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Biomedical subjects

K Fossum

Publications and source records attributed to K Fossum.

At least 19 recordsLinked to original sources
PubMed2004

Ground based studies of gene expression in Arabidopsis exposed to gravity stresses.

As a link in the preparation of the MULTIGEN experiment, which will take place on the International Space Station, ground based studies of the gene expression in Arabidopsis thaliana were performed. Microarray technology was used to screen Arabidopsis seedlings exposed to simulated hypogravity on a Random Positioning Machine and a 1 x g control sample. This screening showed differential expression in 177 out of approximately 8000 genes. Some of these genes can be grouped into functional categories, e.g. general metabolism, biogenesis of cellular components, cellular transport and transport facilitation, and cell rescue and defense response. However, about 50% of the genes encode proteins with unknown function. Based on the above results a new "in-house" cDNA microarray was constructed. Some of the selected genes on this microarray (e.g. Xyloglucan endotransglycosylase, At2g18800) showed differential expression both in Arabidopsis exposed to hypergravity and simulated hypogravity by use of a centrifuge and a Random Positioning Machine.

Arabidopsis↗
PubMed2000

Injectional anthrax in a heroin skin-popper.

Anthrax is rare in western Europe but may arise sporadically in people exposed to animal products from endemic areas. A heroin-injecting drug user presented with a severe soft-tissue infection at the injection site, septic shock, and meningitis. A gram-positive endospore-forming aerobic rod was isolated from the soft tissue and cerebrospinal fluid; confirmation of Bacillus anthracis was made by PCR. Since contaminated heroin was the probable source of infection, this case is of concern and warrants surveillance.

Anthrax↗
PubMed1998

Antibiotic resistance in Escherichia coli of the normal intestinal flora of swine.

Twelve hundred enterobacterial Escherichia coli isolates of porcine origin were screened phenotypically for antibiotic resistance. The bacteria were isolated from 10 herds of swine with different histories of exposure to antimicrobial agents for therapeutic purposes. The bacterial isolates were part of the normal bacterial flora of the intestines of the animals because they were isolated from healthy individuals. The strains were tested for phenotypic antibiotic resistance against sulfonamides, trimethoprim, streptomycin, ampicillin, neomycin, chloramphenicol, and tetracycline. Resistance against streptomycin was found to be most common, followed by resistance against sulfonamides and tetracycline. The highest number of resistant bacteria was found in herds where the use of antimicrobial agents was considered to be high. A selection of multiresistant bacterial isolates were further genetically characterized by hybridization with probes specific for the antibiotic resistance genes; sulI, sulII, dfrI, dfrIIb, dfrIX, and the class A, B, C, and D tetracycline resistance determinants. A PCR was developed and used for detection of the strA-strB gene pair encoding streptomycin resistance in gram-negative bacteria. The strA-strB gene pair was the most frequent resistance determinant in the isolates examined. This study indicates that nonpathogenic E. coli from swine may represent a considerable reservoir of antibiotic resistance genes that might be transferable to pathogens.

Animals↗
PubMed1989

Antibodies to staphylococcal DNases in sera from different animal species, including humans.

An agar diffusion method using microtiter plates was used to detect antibodies to the DNases produced by Staphylococcus aureus, S. intermedius, and S. hyicus. Antibodies to DNase from S. aureus were demonstrated in most of the sera from the species investigated, except dogs, only 11% of whose sera were positive. Positive titers to S. intermedius DNase were found in 84% of deg sera, 61% of Icelandic pony sera, 41% of pig sera, 21% of human sera, and 20% of cow sera but in only 2 and 4% of goat and sheep sera, respectively. Although antibodies to DNase from S. hyicus were not found in sera from humans, dogs, goats, or sheep, 84% of sera from pigs and cows and 29% of sera from Icelandic ponies were positive in this respect. The good accordance between the findings from bacteriological investigations performed elsewhere and the results of serologic tests performed in this study indicates that the results obtained with the serological method in this study properly reflect the actual antigenic exposure to and distribution of the three Staphylococcus spp. in animals and humans.

Animals↗
PubMed1989

Enteropathogenic Escherichia coli serotype O111:HNT isolated from preterm neonates in Nairobi, Kenya.

This investigation was initiated as a consequence of several cases of diarrhea in a nursery ward for preterm babies in Nairobi, Kenya. Ten lactose-positive colonies were isolated from the stools of each of 30 neonates, regardless of whether they had diarrhea; 229 strains were identified as Escherichia coli and 65 strains were identified as Klebsiella pneumoniae. Six strains were lost during laboratory handling. No other bacterial, viral, or parasitic enteropathogens were identified. Using synthetic alkaline phosphatase-labeled probes, the bacterial isolates were found to be negative for the presence of genes coding for heat-stable and heat-labile enterotoxins. Seventy-eight E. coli strains isolated from a total of 13 neonates possessed the E. coli enteropathogenic adhesion factor (EAF) gene, as demonstrated by the use of a cloned radiolabeled DNA fragment probe. These strains possessed similar plasmid profiles constituting a core plasmid profile, and while all adhered to HeLa cells, none produced Vero cell cytotoxins. The EAF gene was located on a 65-megadalton plasmid. Serotyping showed the strains to be of serogroup O111 and serotype H nontypable, a well known enteropathogenic type. Five neonates died during the outbreak, and the fatality rate was 30.7% (4 of 13) for neonates infected with EAF-positive E. coli strains compared with 7.7% (1 of 13) for neonates from whom only EAF-negative E. coli strains were isolated. K. pneumoniae only was isolated from five neonates.

Adhesins, Escherichia coli↗
PubMed1989

Antibacterial spectrum and some other characteristics of an antimicrobial factor produced by Yersinia ruckeri.

Yersinia ruckeri produces an antibacterial factor which inhibits the growth of a wide spectrum of Gram-negative and Gram-positive bacteria, though not other strains of Y. ruckeri. The antibacterial factor was produced at low temperatures (4-20 degrees C), but not at 37 degrees C. The activity was lost after treatment of the supernatant with chloroform, UV-light and after boiling of the supernatant. One did not succeed in obtaining the antibacterial factor in a sterile solution.

Animals↗
PubMed1988

Heat-stable-enterotoxin-producing Escherichia coli strains isolated from dogs.

Five strains of hemolytic Escherichia coli isolated from dogs suffering from diarrhea were shown by radioactive and enzyme-labeled oligonucleotide probes to possess genes coding for heat-stable enterotoxin (STIa). Four of the strains were shown by immunoassay (enzyme-linked immunosorbent assay) and bioassay (infant mouse test) to produce STI in vitro. All five strains, however, were able to induce fluid accumulation in ligated dog intestinal loops. The four STI-producing strains all possessed the K99 fimbrial antigen (F5) and belonged to serotype O42:H37. In these strains, genes encoding STI were located on a 98-megadalton plasmid. In the fifth strain, which produced STI in vitro only after several subcultivations, the STI gene was located on an 80-megadalton plasmid. This strain was nontypable.

Animals↗
PubMed1985

Plasmid characterization of Salmonella typhimurium transmitted from animals to humans.

The transmission of pathogenic bacteria from animals to humans is widely studied because of its public health importance. In this study, we show the transmission of Salmonella typhimurium from cattle which had received no growth-promoting antibiotics to humans who had direct contact with the ill animals. On one cattle farm, the veterinarian attending the sick animals became ill, and two other individuals living on the farm later developed salmonellosis. The strains isolated from both humans and animals at one farm were identical as to antibiotic susceptibility and phage type, and they were specifically traced by the presence of a common 24-megadalton plasmid. Restriction enzyme digests of this plasmid from both human and animal strains were identical. At another farm, tetracycline-resistant S. typhimurium strains possessing a different profile (eight plasmids) were isolated from both animals and humans. The tetracycline-resistant clone was also isolated from animals at a third farm, but with animals and humans having no known contact with those of the other two farms.

Animals↗
PubMed1982

Occurrence and immunogenicity of proteinases from Legionella species.

Proteinases produced by various Legionella species were studied by means of caseinate precipitation. Proteinase production was particularly high in strains of Legionella pneumophila (serogroups 1-6), much lower in other Legionella species, and absent in Legionella micdadei strain Tatlock. Immunoglobulins against proteinases of Legionella pneumophila (serogroup 1, strain Philadelphia 1) inhibited the proteinase activity of all strains of Legionella pneumophila, Legionella bozemanii, Legionella dumoffi and Legionella gormanii. There was no cross-reactivity between these antibodies and proteinases from bacteria belonging to other genera. Antibodies against Legionella pneumophila proteinases were not found in human convalescent sera. The proteinases of Legionella species could possibly be associated with pathogenicity factors.

Antigens, Bacterial↗