scholarly journals Olmesartan Attenuates Single-Lung Ventilation Induced Lung Injury via Regulating Pulmonary Microbiota

2021 ◽  
Author(s):  
Di Lu ◽  
Zhizhi Wang ◽  
Ziming Chen ◽  
Jiayang fan ◽  
Jianxue Zhai ◽  
...  
Keyword(s):  
16S Rrna ◽  
Lung Injury ◽  
16S Rrna Gene ◽  
Sham Group ◽  
Lung Ventilation ◽  
Rrna Gene ◽  
Sequencing Analysis ◽  
Single Lung Ventilation ◽  
Group I ◽  
Injury Group

Abstract Background: Single-lung ventilation (SLV) associated acute lung injury is similar to ischemia reperfusion (IR) injury which is usually occurred during lung surgery. Olmesartan (Olm), a novel angiotensin receptor blocker (ARB), has been reported to ameliorate organ IR injury. Several recent studies have shown that lung microbiota may be involved in pulmonary diseases, but the effect of pulmonary microbiota in SLV-induced lung injury has not been reported. This study aims to determine the mechanism of how Olm attenuates SLV induced lung injury. Results: 24 Sprague Dawley (SD) rats were randomly divided into four groups: S (sham) group; AS (ARB + sham) group, in which the rats were given 7 days Olm treatment before the sham surgery; I (injury) group, in which the rats underwent SLV for 1 h (right lung ventilation and left lung collapsed) and double lungs ventilation for 3 h; and the AI (ARB + injury) group. Our data showed that 7 days Olm treatment before modeling markedly alleviated SLV-induced lung injury by suppressing inflammation and reactive oxygen species. Bronchoalveolar lavage fluid samples from the injured side were collected for 16S rRNA gene-based sequencing analysis. A total of 53 different bacteria at the genus and species levels were identified, among which Burkholderiaceae was more enriched in group I compared with group S, but significantly decreased in AI group after Olm treatment. Fecal samples were then collected for gut microbiota analysis using 16S rRNA gene-based sequencing analysis, which revealed no significant difference between the A and AS group. Furthermore, the injured lung samples were collected for metabolomics analysis using liquid chromatography-mass spectrometry analyses to explore differential metabolites among all groups. The Kyoto Encyclopedia of Genes and Genomes (KEGG) was applied to analyze the correlation between differential metabolites and lung microbiota. A total of 38 pathways were identified according to differential metabolites and 275 relevant pathways were enriched via analyzing the microbial community, 24 pathways were both identified by analyzing either metabolites or microbiota, including pyrimidine metabolism, purine metabolism, aminoacyl-tRNA biosynthesis and ATP-binding cassette transporter. Conclusions: Besides classical blockage of the renin-angiotensin II system, Olm could also alleviate SLV-induced lung injury by rewiring the interaction between pulmonary microbiota and metabolites.

scholarly journals Microbiome of Odontogenic Abscesses

2021 ◽  
Vol 9 (6) ◽  
pp. 1307
Author(s):  
Sebastian Böttger ◽  
Silke Zechel-Gran ◽  
Daniel Schmermund ◽  
Philipp Streckbein ◽  
Jan-Falco Wilbrand ◽  
...  
Keyword(s):  
16S Rrna ◽  
16S Rrna Gene ◽  
Oral Microbiome ◽  
Minor Role ◽  
Rrna Gene ◽  
Sequencing Analysis ◽  
Bacterial Strains ◽  
16S Rrna Gene Analysis ◽  
Odontogenic Infections ◽  
Odontogenic Abscess

Severe odontogenic abscesses are regularly caused by bacteria of the physiological oral microbiome. However, the culture of these bacteria is often prone to errors and sometimes does not result in any bacterial growth. Furthermore, various authors found completely different bacterial spectra in odontogenic abscesses. Experimental 16S rRNA gene next-generation sequencing analysis was used to identify the microbiome of the saliva and the pus in patients with a severe odontogenic infection. The microbiome of the saliva and the pus was determined for 50 patients with a severe odontogenic abscess. Perimandibular and submandibular abscesses were the most commonly observed diseases at 15 (30%) patients each. Polymicrobial infections were observed in 48 (96%) cases, while the picture of a mono-infection only occurred twice (4%). On average, 31.44 (±12.09) bacterial genera were detected in the pus and 41.32 (±9.00) in the saliva. In most cases, a predominantly anaerobic bacterial spectrum was found in the pus, while saliva showed a similar oral microbiome to healthy individuals. In the majority of cases, odontogenic infections are polymicrobial. Our results indicate that these are mainly caused by anaerobic bacterial strains and that aerobic and facultative anaerobe bacteria seem to play a more minor role than previously described by other authors. The 16S rRNA gene analysis detects significantly more bacteria than conventional methods and molecular methods should therefore become a part of routine diagnostics in medical microbiology.

scholarly journals The Termite Group I Phylum Is Highly Diverse and Widespread in the Environment

2007 ◽  
Vol 73 (20) ◽  
pp. 6682-6685 ◽  
Author(s):  
Daniel P. R. Herlemann ◽  
Oliver Geissinger ◽  
Andreas Brune
Keyword(s):  
Phylogenetic Analysis ◽  
16S Rrna ◽  
16S Rrna Gene ◽  
Rrna Gene ◽  
Gene Sequences ◽  
16S Rrna Gene Sequences ◽  
Specific Primers ◽  
Environmental Distribution ◽  
Data Set ◽  
Group I

ABSTRACT The bacterial candidate phylum Termite Group I (TG-1) presently consists mostly of “Endomicrobia,” which are endosymbionts of flagellate protists occurring exclusively in the hindguts of termites and wood-feeding cockroaches. Here, we show that public databases contain many, mostly undocumented 16S rRNA gene sequences from other habitats that are affiliated with the TG-1 phylum but are only distantly related to “Endomicrobia.” Phylogenetic analysis of the expanded data set revealed several diverse and deeply branching lineages comprising clones from many different habitats. In addition, we designed specific primers to explore the diversity and environmental distribution of bacteria in the TG-1 phylum.

scholarly journals First case of an invasive Bacteroides dorei infection detected in a patient with a mycotic aortic aneurysm—raising a rebellion of major indigenous bacteria in humans: a case report and review

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Takayuki Matsuoka ◽  
Takuya Shimizu ◽  
Tadanori Minagawa ◽  
Wakiko Hiranuma ◽  
Miki Takeda ◽  
...  
Keyword(s):  
Aortic Aneurysm ◽  
16S Rrna ◽  
16S Rrna Gene ◽  
Gene Sequencing ◽  
16S Rrna Gene Sequencing ◽  
Resected Specimen ◽  
Rrna Gene ◽  
Sequencing Analysis ◽  
First Case ◽  
Rrna Gene Sequencing

Abstract Background Bacteroides dorei is an anaerobic gram-negative bacterium first described in 2006. Because of the high similarity in mass spectra between B. dorei and Bacteroides vulgatus, discriminating between these species is arduous in clinical practice. In recent decades, 16S rRNA gene sequencing has been a complementary method for distinguishing taxonomically close bacteria, including B. dorei and B. vulgatus, at the genus and species levels. Consequently, B. dorei has been shown to contribute to some diseases, including type 1 autoimmune diabetes mellitus and atherosclerotic diseases. However, there are no reports on invasive infectious diseases caused by B. dorei. This report describes the first case of direct invasion and colonisation of human tissue by B. dorei, thus providing a warning regarding the previously proposed application of B. dorei as a live biotherapeutic for atherosclerotic diseases. Case presentation A 78-year-old Japanese man complained of intermittent chest/back pain and was diagnosed with a mycotic thoracic aortic aneurysm by enhanced computed tomography on admission. Despite strict blood pressure control and empirical antibiotic therapy, the patient’s condition worsened. To prevent aneurysmal rupture and eliminate infectious foci, the patient underwent surgical treatment. The resected specimen was subjected to tissue culture and 16S rRNA gene sequencing analysis to identify pathogenic bacteria. A few days after the surgery, culture and sequencing results revealed that the pathogen was B. dorei/B. vulgatus and B. dorei, respectively. The patient was successfully treated with appropriate antibacterial therapy and after improvement, was transferred to another hospital for rehabilitation on postoperative day 34. There was no recurrence of infection or aneurysm after the patient transfer. Conclusions This report describes the first case of invasive infectious disease caused by B. dorei, casting a shadow over its utilisation as a probiotic for atherosclerotic diseases.

Flavobacterium cutihirudinis sp. nov., isolated from the skin of the medical leech Hirudo verbana

2013 ◽  
Vol 63 (Pt_8) ◽  
pp. 2841-2847 ◽  
Author(s):  
S. P. Glaeser ◽  
H. Galatis ◽  
K. Martin ◽  
P. Kämpfer
Keyword(s):  
16S Rrna ◽  
16S Rrna Gene ◽  
Type Species ◽  
Biochemical Characterization ◽  
Rrna Gene ◽  
Sequencing Analysis ◽  
Respiratory Quinone ◽  
Content Type ◽  
Link Type ◽  
Hirudo Verbana

A Gram-staining-negative, non-endospore-forming, yellow-pigmented strain (E89T) was isolated from the skin of the medical leech Hirudo verbana obtained from a leech farm located in Biebertal, Germany. 16S rRNA gene sequencing analysis showed that the isolate was grouped in the genus Flavobacterium . Strain E89T was most closely related to Flavobacterium chilense LM-09-FpT (98.2 %), Flavobacterium chungangense CJ7T (98.1 %), and Flavobacterium oncorhynchi 631-08T (98.1 %). 16S rRNA gene sequence similarities to all other species of the genus Flavobacterium were ≤97.4 %. A menaquinone of the type MK-6 was found to be the predominant respiratory quinone and the polar lipid profile consisted of the major compounds phosphatidylethanolamine, phosphatidylserine, two unidentified aminolipids, one unknown phospholipid and two unknown lipids. The fatty acid profile was composed of iso-C15 : 0, C15 : 0, summed feature 3 (C16 : 1ω7c and/or iso-C15 : 0 2-OH) found in major amounts and several hydroxylated fatty acids in smaller amounts, among them iso-C15 : 0 3-OH and iso-C17 : 0 3-OH. All these data support the allocation of the isolate in the genus Flavobacterium . Physiological/biochemical characterization and DNA–DNA hybridizations with the type strains of the most closely related species allowed a clear phenotypic and genotypic differentiation of the strain. Based on these data, strain E89T represents a novel species of the genus Flavobacterium , for which the name Flavobacterium cutihirudinis sp. nov. is proposed. The type strain is E89T ( = DSM 25795T = LMG 26922T = CIP 110374T).

scholarly journals Fastidious Gram-Negatives: Identification by the Vitek 2 Neisseria-Haemophilus Card and by Partial 16S rRNA Gene Sequencing Analysis

2010 ◽  
Vol 4 (1) ◽  
pp. 123-131 ◽  
Author(s):  
Jens JØrgen Christensen ◽  
Brita Bruun ◽  
Ute Wolff Sönksen ◽  
Lisbeth Nielsen ◽  
Annemarie Hesselbjerg ◽  
...  
Keyword(s):  
16S Rrna ◽  
16S Rrna Gene ◽  
Gene Sequencing ◽  
16S Rrna Gene Sequencing ◽  
Rrna Gene ◽  
Sequencing Analysis ◽  
Vitek 2 ◽  
Rrna Gene Sequencing

Oxynema aestuarii sp. nov. (Microcoleaceae) isolated from an Indian mangrove forest

Phytotaxa ◽  
2018 ◽  
Vol 374 (1) ◽  
pp. 24 ◽  
Author(s):  
SANDEEP CHAKRABORTY ◽  
VEERABADHRAN MARUTHANAYAGAM ◽  
ANUSHREE ACHARI ◽  
RIDDHI MAHANSARIA ◽  
ARNAB PRAMANIK ◽  
...  
Keyword(s):  
16S Rrna ◽  
16S Rrna Gene ◽  
Sequence Similarity ◽  
Hypersaline Environment ◽  
Phylogenetic Study ◽  
Rrna Gene ◽  
Growth Responses ◽  
Nucleotide Substitutions ◽  
Intertidal Environment ◽  
Group I

Taxonomic characterization by a polyphasic approach was carried out on two cyanobacteria, AP17 and AP24 isolated from soil biofilms of two separate islands, Lothian and Sagar respectively, of the Indian Sundarbans. The strains were studied morphologically by light microscopy, scanning and transmission electron microscopy. Growth responses to various salinities were recorded. Molecular data included sequencing and phylogenetic study of the 16S rRNA gene as well as analysis of the 14 regions of the 16S-23S ITS regions. Morphologically the strains were found to be non-heterocytous, having attenuated trichomes with a narrow, bent terminal cell without any crosswalls. Strains under investigation shared 99–100% 16S rRNA gene sequence similarity with Oxynema thaianum CCALA960, the type species of the novel Oxynema genus, recently separated from the Phormidium-Group I genus. However, cross walls in the apical portion of AP17 and AP24 were totally absent while the same was present in CCALA960. Additionally, optimal growth of AP17 and AP24 was recorded in 5–8% salinity and salinity above 14% inhibited growth of both strains, which were isolated from an intertidal environment; whereas O. thaianum CCALA960 which was found in a hypersaline environment could grow at 40% salinity. Insertion of 9 nucleotides in the D2 with spacer region, insertion of 2 nucleotides in the pre Box B spacer region, deletion of 2 nucleotides in the post Box B spacer region, deletion of 8 nucleotides in the D4 region, deletion of 8 nucleotides in V3 region and insertion of 2 nucleotides in the D5 region of the ITS sequences of AP17 and AP24 were observed in comparison to the analogous regions of CCALA960. Structural details of Box B helices of AP17 and AP24 revealed that although their lengths were identical with the reference, their sequences were completely different from CCALA960. Four nucleotide substitutions were observed in different positions in the Box B helix of O. thaianum CCALA960. Secondary structures of the V3 regions of AP17 and AP24 (containing 51 nucleotides) showed a small terminal bulge and a bigger bilateral bulge while the analogous structure of O. thaianum CCALA 960 (comprising of 59 nucleotides) showed one additional bilateral bulge in comparison to AP17 and AP24. Therefore, based on morphological, ecological and molecular differences in comparison to O. thaianum CCALA960, isolates AP17 and AP24 should be considered as a second novel species in the Oxynema genus, for which the name Oxynema aestuarii sp. nov. is proposed.

scholarly journals Bacterial composition of nasal discharge in children based on highly accurate 16S rRNA gene sequencing analysis

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Kaoru Haro ◽  
Midori Ogawa ◽  
Mitsumasa Saito ◽  
Koichi Kusuhara ◽  
Kazumasa Fukuda
Keyword(s):  
16S Rrna ◽  
16S Rrna Gene ◽  
Gene Sequencing ◽  
16S Rrna Gene Sequencing ◽  
Nasal Discharge ◽  
Rrna Gene ◽  
Respiratory Pathogens ◽  
Sequencing Analysis ◽  
Bacterial Cells ◽  
Rrna Gene Sequencing

AbstractNasopharyngeal colonization by bacteria is a prerequisite for progression to respiratory disease and an important source of horizontal spread within communities. We aimed to perform quantitative analysis of the bacterial cells and reveal the microbiota of the nasal discharge in children at the species level based on highly accurate 16S rRNA gene sequencing. This study enrolled 40 pediatric patients with rhinorrhea. The bacterial cells in the nasal discharge were counted by epifluorescence microscopic analysis. The microbiota was analyzed by using the 16S rRNA gene clone library sequencing method. We demonstrated that a high abundance (median 2.2 × 107 cells/mL) of bacteria was contained in the nasal discharge of children. Of the 40 samples, 37 (92.5%) were dominated by OTUs corresponding to Haemophilus aegyptius/influenzae, Moraxella catarrhalis/nonliquefaciens, or Streptococcus pneumoniae. These samples showed higher cell abundance and lower alpha diversity than the remaining three samples in which the other bacteria coexisted. In addition, 12 sequences with low homology to type strains were considered as previously unknown bacterial lineages. In conclusion, the nasal discharge of most young children contains a large amount of respiratory pathogens and several unknown bacteria, which could not only cause endogenous infection but also be a source of transmission to others.

scholarly journals Molecular Identification of Mycobacterium Species of Public Health Importance in Cattle in Zimbabwe by 16S rRNA Gene Sequencing

2015 ◽  
Vol 9 (1) ◽  
pp. 38-42 ◽  
Author(s):  
Leah Padya ◽  
Nyasha Chin'ombe ◽  
Marcelyn Magwenzi ◽  
Joshua Mbanga ◽  
Vurayai Ruhanya ◽  
...  
Keyword(s):  
16S Rrna ◽  
16S Rrna Gene ◽  
Dna Sequences ◽  
Close Relative ◽  
Cow Dung ◽  
Rrna Gene ◽  
Mycobacterium Fortuitum ◽  
Sequencing Analysis ◽  
Public Health Importance ◽  
Detection And Identification

Mycobacteriumspecies are naturally found in the environment as well as in domestic animals such as cattle. So far, more than 150 species ofMycobacterium, some of which are pathogenic, have been identified. Laboratory isolation, detection and identification ofMycobacteriumspecies are therefore critical if human and animal infections are to be controlled. The objective of this study was to identifyMycobacteriumspecies isolated in cattle in Zimbabwe using 16S ribosomal RNA gene amplification and sequencing. A total of 134 cow dung samples were collected throughout Zimbabwe and mycobacteria were isolated by culture. Only 49 culture isolates that were found to be acid-fast bacilli positive by Ziehl-Neelsen staining. The 16S rRNA gene was successfully amplified by PCR in 41 (84%) of the samples. There was no amplification in 8 (16%) of the samples. Out of the 41 samples that showed amplification, 26 (63%) had strong PCR bands and were selected for DNA sequencing. Analysis of the DNA sequences showed that 7 (27%) belonged toMycobacterium neoaurum, 6 (23%) belonged toMycobacterium fortuitum, 3 (12%) toMycobacterium goodii, 2 (1%) toMycobacterium arupense, 2 (1%) toMycobacterium peregrinumorM. septicumand 1 isolate (0.04%) toMycobacterium elephantis. There were 5 (19%) isolates that were non-mycobacteria and identified as Gordonia terrae, a close relative ofMycobacterium. The study therefore provided a molecular basis for detection and identification ofMycobacteriumspecies in animals and humans.

scholarly journals Nocardia niwae sp. nov., isolated from human pulmonary sources

2011 ◽  
Vol 61 (2) ◽  
pp. 438-442 ◽  
Author(s):  
Benjamin D. Moser ◽  
Hans-Peter Klenk ◽  
Peter Schumann ◽  
Gabriele Pötter ◽  
Brent A. Lasker ◽  
...  
Keyword(s):  
16S Rrna ◽  
16S Rrna Gene ◽  
Gene Sequence ◽  
Novel Species ◽  
Rrna Gene ◽  
Sequencing Analysis ◽  
The Novel ◽  
Gene Sequences ◽  
Sequence Analyses ◽  
Taxonomic Analysis

Members of the genus Nocardia are responsible for cutaneous, pulmonary and disseminated human infections. From 2003 to 2008, four nocardioform strains (W8027, W8681, W9071 and W9241T) were isolated from patients in the state of Florida, USA. Ribosomal gene sequencing analysis suggested that a novel species of the genus Nocardia had been isolated. These strains were subjected to a taxonomic analysis using a polyphasic approach. Phenotypic analyses included morphological examination, biochemical profiling and antimicrobial susceptibility testing. Molecular studies included 16S rRNA and DNA gyrase B subunit (gyrB) gene sequence analyses and DNA–DNA hybridization. Phylogenetic neighbours were determined through 16S rRNA and gyrB gene sequence analyses. Phenotypic characteristics that differentiated the novel isolates from phylogenetically related species were growth at 45 °C, and three of the four novel strains utilized l-rhamnose. The antimicrobial profiles could not reliably distinguish the novel species from related nocardiae. Analysis showed that the 16S rRNA gene sequences of the four novel isolates were identical. The blast analysis of the near full-length 16S rRNA gene showed 99.2 % sequence similarity to Nocardia araoensis DSM 44729T, Nocardia arthritidis DSM 44731T and Nocardia beijingensis JCM 10666T, 98.7 % to Nocardia amamiensis DSM 45066T, 98.2 % to Nocardia pneumoniae JCM 12119T and 97.8 % to Nocardia takedensis JCM 13313T. Analysis of partial gyrB gene sequences showed that the novel isolates had 95.4 % similarity to N. arthritidis DSM 44731T, 95.3 % to Nocardia gamkensis DSM 44956T, 94.4 % to N. pneumoniae JCM 12119T, 93.8 % to Nocardia asiatica DSM 44668T, 93.5 % to N. amamiensis DSM 45066T, 93.4 % to N. beijingensis JCM 10666T and 93.2 % to N. araoensis DSM 44729T. The DNA–DNA relatedness values between the four novel strains were 86–89 %; the relatedness value for strain W9241T compared with N. beijingensis JCM 10666T was 47 % and 46 % with N. araoensis DSM 44729T, 44 % with N. arthritidis DSM 44731T, 32 % with N. amamiensis DSM 45066T and 20 % with N. asiatica DSM 44668T. The results of the taxonomic analysis suggested that the new isolates represent a novel species of the genus Nocardia for which the name Nocardia niwae sp. nov. is proposed. The type strain is W9241T (=DSM 45340T=CCUG 57756T).

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