Isolation of a virulent bacteriophage from a Propionibacterium species in the sheep rumen

2000 ◽  
Vol 51 (1) ◽  
pp. 119 ◽  
Author(s):  
J. P. E. Cheong ◽  
J. P. E. Cheong ◽  
J. D. Brooker ◽  
J. D. Brooker
Keyword(s):  
Rumen Fluid ◽  
Indicator Strain ◽  
Facultative Anaerobe ◽  
Isolation And Identification ◽  
Rumen Epithelium ◽  
Oxygen Scavenging ◽  
Transmission Electron ◽  
Sheep Rumen ◽  
Anaerobic Environment ◽  
Icosahedral Head

Propionibacterium is a facultative anaerobe associated with the rumen epithelium, the presence of which may influence the anaerobic environment through oxygen scavenging, as well as providing a source of propionate. Factors such as bacteriophages that influence Propionibacterium populations may therefore be important regulators of rumen function. This study describes the isolation and identification of a ruminal Propionibacterium bacteriophage. Sheep rumen fluid was screened for Propionibacterium species and 3 isolates were identified and characterised. One isolate, PA1, was used as an indicator strain to screen for the presence of Propionibacterium-specific virulent bacteriophages. A virulent bacteriophage, PB2, was isolated from clear plaques on a lawn of PA1 cells and was shown by transmission electron microscopy to be a siphovirus-like particle comprising an icosahedral head 50 nm in diameter and a tail 140 nm in length. The bacteriophage was visibly attached to and within PA1 cells, and was shown to infect all 3 ruminal isolates of Propionibacterium and 4 of 6 clinical isolates of P. acnes. Restriction mapping of bacteriophage PB2 demonstrated a 30.8 kb genome.

scholarly journals TCTP Promotes Hu Sheep Rumen Epithelial Development before Weaning

2021 ◽  
Author(s):  
kaizhi zheng ◽  
Jianliang Wu ◽  
Liangyong Guo ◽  
Yuyang Ying ◽  
Peng Li ◽  
...  
Keyword(s):  
Molecular Mechanisms ◽  
Rumen Fluid ◽  
Postnatal Life ◽  
Akt Phosphorylation ◽  
Cellular Processes ◽  
Rumen Epithelium ◽  
Epithelial Development ◽  
Stratum Spinosum ◽  
Ruminant Animals ◽  
Sheep Rumen

Abstract BackgroundHu Sheep is a world precious breed of sheep. Rumen is the most important digestive organ for ruminant animals. A better understanding of the molecular mechanisms involved in rumen development help us design better strategies to improve the production of sheep. Translationally controlled tumor protein (TCTP) is a highly conserved protein that involves various cellular processes. However, its role in rumen epithelium development remains unknown.ResultsTCTP was expressed in stratum basale, stratum spinosum and stratum granulosum of rumen epithelium. TCTP mRNA expression was extremely high on the day of birth, it then significantly decreased on day 15 and gradually increased until day 45 of age. TCTP protein expression remained in a relative low level from day 0 to day 15 of age, it then significantly increased on day 30 and gradually decreased until day 60. The ratio of Ki67 positive cell in stratum basale cell followed the similar pattern as the expression of TCTP. The papillae length decreased at first 15 days of postnatal life. Thereafter, the papilla undergo a period of growth from 538.1±17.3μm to 2211.1±56.6μm until 60 days of age. The phosphorylation of AKT is the highest on day 15 of age, then decreased until day 45. The ratio of acetate:propionate in rumen fluid decreased from day 30 to day 60 of age. ConclusionsTCTP participates in rumen papillae growth by promoting rumen stratum basale cell proliferation. We suggest that the translation of TCTP mRNA is regulated by AKT phosphorylation and the development of rumen papillae is associated with acetate:propionate ratio.

scholarly journals Isolation and Identification of Sodium Fluoroacetate Degrading Bacteria from Caprine Rumen in Brazil

2012 ◽  
Vol 2012 ◽  
pp. 1-6 ◽  
Author(s):  
Expedito K. A. Camboim ◽  
Arthur P. Almeida ◽  
Michelle Z. Tadra-Sfeir ◽  
Felício G. Junior ◽  
Paulo P. Andrade ◽  
...  
Keyword(s):  
Rumen Fluid ◽  
16S Rrna Gene Sequencing ◽  
Positive Control ◽  
Control Measures ◽  
Rrna Gene ◽  
Isolation And Identification ◽  
Poisonous Plants ◽  
Degrading Bacteria ◽  
Rrna Gene Sequencing ◽  
Orbital Shaker

The objective of this paper was to report the isolation of two fluoroacetate degrading bacteria from the rumen of goats. The animals were adult goats, males, crossbred, with rumen fistula, fed with hay, and native pasture. The rumen fluid was obtained through the rumen fistula and immediately was inoculated 100 μL in mineral medium added with 20 mmol L−1sodium fluoroacetate (SF), incubated at 39°C in an orbital shaker.Pseudomonas fluorescens(strain DSM 8341) was used as positive control for fluoroacetate dehalogenase activity. Two isolates were identified by 16S rRNA gene sequencing asPigmentiphaga kullae(ECPB08) andAncylobacter dichloromethanicus(ECPB09). These bacteria degraded sodium fluoroacetate, releasing 20 mmol L−1of fluoride ion after 32 hours of incubation in Brunner medium containing 20 mmol L−1of SF. There are no previous reports of fluoroacetate dehalogenase activity forP. kullaeandA. dichloromethanicus. Control measures to prevent plant intoxication, including use of fences, herbicides, or other methods of eliminating poisonous plants, have been unsuccessful to avoid poisoning by fluoroacetate containing plants in Brazil. In this way,P. kullaeandA. dichloromethanicusmay be used to colonize the rumen of susceptible animals to avoid intoxication by fluoroacetate containing plants.

Isolation and identification of rumen bacteria capable of anaerobic rutin degradation

1969 ◽  
Vol 15 (12) ◽  
pp. 1365-1371 ◽  
Author(s):  
K. -J. Cheng ◽  
G. A. Jones ◽  
F. J. Simpson ◽  
M. P. Bryant
Keyword(s):  
Volatile Fatty Acids ◽  
Rumen Fluid ◽  
Anaerobic Bacteria ◽  
Heterocyclic Ring ◽  
Ring Structure ◽  
Water Soluble ◽  
Rumen Bacteria ◽  
Isolation And Identification ◽  
Pure Cultures ◽  
Rutin Degradation

Fifteen strains of bacteria capable of degrading rutin anaerobically were isolated from bovine rumen contents and identified by morphological and biochemical evidence as strains of Butyrivibrio sp. Three cultures from a laboratory collection of 53 strains of rumen bacteria also used rutin anaerobically. Two, Butyrivibrio fibrisolvens D1 and Selenomonas ruminantium GA192, cleaved the glycosidic bond of rutin and fermented the sugar but did not degrade the insoluble aglycone produced; the third strain, Peptostreptococcus sp. B178, degraded the substrate to soluble products. Butyrivibrio sp. C3 degraded rutin, quercitrin, and naringin to water-soluble products, showing that the organism cleaved the heterocyclic ring of these compounds. Butyrivibrio sp. C3 fermented the sugar moiety of hesperidin but did not cleave the heterocyclic ring. It did not attack quercetin, taxifolin, protocatechuic acid, or phloroglucinol. In a medium containing rumen fluid, Butyrivibrio sp. C3 degraded rutin more than twice as fast as it did in a medium containing enzymatic casein hydrolyzate, volatile fatty acids, yeast extract, and hemin in place of rumen fluid.The observations reported in this paper are believed to represent the first recorded demonstration of degradation of the heterocyclic ring structure of rutin and other bioflavonoids in pure cultures of anaerobic bacteria.

scholarly journals Bacteriocin Activity of Lactic Acid Bacteria Isolated from Rumen Fluid of Thin Tail Sheep

2019 ◽  
Vol 43 (3) ◽  
Author(s):  
Okti Widayati ◽  
Zaenal Bachruddin ◽  
Chusnul Hanim ◽  
Lies Mira Yusiati ◽  
Nafiatul Umami
Keyword(s):  
Lactic Acid ◽  
Lactic Acid Bacteria ◽  
Ph Value ◽  
Heating Temperature ◽  
Rumen Fluid ◽  
Bacteriocin Activity ◽  
Significant Difference ◽  
Sheep Rumen ◽  
The Stability ◽  
Range Test

The objective of this study was to determine the activity and the stability of bacteriocin from lactic acid bacteria (BAL) isolated from rumen fluid of thin-tail sheep under the temperature (80, 100, and 121°C), pH (3, 7, and 10), and the length of storage (for 2 weeks under the temperature -8, 11, and 29°C). Lactic acid bacteria obtained by isolation, selection, and identification of thin-tailed sheep rumen fluid were used for bacteriocin production. The crude bacteriocin was partially purified using 70% ammonium sulfate, then was dialysis for 12 hours. The obtained bacteriocin then tested its inhibitory activity against E.coli (representing Gram-negative) and S. aureus (representing Gram-positive) under temperature (80, 100, and 121°C), pH (3, 7, and 10), and the length of storage (for 2 weeks under the temperature -8, 11, and 29°C). The data of bacteriocin activity based on pH, temperature, and the length of storage were analyzed with factorial, then when there was a significant difference of variable because treatment was continued with Duncan's Multiple Range Test (DMRT) test. The results showed that the bacteriocin activity of the three types of BAL against S.aureus is greater than E.coli. The highest activity was shown in pH 3, while the lowest activity was shown at pH 10 (P<0.01). The highest activity was shown at a heating temperature of 100°C, while the lowest activity was shown at a heating temperature of 80°C (P<0.01). The activity of bacteriocin produced by BAL 0 A, BAL 1 A, and BAL 4 C tended to be stable to the heating temperature of 80, 100, and 121°C but decreased with increasing pH value (pH 3, 7, and 10). The best of bacteriocin activity was found at pH 3 (acid), heating at 100°C, and stored at -8°C for 14 days.

scholarly journals Isolation and Identification of Exosomes from Feline Plasma, Urine and Adipose-Derived Mesenchymal Stem Cells

2021 ◽  
Author(s):  
Dongsheng Li ◽  
Huina Luo ◽  
Huimin Ruan ◽  
Zhisheng Chen ◽  
Shengfeng Chen ◽  
...  
Keyword(s):  
Stem Cells ◽  
Mesenchymal Stem Cells ◽  
Transmembrane Protein ◽  
Cell Communication ◽  
Phospholipid Bilayer ◽  
Differential Centrifugation ◽  
Isolation And Identification ◽  
Feasible Method ◽  
Transmission Electron ◽  
Mediate Cell

Abstract Background: Exosomes, internal proteins, lipids, and nucleic acids coated by phospholipid bilayer membranes, are one type of small extracellular vesicles, which can mediate cell-cell communication. In recent years, exosomes have gained considerable scientific interest due to their widely applied prospect in the diagnosis and therapeutics of human and animal diseases. In this study, we describe for the first time a feasible method designed to isolate and characterize exosomes from feline plasma, urine and adipose-derived mesenchymal stem cells. Results: Exosomes from feline plasma, urine and adipose-derived mesenchymal stem cells were successfully isolated by differential centrifugation. Quantification and sizing of exosomes were assessed by transmission electron microscopy, flow nano analysis and western blotting. Detected particles showed the normal size (30-100 nm) and morphology described for exosomes, as well as presence of the transmembrane protein (TSG101, CD9, CD63, and CD81) known as exosomal marker.Conclusions: The results suggest that differential centrifugation is a feasible method for isolation of exosomes from different types of feline samples. Moreover, these exosomes can be used to further diagnosis and therapeutics in veterinary pre-clinical and clinical studies.

Evaluating the In Vitro Metabolism of Docosahexaenoic Acid in Sheep Rumen Fluid

Lipids ◽  
2012 ◽  
Vol 47 (8) ◽  
pp. 821-825 ◽  
Author(s):  
Noelia Aldai ◽  
Gonzalo Hervás ◽  
Álvaro Belenguer ◽  
Pilar Frutos ◽  
Angel R. Mantecón ◽  
...  
Keyword(s):  
Docosahexaenoic Acid ◽  
Rumen Fluid ◽  
In Vitro Metabolism ◽  
Sheep Rumen

Poly-β-hydroxybutyrate accumulation in bacterial consortia from different environments

2012 ◽  
Vol 58 (5) ◽  
pp. 660-667 ◽  
Author(s):  
Rahela Carpa ◽  
Anca Butiuc-Keul ◽  
Iulia Lupan ◽  
Lucian Barbu-Tudoran ◽  
Vasile Muntean ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Polymerase Chain Reaction ◽  
Flood Plain ◽  
Soil Samples ◽  
Chain Reaction ◽  
Isolation And Identification ◽  
Stressful Environment ◽  
Transmission Electron ◽  
Polymerase Chain

The aim of the present study was to examine soil samples from various vegetation zones in terms of physicochemical properties, microbial communities, and isolation and identification (by polymerase chain reaction and transmission electron microscopy) of bacteria producing poly-β-hydroxybutyrates (PHBs). Soil samples were analysed originating from zones with heterogeneous environmental conditions from the Romanian Carpathian Mountains (mountain zone with alpine meadow, karstic zone with limestone meadow, hill zone with xerophilous meadow, and flood plain zone with hygrophilic meadow). Different bacterial groups involved in the nitrogen cycle (aerobic mesophilic heterotrophs, ammonifiers, denitrifiers, nitrifiers, and free nitrogen-fixing bacteria from Azotobacter genus) were analysed. Soil biological quality was assessed by the bacterial indicator of soil quality, which varied between 4.3 and 4.7. A colony polymerase chain reaction technique was used for screening PHB producers. With different primers, specific bands were obtained in all the soil samples. Some wild types of Azotobacter species were isolated from the 4 studied sites. Biodegradable polymers of PHB were assessed by negative staining in transmission electron microscopy. The maximum PHB granules density was obtained in the strains isolated from the xerophilous meadow (10–18 granules/cell), which was the most stressful environment from all the studied sites, as the physicochemical and microbiological tests proved.

A system for analysing the buffer system in the developing rumen of the young calf

1989 ◽  
Vol 1989 ◽  
pp. 162-162
Author(s):  
A.I. Frost ◽  
I.M. Nevison
Keyword(s):  
Rumen Fluid ◽  
Rapid Development ◽  
Salivary Flow ◽  
High Energy ◽  
Chemical Components ◽  
Buffer System ◽  
Young Calf ◽  
Rumen Epithelium ◽  
Rumen Ph ◽  
Number Of Factors

The feeding of rapidly fermentable, high energy, diets to young calves stimulates a rapid development of microbial fermentation. High concentrate diets may not, however, stimulate a corresponding development of salivary flow (Kay, 1966). A number of factors affect the buffering system of ruminal contents, besides saliva, such as the concentration of the end products of fermentation and the rate at which these products are absorbed through the rumen epithelium (Turner and Hodgetts, 1955). Counotte, van Klooster, van der Kuilen and Prins (1979) presented the analysis of the buffer system in the rumen using the first derivative of the titration curve. The results showed that bicarbonate and VFA are the main chemical components of the buffer system in the rumen fluid of adult dairy cattle. The ability to buffer against potentially large deterimental fluctuations, ie rumen pH, may improve rumen stability and be benefical to stimulate solid food intake in the early weaned calf. The present experiment describes a system for analysing the buffer system in the developing rumen of the young calf.

The use of rumen material in culture media for rumen bacteria

1961 ◽  
Vol 12 (5) ◽  
pp. 960 ◽  
Author(s):  
E Munch-Petersen ◽  
CAP Boundy
Keyword(s):  
Culture Media ◽  
Rumen Fluid ◽  
Rumen Bacteria ◽  
Agar Culture ◽  
Sheep Rumen

The suggestion that homologous rumen fluid in culture media results in better growth of rumen bacteria than that obtained with heterologous fluid was tested with samples of rumen material from cows and sheep, with the use of rumen fluid from cows and sheep, and two agar culture media. It is shown that the suggestion cannot be taken as applying in general. With rumen material from the cow, the use of either type of rumen fluid gave the same growth, whereas with rumen material from the sheep, growth was depressed by use of sheep rumen fluid.

Repeatability of in vitro digestibility assays of forages when using fresh, frozen or freeze-dried cow faeces instead of sheep rumen liquor as sources of micro-organisms

1995 ◽  
Vol 1995 ◽  
pp. 110-110 ◽  
Author(s):  
S Akhter ◽  
E Owen ◽  
M K Theodorou ◽  
S L Tembo ◽  
E R Deaville
Keyword(s):  
Freeze Drying ◽  
Rumen Fluid ◽  
In Vitro Digestibility ◽  
Two Stage ◽  
Freeze Dried ◽  
Fresh Frozen ◽  
Sheep Rumen ◽  
Micro Organisms

Previous studies (El Shaer, Omed and Axford, 1987; Akhter, Owen, Fall, O'Donovan and Theodorou, 1994) with the two-stage in vitro procedure of Tilley and Terry (1963) have shown a high correlation between digestibilities of forages as determined using either sheep rumen liquor, sheep faeces or cow faeces as the microbial inoculum. In the first study of the of the present investigation one objective was to examine the repeatability of these digestibility measurements when made on different occasions. A second objective was to assess whether the correlations between faecal and rumen fluid based inocula could be improved if microorganisms were obtained from pairs rather than individual animals. The objective in the second study using forages of known in vivo digestibility, was to investigate the effect of freezing or freeze-drying of faeces on the repeatability of digestibilities of forages determined in vitro using micro-organisms from cow faeces.

Sign in / Sign up

Export Citation Format

Share Document