scholarly journals Metagenomics and Culture Dependent Insights into the Distribution of Firmicutes across Two Different Sample Types Located in the Black Hills Region of South Dakota, USA

2021 ◽  
Vol 9 (1) ◽  
pp. 113
Author(s):  
Tanvi Govil ◽  
Manasi Paste ◽  
Dipayan Samanta ◽  
Aditi David ◽  
Kian Mau Goh ◽  
...  
Keyword(s):  
Sequence Analysis ◽  
16S Rrna ◽  
South Dakota ◽  
Ligninolytic Enzymes ◽  
Operational Taxonomic Unit ◽  
Amplicon Sequencing ◽  
16S Rrna Sequence ◽  
Gene Sequence Analysis ◽  
16S Rrna Sequence Analysis ◽  
Sanford Underground Research Facility

Firmicutes is almost a ubiquitous phylum. Several genera of this group, for instance, Geobacillus, are recognized for decomposing plant organic matter and for producing thermostable ligninolytic enzymes. Amplicon sequencing was used in this study to determine the prevalence and genetic diversity of the Firmicutes in two distinctly related environmental samples—South Dakota Landfill Compost (SDLC, 60 °C), and Sanford Underground Research Facility sediments (SURF, 45 °C). Although distinct microbial community compositions were observed, there was a dominance of Firmicutes in both the SDLC and SURF samples, followed by Proteobacteria. The abundant classes of bacteria in the SDLC site, within the phylum Firmicutes, were Bacilli (83.2%), and Clostridia (2.9%). In comparison, the sample from the SURF mine was dominated by the Clostridia (45.8%) and then Bacilli (20.1%). Within the class Bacilli, the SDLC sample had more diversity (a total of 11 genera with more than 1% operational taxonomic unit, OTU). On the other hand, SURF samples had just three genera, about 1% of the total population: Bacilli, Paenibacillus, and Solibacillus. With specific regard to Geobacillus, it was found to be present at a level of 0.07% and 2.5% in SURF and SDLC, respectively. Subsequently, culture isolations of endospore-forming Firmicutes members from these samples led to the isolation of a total of 117 isolates. According to colony morphologies, and identification based upon 16S rRNA and gyrB gene sequence analysis, we obtained 58 taxonomically distinct strains. Depending on the similarity indexes, a gyrB sequence comparison appeared more useful than 16S rRNA sequence analysis for inferring intra- and some intergeneric relationships between the isolates.

scholarly journals Parapedobacter indicus sp. nov., isolated from hexachlorocyclohexane-contaminated soil

2015 ◽  
Vol 65 (Pt_1) ◽  
pp. 129-134 ◽  
Author(s):  
Roshan Kumar ◽  
Vatsala Dwivedi ◽  
Namita Nayyar ◽  
Helianthous Verma ◽  
Amit Kumar Singh ◽  
...  
Keyword(s):  
Sequence Analysis ◽  
16S Rrna ◽  
Sequence Similarity ◽  
Rrna Gene ◽  
Biochemical Tests ◽  
16S Rrna Sequence ◽  
Content Type ◽  
Link Type ◽  
Gene Sequence Analysis ◽  
16S Rrna Sequence Analysis

Strain RK1T, a Gram-stain-negative, non-spore-forming, rod-shaped, non-motile bacterium was isolated from a hexachlorocyclohexane (HCH) dumpsite, Lucknow, India. 16S rRNA gene sequence analysis revealed that strain RK1T belongs to the family Sphingobacteriaceae and showed highest sequence similarity to Parapedobacter koreensis Jip14T (95.63 %). The major cellular fatty acids of strain RK1T were iso-C15 : 0, summed feature 3 (C16 : 1ω7c and/or C16 : 1ω6c), iso-C17 : 0 3-OH, summed feature 9 (10-methyl C16 : 0 and/or iso-C17 : 1ω9c), iso-C15 : 0 3-OH and C16 : 0. The major respiratory pigment and polyamine of RK1T were menaquinone (MK-7) and homospermidine, respectively. The main polar lipids were phosphatidylethanolamine and sphingolipid. The G+C content of the DNA was 44.5 mol%. The results of physiological and biochemical tests and 16S rRNA sequence analysis clearly demonstrated that strain RK1T represents a novel species of the genus Parapedobacter , for which the name Parapedobacter indicus sp. nov. is proposed. The type strain is RK1T ( = DSM 28470T = MCC 2546T).

scholarly journals Mycobacterium neoaurumBacteremia in a Hemodialysis Patient

2003 ◽  
Vol 14 (1) ◽  
pp. 45-48 ◽  
Author(s):  
Marissa L Becker ◽  
Amar A Suchak ◽  
Joyce N Wolfe ◽  
Ryan Zarychanski ◽  
Amin Kabani ◽  
...  
Keyword(s):  
Sequence Analysis ◽  
16S Rrna ◽  
Hemodialysis Patient ◽  
Immunocompromised Host ◽  
Blood Cultures ◽  
Clinical Suspicion ◽  
Diabetic Woman ◽  
Rrna Sequence ◽  
16S Rrna Sequence ◽  
16S Rrna Sequence Analysis

Bacteremia due toMycobacterium neoaurum, a rapidly growing mycobacterium, is described in a diabetic woman on hemodialysis. This is the first reported case of M neoaurum bacteremia in Canada. The organism initially grew on standard BacT/Alert SA aerobic blood cultures, and was subsequently positively identified using 16S rRNA sequence analysis. The present case serves to reinforce the need for a high index of clinical suspicion of infections caused by unusual microorganisms in the context of an immunocompromised host.

Mycobacterium marinum infections in humans and tracing of its possible environmental sources

2012 ◽  
Vol 58 (1) ◽  
pp. 39-44 ◽  
Author(s):  
Michal Slany ◽  
Petr Jezek ◽  
Vera Fiserova ◽  
Monika Bodnarova ◽  
Jiri Stork ◽  
...  
Keyword(s):  
Sequence Analysis ◽  
16S Rrna ◽  
Correct Diagnosis ◽  
Low Frequency ◽  
Mycobacterium Marinum ◽  
Mycobacterium Fortuitum ◽  
Rrna Sequence ◽  
16S Rrna Sequence ◽  
Mycobacterium Chelonae ◽  
16S Rrna Sequence Analysis

The low frequency of nontuberculous mycobacterial infections, nonspecific symptoms for individual mycobacteria, and the lack of specific identification methods could alter correct diagnosis. This study presents a combined microbiology and molecular-based approach for Mycobacterium marinum detection in four aquarists with cutaneous mycobacterial infection. Simultaneously, ecology screening for M. marinum presence in the aquarists’ fish tanks was performed. A total of 38 mycobacterial isolates originated from four human patients (n = 20), aquarium animals (n = 8), and an aquarium environment (n = 10). Isolate identification was carried out using 16S rRNA sequence analysis. A microbiology-based approach, followed by 16S rRNA sequence analysis, was successfully used for detection of M. marinum in all four patients. Animal and environmental samples were simultaneously examined, and a total of seven mycobacterial species were isolated: Mycobacterium chelonae , Mycobacterium fortuitum , Mycobacterium gordonae , Mycobacterium kansasii , Mycobacterium mantenii , Mycobacterium marinum , and Mycobacterium peregrinum . The presence of M. marinum was proven in the aquarium environments of two patients. Although M. marinum is described as being present in water, it was detected only in fish.

Cleaning and Handling Implements as Potential Reservoirs for Bacterial Contamination of Some Ready-to-Eat Foods in Retail Delicatessen Environments

2007 ◽  
Vol 70 (12) ◽  
pp. 2878-2883 ◽  
Author(s):  
C. A. CHRISTISON ◽  
D. LINDSAY ◽  
A. von HOLY
Keyword(s):  
South Africa ◽  
Sequence Analysis ◽  
16S Rrna ◽  
Rrna Sequence ◽  
Gram Positive ◽  
16S Rrna Sequence ◽  
Bacterial Populations ◽  
16S Rrna Sequence Analysis ◽  
And Staphylococcus Aureus ◽  
Disposable Plastic

This study assessed the association of bacteria with cleaning tools, such as floor mops (n = 25) and cleaning cloths (n = 39), and handling devices, such as disposable plastic gloves (n = 20), used during filled baguette and assorted salad preparation in four selected retail delicatessens in Johannesburg, South Africa. Samples of each cleaning or handling tool were prepared for aerobic (APC), coliform (CC), Escherichia coli (EC), Bacillus cereus (BCC), and Staphylococcus aureus (SAC) counts, as well as tested for the incidence of Listeria monocytogenes (LM) and Salmonella (SALM) by standard plating methods. Bacterial populations attached to the cleaning and handling tools were observed by scanning electron microscopy (SEM). Ten selected gram-positive isolates were further analyzed by 16S rRNA sequence analysis and compared with isolates from filled baguettes and assorted salads. The floor mops consistently yielded the highest APCs, CCs, and ECs (5.7, 4.1, and 3.0 log CFU/g, respectively), while gloves had the lowest corresponding counts (3.6, 2.0, and 1.0 log CFU/g, respectively). Low BCCs and SACs were recorded in this study (ca. 1.2 log CFU/g), while SALM and LM were each detected in five cleaning tool samples. SEM showed rods and cocci attached to handling and cleaning tools. Furthermore, results of 16S rRNA sequence analysis indicated that several gram-positive isolates were identified as S. aureus, Staphylococcus pasteuri, Staphylococcus sciuri, and Enterococcus faecalis. Genetically similar strains (100% similarity) were isolated from cleaning and handling tools and associated ready-to-eat (RTE) foods. Cleaning and handling tools may act as reservoirs of contamination for RTE foods during preparation in retail delicatessens in South Africa. The transfer of potential pathogens, such as S. aureus, to foods from cleaning and handling tools may hold food safety implications.

Haemophilus parainfluenzaeInfective Endocarditis Confirmed by 16S rRNA Sequence Analysis from Culture Negative Tissue

2012 ◽  
Vol 15 (4) ◽  
pp. 139 ◽  
Author(s):  
Kyoung-Jin Park ◽  
Kyung Sun Park ◽  
Soo-Han Choi ◽  
Yae-Jean Kim ◽  
Chang-Seok Ki ◽  
...  
Keyword(s):  
Sequence Analysis ◽  
16S Rrna ◽  
Rrna Sequence ◽  
16S Rrna Sequence ◽  
16S Rrna Sequence Analysis ◽  
Culture Negative
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