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Review
- The Role of Extracellular Vesicles in Pandemic Viral Infections.
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Woosung Shim, Anjae Lee, Jung-Hyun Lee
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J. Microbiol. 2024;62(6):419-427. Published online June 25, 2024
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DOI: https://doi.org/10.1007/s12275-024-00144-x
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Abstract
- Extracellular vesicles (EVs), of diverse origin and content, are membranous structures secreted by a broad range of cell types. Recent advances in molecular biology have highlighted the pivotal role of EVs in mediating intercellular communication, facilitated by their ability to transport a diverse range of biomolecules, including proteins, lipids, DNA, RNA and metabolites. A striking feature of EVs is their ability to exert dual effects during viral infections, involving both proviral and antiviral effects. This review explores the dual roles of EVs, particularly in the context of pandemic viruses such as HIV-1 and SARS-CoV-2. On the one hand, EVs can enhance viral replication and exacerbate pathogenesis by transferring viral components to susceptible cells. On the other hand, they have intrinsic antiviral properties, including activation of immune responses and direct inhibition of viral infection. By exploring these contrasting functions, our review emphasizes the complexity of EV-mediated interactions in viral pathogenesis and highlights their potential as targets for therapeutic intervention. The insights obtained from investigating EVs in the context of HIV-1 and SARS-CoV-2 provide a deeper understanding of viral mechanisms and pathologies, and offer a new perspective on managing and mitigating the impact of these global health challenges.
Journal Articles
- Quorum Quenching Potential of Reyranella sp. Isolated from Riverside Soil and Description of Reyranella humidisoli sp. nov.
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Dong Hyeon Lee, Seung Bum Kim
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J. Microbiol. 2024;62(6):449-461. Published online May 30, 2024
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DOI: https://doi.org/10.1007/s12275-024-00131-2
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Abstract
- Quorum quenching refers to any mechanism that inhibits quorum sensing processes.
In this study, quorum quenching activity among bacteria inhabiting riverside soil was screened, and a novel Gram-stain-negative, rod shaped bacterial strain designated MMS21-HV4-11(T), which showed the highest level of quorum quenching activity, was isolated and subjected to further analysis. Strain MMS21-HV4-11(T) could be assigned to the genus Reyranella of Alphaproteobacteria based on the 16S rRNA gene sequence, as the strain shared 98.74% sequence similarity with Reyranella aquatilis seoho-37(T), and then 97.87% and 97.80% sequence similarity with Reyranella soli KIS14-15(T) and Reyranella massiliensis 521(T), respectively. The decomposed N-acyl homoserine lactone was restored at high concentrations under acidic conditions, implying that lactonase and other enzyme(s) are responsible for quorum quenching. The genome analysis indicated that strain MMS21-HV4-11(T) had two candidate genes for lactonase and one for acylase, and expected protein structures were confirmed. In the quorum sensing inhibition assay using a plant pathogen Pectobacterium carotovorum KACC 14888, development of soft rot was significantly inhibited by strain MMS21-HV4-11(T).
Besides, the swarming motility by Pseudomonas aeruginosa PA14 was significantly inhibited in the presence of strain MMS21-HV4-11(T). Since the isolate did not display direct antibacterial activity against either of these species, the inhibition was certainly due to quorum quenching activity. In an extended study with the type strains of all known species of Reyranella, all strains were capable of degrading N-acyl homoserine lactones (AHLs), thus showing quorum quenching potential at the genus level. This is the first study on the quorum quenching potential and enzymes responsible in Reyranella. In addition, MMS21-HV4-11(T) could be recognized as a new species through taxonomic characterization, for which the name Reyranella humidisoli sp. nov. is proposed (type strain = MMS21-HV4-11( T) = KCTC 82780( T) = LMG 32365(T)).
- Antiviral Activity Against SARS‑CoV‑2 Variants Using in Silico and in Vitro Approaches
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Hee-Jung Lee , Hanul Choi , Aleksandra Nowakowska , Lin-Woo Kang , Minjee Kim , Young Bong Kim
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J. Microbiol. 2023;61(7):703-711. Published online June 26, 2023
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DOI: https://doi.org/10.1007/s12275-023-00062-4
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Abstract
- Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emergence in 2019 led to global health crises and the persistent
risk of viral mutations. To combat SARS-CoV-2 variants, researchers have explored new approaches to identifying
potential targets for coronaviruses. This study aimed to identify SARS-CoV-2 inhibitors using drug repurposing. In silico
studies and network pharmacology were conducted to validate targets and coronavirus-associated diseases to select potential
candidates, and in vitro assays were performed to evaluate the antiviral effects of the candidate drugs to elucidate the
mechanisms of the viruses at the molecular level and determine the effective antiviral drugs for them. Plaque and cytopathic
effect reduction were evaluated, and real-time quantitative reverse transcription was used to evaluate the antiviral activity
of the candidate drugs against SARS-CoV-2 variants in vitro. Finally, a comparison was made between the molecular docking
binding affinities of fenofibrate and remdesivir (positive control) to conventional and identified targets validated from
protein–protein interaction (PPI). Seven candidate drugs were obtained based on the biological targets of the coronavirus,
and potential targets were identified by constructing complex disease targets and PPI networks. Among the candidates,
fenofibrate exhibited the strongest inhibition effect 1 h after Vero E6 cell infection with SARS-CoV-2 variants. This study
identified potential targets for coronavirus disease (COVID-19) and SARS-CoV-2 and suggested fenofibrate as a potential
therapy for COVID-19.
- Relationship Between Mycotoxin Production and Gene Expression in Fusarium graminearum Species Complex Strains Under Various Environmental Conditions
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Wenwen Huang , Ping Zhou , Guanghui Shen , Tao Gao , Xin Liu , Jianrong Shi , Jianhong Xu , Jianbo Qiu
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J. Microbiol. 2023;61(5):525-542. Published online May 2, 2023
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DOI: https://doi.org/10.1007/s12275-023-00046-4
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Abstract
- The Fusarium graminearum species complex (FGSC) can produce various mycotoxins and is a major concern for food
quantity and quality worldwide. In this study, we determined the effects of water activity (
aw), temperature, incubation time
and their interactions on mycotoxin accumulation and the expression levels of biosynthetic genes in FGSC strains from
maize samples in China. The highest deoxynivalenol (DON), 3-acetyldeoxynivalenol(3ADON) and 15-acetyldeoxynivalenol
(15ADON) levels of the F. boothii and F. graminearum strains were observed at 0.98 aw/
30 °C or 0.99 aw/
25 °C. F. asiaticum
and F. meridionale reached maximum nivalenol (NIV) and 4-acetylnivalenol (4ANIV) contents at 0.99 aw
and 30 °C. With
the extension of the incubation time, the concentrations of DON and NIV gradually increased, while those of their derivatives
decreased. F. boothii, F. meridionale and one F. asiaticum strain had the highest zearalenone (ZEN) values at 0.95 aw
and 25 °C, while the optimum conditions for the other F. asiaticum strain and F. graminearum were 0.99 aw
and 30 °C. Four
genes associated with trichothecene and zearalenone synthesis were significantly induced under higher water stress in the
early stage of production. The results indicated independence of mycotoxin production and gene expression, as maximum
amounts of these toxic metabolites were observed at higher aw
in most cases. This study provides useful information for the
monitoring and prevention of such toxins entering the maize production chain.
- Description of Fervidibacillus gen. nov. with Two Species, Fervidibacillus albus sp. nov., and Fervidibacillus halotolerans sp. nov., Isolated from Tidal Flat Sediments and Emendation of Misclassificed Taxa in the Genus Caldibacillus
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Sung , Mi , Hyun , Kae Kyoung Kwon
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J. Microbiol. 2023;61(2):175-187. Published online February 17, 2023
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DOI: https://doi.org/10.1007/s12275-023-00022-y
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Abstract
- Two Gram-stain-positive, motile, endospore-forming, facultatively anaerobic strains, designated MEBiC13591T
and
MEBiC13594T,
were isolated from tidal flat sediment of the Incheon City on the west coast of Korea. Growth of both
novel strains was observed at pH 5–9 (optimum, pH 7–7.5), and in 0–8% NaCl (optimum, 2% for MEBiC13591T
and
3% for MEBiC13594T).
Strains MEBiC13591T
and MEBiC13594T
grew optimally at 50 °C, (37.5–56.1 °C) and 44 °C
(20.7–50.7 °C), respectively. The main cellular fatty acids of strain MEBiC13591T
were iso-C15: 0, anteiso-C15: 0, iso-C16: 0,
iso-C17: 0 and anteiso-C17: 0, while those for strain MEBiC13594T
were C14:
0, iso-C14: 0, iso-C15: 0, anteiso-C15: 0 and C16:
0. In
both taxa, the major isoprenoid was MK-7. The genomic DNA G + C contents were 34.1 and 37.0 mol% for MEBiC13591T
and MEBiC13594T,
respectively. A 16S rRNA gene sequence analysis revealed that the novel strains showed high similarity
with members of the genera Aeribacillus (95.0%) and Caldibacillus (93.5–94.5%); however, showed lower than 90%
with Caldibacillus debilis TfT.
Phylogenetic and Phylogenomic analysis revealed that two novel strains comprised distinct
phyletic line with members formerly assigned to Caldibacillus. Based on genomic indices, such as AAI and ANI, members
formerly affiliated with Caldibacillus and Bacillus as well as the novel strains should be classified into five independent
genera. Based on the phenotypic, genomic and biochemical data, strains MEBiC13591T
and MEBiC13594T
represent two
novel species in the novel genus, for which the names Fervidibacillus albus gen. nov., sp. nov. (
MEBiC13591T [= KCCM
43317T
= KCTC 43181T
= JCM 33662T
= MCCC 1K04565T]),
and Fervidibacillus halotolerans sp. nov. (
MEBiC13594T
[= KCTC 43182T
= JCM 34001T])
are proposed. Three additional genera Caldifermentibacillus, Palidibacillus, and Perspicuibacillus
are also proposed by reclassification of the several species with valid names that formerly affiliated with the
genera Caldibacillus.
- Transcript-specific selective translation by specialized ribosomes bearing genome-encoded heterogeneous rRNAs in V. vulnificus CMCP6
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Younkyung Choi , Minju Joo , Wooseok Song , Minho Lee , Hana Hyeon , Hyun-Lee Kim , Ji-Hyun Yeom , Kangseok Lee , Eunkyoung Shin
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J. Microbiol. 2022;60(12):1162-1167. Published online November 24, 2022
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DOI: https://doi.org/10.1007/s12275-022-2437-9
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Abstract
- Ribosomes composed of genome-encoded heterogeneous
rRNAs are implicated in the rapid adaptation of bacterial
cells to environmental changes. A previous study showed that
ribosomes bearing the most heterogeneous rRNAs expressed
from the rrnI operon (I-ribosomes) are implicated in the preferential
translation of a subset of mRNAs, including hspA
and tpiA, in Vibrio vulnificus CMCP6. In this study, we show
that HspA nascent peptides were predominantly bound to
I-ribosomes. Specifically, I-ribosomes were enriched more
than two-fold in ribosomes that were pulled down by immunoprecipitation
of HspA peptides compared with the proportion
of I-ribosomes in crude ribosomes and ribosomes pulled
down by immunoprecipitation of RNA polymerase subunit
ß peptides in the wild-type (WT) and rrnI-completed strains.
Other methods that utilized the incorporation of an affinity
tag in 23S rRNA or chimeric rRNA tethering 16S and 23S
rRNAs, which generated specialized functional ribosomes
in Escherichia coli, did not result in functional I-ribosomes
in V. vulnificus CMCP6. This study provides direct evidence
of the preferential translation of hspA mRNA by I-ribosomes.
- Comparative analysis of the colistin resistance-regulating gene cluster in Klebsiella species
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Sun Ju Kim , Hongbaek Cho , Kwan Soo Ko
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J. Microbiol. 2022;60(5):461-468. Published online April 18, 2022
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DOI: https://doi.org/10.1007/s12275-022-1640-z
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3
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Abstract
- CrrAB two-component regulatory system is associated with
colistin resistance in Klebsiella pneumoniae. Recently, some
K. pneumoniae isolates lacking crrAB genes have been identified.
In this study, we investigated the distribution and structural
variation of the crrBAC-kexD cluster. To evaluate the
structural variation of the crrBAC-kexD cluster, we explored
59 clinical K. pneumoniae isolates from Korea, and 508 whole
genomes of K. pneumoniae and other strains of Klebsiella
sp. Significant structural variations in crrBAC-kexD and its
surrounding regions were identified among K. pneumoniae
genomes. Within the genus Klebsiella, the cluster was identified
only in K. pneumoniae, K. variicola, and K. quasipneumoniae,
which form the K. pneumoniae complex. Among the
304 available K. pneumoniae genomes, an intact crrBAC-kexD
cluster was identified in 178 isolates (58.6%), while the cluster
was absent in 90 isolates (29.6%). Partial deletions within
the cluster were identified in 22 genomes (7.2%). The most
diverse structural patterns of the crrBAC-kexD cluster were
observed in ST11 strains. Some clades lacked the crrBAC-kexD
cluster. The crrBAC-kexD cluster was identified in the genomes
of other bacterial species, including Citrobacter freundii and
Enterobacter ludwigii. The crrBAC-kexD cluster is proposed
to have been acquired by the ancestor of the K. pneumoniae
complex from other bacterial species and the cluster may have
been lost and re-acquired repeatedly in K. pneumoniae strains
according to the phylogenetic analysis. The dynamic evolution
of the crrBAC-kexD cluster suggests that it may have other
roles, in addition to colistin resistance, in bacterial physiology.
- Prevalence and characteristics of the mcr-1 gene in retail meat samples in Zhejiang Province, China
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Biao Tang , Jiang Chang , Yi Luo , Han Jiang , Canying Liu , Xingning Xiao , Xiaofeng Ji , Hua Yang
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J. Microbiol. 2022;60(6):610-619. Published online March 31, 2022
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DOI: https://doi.org/10.1007/s12275-022-1597-y
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10
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Abstract
- Considering the serious threat to food safety and public
health posed by pathogens with colistin resistance, colistin was
banned as a growth promoter in 2017 in China. In recent years,
the resistance rate of Escherichia coli isolated from animal
intestines or feces to colistin has decreased. However, the prevalence
and characteristics of the mcr-1 gene in retail meat have
not been well explored. Herein, 106 mcr-1-negative and 16 mcr-
1-positive E. coli isolates were randomly recovered from 120 retail
meat samples and screened using colistin. The 106 E. coli
isolates showed maximum resistance to sulfafurazole (73.58%)
and tetracycline (62.26%) but susceptibility to colistin (0.00%).
All 16 mcr-1-positive E. coli isolates showed resistance to colistin,
were extended spectrum beta-lactamase (ESBL)-positive
and exhibited complex multidrug resistance (MDR). For these
16 isolates, 17 plasmid replicons and 42 antibiotic resistance
genes were identified, and at least 7 antibiotic resistance genes
were found in each isolate. Acquired disinfectant resistance
genes were identified in 75.00% (12/16) of the isolates. Furthermore,
comparative genomic and phylogenetic analysis
results
indicated that these 16 mcr-1-positive E. coli isolates
and the most prevalent mcr-1-harboring IncI2 plasmid in
this study were closely related to other previously reported
mcr-1-positive E. coli isolates and the IncI2 plasmid, respectively,
showing their wide distribution. Taken together, our
findings showed that retail meat products were a crucial reservoir
of mcr-1 during the colistin ban period and should
be continuously monitored.
- Down-regulation of microRNA-155 suppressed Candida albicans induced acute lung injury by activating SOCS1 and inhibiting inflammation response
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Xiaohua Li , Yuanzhong Gong , Xin Lin , Qiong Lin , Jianxiong Luo , Tianxing Yu , Junping Xu , Lifang Chen , Liyu Xu , Ying Hu
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J. Microbiol. 2022;60(4):402-410. Published online February 14, 2022
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DOI: https://doi.org/10.1007/s12275-022-1663-5
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Abstract
- Acute lung injury caused by Candida albicans could result in
high mortality and morbidity. MicroRNA-155 (miR-155) and
suppressor of cytokine signaling 1 (SOCS1) have been believed
to play a key in the regulation of inflammatory response.
Whether miR-155/SOCS1 axis could regulate the acute lung
injury caused by C. albicans has not been reported. The acute
lung injury animal model was established with acute infection
of C. albicans. miR-155 inhibitor, miR-155 mimic, and
sh-SOCS1 were constructed. The binding site between miR-
155 and SOCS1 was identified with dual luciferase reporter
assay. Knockdown of miR-155 markedly inhibited the germ
tube formation of C. albicans. Knockdown of miR-155 significantly
up-regulated the expression of SOCS1, and the binding
site between miR-155 and SOCS1 was identified. Knockdown
of miR-155 improved the acute lung injury, suppressed
inflammatory factors and fungus loading through SOCS1.
Knockdown of SOCS1 greatly reversed the influence of miR-
155 inhibitor on the cell apoptosis in vitro. The improvement
of acute lung injury caused by C. albicans, suppression of inflammatory
response and C. albicans infection, and inhibitor
of cell apoptosis were achieved by knocking down miR-155
through SOCS1. This research might provide a new thought
for the prevention and treatment of acute lung injury caused
by C. albicans through targeting miR-155/SOCS1 axis.
- Characterization and validation of an alternative reference bacterium Korean Pharmacopoeia Staphylococcus aureus strain
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Ye Won An , Young Sill Choi , Mi-ran Yun , Chihwan Choi , Su Yeon Kim
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J. Microbiol. 2022;60(2):187-191. Published online January 7, 2022
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DOI: https://doi.org/10.1007/s12275-022-1335-5
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Abstract
- The National Culture Collection of Pathogens (NCCP) is a
microbial resource bank in Korea that collects pathogen resources
causing infectious disease in human and distributes
them for research and education. The NCCP bank attempts
to discover strains with various characteristics and specific
purposes to provide diverse resources to researchers. Staphylococcus
aureus American Type Culture Collection (ATCC)
6538P is used as a reference strain in the microbial assay for
antibiotics in the Korean and in the United States Pharmacopoeias.
We aimed to analyze domestically isolated microbial
resources from the NCCP to replace the S. aureus reference
strain. Staphylococcus aureus strains were identified using matrix-
assisted laser desorption/ionization time-of-flight mass
spectrometry and the VITEK-2 system and characterized by
multilocus sequence typing, 16S rRNA sequencing, and antibiotic
susceptibility testing. Several candidate strains had similar
characteristics as the reference strain. Among them, the
nucleotide sequence of the 16S rRNA region of NCCP 16830
was 100% identical to that of the reference strain; it was sensitive
to six types of antibiotics and showed results most similar
to the reference strain. A validity evaluation was conducted
using the cylinder-plate method. NCCP 16830 presented
valid results and had the same performance as ATCC
6538P; therefore, it was selected as an alternative candidate
strain.
- Zinc-binding domain mediates pleiotropic functions of Yvh1 in Cryptococcus neoformans
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Jae-Hyung Jin , Myung Kyung Choi , Hyun-Soo Cho , Yong-Sun Bahn
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J. Microbiol. 2021;59(7):658-665. Published online July 1, 2021
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DOI: https://doi.org/10.1007/s12275-021-1287-1
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Abstract
- Yvh1 is a dual-specificity phosphatase (DUSP) that is evolutionarily
conserved in eukaryotes, including yeasts and humans.
Yvh1 is involved in the vegetative growth, differentiation,
and virulence of animal and plant fungal pathogens.
All Yvh1 orthologs have a conserved DUSP catalytic domain
at the N-terminus and a zinc-binding (ZB) domain with two
zinc fingers (ZFs) at the C-terminus. Although the DUSP domain
is implicated in the regulation of MAPK signaling in
humans, only the ZB domain is essential for most cellular
functions of Yvh1 in fungi. This study aimed to analyze the
functions of the DUSP and ZB domains of Yvh1 in the human
fungal pathogen Cryptococcus neoformans, whose Yvh1
(CnYvh1) contains a DUSP domain at the C-terminus and
a ZB domain at the N-terminus. Notably, CnYvh1 has an extended
internal domain between the two ZF motifs in the ZB
domain. To elucidate the function of each domain, we constructed
individual domain deletions and swapping strains
by complementing the yvh1Δ mutant with wild-type (WT)
or mutated YVH1 alleles and examined their Yvh1-dependent
phenotypes, including growth under varying stress conditions,
mating, and virulence factor production. Here, we found
that the complementation of the yvh1Δ mutant with the mutated
YVH1 alleles having two ZFs of the ZB domain, but not
the DUSP and extended internal domains, restored the WT
phenotypic traits in the yvh1Δ mutant. In conclusion, the
ZB domain, but not the N-terminal DUSP domain, plays a
pivotal role in the pathobiological functions of cryptococcal
Yvh1.
- Distribution characteristics of fungal communities with depth in paddy fields of three soil types in China
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Xu Li , Huanhuan Wang , Xiang Li , Xinyu Li , Huiwen Zhang
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J. Microbiol. 2020;58(4):279-287. Published online February 27, 2020
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DOI: https://doi.org/10.1007/s12275-020-9409-8
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Abstract
- Little is known about the distribution of fungal communities
with soil depth on relatively large scales. In this study, typical
paddy soils in three regions (Hailun, Changshu, and Yingtan)
from north to south China were selected to investigate the
vertical distribution (0-100 cm) of the fungal community by
Illumina MiSeq sequencing, and to identify the main factors
influencing the fungal community distribution. The results
indicated that the structure of the soil fungal community
changed significantly with region and soil depth. Soil fungal
taxa such as Zygomycota, Glomeromycota, Saccharomycete,
Kazachstania, Mortierella, Massariosphaeria, Hypholoma, and
Zopfiella were enriched at depths of 0–20 cm, whereas Dothideomycetes,
Microbotryomycetes, Tremellomycetes, Sporobolomyces,
Cryptococcus, Rhodotorula, Fusarium, and Pyrenochaetopsis
had high relative abundances at 80–100 cm.
Variance partitioning analysis indicated that the geographic
distance contributed more to the fungal community variation
than environmental variables on a large scale. In addition,
soil total carbon and nitrogen contents were the main
environmental factors driving the vertical distribution of the
fungal community in paddy soils.
- Mucibacter soli gen. nov., sp. nov., a new member of the family Chitinophagaceae producing mucin
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Min-Kyeong Kim , Sewook Park , Tae-Su Kim , Yochan Joung , Ji-Hye Han , Seung Bum Kim
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J. Microbiol. 2019;57(5):356-361. Published online February 22, 2019
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DOI: https://doi.org/10.1007/s12275-019-8512-1
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Abstract
- A Gram-stain-negative, mucus-forming, motile by gliding,
non-spore-forming and short rod-shaped bacterial strain
designated R1-15T was isolated from soil and its taxonomic
position was evaluated using a polyphasic approach. Strain
R1-15T grew at 15–37°C (optimum, 30°C), at pH 6–7 (optimum,
pH 6) and in the presence of 0–1% (w/v) NaCl (optimum,
0%) on 0.1X TSA. On the basis of 16S rRNA gene sequence
similarity, the novel strain was assigned to the family
Chitinophagaceae of the phylum Bacteroidetes, and its closest
related taxa were species of the genera Taibaiella (88.76–
90.02% sequence similarity), Lacibacter (89.24–90.00%), Chitinophaga
(88.61–89.76%), and Terrimonas (89.04%). Flexirubin-
type pigments were produced. The only isoprenoid
quinone was MK-7, and the major polar lipid was phosphatidylethanolamine.
Based on whole genome comparisons
between the strain R1-15T and the type strains of relatives,
the orthologous average nucleotide identity values were 66.9–
67.0%. The DNA G+C content of strain R1-15T was 43.8
mol%. The combination of phylogenetic, chemotaxonomic
and phenotypic data clearly supported separation of strain
R1-15T from related taxa, and thus the name Mucibacter
soli gen. nov., sp. nov. is proposed. The type strain is R1-15T
(= KCTC 62274T = JCM 31190T).
- Growth of cyanobacterial soil crusts during diurnal freeze-thaw cycles
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Steven K. Schmidt , Lara Vimercati
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J. Microbiol. 2019;57(4):243-251. Published online February 5, 2019
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DOI: https://doi.org/10.1007/s12275-019-8359-5
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Abstract
- Various Nostoc spp. and related cyanobacteria are able to survive
extreme temperatures and are among the most successful
colonists of high-elevation sites being exposed due to glacial
retreat. It is unclear, however, if cyanobacteria can grow
during the extreme freeze-thaw cycles that occur on a yearround
basis at high-elevation, peri-glacial sites or if they only
grow during the rare periods when freeze-thaw cycles do not
occur. We conducted several experiments to determine if cyanobacteria
that form biological soil crusts (BSCs) at highelevation
sites (> 5,000 m.a.s.l.) in the Andes can grow during
diurnal freeze-thaw cycles on a par with those that occur in
the field. Here we show that a soil crust that had been frozen
at -20°C for five years was able to increase from 40% to 100%
soil coverage during a 45-day incubation during which the
soil temperature cycled between -12°C and 26°C every day.
In a second, experiment an undeveloped soil with no visible
BSCs showed a statistically significant shift in the bacterial
community from one containing few cyanobacterial sequences
(8% of sequences) to one dominated (27%) by Nostoc,
Microcoleus, and Leptolyngbya phylotypes during a 77-day
incubation with daily freeze-thaw cycles. In addition, counts
of spherical Nostoc-like colonies increased significantly on
the soil surface during the experiment, especially in microcosms
receiving phosphorus. Taken together these results
show that freeze-thaw cycles alone do not limit the growth
of BSCs in high-elevation soils, and provide new insight into
how life is able to thrive in one of the most extreme terrestrial
environments on Earth.
Review
- MINIREVIEW] Dynamics of microbial communities and CO2 and CH4 fluxes in the tundra ecosystems of the changing Arctic
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Min Jung Kwon , Ji Young Jung , Binu M. Tripathi , Mathias Göckede , Yoo Kyung Lee , Mincheol Kim
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J. Microbiol. 2019;57(5):325-336. Published online January 16, 2019
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DOI: https://doi.org/10.1007/s12275-019-8661-2
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Abstract
- Arctic tundra ecosystems are rapidly changing due to the amplified
effects of global warming within the northern high
latitudes. Warming has the potential to increase the thawing
of the permafrost and to change the landscape and its geochemical
characteristics, as well as terrestrial biota. It is important
to investigate microbial processes and community
structures, since soil microorganisms play a significant role
in decomposing soil organic carbon in the Arctic tundra. In
addition, the feedback from tundra ecosystems to climate
change, including the emission of greenhouse gases into the
atmosphere, is substantially dependent on the compositional
and functional changes in the soil microbiome. This article
reviews the current state of knowledge of the soil microbiome
and the two most abundant greenhouse gas (CO2 and CH4)
emissions, and summarizes permafrost thaw-induced changes
in the Arctic tundra. Furthermore, we discuss future directions
in microbial ecological research coupled with its link
to CO2 and CH4 emissions.
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