| 1. |
- Nene, Vishvanath, et al.
(författare)
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Genome sequence of Aedes aegypti, a major arbovirus vector.
- 2007
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Ingår i: Science (New York, N.Y.). - : American Association for the Advancement of Science (AAAS). - 1095-9203 .- 0036-8075. ; 316:5832, s. 1718-23
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Tidskriftsartikel (refereegranskat)abstract
- We present a draft sequence of the genome of Aedes aegypti, the primary vector for yellow fever and dengue fever, which at approximately 1376 million base pairs is about 5 times the size of the genome of the malaria vector Anopheles gambiae. Nearly 50% of the Ae. aegypti genome consists of transposable elements. These contribute to a factor of approximately 4 to 6 increase in average gene length and in sizes of intergenic regions relative to An. gambiae and Drosophila melanogaster. Nonetheless, chromosomal synteny is generally maintained among all three insects, although conservation of orthologous gene order is higher (by a factor of approximately 2) between the mosquito species than between either of them and the fruit fly. An increase in genes encoding odorant binding, cytochrome P450, and cuticle domains relative to An. gambiae suggests that members of these protein families underpin some of the biological differences between the two mosquito species.
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| 2. |
- Andersson, Mikael, et al.
(författare)
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Admission control with service level agreements for a web server
- 2005
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Ingår i: Proceedings of the IASTED International Conference on Internet and Multimedia Systems and Applications, EuroIMSA 2005 : February 21 - 23, 2005, Grindelwald, Switzerland. - 0889864845
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Konferensbidrag (refereegranskat)abstract
- One problem with web servers is that they are sensitive to overload. The servers may become overloaded during temporary traffic peaks when more requests arrive than the server is designed for. Because overload usually occurs rather seldom, it is not economical to overprovision the servers for these traffic peaks, instead admission control mechanisms can be implemented in the servers. This pa per investigates two overload control strategies with per formance bounds for a web server. In service level agree ments, we bound average response times and throughputs for all service classes. Each request is sorted into a class, where each class is assigned a weight representing the in come for the web site owner. Then a linear optimization algorithm is applied so that the total revenue for the web site during overload is maximized.
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| 3. |
- Babiker, Hamza A., et al.
(författare)
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Impaired fitness of drug-resistant malaria parasites : evidence and implication on drug-deployment policies
- 2009
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Ingår i: Expert review of anti-infective therapy. - 1478-7210. ; 7:5, s. 581-593
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Forskningsöversikt (refereegranskat)abstract
- Malaria, a leading parasitic disease, inflicts an enormous toll on human lives and is caused by protozoal parasites belonging to the genus Plasmodium. Antimalarial drugs targeting essential biochemical processes in the parasite are the primary resources for management and control. However, the parasite has established mutations, substantially reducing the efficacy of these drugs. First-line therapy is faced the with the consistent evolution of drug-resistant genotypes carrying these mutations. However, drug-resistant genotypes are likely to be less fit than the wild-type, suggesting that they might disappear by reducing the volume of drug pressure. A substantial body of epidemiological evidence confirmed that the frequency of resistant genotypes wanes when active drug selection declines. Drug selection on the parasite genome that removes genetic variation in the vicinity of drug-resistant genes (hitch-hiking) is common among resistant parasites in the field. This can further disadvantage drug-resistant strains and limit their variability in the face of a mounting immune response. Attempts to provide unequivocal evidence for the fitness cost of drug resistance have monitored the outcomes of laboratory competition experiments of deliberate mixtures of sensitive and resistant strains, in the absence of drug pressure, using isogenic clones produced either by drug selection or gene manipulation. Some of these experiments provided inconclusive results, but they all suggested reduced fitness of drug-resistant clones in the absence of drug pressure. In addition, biochemical analyses provided clearer information demonstrating that the mutation of some antimalarial-targeted enzymes lowers their activity compared with the wild-type enzyme. Here, we review current evidences for the disadvantage of drug-resistance mutations, and discuss some strategies of drug deployment to maximize the cost of resistance and limit its spread.
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