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Effect of Multiple Parasitic Infections on the Tolerance to Pollutant Contamination

https://doi.org/10.1371/journal.pone.0041950

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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INTEGRATED BIOMARKER RESPONSE: A USEFUL TOOL FOR ECOLOGICAL RISK ASSESSMENT

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Gammarus spp. in Aquatic Ecotoxicology and Water Quality Assessment: Toward Integrated Multilevel Tests

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Energetic costs of mate guarding behavior in male stream-dwelling isopods

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Evaluation ofo-phthalaldehyde as bifunctional fluorogenic post-column reagent for glutathione in LC

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Malonaldehyde determination in tissues and biological fluids by ion‐pairing high‐performance liquid chromatography

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Field evidence for non-host predator avoidance in a manipulated amphipod

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Acanthocephalan parasites: help or burden in gammarid amphipods exposed to cadmium?

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[38] Antioxidant effects of carotenoids in Vivo and in Vitro: An overview

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Metallothioneins in metal regulation and toxicity in aquatic animals

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Carotenoid pigments and their possible role in reproduction in the sand crab, Emerita analoga (Stimpson, 1857)

inferredcites →https://doi.org/10.1016/j.anbehav.2009.01.029openalex-snapshot

A manipulative parasite increasing an antipredator response decreases its vulnerability to a nonhost predator

inferredcites →https://doi.org/10.1016/j.beproc.2004.09.005openalex-snapshot

Conflict between co-occurring parasites as a confounding factor in manipulation studies?

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A Wolbachia Symbiont in Aedes aegypti Limits Infection with Dengue, Chikungunya, and Plasmodium

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Metallothionein quantification in clams by reversed-phase high-performance liquid chromatography coupled to fluorescence detection after monobromobimane derivatization

inferredcites →https://doi.org/10.1016/j.envpol.2011.09.021openalex-snapshot

Microsporidia parasites disrupt the responses to cadmium exposure in a gammarid

inferredcites →https://doi.org/10.1016/j.envres.2009.07.012openalex-snapshot

Interactions between parasitism and biological responses in zebra mussels (Dreissena polymorpha): Importance in ecotoxicological studies

inferredcites →https://doi.org/10.1016/j.ijpara.2003.10.005openalex-snapshot

Larval morphology, genetic divergence, and contrasting levels of host manipulation between forms of Pomphorhynchus laevis (Acanthocephala)

inferredcites →https://doi.org/10.1016/j.ijpara.2004.06.006openalex-snapshot

Coexistence of three microsporidia parasites in populations of the freshwater amphipod Gammarus roeseli: evidence for vertical transmission and positive effect on reproduction

inferredcites →https://doi.org/10.1016/j.ijpara.2006.07.001openalex-snapshot

Host manipulation of a freshwater crustacean (Gammarus roeseli) by an acanthocephalan parasite (Polymorphus minutus) in a biological invasion context

inferredcites →https://doi.org/10.1016/j.jip.2008.10.001openalex-snapshot

Effects of two acanthocephalan species on the reproduction of Hyalella patagonica (Amphipoda, Hyalellidae) in an Andean Patagonian Lake (Argentina)

inferredcites →https://doi.org/10.1016/j.jtbi.2006.12.007openalex-snapshot

Interference and the persistence of vertically transmitted parasites

inferredcites →https://doi.org/10.1016/j.pt.2004.01.014openalex-snapshot

Environmental parasitology: relevancy of parasites in monitoring environmental pollution

inferredcites →https://doi.org/10.1016/j.pt.2010.11.002openalex-snapshot

Combined effects of parasites and contaminants on animal health: parasites do matter

inferredcites →https://doi.org/10.1016/j.talanta.2005.09.043openalex-snapshot

A “toolbox” for biological and chemical monitoring requirements for the European Union's Water Framework Directive

inferredcites →https://doi.org/10.1016/j.tree.2006.11.005openalex-snapshot

Emphasizing the ecology in parasite community ecology

inferredcites →https://doi.org/10.1016/s0020-7519(00)00138-7openalex-snapshot

Differential influence of Pomphorhynchus laevis (Acanthocephala) on the behaviour of native and invader gammarid species

inferredcites →https://doi.org/10.1016/s0020-7519(01)00115-1openalex-snapshot

The effect of the acanthocephalan parasite Pomphorhynchus laevis on the lipid and glycogen content of its intermediate host Gammarus pulex

inferredcites →https://doi.org/10.1016/s0022-2011(02)00027-7openalex-snapshot

Effects of two acanthocephalan parasites on the fecundity and pairing status of female Gammarus pulex (Crustacea: Amphipoda)

inferredcites →https://doi.org/10.1016/s0076-6879(00)x0142-5openalex-snapshot

Carotenoids Part A: Chemistry, Separation, Quantitation, and Antioxidation

inferredcites →https://doi.org/10.1016/s0378-4347(98)00414-9openalex-snapshot

Determination of cellular thiols and glutathione-related enzyme activities: versatility of high-performance liquid chromatography–spectrofluorimetric detection

inferredcites →https://doi.org/10.1016/s0966-842x(02)02413-7openalex-snapshot

Does multiple infection select for raised virulence?

inferredcites →https://doi.org/10.1017/cbo9780511541902openalex-snapshot

Ecology of the Acanthocephala

inferredcites →https://doi.org/10.1017/s0022149x00003771openalex-snapshot

The Importance of the Acanthocephalan Polymorphus minutus as a Parasite of Domestic Ducks in the United Kingdom

inferredcites →https://doi.org/10.1017/s0022149x07751465openalex-snapshot

Pollution-induced heat shock protein expression in the amphipod Gammarus roeseli is affected by larvae of Polymorphus minutus (Acanthocephala)

inferredcites →https://doi.org/10.1017/s0031182006001375openalex-snapshot

Evidence of an altered protective effect of metallothioneins after cadmium exposure in the digenean parasite-infected cockle (Cerastoderma edule)

inferredcites →https://doi.org/10.1017/s0031182010000296openalex-snapshot

Prior residency does not always pay off – co-infections inDaphnia

inferredcites →https://doi.org/10.1017/s0031182012000315openalex-snapshot

Does the acanthocephalan parasite Polymorphus minutus modify the energy reserves and antitoxic defences of its intermediate host Gammarus roeseli?

inferredcites →https://doi.org/10.1017/s0031182099005910openalex-snapshot

Conflict between co-occurring manipulative parasites? An experimental study of the joint influence of two acanthocephalan parasites on the behaviour of Gammarus pulex

inferredcites →https://doi.org/10.1046/j.1365-2761.2003.00446.xopenalex-snapshot

Influence of enteric helminths on the distribution of intestinal endocrine cells belonging to the diffuse endocrine system in brown trout, Salmo trutta L.

inferredcites →https://doi.org/10.1046/j.1461-0248.2003.00414.xopenalex-snapshot

Mixed infections and insect–pathogen interactions

inferredcites →https://doi.org/10.1073/pnas.0335320100openalex-snapshot

Facultative bacterial symbionts in aphids confer resistance to parasitic wasps

inferredcites →https://doi.org/10.1080/03949370.2010.502321openalex-snapshot

Bird and amphipod parasites illustrate a gradient from adaptation to exaptation in complex life cycle

inferredcites →https://doi.org/10.1098/rsbl.2003.0115openalex-snapshot

Let your enemy do the work: within–host interactions between two fungal parasites of leaf–cutting ants

inferredcites →https://doi.org/10.1098/rspb.2005.3244openalex-snapshot

Conflict between parasites with different transmission strategies infecting an amphipod host

inferredcites →https://doi.org/10.1098/rspb.2007.1211openalex-snapshot

Symbiont-mediated protection

inferredcites →https://doi.org/10.1098/rspb.2010.1163openalex-snapshot

Parasite and host assemblages: embracing the reality will improve our knowledge of parasite transmission and virulence

inferredcites →https://doi.org/10.1111/j.1365-2427.1985.tb00215.xopenalex-snapshot

The role of lipids as feeding stimulants for shredding aquatic insects

inferredcites →https://doi.org/10.1111/j.1365-2427.1991.tb01393.xopenalex-snapshot

The effect of the acanthocephalan parasite (Pomphorhynchus laevis) on the drift of its intermediate host (Gammarus pulex)

inferredcites →https://doi.org/10.1111/j.1420-9101.2011.02264.xopenalex-snapshot

The expression of virulence during double infections by different parasites with conflicting host exploitation and transmission strategies

inferredcites →https://doi.org/10.1111/j.1558-5646.2010.00992.xopenalex-snapshot

THE EVOLUTIONARY IMPLICATIONS OF CONFLICT BETWEEN PARASITES WITH DIFFERENT TRANSMISSION MODES

inferredcites →https://doi.org/10.1111/j.1558-5646.2011.01330.xopenalex-snapshot

PROTECTION FIRST THEN FACILITATION: A MANIPULATIVE PARASITE MODULATES THE VULNERABILITY TO PREDATION OF ITS INTERMEDIATE HOST ACCORDING TO ITS OWN DEVELOPMENTAL STAGE

inferredcites →https://doi.org/10.1890/06-2105.1openalex-snapshot

MODIFICATION OF HOSTS' BEHAVIOR BY A PARASITE: FIELD EVIDENCE FOR ADAPTIVE MANIPULATION

inferredcites →https://doi.org/10.2307/3284656openalex-snapshot

Parasite-Altered Behavior in a Crustacean Intermediate Host: Field and Laboratory Studies

inferredcites →https://doi.org/10.3354/dao063077openalex-snapshot

Joint effects of parasitism and pollution on oxidative stress biomarkers in yellow perch Perca flavescens

inferredcites →https://doi.org/10.5860/choice.44-6852openalex-snapshot

Ecology of the acanthocephala

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Wide geographic distribution of overlooked parasites: Rare Microsporidia in Gammarus balcanicus, a species complex with a high rate of endemism

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Biochemical and morphological responses in Chironomus riparius (Diptera, Chironomidae) larvae exposed to lead-spiked sediment

inferred← citeshttps://doi.org/10.1002/etc.5689openalex-snapshot

Parasites and Pollutants: Effects of Multiple Stressors on Aquatic Organisms

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Anthropogenic Stressor and Parasite Interactions in Aquatic Environments

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Does fish reproduction and metabolic activity influence metal levels in fish intestinal parasites, acanthocephalans, during fish spawning and post-spawning period?

inferred← citeshttps://doi.org/10.1016/j.ecoenv.2026.120199openalex-snapshot

Parasitic interactions modulate the physiological responses of Gammarus fossarum to the herbicide metazachlor

inferred← citeshttps://doi.org/10.1016/j.envpol.2017.03.006openalex-snapshot

Ecotoxicoproteomic assessment of the functional alterations caused by chronic metallic exposures in gammarids

inferred← citeshttps://doi.org/10.1016/j.ijppaw.2015.08.001openalex-snapshot

Host manipulation in the face of environmental changes: Ecological consequences

inferred← citeshttps://doi.org/10.1016/j.marpolbul.2020.111905openalex-snapshot

Preliminary study of oxidative stress biomarkers and trace elements in North Sea Harbour Seals

inferred← citeshttps://doi.org/10.1016/j.scitotenv.2013.06.041openalex-snapshot

Effect of acanthocephalan infection on metal, total protein and metallothionein concentrations in European chub from a Sava River section with low metal contamination

inferred← citeshttps://doi.org/10.1016/j.scitotenv.2018.07.227openalex-snapshot

High stoichiometric food quality increases moulting organism vulnerability to pollutant impacts: An experimental test with Gammarus fossarum (Crustacea: Amphipoda)

inferred← citeshttps://doi.org/10.1017/s003118202100038xopenalex-snapshot

Effects of multiple stressors on northern leopard frogs in agricultural wetlands

inferred← citeshttps://doi.org/10.1139/er-2014-0026openalex-snapshot

Testing for dual impacts of contaminants and parasites on hosts: the importance of skew

inferred← citeshttps://doi.org/10.1186/1756-3305-7-170openalex-snapshot

Effect of multiple microsporidian infections and temperature stress on the heat shock protein 70 (hsp70) response of the amphipod Gammarus pulex

inferred← citeshttps://doi.org/10.1186/s13071-015-1036-6openalex-snapshot

Invaders, natives and their enemies: distribution patterns of amphipods and their microsporidian parasites in the Ruhr Metropolis, Germany

inferred← citeshttps://doi.org/10.1186/s13071-019-3571-zopenalex-snapshot

Microsporidian infections in the species complex Gammarus roeselii (Amphipoda) over its geographical range: evidence for both host–parasite co-diversification and recent host shifts

inferred← citeshttps://doi.org/10.1371/journal.pone.0231247openalex-snapshot

Origin of the natural variation in the storage of dietary carotenoids in freshwater amphipod crustaceans

inferred← citeshttps://doi.org/10.1371/journal.ppat.1005459openalex-snapshot

When Parasites Are Good for Health: Cestode Parasitism Increases Resistance to Arsenic in Brine Shrimps

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Widespread infection, diversification and old host associations of Nosema Microsporidia in European freshwater gammarids (Amphipoda)

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Amphipod parasites may bias results of ecotoxicological research

inferred← citeshttps://doi.org/10.3389/fmicb.2014.00248openalex-snapshot

Cooperation and conflict in host manipulation: interactions among macro-parasites and micro-organisms

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Evolutionary histories of symbioses between microsporidia and their amphipod hosts : contribution of studying two hosts over their geographic ranges.

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Effect of the environment on the interaction between gammarids (Crustacea : Amphipoda) and their manipulative acanthocephalan parasites

inferred← citeshttps://doi.org/10.7287/peerj.1353v0.1/reviews/1openalex-snapshot

Peer Review #1 of "Effects of the acanthocephalan Polymorphus minutus and the microsporidian Dictyocoela duebenum on energy reserves and stress response of cadmium exposed Gammarus fossarum (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.1353v0.1/reviews/2openalex-snapshot

Peer Review #2 of "Effects of the acanthocephalan Polymorphus minutus and the microsporidian Dictyocoela duebenum on energy reserves and stress response of cadmium exposed Gammarus fossarum (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.1353v0.2/reviews/1openalex-snapshot

Peer Review #1 of "Effects of the acanthocephalan Polymorphus minutus and the microsporidian Dictyocoela duebenum on energy reserves and stress response of cadmium exposed Gammarus fossarum (v0.2)"

inferred← citeshttps://doi.org/10.7287/peerj.1353v0.2/reviews/2openalex-snapshot

Peer Review #2 of "Effects of the acanthocephalan Polymorphus minutus and the microsporidian Dictyocoela duebenum on energy reserves and stress response of cadmium exposed Gammarus fossarum (v0.2)"

inferred← citeshttps://doi.org/10.7717/peerj.1353openalex-snapshot

Effects of the acanthocephalan Polymorphus minutus and the microsporidian Dictyocoela duebenum on energy reserves and stress response of cadmium exposed Gammarus fossarum

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.