Analyze Diet

Topic:Colony-Forming Units

Colony-Forming Units (CFUs) are a measurement used to estimate the number of viable bacteria or fungal cells in a sample. In equine research, CFUs are often utilized to assess microbial populations in various contexts, such as the gastrointestinal tract, respiratory system, or wound sites of horses. This measurement helps in understanding the microbial environment and its potential impact on equine health. CFUs provide insights into the presence and concentration of specific microorganisms, which can be important for diagnosing infections, evaluating the effectiveness of antimicrobial treatments, or studying the microbiome of horses. This page compiles peer-reviewed research studies and scholarly articles that explore the application, methodology, and implications of using CFUs in equine microbiological studies.
The health enhancer yeast Saccharomyces cerevisiae in two types of commercial products for animal nutrition.
Letters in applied microbiology    March 19, 2019   Volume 68, Issue 5 472-478 doi: 10.1111/lam.13141
Garcia-Mazcorro JF, Rodriguez-Herrera MV, Marroquin-Cardona AG, Kawas JR.The health enhancer yeast Saccharomyces cerevisiae (SC) is widely used in diets for different animals. Two main types of SC-based products are commercially available, one containing live yeasts and one containing SC fermentation by-products, which are supposedly not dependent on live yeasts for their physiological effects in vivo. Culture-based techniques were applied to study yeasts in two types of commercial products: a product containing live SC (LSC) and a SC fermentation product (SCFP). Three temperatures (25, 30 and 39°C) and two pH levels (4 and 7) were tested. The product with LSC co...
Colloid centrifugation of fresh stallion semen before cryopreservation decreased microorganism load of frozen-thawed semen without affecting seminal kinetics.
Theriogenology    September 16, 2014   Volume 83, Issue 2 186-191 doi: 10.1016/j.theriogenology.2014.09.003
Guimarães T, Lopes G, Pinto M, Silva E, Miranda C, Correia MJ, Damásio L, Thompson G, Rocha A.Freezability of equine semen may be influenced by microorganism population of semen. The objective of this study was to verify the effect of single-layer density gradient centrifugation (SLC) of fresh semen before cryopreservation on semen's microbial load (ML) and sperm cells kinetics after freezing-thawing. For that, one ejaculate was collected from 20 healthy stallions and split into control (C) samples (cryopreserved without previous SLC) and SLC samples (subjected to SLC). Semen cryopreservation was performed according to the same protocol in both groups. Microbial load of each microorgan...
Optimisation of bone marrow aspiration from the equine sternum for the safe recovery of mesenchymal stem cells.
Equine veterinary journal    September 23, 2010   Volume 43, Issue 3 288-294 doi: 10.1111/j.2042-3306.2010.00215.x
Kasashima Y, Ueno T, Tomita A, Goodship AE, Smith RK.Mesenchymal stem cell (MSC) therapy for orthopaedic disease is being used with increasing frequency; there is a need to define a safe, reliable and effective technique for the recovery of MSCs from the sternum of the horse. Objective: To describe an optimised safe technique for obtaining bone marrow-derived MSCs from the sternum of the Thoroughbred horse. Methods: The anatomical relationship of the sternum with the heart and internal anatomy was demonstrated in cadavers. Sternal anatomy was evaluated ultrasonographically and after midline sectioning. Sternebrae were examined histologically aft...
Characterization of equine adipose tissue-derived stromal cells: adipogenic and osteogenic capacity and comparison with bone marrow-derived mesenchymal stromal cells.
Veterinary surgery : VS    September 27, 2007   Volume 36, Issue 7 613-622 doi: 10.1111/j.1532-950X.2007.00313.x
Vidal MA, Kilroy GE, Lopez MJ, Johnson JR, Moore RM, Gimble JM.To characterize equine adipose tissue-derived stromal cell (ASC) frequency and growth characteristics and assess of their adipogenic and osteogenic differentiation potential. Methods: In vitro experimental study. Methods: Horses (n=5; aged, 9 months to 5 years). Methods: Cell doubling characteristics of ASCs harvested from supragluteal subcutaneous adipose tissue were evaluated over 10 passages. Primary, second (P2), and fourth (P4) passage ASCs were induced under appropriate conditions to undergo adipogenesis and osteogenesis. Limit dilution assays were performed on each passage to determine ...
Conjunctival fungal flora in healthy donkeys.
Veterinary ophthalmology    June 15, 2007   Volume 10, Issue 4 207-210 doi: 10.1111/j.1463-5224.2007.00537.x
Nardoni S, Sgorbini M, Barsotti G, Corazza M, Mancianti F.To identify and quantify ocular fungi from healthy donkeys living in the center of Italy. Methods: One hundred and two Amiata donkeys were examined. Methods: Conjunctival swabs from both eyes were seeded onto Sabouraud dextrose agar (SDA) and malt extract agar (MEA), and incubated at 25 degrees C over a 10-day period. Filamentous fungi identification was achieved to the genus level; yeast colonies were identified for macro-micromorphologic and physiological characteristics. Results: Eighty-one donkeys out of 102 (79.4%) were positive for fungi; 47/102 (46.1%) had positive cultures from both ey...
Evaluation of arthrocentesis site bacterial flora before and after 4 methods of preparation in horses with and without evidence of skin contamination.
Veterinary surgery : VS    September 15, 2004   Volume 33, Issue 5 525-530 doi: 10.1111/j.1532-950X.2004.04074.x
Zubrod CJ, Farnsworth KD, Oaks JL.To evaluate the effectiveness of four methods of povidone-iodine preparation on skin bacterial flora of arthrocentesis sites, in horses, with and without evidence of skin contamination. Methods: Prospective randomized study. Methods: Twenty-four adult horses. Methods: Horses were assigned to either the clean or contaminated group based on housing environment and visual evidence of contamination. Using a moist sterile swab, microbial culture samples were obtained from the skin over the distal interphalangeal joints immediately before and after preparation. Each site was aseptically prepared wit...
Prevalence of virulent Rhodococcus equi in isolates from soil collected from two horse farms in South Africa and restriction fragment length polymorphisms of virulence plasmids in the isolates from infected foals, a dog and a monkey.
The Onderstepoort journal of veterinary research    October 5, 2001   Volume 68, Issue 2 105-110 
Takai S, Henton MM, Picard JA, Guthrie AJ, Fukushi H, Sugimoto C.The prevalence of virulent Rhodococcus equi in soil isolates from two horse farms in South Africa and nine clinical isolates from six foals, a foal foetus, a dog, and a monkey was investigated. The isolates were tested for the presence of virulence plasmid DNA and 15- to 17-kDa antigens by immunoblotting. Rhodococcus equi was isolated from almost all of the soil samples obtained from the two farms with 5.0 x 10(1) to 3.3 x 10(4) colony forming units per gram of soil. Virulent R. equi was isolated from three soil samples from one of the farms and appeared in 3.8% (three of 80 isolates), but not...
Effects of equine infectious anemia virus on hematopoietic progenitors in vitro.
American journal of veterinary research    July 1, 1992   Volume 53, Issue 7 1176-1179 
Swardson CJ, Kociba GJ, Perryman LE.Direct effects of equine infectious anemia virus (EIAV) on hematopoiesis in vitro were studied. Bone marrow mononuclear cells from clinically normal horses were incubated with 100 TCID50 of EIAV/10(7) cells. These cells were cultured to assay for colonies derived from erythroid progenitors, granulocyte/monocyte progenitors, and fibroblastic progenitors. The EIAV had a selective suppressive effect on the erythroid progenitors. Colony-forming units-erythroid were suppressed to 80% of that for medium controls (P = 0.011). Burst-forming units-erythroid were suppressed to 70% of that for medium con...
An assay to quantitate the binding of Rhodococcus equi to macrophages.
Veterinary immunology and immunopathology    May 1, 1992   Volume 32, Issue 3-4 339-350 doi: 10.1016/0165-2427(92)90055-u
Hondalus MK, Sweeney CR, Mosser DM.A Rhodococcus equi radiobinding assay has been developed using organisms labeled with 3H-uracil. These labeled organisms resemble their unlabeled counterparts with respect to colony morphology, viability, and buoyant density. Bacteria routinely incorporate between 5 x 10(-3) and 5 x 10(-2) counts per minute per colony forming unit (cfu) which in this assay allows the detection of fewer than 0.2 cfu per macrophage. Once incorporated, greater than 90% of the label remains bacterial associated for at least 4 h postlabeling. The majority of the label is trichloroacetic acid precipitable, partition...
Ecology of Rhodococcus (Corynebacterium) equi in soil on a horse-breeding farm.
Veterinary microbiology    July 1, 1986   Volume 12, Issue 2 169-177 doi: 10.1016/0378-1135(86)90078-7
Takai S, Narita K, Ando K, Tsubaki S.The ecology of Rhodococcus (Corynebacterium) equi in soil was studied on a horse-breeding farm. R. equi was cultured from soil at a depth of 0, 10, and 20 cm on the six sites of the farm at monthly intervals for 10 months from March to December of 1983. The highest numbers of R. equi were found in the surface soil. The mean number of bacteria in soil samples at every depth increased remarkably from 0 or 10(2) to 10(4) colony-forming units (CFU) g-1 of soil in the middle of April, and later decreased gradually. R. equi inoculated into six soil exudate broths prepared from surface soils at separ...