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PubMed2003

Immunological anomalies and thrombocytopenia in 117 dogs and cats diagnosed with chronic fatigue syndrome (CFS).

Retrospective analysis of immune dysfunctions found in 55 dogs and 62 cats diagnosed with Chronic Fatigue Syndrome (CFS), revealed leukopenia in 11% of dogs (n = 6) and 22.5% of cats (n = 14), lymphopenia in 14.5% of dogs (n = 8) and 10% of cats (n = 6), hypogammaglobulinaemia in 9% of dogs (n = 5) and 13% of cats (n = 8) and thrombocytopenia in 20% of dogs (n = 11) and 68% of cats (n = 42). All patients had creatine kinase enzyme levels above the normal range (CK = 5-100 IU/L) and carried micrococcus-like organisms on erythrocytes. Blood cultures proved positive for Staphylococcus spp. in 16 cases. After low-dosage arsenic-based therapy (thiacetarsamide sodium) all animals experienced complete clinical remission. Subsequent controls demonstrated immune restoration in 4 representative FIV-FeLV negative cats, previously diagnosed with CFS associated with leukopenia, lymphopenia, hypogammaglobulinaemia and thrombocytopenia. The main conclusion is that a CFS-like disease in dogs and cats, characterised by the common hallmarks of high CK levels, absence of known causes of chronic fatigue in animals and presence of micrococcus-like organisms in the blood, can be associated with humoral and/or cellular immune deficiencies in 9-22.5% of cases and with thrombocytopenia in 20-68% of cases. Considerations are made on the possible role of micrococci in the aetiology of the condition and on the similarities with CFS in humans.

Agammaglobulinemia↗
PubMed1997

Bacteriologic studies of skin, tissue fluid, lymph, and lymph nodes in patients with filarial lymphedema.

Filarial lymphedema is complicated by frequent episodes of dermatolymphangioadenitis (DLA). It is not certain whether DLA is of filarial or bacterial etiology. The frequency of episodic DLA does not depend on the presence or absence of microfilariae. Antibiotic therapy is effective in prevention and treatment of DLA. These observations point to the bacterial rather than filarial etiology of DLA. Skin and lymph node biopsies, tissue fluid, lymph, and blood from patients with chronic filarial lymphedema, and during acute episodes of DLA, were cultured for detection of bacteria. A high prevalence of bacterial isolates from the tissue fluid (64%), lymph (75%), and inguinal lymph nodes (66%) of limbs with filarial lymphedema was found. Bacillus cereus, Staphylococcus epidermidis, S. hominis, S. capitis, S. xylosus, and Micrococcus spp. were the most common isolates. Bacteria were also isolated from the blood of patients with recent episodes of DLA, with strains of the same phenotype and antibiotic sensitivity in all specimens from patients with DLA. Bacterial strains of the same phenotype and antibiotic sensitivity were documented on the toe web surface and in tissue fluid (25%), lymph (26%), or lymph nodes (41%). Increasing prevalence of bacterial isolates in tissue fluid, lymph, and lymph nodes was observed in advanced stages of lymphedema. Bacilli and cocci were sensitive to gentamicin, tetracyline, rifampicin, vancomycin, kanamycin and cotrimoxazole, and least sensitive to penicillin. Blood cultures of patients in the periods between DLA attacks were negative. In healthy controls without edema and episodes of DLA, tissue fluid did not contain bacteria. In lymph, only single colonies of Micrococcus and Acinetobacter were cultured in 12% of the cases. Impaired lymph drainage and lack of elimination of penetrating bacteria may be responsible for progression of lymphedema and recurrent attacks of DLA.

Adolescent↗
PubMed1982

A preferential isolation procedure for asporogenous Gram-positive bacteria.

A preferential isolation procedure was devised for asporogenous (Asp), Gram-positive (Gp), aerobic or facultative anaerobic bacteria which included the genera Arthrobacter, Corynebacterium, Brevibacterium, Microbacterium, Mycobacterium, and Micrococcus (Asp-Gp bacteria). An antibiotics-mixture agar which contained 5 to 10 micrograms per ml of colistin, 10 to 20 micrograms per ml of nalidixic acid and 30 micrograms per ml of cycloheximide was used in the isolation. Using this technique 47 Asp-Gp bacteria representing 26 subgroups of coryneform bacteria and Micrococcus were isolated from 3 soil samples. The method was far more efficient than the standard dilution-plate technique. This preferential method is available to isolate Asp-Gp bacteria from a sample containing about 500-fold more of other Gram-positive and negative bacteria.

Bacteria↗
PubMedDate not supplied

[Microbial biocenosis of the nasal mucosa in healthy persons and in Staphylococcus carriers].

The normal microflora of the nasal mucosa in man is differentiated into main, complementary and casual microflora, taking into account its isolation rate and characteristics of microbial contamination. The main microflora of adults, in contrast to children, is represented, in addition to coagulaso-negative (CN) staphylococci, by bacteria of the genus Corynebacterium. In staphylococcal carrier state a decrease in the isolation rate and the amount of bacteria belonging to the main and complementary microflora (CN staphylococci, Micrococcus, Streptococcus, Bacillus) was observed. Moreover, in carriers the weakening of the degree of association between CN staphylococci, Micrococcus, Corynebacterium, Streptococcus in symbiotic pairs was noted. In the absence of S. aureus carrier state the main and complementary microflora was characterized by the combination of the factors of antagonism and persistence, while in carrier state the complex of colonization factors was defective in the main microflora and well pronounced in coagulase-positive staphylococcal strains and enterobacteria.

Adult↗
PubMedDate not supplied

Bacterial flora of the conjunctiva and nasal cavity in normal and diseased captive bustards.

A survey was carried out to describe the normal aerobic bacterial flora of the conjunctiva and nasal cavity of captive houbara bustards (Chlamydotis undulata), kori bustards (Ardeotis kori), and white-bellied bustards (Eupodotis senegalensis) maintained at the National Avian Research Center, Abu Dhabi, United Arab Emirates. A total of 58 samples were examined from the nasal cavity and 55 samples from the conjunctiva of healthy bustards. There was no bacterial growth in 45% of conjunctival samples. Bacteria isolated from the conjunctiva of healthy birds included Micrococcus spp., Staphylococcus auricularis, Staphylococcus xylosus, Staphylococcus capitis, Staphylococcus warneri, Bacillus spp., and Enterobacter amigenus. Bacteria isolated from the nasal cavity of healthy birds included Bacillus spp., Micrococcus spp., S. auricularis, S. xylosus, Staphylococcus simulans, Staphylococcus saprophyticus, Staphylococcus hyicus, Staphylococcus cohnii, Staphylococcus sciuri, Aerococcus spp., and Providencia rettgeri. These findings were compared with bacterial isolates from bustards with clinical signs of ocular or upper respiratory tract diseases. Mycoplasma spp., Pseudomonas aeruginosa, Pseudomonas stutzeri, Proteus mirabilis, Escherichia coli, Klebsiella spp., Aeromonas hydrophila, and Staphylococcus aureus were the pathogenic bacteria isolated from the conjunctiva of 34.3% bustards with ocular discharges. Mycoplasma spp., P. aeruginosa, Pseudomonas spp., P. mirabilis, E. coli, Klebsiella pneumoniae, and S. aureus were the pathogenic bacteria isolated from the nasal cavity of 74% bustards with upper respiratory tract diseases.

Animals↗
PubMed2004

Isolation and characterization of microorganisms from instruments used by pedicurists operating within Lagos metropolis, Nigeria.

Eight bacterial and five fungal species were isolated from swab samples taken from instruments used by pedicurists operating at three different sites in Lagos, Nigeria. The bacterial isolates included Micrococcus luteus, Micrococcus roseus, Staphylococcus epidermidis, Staphylococcus aureus, Hafnia spp, Shigella spp, Bacillus subtilis and Bacillus spp. The five fungal isolates were identified as Aspergillus niger, Aspergillus flavus, Mucor spp, Trichophyton spp and Candida albicans. The presence of these microorganisms, some of which are pathogenic, is an indication that pedicurists could be contributing towards the spread of skin and nail infections within the Lagos metropolis.

Bacteria↗
PubMed2004

Antimicrobial spectrum, production and mode of action of staphylococcin 188 produced by Staphylococcus aureus 188.

Staphylococcus aureus 188 has been shown to produce bacteriocin-like inhibitory substance known as staphylococcin 188. It has a broad-activity spectrum against Micrococcus luteus, Streptococcus pneumoniae, Streptococcus faecalis, Streptococcus viridans, Corynebacterium diphtheriae and several staphylococcus species. The arbitrary unit of staphylococcin 188 against Micrococcus luteus was 1280 AU/mL. Its production with simultaneous measurement of activity was monitored and was found to produce maximum amount of staphylococcin after 7 hours of incubation. Mode of action of the staphylococcin 188 on the sensitive cells was bactericidal rather than bacterioloytic.

Journal Article↗
PubMed2006

Bacterial decontamination of DUWL biofilm using Oxygenal 6.

The aim of this study was bacteriological assessment of the dental unit waterlines (DUWL) biofilm - concentration and composition of the aerobe and facultative anaerobe bacterial microflora, and evaluation of the influence of a disinfecting product, Oxygenal 6, on the biofilm composition. Tubing fragments were taken from 25 units twice, before and after disinfection, and bacterial suspension of the biofilm was obtained from the samples. The bacterial flora was determined with the plate culture method. Bacteria were identified with biochemical microtests: API 20E, API 20NE (bioMerieux, France) and GP2 MicroPlate(TM) (BIOLOG, USA). Before disinfection, the following bacteria were identified: Gram-negative bacteria - Ralstonia pickettii, Pseudomonas vesicularis, Sphingomonas paucimobilis, Xanthomonas maltophilia; Gram-positive cocci - Micrococcus luteus, Micrococcus lylae, Staphylococcus cohnii, Staphylococcus lentus, Staphylococcus spp., Streptococcus spp.; Actinomycetes - Streptomyces albus. The prevailing bacteria were: Ralstonia pickettii (78.62%), found in all the units, and Sphingomonas paucimobilis (20.45%). After DUWL disinfection, Sphingomonas paucimobilis (88.79%) dominated in the biofilm, Staphylococcus spp. - 5.61% and Pseudomonas spp. - 3.74% were next most frequently occurring bacteria, and in more than a half of the biofilm samples 100% reduction of the bacterial microflora occurred. This study confirms effectiveness of Oxygenal 6 in bacterial decontamination of the DUWL biofilm.

Anti-Bacterial Agents↗
PubMed2006

Effectiveness of biodegradation of petroleum products by mixed bacterial populations in liquid medium at different pH values.

The possibility of using mineral oils as a carbon source by bacteria adapted to high oil concentrations was tested in liquid media with different pH values (pH = 5, 7 and 9). Two types of inocula were tested: inoculum I consisted of selected strains used in the bioremediation of oil-contaminated soils and inoculum II contained bacteria isolated from soil samples previously bioremediated at pH = 5, 7 and 9. Biodegradation was observed in all the investigated media independently of initial pH value and type of inoculum used. After 21 days of cultivation the reduction of oil content reached 60-70% in medium with pH = 5 and 80-90% in medium with pH = 7 and 9, respectively. Inoculum I consisted of strains of Arthrobacter, Pseudomonas, Agrobacter, Xanthomonas spp. After 21 days of incubation the elimination of some strains was observed. In cultures conducted at pH = 5 Agrobacter strain was no longer found, at pH 9 - the Pseudomonas strain was lost. In cultures maintained at pH = 7 all the introduced strains survived. Prolonged incubation in liquid medium at pH = 5 of strains isolated from bioremediated soils (type II inoculum) leads to the elimination of Bacillus from initial consortium of Arthrobacter, Bacillus and Pseudomonas. In cultures containing bacteria of type II inoculum (Arthrobacter, Bacillus, Achromobacter, Agrobacter, Alcaligenes, Pseudomonas, Xanthomonas, Micrococcus) conducted in liquid media at pH = 9 the Micrococcus strain was no longer present. In liquid cultures incubated at pH = 7 all introduced strains were recovered (Arthrobacter, Bacillus, Achromobacter).

Bacteria↗
PubMed1991

Comparison of three commercial rapid agglutination test kits for identification of coagulase positive staphylococci from foods and animals.

Three rapid agglutination assays for the identification of Staphylococcus aureus Monostaph (Bionor A/S, Skien, Norway), Staphyslide-Test (BioMerieux, Lyon, France) and Staph-Rapid-Test (Roche, Basel, Switzerland), were compared. A total of 104 Gram-positive, catalase positive cocci were tested: Nineteen Staphylococcus reference strains comprising 15 spp. (4 strains were coagulase positive), and 7 Micrococcus reference strains comprising 4 spp.; 22 food isolates comprising 13 S. aureus, 8 coagulase positive Staphylococcus spp., and 1 Micrococcus sp.; 56 animal isolates comprising 11 S. aureus, 9 S. hyicus subsp. hyicus, 2 S. intermedius, 15 coagulase positive and 19 coagulase negative Staphylococcus spp. Totally 54 strains were coagulase positive. Considering agglutination of a coagulase positive strain as a correct identification, Monostaph, Staph-Rapid-Test, and Staphyslide-Test correctly identified 52 (96.3%), 47 (87.0%) and 48 (89.0%) of the coagulase positive staphylococci, respectively. Monostaph, Staph-Rapid-Test and Staphyslide-Test showed 1 (2.0%), 4 (8.0%) and 4 (8.0%) false positive reactions respectively. Monostaph, Staph-Rapid-Test and Staphyslide-Test gave 0 (0.0%), 6 (5.8%) and 7 (6.7%) non-interpretable reactions, respectively. Monostaph may be a good alternative to the tube-coagulase test for rapid and reliable identification of coagulase positive staphylococci from both food and veterinary sources. However, false negative reactions may occur with coagulase positive strains of S. hyicus subsp. hyicus and S. intermedius.

Agglutination Tests↗
PubMed1989

Hygienic status of food handlers.

The study demonstrated bacterial species on hands and nails of food-handlers before and after hand-washing. Those were Staphylococcus spp., Streptococcus spp., Micrococcus spp., Bacillus spp., Diphtheroid, Aeromonas hydrophila, Klebsiella pneumoniae, Acinetobacter, Enterobacter cloacae, Escherichia coli, Pseudomonas spp., Proteus mirabilis, Serratia spp., Citrobacter freundii. Before hand washing, each food-handler harboured one to eight bacterial species. After hand-washing (eight with water from plastic boxes, 97 from pipe water, 57 out of 97 (58.8%) used soap or detergent with water), disappearance of one to four bacterial strains from hands and nails were found in 47.6 per cent of food-handlers. Cultures of water used for washing from eight plastic boxes yielded Staph. spp., Strep. spp., Aeromonas hydrophila, Kleb.pneumoniae, Acinetobacter anitratus, Enterobacter cloacae. From pipe water, Diphtheroid in 4, 4.1 per cent Micrococcus in 1, 1.03 per cent were shown. Comparing bacterial species found in food-handlers with long nails and short nails, 4-8 more species were revealed in the former than the latter for 35.7 per cent. After hand-washing, there was recontamination of bacterial species in 17 food-handlers. This was probably due to dirty napkins or dresses during hand-drying or from water in plastic boxes.

Adolescent↗
PubMedDate not supplied

[Participation of the NAD-poly(ADP ribose) system in the degradation of chromatin in irradiated thymocytes].

The diminution of NAD level in mouse thymus lymphocytes precedes their death under the effect of various genotoxic agents and manifests itself by the time of the onset of chromatin degradation. At the same time, in vitro, NAD does not influence the activity of micrococcus nuclease of Ca2+,Mg2+-dependent endonuclease from human spleen. Stimulation of protein poly(ADP-ribosylation) by exogenous NAD does not change the sensitivity of chromatin to micrococcus nuclease. In contrast to hepatocytes, in the thymus, no inhibition of Ca2+,Mg2+-endonuclease, resulting from ADP-ribosylation, occurs which may be due to low activity of ADP-ribosyl transferase in thymocytes. Incubation of thymus lymphocytes with benzamide prior to irradiation does not inhibit chromatin degradation. It is suggested that the decrease in the NAD level is one of the indications of the injury to thymocytes which is not related to the induction of their death. In contrast to thymocytes, the pretreatment of Ehrlich ascites tumor cells with benzamide produces a radiosensitizing effect.

Animals↗
PubMedDate not supplied

[Value of different diagnostic tests for Micrococcaceae and their implication in pathology].

A number of 1431 products were examined and 200 coagulase-negative micrococcaceae strains were isolated and identified. On the basis of morphological aspects, enzymatic reactions and behavioural testing to antibiotics 18 strains (9%) were listed as Micrococcus and 182 (91%) as Staphylococcus strains. Efficient among the tests used for differentiating between the two genera were : microscopic aspects, pigmentogenesis, resistance to ClNa, anaerobic glucose fermentation, glycerol fermentation in the presence of erythromycin, reduction of nitrates to nitrites, and testing to novobiocin. Other tests, due to their variability, could only be used conjointly, and, finally, a further category had no diagnostic value, such as oxidase and catalase tests or the rhamnose fermentation reaction. Both the Micrococcus and the Staphylococcus strains were isolated from pathological cases and from healthy carriers, and can therefore be listed in the group of potential pathogens.

Bacterial Infections↗
PubMed1985

[Microorganisms of the fam. Micrococcaceae in the production and storage of prepackaged veal].

Studies were carried out on the numbers and composition of organisms belonging to family Micrococcaceae in the production and storing of calf meat on a dressing combine supplied with modern equipment. Investigated were a total of 60 samples taken from small cuts of veal of the various carcass parts. The samples were packed either under vacuum or without such, and were studied immediately after cutting in small parts or after storing for 48 and 72 hours at 4 to 6 degrees C. It was found that the amount of Micrococcaceae organisms on the surface of cut meat packed out or in vacuum was within the range of 10(3) up to 10(4)/g, and it was shown to be in close relation to the microbial contamination of the initial raw material. There was no rise of the numbers of micrococci and staphylococci of veal that was cut and packed out of vacuum and kept for 48 hours at 4 to 6 degrees C. At refrigerator storing of veal that was packed under vacuum there was no increase in the microbial numbers at the 72nd hour. This pointed to the advantage of using the introduced technology of packing the meat under vacuum. Micrococcus luteus (56.7%), Micrococcus varians (41.8%), and Staphylococcus saprophyticus (1.5%) were isolated from cuts of veal packed both in and out of vacuum. No pathogenic staphylococci were found.

Animals↗
PubMed1966

Exudative epidermitis in pigs: etiological studies and pathology.

The experimental production of exudative epidermitis of pigs following the inoculation of skin scrapings or cultures from field or experimentally-produced cases of the disease is described. Typical lesions of exudative epidermitis were produced following inoculation, either intravenously or by scarification, of broth cultures of 4 strains of a micrococcus isolated from field cases of the disease. The experimental inoculation of pigs with skin scrapings sterilized by filtration or antibiotic treated, yielded negative results. Cultures of CORYNEBACTERIUM PYOGENES and of STREPTOCOCCUS SP. also isolated from the affected pigs, likewise yielded negative results on experimental inoculation of pigs. The conclusion is drawn, that the micrococcus isolated from field cases and which produced the disease experimentally is the primary etiological agent of exudative epidermitis as seen in weaned pigs in this area. The histopathology of the experimentally produced disease is described.

Animals↗
PubMed1983

Genetic relatedness of Haemophilus somnus to select genera of bacteria.

The degree of DNA homology from Haemophilus somnus and DNA from select members of the genera Haemophilus, Actinobacillus, Pasteurella, Escherichia, and Micrococcus was determined. Hybridization tests indicated that H somnus DNA has a 46%, 58%, and 43% homology with the DNA from H influenzae, H parainfluenzae, and A lignieresii, respectively. These percentages of homology values indicate that H somnus was moderately related to 2 members of the genus Haemophilus and 1 member of the genus Actinobacillus. Haemophilus somnus DNA did not show any hybridization with DNA from the genera of Escherichia, Micrococcus, or Pasteurella.

DNA, Bacterial↗
PubMed1982

Microbiological sampling of towels: comparison of 7 methods.

Pull-out roller towels were infected with bacteria and examined with 5 non-destructive methods. In addition to three traditional methods, the agar contact method (A), the swab method (S) and the tape method (T), two lesser known methods have been applied: the rinsing box method (R), new developed in the laboratory, and the filter method (F). In the first (R), the towel is fixed between the lid and the cup of a metal box containing a rinsing liquid; shaking the box completes the test. In the second (F) the liquid is forced through the towel by vacuum. In both experiments the rinsing liquid is tested for contamination. Destructive methods, mainly with a peristaltic blender ("stomacher") (P) or rotary mixer (M), were used as reference for calculating ratios of recovery. With the methods A, S and T, a low ratio of recovery, resp. 5, 10 and 2%, was obtained for Escherichia coli and Staphylococcus aureus. With method R, ratios for the two species were 60-90%, and also for a Micrococcus species and for spores of Bacillus subtilis. With method F the ratio for E. coli and Micrococcus sp. was even slightly higher than 100%. Recovery with method M was about the same as with P. It is concluded that the rinsing box method as well as the filter method are well suited to the purpose of microbiologically testing towels; the lower recovery of the first is compensated by its simplicity.

Bacteria↗
PubMedDate not supplied

[Resistance of microorganisms of upper layers of the atmosphere to ultraviolet radiation and a high vacuum].

Solar radiation and high vacuum are the main factors affecting the incidence of microorganisms in the stratosphere and mesophere. It has been established in experiments that the conidia of Aspergillus niger are most resistant of UV irradiation. The conidia of Penicillium, the spores of Papulaspora anomala and Circinella muscae, and the vegetative cells of Micrococcus and Mycobacterium are more susceptible to UV radiation. All of the isolated microorganisms have been shown to be resistant to high vacuum. Their inactivation varied within the range of 2 to 16%, with an exception of Micrococcus cells (40%).

Air Microbiology↗