Coevolution and maladaptation

Many of the most commonly cited examples of exquisite adaptationare of coevolved symbioses. As we learn more about the coevolutionaryprocess, however, it is becoming increasingly evident that coevolutionmay also keep populations moderately maladapted much of thetime. As a result, coevolving populations may only rarely occupyadaptive peaks, because the selective landscape is under continualchange through reciprocal selection on the species themselves.These shifting patterns of coadaptation are further shaped bythe geographic structure of most species. Selection mosaicsacross landscapes and coevolutionary hotspots can favor differentevolutionary trajectories in different populations. The combinedaction of gene flow, random genetic drift, and local extinctionof populations may then continually remold these local patterns,creating a geographic mosaic in the degrees of maladaptationfound within local interactions. Recent mathematical modelsof the geographic mosaic of coevolution suggest that complexmosaics of maladaptation are a likely consequence of spatiallystructured species interactions. These models indicate thatthe spatial structure of maladaptation may depend upon the typeof coevolutionary interaction, the underlying selection mosaic,and patterns of gene flow across landscapes. By maintaininglocal polymorphisms and driving the divergence of populations,coevolution may produce spatial patterns of maladaptation thatare a source of ongoing innovation and diversification in speciesinteractions.     

Getting Worse: The Stigmatization of Obese Children

Objective: The prevalence of childhood obesity more than doubled in the period from 1961 to 2001. We replicated a 1961 study of stigma in childhood obesity to see what effect this increased prevalence has had on this stigma. Research Methods and Procedures: Participants included 458 5th‐ and 6th‐grade children attending upper‐middle and lower‐middle income U.S. public schools. Children ranked six drawings of same‐sex children with obesity, various disabilities, or no disability (“healthy”), in order of how well they liked each child. Results: Children in both the present and the 1961 study liked the drawing of the obese child least. The obese child was liked significantly less in the present study than in 1961 [Kruskal‐Wallis H (1) = 130.53, p < 0.001]. Girls liked the obese child less than boys did [H (1) = 5.23, p < 0.02]. Children ranked the healthy child highest and significantly higher than in 1961 [H (1) = 245.40, p < 0.001]. The difference in liking between the healthy and obese child was currently 40.8% greater than in 1961. Discussion: Stigmatization of obesity by children appears to have increased over the last 40 years.     

Antagonistic Coevolution and Sex

One of the leading hypotheses for the maintenance of sexual reproduction is the Red Queen hypothesis. The underlying premise of the Red Queen hypothesis is that parasites rapidly evolve to infect common host genotypes. This response by parasites could result in the long-term maintenance of genetic variation and may favor sexual reproduction over asexual reproduction. The underlying ideas present a wonderful microcosm for teaching evolution. Here I present the reasons for why sex is anomalous for evolutionary theory, the rationale underlying the Red Queen hypothesis, and some empirical studies of the Red Queen hypothesis using a freshwater snail. The empirical results are consistent with the Red Queen hypothesis. In addition, the distribution of sexual and asexual reproduction in the snail leads naturally to thinking about coevolution in a geographic mosaic of parasite-mediated natural selection.     

食虫蝙蝠与昆虫之间的相互作用和协同进化关系

食虫蝙蝠与昆虫之间是捕食和被捕食的关系,夜行性昆虫是食虫蝙蝠主要的食物来源。在漫长的协同进化中,蝙蝠施加的捕食压力导致夜行性昆虫一系列特征的进化,其中一部分昆虫进化出能听到蝙蝠的超声波信号并采取逃跑行为或者能通过其它方式躲避蝙蝠,同时昆虫的适应性特征同样影响着蝙蝠的回声定位和捕食策略。本文从蝙蝠捕食昆虫的种类、昆虫对蝙蝠捕食的反应和食虫性蝙蝠对昆虫防卫的适应对策等三个方面对食虫蝙蝠与昆虫之间的相互关系进行了概述。     

Molecular Phylogeny and Coevolution

Abstract Recent advances in molecular phylogenetic estimation in diverse organisms have improved our understanding of coevolution. From the phylogenies of interacting organisms, we can interpret the evolution of adaptive characters, and the history of interaction. Molecular approaches are generally more informative than these based solely on phenotypic characters. Molecular genetic method can be applied to organisms that have only simple morphological features and can be used for comparisons at any taxonomic level. Estimation of divergence time is also possible but still difficult because evolutionary rates of macromolecules are not always constant and suitable fossil records are often not available for calibrating rates of change. Here I review recent progress in the application of molecular techniques to the interpretation of coevolutionary relationships.     

The Coevolution of Virulence: Tolerance in Perspective

Coevolutionary interactions, such as those between host and parasite, predator and prey, or plant and pollinator, evolve subject to the genes of both interactors. It is clear, for example, that the evolution of pollination strategies can only be understood with knowledge of both the pollinator and the pollinated. Studies of the evolution of virulence, the reduction in host fitness due to infection, have nonetheless tended to focus on parasite evolution. Host-centric approaches have also been proposed—for example, under the rubric of “tolerance”, the ability of hosts to minimize virulence without necessarily minimizing parasite density. Within the tolerance framework, however, there is room for more comprehensive measures of host fitness traits, and for fuller consideration of the consequences of coevolution. For example, the evolution of tolerance can result in changed selection on parasite populations, which should provoke parasite evolution despite the fact that tolerance is not directly antagonistic to parasite fitness. As a result, consideration of the potential for parasite counter-adaptation to host tolerance—whether evolved or medially manipulated—is essential to the emergence of a cohesive theory of biotic partnerships and robust disease control strategies.     

Coevolution of insect trypsins and inhibitors

Many plant proteinase inhibitors have lysine at the P1 position, presumably to avoid hydrolysis by insect trypsins. Lepidopteran trypsins appear to have adapted to resist proteinase inhibitors through increased inhibitor hydrolysis and decreased binding to inhibitor hydrophilic reactive sites. Lepidopteran digestive trypsins prefer lysine at the P1 position and have substrate binding subsites more hydrophobic than trypsins from insects in other orders. All available sequences of sensitive and inhibitor-insensitive insect trypsins were aligned with porcine trypsin, for which interactions with Kunitz and Bowman-Birk inhibitor are known. After discounting conserved positions and positions not typical of sensitive or insensitive trypsins, the following residues were considered important to insect trypsin-PI interactions (chymotrypsin numbering): 60, 94, 97, 98, 99, 188, 190, 213, 215, 217, 219, 228. These residues support the Neighbor Joining analysis tree branches separating sensitive and insensitive trypsin sequences. Primary sequences interacting with PIs are around the active site, with some forming part of the S1 (188, 217, 219 and 228) or S4 (99, 215) pockets.     

Stigmatization of patients suffering from schizophrenia

For the general public, but also for healthcare professionals, schizophrenia is still one of those areas of medicine connected with feelings of unease, fear and prejudice. These feelings lead to stigmatization and discrimination which are unjust processes which put patients suffering from mental illnesses into undesirable and unequal positions. Aim of this research was to establish the extent of stigmatization of mentally ill patients among the population of healthcare professionals and future healthcare professionals and if they differ from general population. Results show that stigmatization of schizophrenic patients is high among all included populations. Although there were no statistical differences between groups regarding the assessment of schizophrenic patients, nurses employed in psychiatric wards exhibited a tendency towards higher acceptance of schizophrenic patients, as well as better understanding of that illness. This data emphasizes a growing need for continuous education of general population but also of healthcare professionals.     

Coevolution of physiological systems

Coevolution is the interaction in the process of evolution of different species that are closely related biologically but do not exchange genetic information. In this paper, we address the problem of coevolution of the whole organism’s physiological systems as a process of the interrelated development of structure and function as well as their regulatory systems during the formation of living organisms. We consider the coevolution of osmoregulation and the nitrogen metabolism type, systemic and individual coevolutionary strategies of cell volume regulation in poikiloosmotic and homoiosmotic animals, coevolution of effectory organs and endocrine factors in the development of water–salt homeostasis, co-involvement of neurohypophyseal nonapeptides and glucagon-like peptide-1 in the regulation of the renal function aimed at stabilizing physico-chemical parameters of extracellular fluids which make up the internal environment of the organism.     

Coevolution of bacteria and their viruses

Coevolution between bacteria and bacteriophages can be characterized as an infinitive constant evolutionary battle (phage-host arm race), which starts during phage adsorption and penetration into host cell, continues during phage replication inside the cells, and remains preserved also during prophage lysogeny. Bacteriophage may exist inside the bacterial cells in four forms with different evolutionary strategies: as a replicating virus during the lytic cycle, in an unstable carrier state termed pseudolysogeny, as a prophage with complete genome during the lysogeny, or as a defective cryptic prophage. Some defensive mechanisms of bacteria and virus countermeasures are characterized, and some evolutionary questions concerning phage–host relationship are discussed.     

中国种子植物内生真菌资源及菌植协同进化

综述了中国种子植物内生真菌资源研究概况,比较了裸子植物和被子植物内生真菌种类,它们都具有肉座菌目(Hypocreales),粪壳菌目(Sordariales),散囊菌目(Eurotiales),毛霉目(Mucorales)及不产孢类(Myceliasterilia)内生真菌。裸子植物内生真菌涉及52个属,既包括高等的子囊菌和担子菌,也包括低等的卵菌(Oomycetes)和接合菌(Zygomycetes)类。被子植物涉及60个属,主要为高等的子囊菌(Ascomycetes)和担子菌(Basidiomycetes),低等的卵菌和接合菌报道很少。双子叶植物涉及40个属,单子叶植物内生真菌涉及30个属,两类被子植物所报道的内生真菌只有11个属相同。裸子植物与双子叶植物内生真菌相似程度较高,都具有炭角菌目(Xylariales)、格孢腔菌目(Pleosporales)、柔膜菌目(Helotiales)和白粉菌目(Erysiphales),刺盘孢菌属(Colletotrichum)、拟茎点霉属(Phomopsis)、枝孢霉属(Cladosporium)、地霉属(Geotrichum)等内真菌,共20个属相同。各类种子植物具有自己独特的一些内生真菌。还对植物与其内生真菌的协同进化关系进行了分析。     

Coevolution of Interacting Fertilization Proteins

Reproductive proteins are among the fastest evolving in the proteome, often due to the consequences of positive selection, and their rapid evolution is frequently attributed to a coevolutionary process between interacting female and male proteins. Such a process could leave characteristic signatures at coevolving genes. One signature of coevolution, predicted by sexual selection theory, is an association of alleles between the two genes. Another predicted signature is a correlation of evolutionary rates during divergence due to compensatory evolution. We studied female–male coevolution in the abalone by resequencing sperm lysin and its interacting egg coat protein, VERL, in populations of two species. As predicted, we found intergenic linkage disequilibrium between lysin and VERL, despite our demonstration that they are not physically linked. This finding supports a central prediction of sexual selection using actual genotypes, that of an association between a male trait and its female preference locus. We also created a novel likelihood method to show that lysin and VERL have experienced correlated rates of evolution. These two signatures of coevolution can provide statistical rigor to hypotheses of coevolution and could be exploited for identifying coevolving proteins a priori. We also present polymorphism-based evidence for positive selection and implicate recent selective events at the specific structural regions of lysin and VERL responsible for their species-specific interaction. Finally, we observed deep subdivision between VERL alleles in one species, which matches a theoretical prediction of sexual conflict. Thus, abalone fertilization proteins illustrate how coevolution can lead to reproductive barriers and potentially drive speciation.