Evidence map›Paper›PMID 35655150›Full record

ArticleBMC ecology and evolution2022

Reciprocal positive effects on parasitemia between coinfecting haemosporidian parasites in house sparrows.

Luz Garcia-Longoria, Sergio Magallanes, Xi Huang, Anna Drews, Lars Råberg, Alfonso Marzal, Staffan Bensch, Helena Westerdahl

Open access · goldAbstract read
In one paragraph

Article in BMC ecology and evolution, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.3field-weighted citation impact, top 13% of its field
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

5 citing papers in PubMed, 13 citations in OpenAlex.

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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

8 authors at 3 institutions in 3 countries.

Luz Garcia-LongoriaDepartment of Anatomy, Cellular Biology and Zoology, University of Extremadura, E-06071, Badajoz, Spain.
Sergio MagallanesDepartment of Anatomy, Cellular Biology and Zoology, University of Extremadura, E-06071, Badajoz, Spain.
Xi HuangMolecular Ecology and Evolution Lab, Department of Biology, Lund University, Sölvegatan 37, SE-22362, Lund, Sweden.
Anna DrewsMolecular Ecology and Evolution Lab, Department of Biology, Lund University, Sölvegatan 37, SE-22362, Lund, Sweden.
Lars RåbergMolecular Ecology and Evolution Lab, Department of Biology, Lund University, Sölvegatan 37, SE-22362, Lund, Sweden.
Alfonso MarzalDepartment of Anatomy, Cellular Biology and Zoology, University of Extremadura, E-06071, Badajoz, Spain.
Staffan BenschMolecular Ecology and Evolution Lab, Department of Biology, Lund University, Sölvegatan 37, SE-22362, Lund, Sweden.
Helena WesterdahlMolecular Ecology and Evolution Lab, Department of Biology, Lund University, Sölvegatan 37, SE-22362, Lund, Sweden. helena.westerdahl@biol.lu.se.
Lund University · SEUniversidad de Extremadura · ESBeijing Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHosts are often simultaneously infected with several parasite species. These co-infections can lead to within-host interactions of parasites, including mutualism and competition, which may affect both virulence and transmission. Birds are frequently co-infected with different haemosporidian parasites, but very little is known about if and how these parasites interact in natural host populations and what consequences there are for the infected hosts. We therefore set out to study Plasmodium and Haemoproteus parasites in house sparrows Passer domesticus with naturally acquired infections using a protocol where the parasitemia (infection intensity) is quantified by qPCR separately for the two parasites. We analysed infection status (presence/absence of the parasite) and parasitemia of parasites in the blood of both adult and juvenile house sparrows repeatedly over the season.

resultsHaemoproteus passeris and Plasmodium relictum were the two dominating parasite species, found in 99% of the analyzed Sanger sequences. All birds were infected with both Plasmodium and Haemoproteus parasites during the study period. Seasonality explained infection status for both parasites in the adults: H. passeris was completely absent in the winter while P. relictum was present all year round. Among adults infected with H. passeris there was a positive effect of P. relictum parasitemia on H. passeris parasitemia and likewise among adults infected with P. relictum there was a positive effect of H. passeris parasitemia on P. relictum parasitemia. No such associations on parasitemia were seen in juvenile house sparrows.

conclusionsThe reciprocal positive relationships in parasitemia between P. relictum and H. passeris in adult house sparrows suggests either mutualistic interactions between these frequently occurring parasites or that there is variation in immune responses among house sparrow individuals, hence some individuals suppress the parasitemia of both parasites whereas other individuals suppress neither. Our detailed screening of haemosporidian parasites over the season shows that co-infections are very frequent in both juvenile and adult house sparrows, and since co-infections often have stronger negative effects on host fitness than the single infection, it is imperative to use screening systems with the ability to detect multiple parasites in ecological studies of host-parasite interactions.

Indexed as

CoinfectionHaemosporidaMalaria, AvianParasitesPlasmodiumSparrowsAnimalsHumansParasitemiaCo-infectionHaemoproteusHouse sparrowPlasmodium

Identifiers

PMID35655150
PMCPMC9164529
OpenAlexW4281837673

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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.