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101.
Disease spread in small-size directed networks: Epidemic threshold, correlation between links to and from nodes, and clustering 总被引:1,自引:0,他引:1
Mathieu Moslonka-Lefebvre Marco Pautasso Mike J. Jeger 《Journal of theoretical biology》2009,260(3):402-411
Network epidemiology has mainly focused on large-scale complex networks. It is unclear whether findings of these investigations also apply to networks of small size. This knowledge gap is of relevance for many biological applications, including meta-communities, plant–pollinator interactions and the spread of the oomycete pathogen Phytophthora ramorum in networks of plant nurseries. Moreover, many small-size biological networks are inherently asymmetrical and thus cannot be realistically modelled with undirected networks. We modelled disease spread and establishment in directed networks of 100 and 500 nodes at four levels of connectance in six network structures (local, small-world, random, one-way, uncorrelated, and two-way scale-free networks). The model was based on the probability of infection persistence in a node and of infection transmission between connected nodes. Regardless of the size of the network, the epidemic threshold did not depend on the starting node of infection but was negatively related to the correlation coefficient between in- and out-degree for all structures, unless networks were sparsely connected. In this case clustering played a significant role. For small-size scale-free directed networks to have a lower epidemic threshold than other network structures, there needs to be a positive correlation between number of links to and from nodes. When this correlation is negative (one-way scale-free networks), the epidemic threshold for small-size networks can be higher than in non-scale-free networks. Clustering does not necessarily have an influence on the epidemic threshold if connectance is kept constant. Analyses of the influence of the clustering on the epidemic threshold in directed networks can also be spurious if they do not consider simultaneously the effect of the correlation coefficient between in- and out-degree. 相似文献
102.
Mike S. Fowler 《Oikos》2009,118(4):604-614
The decision to move between patches in the environment is among the most important life history choices an organism can make. I derive a new density dependent dispersal rule, and examine how dispersal decisions based on avoiding fitness loss associated with an Allee effect or competitive effects impact upon population dynamics in spatially structured populations with qualitatively different dynamics. I also investigate the effects of the number of patches in the system and a limit to the patch sampling time available to dispersers. Dispersing to avoid competitive pressures can destabilise otherwise stable population dynamics, and stabilise chaotic dynamics. Dispersing to avoid an Allee effect does not qualitatively change local population dynamics until eventually driving unstable populations to global extinction with a sufficiently high fitness threshold. A time limit for sampling can stabilise dynamics if dispersal is based on escaping the Allee effect, and rescue populations from global extinction. The results are sensitive to the number of patches available in the environment and suggest that dispersal to avoid an Allee effect will only arise under biologically plausible conditions, i.e. where there is a limit to the number of dispersal attempts that can be made between generations. 相似文献
103.
Epithelial sodium channels (ENaCs) are sodium‐conducting ion channels that are located in the apical membrane of various epithelia. They represent the rate‐limiting step for transeptihelial sodium‐ and thereby water‐transport. ENaCs contribute to a variety of physiological processes including the regulation of salt and water homeostasis, blood pressure or the water content of the lung. Further, malfunctions in ENaC regulation contribute to the pathogenesis of diseases like hypertension or pulmonary oedema. This article describes the function and physiology of epithelial sodium channels as well as cellular mechanisms that determine the activity of these ion channels. 相似文献
104.
Ray C. Bartolo Natalie Harfoot Mike Gill Kristy Demmers Bernie McLeod A. Grant Butt 《Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology》2009,179(8):997-1010
The colon of the brushtail possum does not have an electrogenic secretory response. Given the functional significance of electrogenic
Cl− secretion in the intestine of eutherian mammals, we have investigated the secretory response in the small intestine of this
marsupial. In the Ussing chamber cAMP-dependent secretagogues stimulated a sustained increase in ileal short-circuit current
(Isc), whereas Ca2+-dependent secretagogues induced a transient increase. Both the responses were inhibited by mucosal addition of the anion
channel blocker 5-nitro-2-(3-phenylpropylamino) benzoic acid (100 μmol l−1), consistent with an anion secretory response. However, the responses were not inhibited by serosal bumetanide (10 μmol l−1) and were independent of bath Cl−, indicating that the stimulated ileal Isc does not involve electrogenic Cl− secretion driven by the NaK2Cl cotransporter, NKCC1. Consistent with this, there were low levels of NKCC1 expression in the
ileal epithelium. In particular, NKCC1 expression in the ileal crypt cells was comparable to that of the villous cells. This
differs from eutherian mammals where high levels of NKCC1 expression in the ileal crypt cells are associated with their role
in Cl− secretion. The cAMP- and Ca2+-dependent secretory responses were inhibited by the removal of HCO3
− suggesting that these responses were due to electrogenic HCO3
− secretion. We conclude that the ileum of the possum does not secrete Cl− due to low levels of NKCC1 expression. It does however appear to secrete HCO3
−. These results are further significant examples of differences in the transport function of the possum intestinal epithelium
compared with eutherian mammals. 相似文献
105.
Robert O. Hughes John K. Walker D. Joseph Rogier Steve E. Heasley Rhadika M. Blevis-Bal Alan G. Benson E. Jon Jacobsen Jerry W. Cubbage Yvette M. Fobian Dafydd R. Owen John N. Freskos John M. Molyneaux David L. Brown Brad A. Acker Todd M. Maddux Mike B. Tollefson Joseph B. Moon Brent V. Mischke Jeanne M. Rumsey Yi Zheng Ying Yu 《Bioorganic & medicinal chemistry letters》2009,19(17):5209-5213
We describe efforts to improve the pharmacokinetic profile of the aminopyridopyrazinone class of PDE5 inhibitors. These efforts led to the discovery of 3-[(trans-4-hydroxycyclohexyl)amino]-7-(6-methoxypyridin-3-yl)-1-(2-propoxyethyl)pyrido[3,4-b]pyrazin-2(1H)-one, a potent and selective inhibitor of PDE5 with an excellent PK profile. 相似文献
106.
Jiwen Liu Zice Fu Yingcai Wang Mike Schmitt Alan Huang Derek Marshall George Tonn Lisa Seitz Tim Sullivan H. Lucy Tang Tassie Collins Julio Medina 《Bioorganic & medicinal chemistry letters》2009,19(22):6419-6423
A series of phenylacetic acid derivatives was discovered as CRTH2 antagonists. Modification of the series led to compounds that are also antagonists of DP. Since activation of CRTH2 and DP are believed to play key roles in mediating responses of asthma and other immune diseases, this series was optimized to increase the dual antagonistic activities and improve pharmacokinetic properties. These efforts led to selection of AMG 009 as a clinical candidate. 相似文献
107.
Ian Sorrell Andrew White Amy B. Pedersen Rosemary S. Hails Mike Boots 《Proceedings. Biological sciences / The Royal Society》2009,276(1665):2217-2226
Many parasites and pathogens cause silent/covert infections in addition to the more obvious infectious disease-causing pathology. Here, we consider how assumptions concerning superinfection, protection and seasonal host birth and transmission rates affect the evolution of such covert infections as a parasite strategy. Regardless of whether there is vertical infection or effects on sterility, overt infection is always disadvantageous in relatively constant host populations unless it provides protection from superinfection. If covert infections are protective, all individuals will enter the covert stage if there is enough vertical transmission, and revert to overt infections after a ‘latent’ period (susceptible, exposed, infected epidemiology). Seasonal variation in transmission rates selects for non-protective covert infections in relatively long-lived hosts with low birth rates typical of many mammals. Variable host population density caused by seasonal birth rates may also select for covert transmission, but in this case it is most likely in short-lived fecund hosts. The covert infections of some insects may therefore be explained by their outbreak population dynamics. However, our models consistently predict proportions of covert infection, which are lower than some of those observed in nature. Higher proportions of covert infection may occur if there is a direct link between covert infection and overt transmission success, the covert infection is protective or the covert state is the result of suppression by the host. Relatively low proportions of covert transmission may, however, be explained as a parasite strategy when transmission opportunities vary. 相似文献
108.
Thomas Koeck Belinda Willard John W. Crabb Mike Kinter Dennis J. Stuehr Kulwant S. Aulak 《Free radical biology & medicine》2009,46(7):884-892
Hyperglycemia, a key factor in insulin resistance and diabetic pathology, is associated with cellular oxidative stress that promotes oxidative protein modifications. We report that protein nitration is responsive to changes in glucose concentrations in 3T3-L1 adipocytes. Alterations in the extent of tyrosine nitration as well as the cellular nitroproteome profile correlated tightly with changing glucose concentrations. The target proteins we identified are involved in fatty acid binding, cell signaling, protein folding, energy metabolism, antioxidant capacity, and membrane permeability. The nitration of adipocyte fatty acid binding protein (FABP4) at Tyr19 decreases, similar to phosphorylation, the binding of palmitic acid to the fatty acid-free protein. This potentially alters intracellular fatty acid transport, nuclear translocation of FABP4, and agonism of PPAR gamma. Our results suggest that protein tyrosine nitration may be a factor in obesity, insulin resistance, and the pathogenesis of diabetes. 相似文献
109.
Cell division ring, a new cell division protein and vertical inheritance of a bacterial organelle in anammox planctomycetes 总被引:2,自引:1,他引:1
Laura van Niftrik Willie J. C. Geerts Elly G. van Donselaar Bruno M. Humbel Richard I. Webb Harry R. Harhangi Huub J. M. Op den Camp John A. Fuerst Arie J. Verkleij Mike S. M. Jetten Marc Strous 《Molecular microbiology》2009,73(6):1009-1019
Anammox bacteria are members of the phylum Planctomycetes that oxidize ammonium anaerobically and produce a significant part of the atmosphere's dinitrogen gas. They contain a unique bacterial organelle, the anammoxosome, which is the locus of anammox catabolism. While studying anammox cell and anammoxosome division with transmission electron microscopy including electron tomography, we observed a cell division ring in the outermost compartment of dividing anammox cells. In most Bacteria, GTP hydrolysis drives the tubulin-analogue FtsZ to assemble into a ring-like structure at the cell division site where it functions as a scaffold for the molecular machinery that performs cell division. However, the genome of the anammox bacterium ' Candidatus Kuenenia stuttgartiensis' does not encode ftsZ . Genomic analysis of open reading frames with potential GTPase activity indicated a possible novel cell division ring gene: kustd1438, which was unrelated to ftsZ . Immunogold localization specifically localized kustd1438 to the cell division ring. Genomic analyses of other members of the phyla Planctomycetes and Chlamydiae revealed no putative functional homologues of kustd1438, suggesting that it is specific to anammox bacteria. Electron tomography also revealed that the bacterial organelle was elongated along with the rest of the cell and divided equally among daughter cells during the cell division process. 相似文献
110.
Electron shuttles in biotechnology 总被引:1,自引:0,他引:1