Why Helicobacter pylori has Lewis antigens

In mimicry with human gastric epithelial cells, the lipopolysaccharide of Helicobacter pylori expresses Lewis blood group antigens. Recent data suggest that molecular mimicry does not promote immune evasion, nor does it lead to induction of autoantibodies, but that H. pylori Lewis X mediates adhesion to gastric epithelial cells and is essential for colonization.     

Pollinator-mediated interactions between a pathogenic fungus, Uromyces pisi (Pucciniaceae), and its host plant,Euphorbia cyparissias (Euphorbiaceae)

The plant Euphorbia cyparissias is commonly infected by rust fungi of the species complex Uromyces pisi. When infected, E. cyparissias is unable to flower, but instead is induced by the fungus to form pseudoflowers. Pseudoflowers are rosettes of yellow leaves upon which the fungus presents its gametes in a sweet-smelling fungal nectar. We hypothesized that the fungi, as they are heterothallic, are dependent on insect visitation to cross-fertilize their mating types. We confirmed that insects are required with an insect exclusion experiment. We further hypothesized that pseudoflowers of U. pisi interact with uninfected true host flowers through insects during their period of co-"flowering" in early spring. We conducted artificial array experiments in the field to test whether the two species share insects and whether they influenced each other's insect visitation. Insects moved between true flowers and pseudoflowers, but true flowers received more visits over all. Pseudoflowers and true flowers did not influence each other's visitation rates in mixtures. However, shorter visits were observed on pseudoflowers in mixtures than monocultures, suggesting that true flowers might be competitors for pseudoflowers. Further experiments are needed to determine whether the similarity of pseudoflowers to true flowers is adaptive.     

Plant defence signals and Batesian mimicry

In a game theory context, we investigated conditions for an evolutionarily stable equilibrium of defended, signalling plants, and plants mimicking these signals – that is, conditions for a stable mimicry complex. We modelled this in three steps. First, we analysed conditions for selection for defended, signalling plants, in a population of undefended plants. Second, we analysed conditions for when mimicking plants can invade a population of defended, signalling plants, leading to a stable equilibrium between the two strategies. Third, we analysed how sampling of signalling plants by herbivores affects the equilibrium between the strategies. The predictions show that mimicry of plant defence signals may be common, and even imperfect mimics could invade a population of defended, signalling plants. Whether the latter prediction holds or not depends on how herbivores generalize over signals, and on the length of their avoidance sequence'. The length of the avoidance sequence is the number of signalling plants that a herbivore avoids to attack, after attacking a defended plant. If herbivores always sample signalling plants, then mimicry cannot evolve, whereas if herbivores have a long avoidance sequence, this may allow selection even for imperfect mimics.     

The adaptive bases of ant-mimicry in a neotropical aphantochilid spider (Araneae: Aphantochilidae)

The aphantochilid spider Aphanlochilus rogersi accurately mimics black ants of tribe Cephalotini, and is commonly found in the neighbourhood of its models' nests. The mimic seems to be a specialized predator of this type of ant, rejecting any insect offered as prey other than cephalotines. In the field, A. rogersi was observed preying on the model species Zacryptocerus pusillus. In captivity, the spider preyed on the models Z. pusillus and Z. depressus, as well as on the yellow non-model Z. clypeatus. Recognition of correct prey by A. rogersi appears to be based primarily on visual and tactile stimuli. Capturing ant prey from behind was the most common attack tactic observed in A. rogersi, and is probably safer than frontal attacks, as in this case the spider can be bitten on the legs before the ant is immobilized. Aphanlochilus rogersi, when feeding on the hard-bodied ant models, uses the ant corpses as a ‘protective shield’ against patrolling ants of the victim's colony and resembles an ant carrying a dead companion. Certain types of mimetic traits in A. rogersi (close similarity to ant models in integument texture and pilosity of body and legs), together with ‘shielding behaviour’, are thought to function as ant-deceivers, facilitating the obligatory intimate contact the mimic must make with cephalotines in order to capture a prey among other ants. The close similarity in the arrangement of dorsal spines, body shape, integument brightness and locomotion, together with antennal illusion, is regarded as a strategy of A. rogersi for deceiving visually-hunting predators that avoid its sharp spined ant models. It is proposed that ant-mimicry in A. rogersi has both an aggressive and a Batesian adaptive component, and evolved as a result of combined selective pressures exerted both by Cephalotini ant models (through defensive behaviour towards the mimics which attack them) and predators that avoid cephalotines (through predatory behaviour toward imperfect mimics). This suggestion is schematized and discussed in terms of two tripartite mimicry systems.     

Stable Heliconius butterfly hybrid zones are correlated with a local rainfall peak at the edge of the Amazon basin

Multilocus clines between Müllerian mimetic races of Heliconius butterflies provide a classic example of the maintenance of hybrid zones and their importance in speciation. Concordant hybrid zones in the mimics Heliconius erato and H. melpomene in northern Peru were carefully documented in the 1980s, and this prior work now permits a historical analysis of the movement or stasis of the zones. Previous work predicted that these zones might be moving toward the Andes due to selective asymmetry. Extensive deforestation and climate change might also be expected to affect the positions and widths of the hybrid zones. We show that the positions and shapes of these hybrid zones have instead remained remarkably stable between 1985 and 2012. The stability of this interaction strongly implicates continued selection, rather than neutral mixing following secondary contact. The stability of cline widths and strong linkage disequilibria (gametic correlation coefficients R_max = 0.35–0.56 among unlinked loci) over 25 years suggest that mimetic selection pressures on each color pattern locus have remained approximately constant (s ≈ 0.13–0.40 per locus in both species). Exceptionally high levels of precipitation at the edge of the easternmost Andes may act as a population density trough for butterflies, trapping the hybrid zones at the foot of the mountains, and preventing movement. As such, our results falsify one prediction of the Pleistocene Refugium theory: That the ranges of divergent species or subspecies should be centered on regions characterized by maxima of rainfall, with hybrid zones falling in more arid regions between them.     

Canstatin基因转染对人肝癌HepG-2细胞体外血管生成拟态的影响

目的:探讨转染Canstatin基因对人肝癌HepG-2细胞体外形成血管生成拟态的影响。方法:将Canstatin基因通过脂质体法转染人肝癌HepG-2细胞,行G418筛选获得转基因细胞克隆。用SDS-PAGE电泳检测Canstatin蛋白在转基因细胞培养上清液中的表达;建立HepG-2细胞人工基底膜基质凝胶体外三维细胞培养模型,观察HepG-2细胞能否形成血管生成拟态,并比较转基因和未转基因细胞的管道形成能力。结果:Canstatin在转染人HepG-2细胞中表达并分泌至上清液中,人肝癌HepG-2细胞在体外三维培养条件下能够形成血管生成拟态。Canstatin基因转染HepG-2细胞组的管状结构数量高于空载体组和HepG-2细胞组,转染细胞管道形成能力明显受抑制。结论:人肝癌HepG-2细胞株可形成血管生成拟态,Canstatin能抑制人肝癌细胞株HepG-2体外血管生成拟态形成。     

The evolution and diversification of oakleaf butterflies

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A Learning Strategy for Predator Preying on Edible and Inedible Prey

In this paper I propose a reinforcement learning model for a predator preying upon two types of prey, the unpalatable (noxious) models, and the palatable mimics. The latter type of prey resembles the models in appearance so as to derive some protection from the predator who must avoid the unpalatable models. Essentially the predator is treated as a learning automaton adopting a simple reinforcement learning strategy in order to increase its consumption of palatable prey and reduce the consumption of unpalatable ones. The populations of both mimics and models are assumed to grow logistically.     

Vision-based ability of an ant-mimicking jumping spider to discriminate between models,conspecific individuals and prey

Myrmarachne assimilis, an ant-like (myrmecomorphic) jumping spider (Araneae, Salticidae) from the Philippines, is a Batesian mimic of Oecophylla smaragdina, the Asian weaver ant. Salticids are well known for their acute eyesight and the elaborate vision-based display behaviour they adopt during encounters with conspecific individuals, but most salticids are not myrmecomorphic. Despite its unusual morphology, M. assimilis adopts display behaviour during intraspecific interactions that is similar to the display behaviour of more typical salticids. The specificity with which M. assimilis deploys display behaviour is investigated and provides insights into this mimic’s ability to differentiate, by sight alone, between models, conspecific individuals and prey. During each standardized test, an adult M. assimilis female was in a large cage along with a small transparent glass vial, a stimulus animal being enclosed in the vial such that potential optical cues, but not potential chemical cues, were available to the tested M. assimilis individual. Depending on the test, the stimulus animal was another adult M. assimilis female, a house fly (prey) or an ant (Camponotus sp. or O. smaragdina). Only the conspecific female consistently elicited display from M. assimilis, implying that M. assimilis is a Batesian mimic that can, when relying on vision alone, discriminate between conspecific individuals, models and prey. Received 12 June 2006; revised 22 September 2006; accepted 26 September 2006.     

Predator perception and the interrelation between different forms of protective coloration

Animals possess a range of defensive markings to reduce the risk of predation, including warning colours, camouflage, eyespots and mimicry. These different strategies are frequently considered independently, and with little regard towards predator vision, even though they may be linked in various ways and can be fully understood only in terms of predator perception. For example, camouflage and warning coloration need not be mutually exclusive, and may frequently exploit similar features of visual perception. This paper outlines how different forms of protective markings can be understood from predator perception and illustrates how this is fundamental in determining the mechanisms underlying, and the interrelation between, different strategies. Suggestions are made for future work, and potential mechanisms discussed in relation to various forms of defensive coloration, including disruptive coloration, eyespots, dazzle markings, motion camouflage, aposematism and mimicry.