To study the role of intestinal flora in the development of bloodstream infections (BSIs). 42 patients and 19 healthy controls (HCs) were screened into the study and their intestinal flora was measured by 16S rRNA gene sequencing.
The bacterial diversity was significantly lower in the BSI group compared with that in the HCs (P < 0.001), and beta diversity was significantly differentiated between the two groups (PERMANOVA, P = 0.001). The four keystone species [Roseburia, Faecalibacterium, Prevotella, and Enterococcus (LDA > 4)] differed significantly between the two groups. Dysbiosis of fecal microbial ecology is a common condition present in patients with BSI. The proliferation of certain pathogens or reduction of SCFA-producing bacteria would cause susceptibility to BSI.
Many freshwater cyanobacteria, including Microcystis aeruginosa, lack several known antibiotic resistance genes; however,
both axenic and xenic M. aeruginosa strains exhibited high antibiotic resistance against many antibiotics under our tested
concentrations, including colistin, trimethoprim, and kanamycin. Interestingly, axenic PCC7806, although not the xenic
NIBR18 and NIBR452 strains, displayed susceptibility to ampicillin and amoxicillin, indicating that the associated bacteria
in the phycosphere could confer such antibiotic resistance to xenic strains. Fluorescence and scanning electron microscopic
observations revealed their tight association, leading to possible community-level β-lactamase activity. Combinatory treatment
of ampicillin with a β-lactamase inhibitor, sulbactam, abolished the ampicillin resistance in the xenic stains. The
nitrocefin-based assay confirmed the presence of significant community-level β-lactamase activity. Our tested low ampicillin
concentration and high β-lactamase activity could potentially balance the competitive advantage of these dominant species
and provide opportunities for the less competitive species, thereby resulting in higher bacterial diversity under ampicillin
treatment conditions. Non-PCR-based metagenome data from xenic NIBR18 cultures revealed the dominance of blaOXArelated
antibiotic resistance genes followed by other class A β-lactamase genes (AST-1 and FAR-1). Alleviation of ampicillin
toxicity could be observed only in axenic PCC7806, which had been cocultured with β-lactamase from other freshwater
bacteria. Our study suggested M. aeruginosa develops resistance to old-class β-lactam antibiotics through altruism, where
associated bacteria protect axenic M. aeruginosa cells.
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in Korea and whether the composition of MAFs is affected by ocean currents, we isolated and analyzed the fungal community
from the western, southern, and eastern seasides of the Korean Peninsula. In total, 603 strains were isolated and identified
as 259 species based on appropriate molecular markers for each genus (ITS, BenA, CaM, tef1, and act). The composition of
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Two Gram-stain-positive, catalase-negative, non-spore-forming,
cocci-shaped strains (dk850T and JY899) were isolated
from the feces of Equus kiang in the Qinghai-Tibet Plateau of
China. 16S rRNA gene sequence-based phylogenetic analyses
showed that strains dk850T and JY899 belong to the genus
Flaviflexus, closest to F. salsibiostraticola KCTC 33148T, F. ciconiae
KCTC 49253T and F. huanghaiensis H5T. The DNA
G + C content of strain dk850T was 62.9%. The digital DNADNA
hybridization values of strain dk850T with the closely related
species were below the 70% threshold for species demarcation.
The two strains grew best at 28°C on brain heart infusion
(BHI) agar with 5% sheep blood. All strains had C18:1ω9c
and C16:0 as the major cellular fatty acids. MK-9(H4) was the
major menaquinone in strain dk850T. The major polar lipids
included diphosphatidylglycerol and an unidentified phospholipid.
Strains dk850T and JY899 were identified as carrying
a class 1 integron containing the aminoglycoside resistance
gene aadA11, both strains were resistant to spectinomycin
and streptomycin. Based on several lines of evidence
from phenotypic and phylogenetic analyses, strains dk850T
and JY899 represent a novel species of the genus Flaviflexus,
for which the name Flaviflexus equikiangi sp. nov. is proposed.
The type strain is dk850T (= CGMCC 1.16593T = JCM 33598T).
We have identified three Microbacterium strains, A18JL200T,
NY27T, and WY121T, that produce C50 carotenoids. Taxonomy
shows they represent three novel species. These strains
shared < 98.5% 16S rRNA gene sequence identity with each
other and were closely related to Microbacterium aquimaris
JCM 15625T, Microbacterium yannicii JCM 18959T, Microbacterium
ureisolvens CFH S00084T, and Microbacterium
hibisci CCTCC AB 2016180T. Digital DNA-DNA hybridization
(dDDH) values and average nucleotide identity (ANI)
showed differences among the three strains and from their
closest relatives, with values ranging from 20.4% to 34.6%
and 75.5% to 87.6%, respectively. These values are below the
threshold for species discrimination. Both morphology and
physiology also differed from those of phylogenetically related
Microbacterium species, supporting that they are indeed novel
species. These strains produce C50 carotenoids (mainly decaprenoxanthin).
Among the three novel species, A18JL200T
had the highest total yield in carotenoids (6.1 mg/L or 1.2 mg/g
dry cell weight). Unusual dual isoprenoid biosynthetic pathways
(methylerythritol phosphate and mevalonate pathways)
were annotated for strain A18JL200T. In summary, we found
strains of the genus Microbacterium that are potential producers
of C50 carotenoids, but their genome has to be investigated
further.
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A Gram-stain-negative, strictly aerobic, marine bacterium,
designated GH2-2T, was isolated from a rhizosphere mudflat
of a halophyte (Carex scabrifolia) in Gangwha Island,
the Republic of Korea. The cells of the organism were oxidase-
positive, catalase-positive, flagellated, short rods that
grew at 10–40°C, pH 4–10, and 0–13% (w/v) NaCl. The predominant
ubiquinone was Q-10. The major polar lipids were
phosphatidylcholine, phosphatidylethanolamine, and phosphatidylglycerol.
The major fatty acid is C18:1. Phylogenetic
analysis based on 16S rRNA gene sequences revealed that the
novel isolate formed an independent lineage at the base of
the radiation encompassing members of the genus Thioclava,
except for Thioclava arenosa. The closest relatives were T.
nitratireducens (96.03% sequence similarity) and T. dalianensis
(95.97%). The genome size and DNA G+C content
were 3.77 Mbp and 59.6 mol%, respectively. Phylogenomic
analysis supported phylogenetic distinctness based on 16S
rRNA gene sequences. Average nucleotide identity values
were 73.6–74.0% between the novel strain and members of
the genus Thioclava. On the basis of data obtained from a
polyphasic approach, the strain GH2-2T (= KCTC 62124T =
DSM 105743T) represents a novel species of a new genus for
which the name Hahyoungchilella caricis gen. nov., sp. nov. is
proposed. Moreover, the transfer of Thioclava arenosa Thongphrom
et al. 2017 to Pseudothioclava gen. nov. as Pseudothioclava
arenosa comb. nov. is also proposed. Finally, Thioclava
electrotropha Chang et al. 2018 is proposed to be a later
heterosynonym of Thioclava sediminum Liu et al. 2017.
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A novel, Gram-stain-negative, marine bacterium, designated
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(Carex scabrifolia) collected in Gangwha Island, the
Republic of Korea. The cells of the organism were strictly
aerobic, oxidase- and catalase-positive, non-flagellated rods.
Growth occurred at 20–45°C, pH 5–10, and 0.5–9 (w/v) NaCl.
The requirement of Na+ for growth (0.5–3%) was observed.
The major respiratory quinone was Q-10. The major polar
lipids were phosphatidylcholine, phosphatidylethanolamine,
phosphatidylglycerol, an aminolipid and a glycolipid. The
predominant fatty acids were C18:1 ω7c, C18:0, C16:0, C19:0 cyclo
ω8c, C18:1 ω7c 11-methyl and summed feature 2 (C14:0 3-OH
and/or C16:1 iso I). The genome size was 4.45 Mb and the G+C
content of the genomic DNA was 61.9 mol%. Phylogenetic
analyses based on 16S rRNA gene sequences revealed that
strain GH2-6T belonged to genus Martelella and formed a tight
cluster with M. radicis BM5-7T and M. endophytica YC6887T.
Levels of 16S rRNA gene sequence similarity between the novel
isolate and members of the genus were 99.3–95.5%, but strain
GH2-6T possessed an extended loop (49 nucleotides in length)
between positions 187 and 213 of the 16S rRNA gene sequence
(E. coli numbering). DDH values in vitro between the novel
isolate and the closest relatives were 23.2±12.8 – 46.3±5.2%.
On the basis of polyphasic data presented in this study, the
type strain GH2-6T (= KACC 19403T = KCTC 62125T = NBRC
113212T) represents a novel species of the genus Martelella
for which the name Martelella lutilitoris sp. nov. is proposed.
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To compare the ocular surface (OS) microbial communities
and diversity between dry eye (DE) and non-DE (NDE). Furthermore,
we compared meibomian gland dysfunction (MGD)
and non-MGD (NMGD) among DE subjects. The V3-V4 region
of 16S rRNA gene high-throughput sequencing was performed
in the conjunctival swab samples to investigate the
composition of the OS bacterial community in DE (n=35) and
NDE (n=54) and compared the composition of MGD (n=25)
and NMGD (n=10) among DE subjects. Deep sequencing
of OS 16S rDNA from DE (n=35) and NDE (n=54) demonstrated
great a difference in alpha and beta diversity between
the OS bacterial flora (P < 0.05). The similar OS microbial
structures were shown at the phylum and genus levels by bioinformatics
analysis between them, and in LEfSe (linear discriminant
analysis effect size) analysis, Bacteroidia and Bacteroidetes
were enriched in DE, while Pseudomonas was plentiful
in NDE (linear discriminant analysis [LDA] > 4.0). Among
the DE group, there was no significant difference in α and β
diversity between MGD and NMGD (P > 0.05). Surprisingly,
Bacilli was the dominant microbe in MGD, and Bacteroidetes
was the superior bacteria in NMGD among DE subjects (LDA
> 4.0). Different diversity of OS bacteria composition between
DE and NDE and the altered diversity of OS bacteria may
play an important role in DE. Moreover, the lower dominance
of OS bacteria in DE may be associated with the occurrence
and development of DE. Although there was no significant
difference in alpha and beta analysis, the OS dominant microbe
between MGD and NMGD among DE was different.
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A Gram-stain-negative, non-spore-forming, facultative, rodshaped
bacterium (designated LA-28T) was isolated from a
sludge sample from a wastewater treatment plant in Hanam
city, Republic of Korea. On the basis of 16S rRNA gene sequencing,
strain LA-28T clustered with species of the genus
Mesorhizobium and appeared closely related to M. jarvisii
LMG 28313T (96.8%), M. waimense ICMP 19557T (96.7%),
and M. huakuii LMG 14107T (96.7%). Growth occurs at 18–
40°C on R2A medium in the presence of 1–4% NaCl (w/v)
and at pH 6–8. The DNA G+C content was 61.2 mol%, and
the predominant quinone was ubiquinone-10 (Q-10). The
major cellular fatty acids (> 5%) were C16:0, C19:0 ω8c cyclo,
C18:1 ω7c 11-methyl, and C18:1 ω7c and/or C18:1 ω6c (summed
feature 8). Major polar lipids were phosphatidylglycerol (PG),
phosphatidylethanolamine (PE), phosphatidyl-N-methylethanolamine
(PME), and phosphatidylcholine (PC). Physiological
and biochemical characteristics indicated that strain
LA-28T represents a novel species of the genus Mesorhizobium,
for which the name Mesorhizobium denitrificans sp.
nov. is proposed. The type strain is LA-28T (= KACC 19675T
= LMG 30806T).
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A Gram-negative, non-motile, aerobic, catalase-, and oxidasepositive
bacterial strain, designated DCY117T, was isolated
from ginseng cultivated soil in Gochang-gun, Republic of
Korea, and was characterized taxonomically using a multifaceted
approach. 16S rRNA gene sequence analysis revealed
that strain DCY117T showed highest similarity to Lysobacter
ruishenii CTN-1T (95.3%). Phylogenetic analysis revealed
that closely related relatives of strain DCY117T were L. aestuarii
S2-CT (95.1%), L. daejeonensis GH1-9T (95.0%), and
L. caeni BUT-8T (94.9%). Diphosphatidylglycerol (DPG),
phosphatidylglycerol (PG), and phosphatidylethanolamine
(PE) were the major polar lipids of strain DCY117T. The major
isoprenoid quinone was Q-8. The major cellular fatty
acids of strain DCY117T were iso-C15:0, iso-C16:0, and summed
feature 9 (comprising iso-C17:1 ω9c and/or 10-methyl-C16:0).
Genomic DNA G + C content was 61.8 mol%. On the basis of
our findings, strain DCY117T is a novel species in the genus
Lysobacter. We propose the name Lysobacter panacihumi sp.
nov., and the type strain is DCY117T (= KCTC 62019T = JCM
32168T).
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The group of butyrate-producing bacteria within the human
gut microbiome may be associated with positive effects on
memory improvement, according to previous studies on dementia-
associated diseases. Here, fecal samples of four elderly
Japanese diagnosed with Alzheimer’s disease (AD) were
used to isolate butyrate-producing bacteria. 226 isolates were
randomly picked, their 16S rRNA genes were sequenced,
and assigned into sixty OTUs (operational taxonomic units)
based on BLASTn results. Four isolates with less than 97%
homology to known sequences were considered as unique
OTUs of potentially butyrate-producing bacteria. In addition,
12 potential butyrate-producing isolates were selected
from the remaining 56 OTUs based on scan-searching against
the PubMed and the ScienceDirect databases. Those belonged
to the phylum Bacteroidetes and to the clostridial clusters I,
IV, XI, XV, XIVa within the phylum Firmicutes. 15 out of
the 16 isolates were indeed able to produce butyrate in culture
as determined by high-performance liquid chromatography
with UV detection. Furthermore, encoding genes for butyrate
formation in these bacteria were identified by sequencing
of degenerately primed PCR products and included the
genes for butyrate kinase (buk), butyryl-CoA: acetate CoAtransferase
(but), CoA-transferase-related, and propionate
CoA-transferase. The results showed that eight isolates possessed
buk, while five isolates possessed but. The CoA-transfer-
related gene was identified as butyryl-CoA:4-hydroxybutyrate
CoA transferase (4-hbt) in four strains. No strains
contained the propionate CoA-transferase gene. The biochemical
and butyrate-producing pathways analyses of butyrate
producers presented in this study may help to characterize
the butyrate-producing bacterial community in the gut of AD patients.
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A Gram-positive, aerobic, non-motile, pale-yellow, and rodshaped
bacterium, designated as Gsoil 188T, was isolated from
the soil of a ginseng field in Pocheon, South Korea. A phylogenetic
analysis based on 16S rRNA gene sequence comparison
revealed that the strain formed a distinct lineage within
the genus Brevibacterium and was most closely related to B.
epidermidis NBRC 14811T (98.4%), B. sediminis FXJ8.269T
(98.2%), B. avium NCFB 3055T (98.1%), and B. oceani BBH7T
(98.1%), while it shared less than 98.1% identity with the other
species of this genus. The DNA G + C content was 68.1 mol%.
The predominant quinone was MK-8(H2). The major fatty
acids were anteiso-C15:0 and anteiso-C17:0. The cell wall peptidoglycan
of strain Gsoil 188T contained meso-diaminopimelic
acid. The major polar lipids were phosphatidylglycerol, diphosphatidylglycerol,
and an unidentified aminolipid. The
physiological and biochemical characteristics, low DNA-DNA
relatedness values, and taxonomic analysis allowed the differentiation
of strain Gsoil 188T from the other recognized
species of the genus Brevibacterium. Therefore, strain Gsoil
188T represents a novel species of the genus Brevibacterium,
for which the name Brevibacterium anseongense sp. nov. is
proposed, with the type strain Gsoil 188T (= KACC 19439T
= LMG 30331T).
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A Gram-positive, strictly aerobic, nonmotile, yellowish, coccus-
rod-shaped bacterium (designated Gsoil 653T) isolated
from ginseng cultivating soil was characterized using a polyphasic
approach to clarify its taxonomic position. The strain
Gsoil 653T exhibited optimal growth at pH 7.0 on R2A agar
medium at 30°C. Phylogenetic analysis based on 16S rRNA
gene sequence similarities, indicated that Gsoil 653T belongs
to the genus Terrabacter of the family Humibacillus, and was
closely related to Terrabacter tumescens DSM 20308T (98.9%),
Terrabacter carboxydivorans PY2T (98.9%), Terrabacter terrigena
ON10T (98.8%), Terrabacter terrae PPLBT (98.6%), and
Terrabacter lapilli LR-26T (98.6%). The DNA G + C content
was 70.5 mol%. The major quinone was MK-8(H4). The primary
polar lipids were phosphatidylglycerol, diphosphatidylglycerol,
phosphatidyl-ethanolamine. The predominant
fatty acids were iso-C15:0, iso-C16:0, iso-C14:0, and anteiso-C15:0,
as in the case of genus Terrabacter, thereby supporting the
categorization of strain Gsoil 653T. However, the DNA-DNA
relatedness between Gsoil 653T and closely related strains of
Terrabacter species was low at less than 31%. Moreover, strain
Gsoil 653T could be both genotypically and phenotypically distinguished
from the recognized species of the genus Terrabacter.
This isolate, therefore, represents a novel species, for
which the name Terrabacter ginsengisoli sp. nov. is proposed
with the type strain Gsoil 653T (= KACC 19444T = LMG
30325T).
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Phosphorus fertilizer application and tillage practices influence bacterial community composition: implication for soil health R.A. Adeleke, C. C. Obieze, C. Mukoro, C. B. Chikere, S. Tsipinana, A. Nciizah Archives of Agronomy and Soil Science.2023; 69(5): 803. CrossRef
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A Gram-reaction-positive, strictly aerobic, motile, endospore-
forming, and rod-shaped bacterial strain designated
135PIL107-10T was isolated from a sponge on Jeju Island, and
its taxonomic position was investigated using a polyphasic
approach. Strain 135PIL107-10T grew at 20–37°C (optimum
temperature, 25°C) and pH 6.0–10.0 (optimum pH, 6.0) on
marine and R2A agars. Based on 16S rRNA gene phylogeny
analysis, the novel strain formed a new branch within the genus
Bacillus of the family Bacillaceae, and formed clusters
with Bacillus thaohiensis NHI-38T (96.8%), Bacillus fengqiuensis
NPK15T (96.7%), and Bacillus songklensis CAU 1033T
(96.7%). Lower sequence similarities (97.0%) were found
with the type strains of all other recognized members of the
genus Bacillus (95.6–96.8% similarity). The G + C content
of the genomic DNA was 43.6 mol%. The predominant respiratory
quinone was menaquinone-7 and the major fatty
acids were iso-C15:0 and iso-C17:1ω10c. The overall polar lipid
patterns were diphosphatidylglycerol, phosphatidylglycerol,
and phosphatidylethanolamine. The diagnostic diamino acid
in the cell-wall peptidoglycan was meso-diaminopimelic acid.
The isolate therefore represents a novel species, for which
the name Bacillus spongiae sp. nov. is proposed, with the type
strain 135PIL107-10T (= KACC 19275T = LMG 30080T).
Citations
Citations to this article as recorded by
Antimicrobial Biosynthetic Potential and Phylogenetic Analysis of Culturable Bacteria Associated with the Sponge Ophlitaspongia sp. from the Yellow Sea, China Lei Chen, Xue-Ning Wang, Hong-Yu Bi, Guang-Yu Wang Marine Drugs.2022; 20(10): 588. CrossRef
List of new names and new combinations previously effectively, but not validly, published Aharon Oren, George M. Garrity
International Journal of Systematic and Evolutionary Microbiology
.2019; 69(5): 1247. CrossRef
A Gram-negative, motile, aerobic and rod-shaped bacterial
strain designated 119BY6-57T was isolated from spongin. The
taxonomic position of the novel isolate was confirmed using
the polyphasic approach. Strain 119BY6-57T grew well at 25–
30°C on marine agar. On the basis of 16S rRNA gene sequence
similarity, strain 119BY6-57T belongs to the family Xanthomonadaceae
and is related to Lysobacter aestuarii S2-CT
(99.8% sequence similarity), L. maris KMU-14T (97.5%), and
L. daejeonensis GH1-9T (97.3%). Lower sequence similarities
(97.0%) were found with all of the other recognized members
of the genus Lysobacter. The G + C content of the genomic
DNA was 69.9 mol%. The major respiratory quinone was Q-8
and the major fatty acids were C16:0 iso, C15:0 iso, summed feature
9 (comprising C17:1 iso ω9c and/or C16:0 10-methyl), summed
feature 3 (comprising C16:1 ω7c and/or C16:1 ω6c), and
C11:0 iso 3-OH. The polar lipids were phosphatidylglycerol,
phosphatidylethanolamine, diphosphatidylglycerol, three unidentified
phospholipids, and an unidentified polar lipid. DNADNA
relatedness values between strain 119BY6-57T and its
closest phylogenetically neighbors were below 48.0 ± 2.1%.
Based on genotypic and phenotypic characteristics, it is concluded
that strain 119BY6-57T is a new member within the genus
Lysobacter, for which the name Lysobacter spongiae sp.
nov. is proposed. The type strain is 119BY6-57T (= KACC
19276T = LMG 30077T).
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Huibin Lu, Li Chen, Yujing Wang, Peng Xing, Qinglong Wu
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List of new names and new combinations previously effectively, but not validly, published Aharon Oren, George M. Garrity
International Journal of Systematic and Evolutionary Microbiology
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