Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:2.7.7.49 (reverse transcriptase)
 31,746 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Avian bornaviruses are the causative agents of proventricular dilatation disease (PDD), a fatal neurological disease considered to be a major threat to psittacine bird populations. We performed a survey of the presence of avian bornaviruses and PDD in pet psittacines in Brazil and also studied PDD's clinical presentation as well as the genomic variability of the viruses. Samples from 112 psittacines with clinical signs compatible with PDD were collected and tested for the presence of bornaviruses. We found 32 birds (28.6%) positive for bornaviruses using reverse transcriptase polymerase chain reaction (RT-PCR). Twenty-one (65.6%) of the 32 bornavirus-positive birds presented neurological signs, seven (21.9%) presented undigested seeds in feces, four (12.5%) showed proventricular dilatation, six (18.8%) regurgitation, three (9.4%) feather plucking and three (9.4%) sudden death. The results confirm that avian bornaviruses are present in pet psittacines in Brazil, and sequence analysis identified a distinct virus, named parrot bornavirus 8 (PaBV-8).
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PMID:Survey of bornaviruses in pet psittacines in Brazil reveals a novel parrot bornavirus. 2546 70

Induced pluripotent stem cell (iPSC)-derived cortical neurons potentially present a powerful new model to understand corticogenesis and neurological disease. Previous work has established that differentiation protocols can produce cortical neurons, but little has been done to characterize these at cellular resolution. In particular, it is unclear to what extent in vitro two-dimensional, relatively disordered culture conditions recapitulate the development of in vivo cortical layer identity. Single-cell multiplex reverse transcriptase-quantitative polymerase chain reaction (RT-qPCR) was used to interrogate the expression of genes previously implicated in cortical layer or phenotypic identity in individual cells. Totally, 93.6% of single cells derived from iPSCs expressed genes indicative of neuronal identity. High proportions of single neurons derived from iPSCs expressed glutamatergic receptors and synaptic genes. And, 68.4% of iPSC-derived neurons expressing at least one layer marker could be assigned to a laminar identity using canonical cortical layer marker genes. We compared single-cell RNA-seq of our iPSC-derived neurons to available single-cell RNA-seq data from human fetal and adult brain and found that iPSC-derived cortical neurons closely resembled primary fetal brain cells. Unexpectedly, a subpopulation of iPSC-derived neurons co-expressed canonical fetal deep and upper cortical layer markers. However, this appeared to be concordant with data from primary cells. Our results therefore provide reassurance that iPSC-derived cortical neurons are highly similar to primary cortical neurons at the level of single cells but suggest that current layer markers, although effective, may not be able to disambiguate cortical layer identity in all cells.
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PMID:Assessing similarity to primary tissue and cortical layer identity in induced pluripotent stem cell-derived cortical neurons through single-cell transcriptomics. 2674 May 50


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