission and Control of Schistosomiasis in KenyaR01AI101438 · NIAID · UNIVERSITY OF NEW MEXICO · PI LOKER, ERIC SAMUEL · 2012 to 2016
$1.7M
Evo-epidemiology of Scistosoma mansoni in children in KenyaR03TW008127 · FIC · UNIVERSITY OF NEW MEXICO · PI LOKER, ERIC SAMUEL · 2008 to 2010
$110k
FIC NIH HHS I RO3 TW008127FIC NIH HHS R03 TW008127NCRR NIH HHS 1P20RR18754NCRR NIH HHS P20 RR018754NIAID NIH HHS AI044913NIAID NIH HHS R01 AI044913NIAID NIH HHS R01 AI053695NIAID NIH HHS R01AI053695NIAID NIH HHS R01 AI101438
6 · The paper itself

Abstract

For ethical and logistical reasons, population-genetic studies of parasites often rely on the non-invasive sampling of offspring shed from their definitive hosts. However, if the sampled offspring are naturally derived from a small number of parents, then the strong family structure can result in biased population-level estimates of genetic parameters, particularly if reproductive output is skewed. Here, we document and correct for the strong family structure present within schistosome offspring (miracidia) that were collected non-invasively from humans in western Kenya. By genotyping 2,424 miracidia from 12 patients at 12 microsatellite loci and using a sibship clustering program, we found that the samples contained large numbers of siblings. Furthermore, reproductive success of the breeding schistosomes was skewed, creating differential representation of each family in the offspring pool. After removing the family structure with an iterative jacknifing procedure, we demonstrated that the presence of relatives led to inflated estimates of genetic differentiation and linkage disequilibrium, and downwardly-biased estimates of inbreeding coefficients (FIS). For example, correcting for family structure yielded estimates of FST among patients that were 27 times lower than estimates from the uncorrected samples. These biased estimates would cause one to draw false conclusions regarding these parameters in the adult population. We also found from our analyses that estimates of the number of full sibling families and other genetic parameters of samples of miracidia were highly intercorrelated but are not correlated with estimates of worm burden obtained via egg counting (Kato-Katz). Whether genetic methods or the traditional Kato-Katz estimator provide a better estimate of actual number of adult worms remains to be seen. This study illustrates that family structure must be explicitly accounted for when using offspring samples to estimate the genetic parameters of adult parasite populations.

Indexed as

Genetic VariationAdultAnimalsCluster AnalysisGenotypeHumansKenyaMaleMicrosatellite RepeatsSchistosomaSchistosomiasis

Identifiers

PMID24069499
PMCPMC3777896

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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.