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      Malarial pathocoenosis: beneficial and deleterious interactions between malaria and other human diseases

      review-article
      Frontiers in Physiology
      Frontiers Media S.A.
      malaria, pathocoenosis, comorbidity, malaria-therapy, syphilis, plague, cholera

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          Abstract

          In nature, organisms are commonly infected by an assemblage of different parasite species or by genetically distinct parasite strains that interact in complex ways. Linked to co-infections, pathocoenosis, a term proposed by M. Grmek in 1969, refers to a pathological state arising from the interactions of diseases within a population and to the temporal and spatial dynamics of all of the diseases. In the long run, malaria was certainly one of the most important component of past pathocoenoses. Today this disease, which affects hundreds of millions of individuals and results in approximately one million deaths each year, is always highly endemic in over 20% of the world and is thus co-endemic with many other diseases. Therefore, the incidences of co-infections and possible direct and indirect interactions with Plasmodium parasites are very high. Both positive and negative interactions between malaria and other diseases caused by parasites belonging to numerous taxa have been described and in some cases, malaria may modify the process of another disease without being affected itself. Interactions include those observed during voluntary malarial infections intended to cure neuro-syphilis or during the enhanced activations of bacterial gastro-intestinal diseases and HIV infections. Complex relationships with multiple effects should also be considered, such as those observed during helminth infections. Moreover, reports dating back over 2000 years suggested that co- and multiple infections have generally deleterious consequences and analyses of historical texts indicated that malaria might exacerbate both plague and cholera, among other diseases. Possible biases affecting the research of etiological agents caused by the protean manifestations of malaria are discussed. A better understanding of the manner by which pathogens, particularly Plasmodium, modulate immune responses is particularly important for the diagnosis, cure, and control of diseases in human populations.

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          Most cited references84

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          Understanding quantitative genetic variation.

          Until recently, it was impracticable to identify the genes that are responsible for variation in continuous traits, or to directly observe the effects of their different alleles. Now, the abundance of genetic markers has made it possible to identify quantitative trait loci (QTL)--the regions of a chromosome or, ideally, individual sequence variants that are responsible for trait variation. What kind of QTL do we expect to find and what can our observations of QTL tell us about how organisms evolve? The key to understanding the evolutionary significance of QTL is to understand the nature of inherited variation, not in the immediate mechanistic sense of how genes influence phenotype, but, rather, to know what evolutionary forces maintain genetic variability.
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            The ecology of genetically diverse infections.

            Microparasite infections often consist of genetically distinct clonal lineages. Ecological interactions between these lineages within hosts can influence disease severity, epidemiology, and evolution. Many medical and veterinary interventions have an impact on genetic diversity within infections, but there is little understanding of the long-term consequences of such interventions for public and animal health. Indeed, much of the theory in this area is based on assumptions contradicted by the available data.
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              Multiple infections and the evolution of virulence.

              Infections that consist of multiple parasite strains or species are common in the wild and are a major public health concern. Theory suggests that these infections have a key influence on the evolution of infectious diseases and, more specifically, on virulence evolution. However, we still lack an overall vision of the empirical support for these predictions. We argue that within-host interactions between parasites largely determine how virulence evolves and that experimental data support model predictions. Then, we explore the main limitation of the experimental study of such 'mixed infections', which is that it draws conclusions on evolutionary outcomes from studies conducted at the individual level. We also discuss differences between coinfections caused by different strains of the same species or by different species. Overall, we argue that it is possible to make sense out of the complexity inherent to multiple infections and that experimental evolution settings may provide the best opportunity to further our understanding of virulence evolution. © 2013 Blackwell Publishing Ltd/CNRS.
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                Author and article information

                Contributors
                Journal
                Front Physiol
                Front Physiol
                Front. Physiol.
                Frontiers in Physiology
                Frontiers Media S.A.
                1664-042X
                21 November 2014
                2014
                : 5
                : 441
                Affiliations
                Aix-Marseille Université, Centre National de la Recherche Scientifique, Centrale Marseille, I2M, UMR 7373 Marseille, France
                Author notes

                Edited by: Anaïs Baudot, Centre National de la Recherche Scientifique, France

                Reviewed by: Satyaprakash Nayak, Pfizer Inc., USA; Jose-Luis Portero, HM Sanchinarro Norte, Spain

                *Correspondence: Eric Faure, Aix Marseille Université, Centre National de la Recherche Scientifique, Centrale Marseille, I2M, UMR 7373, 3 Place Victor Hugo, 13453 Marseille, France e-mail: eric.faure@ 123456univ-amu.fr

                This article was submitted to Systems Biology, a section of the journal Frontiers in Physiology.

                Article
                10.3389/fphys.2014.00441
                4240042
                25484866
                3a457a5d-2f2f-4469-a295-c071879fe720
                Copyright © 2014 Faure.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 15 May 2014
                : 28 October 2014
                Page count
                Figures: 0, Tables: 0, Equations: 0, References: 146, Pages: 13, Words: 12897
                Categories
                Physiology
                Review Article

                Anatomy & Physiology
                malaria,pathocoenosis,comorbidity,malaria-therapy,syphilis,plague,cholera
                Anatomy & Physiology
                malaria, pathocoenosis, comorbidity, malaria-therapy, syphilis, plague, cholera

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