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Review
- Minor and major circRNAs in virus and host genomes
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Zhihao Lou , Rui Zhou , Yinghua Su , Chun Liu , Wenting Ruan , Che Ok Jeon , Xiao Han , Chun Lin , Baolei Jia
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J. Microbiol. 2021;59(3):324-331. Published online February 23, 2021
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DOI: https://doi.org/10.1007/s12275-021-1021-z
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Abstract
- As a special type of noncoding RNA, circular RNAs (circRNAs)
are prevalent in many organisms. They can serve as sponges
for microRNAs and protein scaffolds, or templates for protein
translation, making them linked to cellular homeostasis
and disease progression. In recent years, circRNAs have been
found to be abnormally expressed during the processes of
viral infection and pathogenesis, and can help a virus escape
the immune response of a host. Thus, they are now considered
to play important functions in the invasion and development
of viruses. Moreover, the potential application of circRNAs
as biomarkers of viral infection or candidates for therapeutic
targeting deserves consideration. This review summarizes
circRNAs in the transcriptome, including their classification,
production, functions, and value as biomarkers. This review
paper also describes research progress on circRNAs in viral
infection (mainly hepatitis B virus, HIV, and some human
herpes viruses) and aims to provide new ideas for antiviral
therapies targeting circRNAs.
Journal Article
- Azohydromonas aeria sp. nov., isolated from air
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Han Xue , Chun-gen Piao , Dan-ran Bian , Min-wei Guo , Yong Li
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J. Microbiol. 2020;58(7):543-549. Published online June 27, 2020
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DOI: https://doi.org/10.1007/s12275-020-9423-x
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Abstract
- A grey pink colored bacterium, strain t3-1-3T, was isolated
from the air at the foot of the Xiangshan Mountain in Beijing,
China. The cells are aerobic, Gram-stain-negative, non-sporeforming,
motile and coccoid-rod shaped (0.9–1.2 × 1.9–2.1
μm). Strain t3-1-3T was catalase-positive and oxidase-negative
and this strain grew at 4–42°C (optimum 28°C), a pH
of 4.0–9.0 (optimum pH 7.0) and under 0–2% (w/v) NaCl
(optimum 0–1% NaCl). A phylogenetic analysis based on 16S
rRNA gene sequences revealed that strain t3-1-3T was closely
related to Azohydromonas riparia UCM-11T (97.4% similarity),
followed by Azohydromonas australica G1-2T (96.8%)
and Azohydromonas ureilytica UCM-80T (96.7%). The genome
of strain t3-1-3T contains 6,895 predicted protein-encoding
genes, 8 rRNA genes, 62 tRNA genes and one sRNA
gene, as well as five potential biosynthetic gene clusters, including
clusters of genes coding for non-ribosomal peptide
synthetase (NRPS), bacteriocin and arylpolyene and two clusters
of genes for terpene. The predominant cellular fatty acids
(> 10.0% of the total) in strain t3-1-3T were summed feature
3 (C16:1ω7c and/or C16:1ω6c, 37.8%), summed feature 8
(C18:1ω7c and/or C18:1ω6c, 29.7%) and C16:0 (17.3%). Strain
t3-1-3T contained ubiquinone-8 (Q-8) as the predominant
respiratory quinone. The polar lipids of strain t3-1-3T comprised
phosphatidyl ethanolamine (PE), phosphatidyl glycerol
(PG), diphosphatidyl glycerol (DPG), an unidentified
glycolipid (GL), an unidentified aminophospholipid (APL),
two unidentified phospholipid (PL1-2) and five unidentified
lipid (L1-5). The DNA G + C content of the type strain
is 70.3%. The broader range of growth temperature, assimilation
of malic acid and trisodium citrate, presence of C18:3ω6c
and an unidentified glycolipid and absence of C12:0 2-OH and
C16:0iso differentiate strain t3-1-3T from related species. Based
on the taxonomic data presented in this study, we suggest
that strain t3-1-3T represents a novel species within the genus
Azohydromonas, for which the name Azohydromonas
aeria sp. nov. is proposed. The type strain of Azohydromonas
aeria is t3-1-3T (= CFCC 13393T = LMG 30135T).
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