scholarly journals Animal-to-Animal Variation in Fecal Microbial Diversity among Beef Cattle

2010 ◽  
Vol 76 (14) ◽  
pp. 4858-4862 ◽  
Author(s):  
Lisa M. Durso ◽  
Gregory P. Harhay ◽  
Timothy P. L. Smith ◽  
James L. Bono ◽  
Todd Z. DeSantis ◽  
...  

ABSTRACT The intestinal microbiota of beef cattle are important for animal health, food safety, and methane emissions. This full-length sequencing survey of 11,171 16S rRNA genes reveals animal-to-animal variation in communities that cannot be attributed to breed, gender, diet, age, or weather. Beef communities differ from those of dairy. Core bovine taxa are identified.

Genes ◽  
2020 ◽  
Vol 12 (1) ◽  
pp. 40
Author(s):  
Liang Cui ◽  
Bitong Zhu ◽  
Xiaobo Zhang ◽  
Zhuhua Chan ◽  
Chungui Zhao ◽  
...  

The elevated NH3-N and NO2-N pollution problems in mariculture have raised concerns because they pose threats to animal health and coastal and offshore environments. Supplement of Marichromatium gracile YL28 (YL28) into polluted shrimp rearing water and sediment significantly decreased ammonia and nitrite concentrations, showing that YL28 functioned as a novel safe marine probiotic in the shrimp culture industry. The diversity of aquatic bacteria in the shrimp mariculture ecosystems was studied by sequencing the V4 region of 16S rRNA genes, with respect to additions of YL28 at the low and high concentrations. It was revealed by 16S rRNA sequencing analysis that Proteobacteria, Planctomycete and Bacteroidetes dominated the community (>80% of operational taxonomic units (OTUs)). Up to 41.6% of the predominant bacterial members were placed in the classes Gammaproteobacteria (14%), Deltaproteobacteria (14%), Planctomycetacia (8%) and Alphaproteobacteria (5.6%) while 40% of OTUs belonged to unclassified ones or others, indicating that the considerable bacterial populations were novel in our shrimp mariculture. Bacterial communities were similar between YL28 supplements and control groups (without addition of YL28) revealed by the β-diversity using PCoA, demonstrating that the additions of YL28 did not disturb the microbiota in shrimp mariculture ecosystems. Instead, the addition of YL28 increased the relative abundance of ammonia-oxidizing and denitrifying bacteria. The quantitative PCR analysis further showed that key genes including nifH and amoA involved in nitrification and nitrate or nitrite reduction significantly increased with YL28 supplementation (p < 0.05). The supplement of YL28 decreased the relative abundance of potential pathogen Vibrio. Together, our studies showed that supplement of YL28 improved the water quality by increasing the relative abundance of ammonia-oxidizing and denitrifying bacteria while the microbial community structure persisted in shrimp mariculture ecosystems.


Geofluids ◽  
2019 ◽  
Vol 2019 ◽  
pp. 1-17 ◽  
Author(s):  
Malin Bomberg ◽  
Jarno Mäkinen ◽  
Marja Salo ◽  
Päivi Kinnunen

Microbial communities of iron-rich water in the Pyhäsalmi mine, Finland, were investigated with high-throughput amplicon sequencing and qPCR targeting bacteria, archaea, and fungi. In addition, the abundance ofLeptospirillumandAcidithiobacilluswas assessed with genus-specific qPCR assays, and enrichment cultures targeting aerobic ferrous iron oxidizers and ferric iron reducers were established. The acidic (pH 1.4–2.3) mine water collected from 240 m, 500 m, and 600 m depth from within the mine had a high microbial diversity consisting of 63-114 bacterial, 10-13 archaeal, and 104-117 fungal genera. The most abundant microorganisms in the mine water were typical acid mine drainage (AMD) taxa, such as acidophilic, iron-oxidizingLeptospirillum,Acidiphilum,Acidithiobacillus,Ferrovum, andThermoplasma. The fungi belonged mostly to the phylum Ascomycetes, although a great part of the fungal sequences remained unclassified. The number of archaeal 16S rRNA genes in the mine water was between 0.3 and 1.2 × 107copies mL−1in the samples from 500 m and 600 m, but only 3.9 × 103at 240 m and archaea were in general not enriched in cultures. The number of fungal 5.8S rRNA genes was high only in the mine water from 500 m and 600 m, where 0.2–3.4 × 104spore equivalents mL−1were detected. A high number ofLeptospirillum16S rRNA genes, 0.6–1.6 × 1010copies mL−1, were detected at 500 m and 600 m depth and in cultures containing ferrous iron, showing the importance of iron oxidizers in this environment. The abundance of bacteria in general was between 103and 10616S rRNA gene copies mL−1. Our results showed a high microbial diversity in the acid- and iron-impacted waters of the Pyhäsalmi mine, whereLeptospirillumbacteria were especially prominent. These iron oxidizers are also the main nitrogen-fixing microorganisms in this ecosystem.


2006 ◽  
Vol 72 (9) ◽  
pp. 6271-6276 ◽  
Author(s):  
Yusuke Nakanishi ◽  
Koichiro Murashima ◽  
Hiroki Ohara ◽  
Takahisa Suzuki ◽  
Hidenori Hayashi ◽  
...  

ABSTRACT It is well known that short chain fructooligosaccharides (scFOS) modify intestinal microbiota in animals as well as in humans. Since most murine intestinal bacteria are still uncultured, it is difficult for a culturing method to detect changes in intestinal microbiota after scFOS administration in a mouse model. In this study, we sought markers of positive change in murine intestinal microbiota after scFOS administration using terminal restriction fragment length polymorphism (T-RFLP) analysis, which is a culture-independent method. The T-RFLP profiles showed that six terminal restriction fragments (T-RFs) were significantly increased after scFOS administration. Phylogenetic analysis of the 16S rRNA partial gene sequences of murine fecal bacteria suggested that four of six T-RFs that increased after scFOS administration were derived from the 16S rRNA genes of the class Bacteroidetes. Preliminary quantification of Bacteroidetes by real-time PCR suggests that the 16S rRNA genes derived from Bacteroidetes were increased by scFOS administration. Therefore, the T-RFs derived from Bacteroidetes are good markers of change of murine intestinal microbiota after scFOS administration.


2007 ◽  
Vol 28 (3) ◽  
pp. 127
Author(s):  
Peter H Janssen

Unculturable microorganisms are those that have been identifiedby microscopy, by their activity or by detection of phylogenetic markers such as their 16S rRNA genes, and have not been able to be cultured, despite reasonable efforts having been made. Recent successes in the cultivation of so-called unculturable microorganisms have revealed that the key ingredient in therecipe for growing them in the laboratory is patience. Beyond that, there is probably no single secret to success and microbial diversity must be matched by experimental ingenuity.


2021 ◽  
Vol 10 (27) ◽  
Author(s):  
Nur Indradewi Oktavitri ◽  
Jong-Oh Kim ◽  
Kyunghoi Kim

Benthic microbial diversity in Tongyeong, South Korea, was analyzed using next-generation sequencing of the 16S rRNA genes, to reveal the effects of seasonal variations on the microbial community in sediment. Proteobacteria was the dominant phylum, with a relative abundance of 61.5 to 68.1%.


2009 ◽  
Vol 71-73 ◽  
pp. 117-120 ◽  
Author(s):  
L. Alves ◽  
C. Bernardelli ◽  
V.A. Leão ◽  
Monica Teixeira ◽  
Edgardo R. Donati

The aim of this work was to determine the microbial diversity of the acid mine drainage (AMD) material collected at an abandoned pyrite mine in Ouro Preto, Brazil. AMD samples were compared to a nickel sulfide column bioleaching pregnant solution which was used as reference. Fluorescent in situ hybridization analyses (FISH) and Denaturing Gradient Gel Electrophoresis (DGGE) were used. FISH analysis was carried out using specific 16S rRNA probes. The extracted DNA was amplified using universal primers for bacterial 16S rRNA genes and analyzed by DGGE. Acidithiobacillus. ferrooxidans was not detected in AMD samples. However, the presence of Acidithiobacillus thiooxidans was confirmed. In other hand, in the bioleaching tanks samples studied, both bacteria species were detected. The non-identified DNA bands were cloned and sequenced for complete characterization.


Diversity ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 138
Author(s):  
Stuart Donachie ◽  
Claire Fraser ◽  
Ethan Hill ◽  
Marguerite Butler

The term “microbiome” is currently applied predominantly to assemblages of organisms with 16S rRNA genes. In this context, “microbiome” is a misnomer that has been conferred a wide-ranging primacy over terms for community members lacking such genes, e.g., mycobiome, eukaryome, and virome, yet these are also important subsets of microbial communities. Widespread convenient and affordable 16S rRNA sequencing pipelines have accelerated continued use of such a “microbiome”, but at what intellectual and practical costs? Here we show that the use of “microbiome” in ribosomal gene-based studies has been egregiously misapplied, and discuss potential impacts. We argue that the current focus of “microbiome” research, predominantly on only ‘bacteria’, presents a dangerous narrowing of scope which encourages dismissal and even ignorance of other organisms’ contributions to microbial diversity, sensu stricto, and as etiologic agents; we put this in context by discussing cases in both marine microbial diversity and the role of pathogens in global amphibian decline. Fortunately, the solution is simple. We must use descriptive nouns that strictly reflect the outcomes attainable by the methods used. “Microbiome”, as a descriptive noun, should only be used when diversity in the three recognized domains is explored.


2021 ◽  
Vol 16 (2) ◽  
pp. 35-43
Author(s):  
Yu.V. Yudina ◽  
◽  
A.I. Aminova ◽  
A.P. Prodeus ◽  
G.D. Abdullaeva ◽  
...  

Objective. To evaluate the composition of intestinal microbiota in children with atopic dermatitis (AD) aged 1–5 years depending on the disease severity. Patients and methods. We have examined 60 children aged between 1 and 5 years diagnosed with AD. In outpatient settings, they have undergone comprehensive clinical and laboratory examination that included analysis of patient's medical history, physical examination, assessment of clinical status using the SCORAD scale, complete blood count, urinalysis, analysis of feces, liver function tests, measurement of total IgE and specific IgE, and bacteriological analysis of feces. The composition of intestinal microbiota was assessed using bacterial 16S rRNA gene sequencing with subsequent bioinformatic and statistical analysis. Results. The analysis of intestinal microbiota in 60 AD children aged 1–5 years using 16S rRNA sequencing demonstrated an association between the composition of intestinal microflora and disease severity. Both bacterial count and species diversity directly depend on the disease course. Children with complicated AD had a very poor diversity of intestinal microorganisms compared to those in remission (р ≤ 0.002). Children with signs of AD exacerbation demonstrated an increased count of Actinobacteria species (р = 0.018) and a decreased count of Proteobacteria species compared to children without clinical manifestations of AD (р = 0.033). We also observed a decrease in the amount of bacteria belonging to Oscillospiraceae and Erysipelatoclostridiaceae families (р = 0.03 : 0.034) in children with AD exacerbation and children with signs of secondary infection. Patients with acute disease and patients with signs of secondary infection were also more likely to have lower level of Bifidobacterium longum (р = 0.03 : 0.034) than patients in remission. Conclusion. Our findings suggest that the intestinal microbiota of children in remission differs from that in children with AD exacerbation or complicated AD. The composition of commensal flora, as well as species richness directly depend on the disease severity. Children with AD exacerbation were found to have lower concentration of Oscillospiraceae species and B. longum that are crucial for normal functioning of the gastrointestinal tract and modulation of the immune response. Understanding of the metabolic potential of bacteria will enable adequate diet correction of the intestinal microbiota. Thus, sequencing of bacterial 16S rRNA genes is very helpful in the diagnosis of AD. It also opens new horizons in the search for new treatment methods. Key words: alpha diversity, atopic dermatitis, children, intestinal microbiota, molecular genetic methods, 16S sequencing


Sign in / Sign up

Export Citation Format

Share Document