Second, our results show that PCR assays for
human adenoviruses in common use are capable of detecting TMAdV.
Not exact matches
But the new test found another seven, including a respiratory virus called
human adenovirus B type 3A, which usually is harmless but can cause severe infections
in some patients.
«No data from
humans vaccinated with
adenovirus 5 vectors are described
in this paper,» says one of them, Dan Barouch of the Beth Israel Deaconess Medical Center at Harvard Medical School.
Adenovirus 5 has 50 or so known relatives that infect
humans and so
in principle could also be used as a basis for vaccines, as could one from a chimpanzee.
Despite their popularity — several HIV vaccines are
in development using
human adenoviruses — the approach has a significant drawback.
The work skirts a problem that has cropped up
in experimental vaccines made from a similar
human adenovirus — they don't work if you've already been exposed to the natural virus.
But
in mice that had been exposed to
human adenovirus, only the chimp virus - based vaccine worked, the researchers report
in the March issue of the Journal of Virology.
Chimp
adenovirus vaccines may have an edge over those that use the
human version, shown here
in an electron micrograph (hexagon shapes).
Adenoviruses, first isolated
in the 1950s from explanted adenoid tissue, are double - stranded nonenveloped DNA viruses that naturally infect many vertebrates, including
humans and nonhuman primates.
To assess cross-neutralization of TMAdV by known
human adenoviruses, 7 pools of
in - house reference sera at the VRDL (rabbit hyperimmune sera) and collectively containing antibodies to
human adenovirus serotypes 1 through 35 were available for testing.
However, the high sequence divergence
in the fiber protein (Table 2), as well as the absence of fiber motifs conserved among
adenoviruses that bind CAR [36], [37](coxsackievirus -
adenovirus receptor) or CD46 [38], [39], [40](data not shown), suggest that neither of these two
human adenoviral receptors may be the attachment receptor for TMAdV.
We used the Virochip, a microarray designed to detect all viruses, to identify a new species of
adenovirus (TMAdV, or titi monkey
adenovirus) that caused a deadly outbreak
in a colony of New World titi monkeys at the California National Primate Research Center (CNPRC), and also infected a
human researcher.
Adenoviruses are DNA viruses that naturally infect many vertebrates, including
humans and monkeys, and cause a wide range of clinical illnesses
in humans.
After removal of similar viral genomes, bootscan plots of the whole genome and individual genes from a subset representing
human / simian
adenoviruses in species A — G and all non-primate vertebrate
adenoviruses were generated.
Human adenoviruses do not usually replicate
in monkey cells
in the absence of helper viruses [11], and do not productively infect rodents (and vice versa)[12].
Some serotypes, such as
human adenovirus type 14 (HAdV - 14), have been associated with severe and potentially fatal outbreaks of pneumonia
in residential facilities and military bases [4].
The fragment shared ∼ 86 % nucleotide identity with its closest phylogenetic relatives
in GenBank, SAdV - 18, an Old World vervet monkey
adenovirus, and the
human species D
adenoviruses.
In this regard, the high sequence divergence of TMAdV relative to the known human / simian adenoviruses (Fig. 3), and comparable sequence similarity in the polymerase gene to a porcine adenovirus (Figs. 3 and S1) are strikin
In this regard, the high sequence divergence of TMAdV relative to the known
human / simian
adenoviruses (Fig. 3), and comparable sequence similarity
in the polymerase gene to a porcine adenovirus (Figs. 3 and S1) are strikin
in the polymerase gene to a porcine
adenovirus (Figs. 3 and S1) are striking.
Although sequencing of PCR amplicons for
human adenoviruses is not performed routinely
in diagnostic virology, TMAdV would presumably have been detected previously
in large - scale studies of hexon sequencing of Ad field isolates if it were circulating
in the community [46], [47].
Interestingly, pleurisy has been specifically reported
in association with certain
human adenovirus infections [44].
The decreased levels of neutralizing Abs to TMAdV
in the researcher (1 ∶ 32) and a family member (1 ∶ 8) relative to those
in infected titi monkeys (up to > 1 ∶ 512) are consistent with a recent study showing much higher levels of neutralizing antibodies
in chimpanzees than
in humans with
adenovirus infections, possibly due to more robust
adenovirus - specific T - cell responses
in humans than
in monkeys [45].
However, recent serological surveys have found antibodies to New World and Old World monkey
adenoviruses in donor
human sera from regions where the monkeys are endemic [14], [15].
The scanning nucleotide pairwise identities of TMAdV relative to representative
human (yellow) or simian (brown)
adenoviruses in species A — G, porcine
adenovirus (red), and fowl
adenovirus (green) are shown.
A defective
adenovirus (one that can not grow or cause
adenovirus infections
in humans) is sometimes used as a vector
in HIV vaccines.
Open Reading Frame E3 - 10.9 K of Subspecies B1
Human Adenoviruses Encodes a Family of Late Orthologous Proteins That Vary
in Their Predicted Structural Features and Subcellular Localization.
Such antibodies are expected to reduce the efficacy of vaccines based on common
human serotypes of
adenovirus in a
human target population.
These viruses do not circulate
in the
human population and fail to carry neutralizing B cell epitopes that cross-react with the common serotypes of
human adenoviruses.
Posttranscriptional block to synthesis of a
human adenovirus capsid protein
in abortively infected monkey cells
Synthesis of
human adenovirus early RNA species is similar
in productive and abortive infections of monkey and
human cells
Normal translation of
human adenovirus mRNA
in cell - free lysates prepared from abortively as well as productively infected monkey cells
Characterization of a variant of
human adenovirus type 2 which multiples efficiently
in simian cells
Characterization of the translational defect to fiber synthesis
in monkey cells abortively infected with
human adenovirus: Role of ancillary leaders
Scale - Up of the
Adenovirus Expression System for the Production of Recombinant Protein
in Human 293S Cells.
Partial block to transcription of
human adenovirus type 2 late genes
in abortively infected monkey cells
Both transient transfection with Lipofectamine and transduction with
adenovirus resulted
in a subpopulation of cells that experessed
human IgG, as shown by the increased fluorescence intensity.
Improving the oncolytic potency of agents has been hampered by the inability to study host - vector interactions
in immune - competent systems, since
human serotype
adenoviruses do not productively replicate
in animal tissues.
In group two, eight children with unexplained fevers were tested; standard testing found 11 viruses, the new test found an additional seven, including the respiratory virus
human adenovirus B type 3A.