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Construction and applications of yellow fever virus replicons.

Subgenomic replicons of yellow fever virus (YFV) were constructed to allow expression of heterologous reporter genes in a replication-dependent manner. Expression of the antibiotic resistance gene neomycin phosphotransferase II (Neo) from one of these YFV replicons allowed selection of a stable population of cells (BHK-REP cells) in which the YFV replicon persistently replicated. BHK-REP cells were successfully used to trans-complement replication-defective YFV replicons harboring large internal deletions within either the NS1 or NS3 proteins. Although replicons with large deletions in either …

Энцотическая передача вируса желтой лихорадки в Перу.

Преобладающей парадигмой экологии вируса желтой лихорадки (YFV) в Южной Америке является блуждающая эпизоотика. Считается, что вирус перемещается из одного места в другое в эпизоотических волнах с участием обезьян и комаров, вместо того чтобы постоянно циркулировать внутри конкретных мест. После крупной вспышки болезни YFV в Перу в 1995 году мы использовали филогенетические анализы вирусов для повторного изучения гипотезы движения вирусов. Мы секвенировали 670-нуклеотидный фрагмент геновой области prM/E из 25 образцов перуанского YFV, собранных в 1977-1999 годах, и выделили шесть клинков, пред

Совпадение в аннотации оригинала
The prevailing paradigm of yellow fever virus (YFV) ecology in South America is that of wandering epizootics. The virus is believed to move from place to place in epizootic waves involving monkeys and mosquitoes, rather than persistently circulating within particular locales. After a large outbreak of YFV illness in Peru in 1995, we used phylogenetic analyse…

THE MULTIPLICATION OF THE VIRUS OF YELLOW FEVER IN AEDES AEGYPTI.

Aëdes aegypti have been shown to be capable of multiplying the Asibi strain of yellow fever virus in their bodies. Following the ingestion of infected blood, the content of virus falls for several days, reaching a minimum during the 1st week. It then increases rapidly until quantities of virus greater than those previously encountered can be demonstrated. The actual final amount of virus demonstrable, however, is subject to variations of which we know little.

THE TITRATION OF YELLOW FEVER VIRUS IN STEGOMYIA MOSQUITOES.

Titrations were made of yellow fever virus in stegomyia mosquitoes, using rhesus monkeys as test animals. It was found that: (a) The average mosquito immediately after engorging on highly infectious blood contained between 1 and 2 million lethal doses of virus. The titer of freshly ingested blood was as high as 1 billion lethal doses of virus per cubic centimeter. (b) During the fortnight succeeding a meal on infectious blood there occurred a reduction of titratable virus to not more than 1 per cent of that present in the freshly fed insects. (c) The titer was somewhat higher at later periods.…

THE FILTRABILITY OF YELLOW FEVER VIRUS AS EXISTING IN THE MOSQUITO.

The virus of yellow fever as it exists in Aëdes aegypti mosquitoes, both in their so-called infective stage and in the intermediate condition termed the "incubation period", is capable of passing through Berkefeld N filters when suspended in normal monkey serum, although earlier investigators have shown that the virus from infective mosquitoes will not do so when suspended in physiological salt solution. The virus of yellow fever as it exists in mosquitoes behaves with regard to filtration through Berkefeld N filters as does the virus in the blood of infective monkeys.

Molecular Characterization of Hamster-Adapted Yellow Fever Virus.

We previously reported two hamster models for viscerotropic yellow fever virus (YFV) infection: one using a YFV strain (Jiménez), isolated from a fatal human case in Panama in 1974, and the other using the prototype YFV strain (Asibi). Asibi hamster passage 7 (P7) was associated with accumulation of seven amino acid substitutions, including five in the envelope protein. In this study we report the genome sequences of the hamster Jiménez P0 and P10 viruses in which we identified only two amino acid substitutions during passage, one each in the nonstructural proteins NS3 and NS5, indicating a ro…

Genetic variability among yellow fever virus 17D substrains.

The complete nucleotide sequence of the genome from two yellow fever (YF) virus strains, 17DD and 17D-213 was determined. Comparison of these sequences with those of other YF viruses, including the parental virulent Asibi strain, allowed the identification of 48 nucleotide sequence differences which are 17D strain-specific and potentially related to viral attenuation. Another 43 nucleotide sequence differences were not common to all 17D substrains and are therefore substrain specific. Of the 21 changes between 17DD and Asibi 15 only five led to amino acid substitutions whereas 13 substrain dif

LRP8 is a functional receptor for yellow fever virus.

Yellow fever virus (YFV) is an arbovirus causing substantial human morbidity and mortality. The live-attenuated 17D strain serves as vaccine and is one of the most successful vaccines so far. Receptor usage between attenuated and pathogenic YFV strains remains unclear. Here we performed a barcoded, genome-wide human open-reading frame library screen and identified LRP8 (also named APOER2) as a receptor for YFV. We show that LRP8 expression increases YFV infection (17D and two clinical strains, BJ01 and Asibi) in cell lines by promoting entry. Adeno-associated virus-mediated expression of human…