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J M Kramer

Publications and source records attributed to J M Kramer.

At least 91 records · Page 5Linked to original sources

Dissemination of Bacillus cereus in a maternity unit.

During a period of 4 months, 54 of 1059 (5%) specimens received for bacterial culture from neonates in a maternity unit yielded Bacillus cereus. Of the strains isolated, 48 originated from 259 umbilical cord swabs examined. Furthermore, 88% of the isolates belonged to a single, previously undescribed serotype. Strains of the same serotype were also found to be widely distributed in the environment throughout the maternity unit. The primary source of the organism, however, could not be established.

Bacillus cereus↗

Intestinal carriage of Bacillus cereus: faecal isolation studies in three population groups.

The results of examinations of stools for Bacillus cereus among three unrelated groups of individuals are presented. The groups consisted of (1) healthy school-children aged 6-11 years in a rural region of South Africa examined during each of the four seasons of the year; (2) 15 healthy volunteers comprising staff of a London microbiology laboratory and their families examined on each of 3 consecutive weeks; (3) 75 unrelated young children, 2 months to 5 years of age, in a second rural region of South Africa examined during a pilot study of 1 week's duration on the aetiology of rural gastroenteritis. The stools of the last group were submitted as being related to present or recent diarrhoea in the respective children. In group 1, B. cereus isolation rates ranged from 24.3% at the autumn visit to 43% at the summer visit with a significantly higher rate of isolation in the summer than at other seasons of the year (P less than 0.05). B. cereus was isolated from 40% of group 2 volunteers on week 1, none on week 2 and 20% on week 3. The organism was detected in the 12 positive specimens at levels of approximately 10(2)/g and constituted 2.5-30% of the total aerobic spore-forming bacillus population in the stools. In group 3, B. cereus was recovered from 18.7% of the stool samples and was isolated consecutively with other pathogens (enteropathogenic Escherichia coli and rotavirus) on only five occasions. In groups 1 and 3, less than 5% of the stools had '3+' levels of B. cereus (greater than 10 colonies per direct plate culture). B. cereus was readily isolated from all of 10 food samples, representative of the typical diet of the group 1 individuals, and was present in substantial numbers (10(4) to 5.5 X 10(6)/g) in half of them. The isolation results, supported by serotyping, indicated that carriage of B. cereus in stools is transient and its presence at any one time reflects solely its intake with foods.

Adult↗

Genetic mapping of Caenorhabditis elegans collagen genes using DNA polymorphisms as phenotypic markers.

In Caenorhabditis elegans collagens comprise a dispersed family of 40-150 genes, the majority of which probably code for collagen proteins found in the animal's cuticle. The conserved (Gly-X-Y)n triple helix coding sequence of collagen genes has facilitated the isolation of a large number of C. elegans collagen genes by recombinant DNA methods. We have begun a study of the chromosomal organization of these genes by screening laboratory strains of C. elegans for DNA polymorphisms in the regions surrounding collagen genes. Polymorphisms near seven genes have been identified and have been used as phenotypic markers in genetic crosses to assign the genes to linkage groups II, III, IV, and X. Four genes are shown by multifactor crosses to map to a 2-3 map unit interval between unc-24 and unc-22 on chromosome IV.

Animals↗

Number and organization of collagen genes in Caenorhabditis elegans.

We analyzed the number and organization of collagen genes in the nematode Caenorhabditis elegans. Genomic Southern blot hybridization experiments and recombinant phage library screenings indicated that C. elegans has between 40 and 150 distinct collagen genes. A large number of recombinant phages containing collagen genes were isolated from C. elegans DNA libraries. Physical mapping studies indicated that most phage contained a single small collagen gene less than 3 kilobases in size. A few phage contained multiple collagen hybridizing regions and may contain a larger collagen gene or several tightly linked small collagen genes. No overlaps were observed between phages containing different collagen genes, implying that the genes are dispersed in the C. elegans genome. Consistent with the small size of most collagen genes, we found that the predominant class of collagen mRNA in C. elegans is 1.2 to 1.4 kilobases in length. Genomic Southern blot experiments under stringent hybridization conditions revealed considerable sequence diversity among collagen genes. Our data suggest that most collagen genes are unique or are present in only a few copies.

Animals↗

Haploid accumulation and translational control of phosphoglycerate kinase-2 messenger RNA during mouse spermatogenesis.

The intracellular location of the mRNA for the testis-specific isozyme of phosphoglycerate kinase-2 (PGK-2) has been determined for two spermatogenic cell types. The mRNA activity for PGK-2 from the polysomal and nonpolysomal fractions of pachytene primary spermatocytes or round spermatids has been assayed by cell-free translation with the polypeptide products monitored by immunoprecipitation, followed by one-dimensional or two-dimensional electrophoresis and fluorography. The results reveal that the majority of PGK-2 mRNA activity of round spermatids was present in the polysomal fraction while the relatively less abundant PGK-2 mRNA of pachytene primary spermatocytes was present in the nonpolysomal fraction. No PGK-2 mRNA activity was observed in the cytoplasmic RNA from primitive type A spermatogonia or prepubertal Sertoli cells. These data indicate that mature PGK-2 mRNA first appears in the cytoplasm of spermatogenic cells during the prophase of meiosis and increases in amount after meiosis. Although mature PGK-2 mRNA is present in meiotic cells it is not actively translated until after meiosis has been completed. Thus, mRNA accumulation and translational mechanisms are involved in the control of phosphoglycerate kinase-2 synthesis during spermatogenesis.

Animals↗

Identification of an autosomal locus affecting steroid sulfatase activity among inbred strains of mice.

We have found an activity variant for testicular and liver steroid sulfatase among inbred strains of mice that is not X-linked. C57BL/6J, SM/J and SWR/J testicular extracts hydrolyze 3H-dehydroepiandrosterone sulfate twice as rapidly as do A/J extracts. The C3H/HeJ and DBA/2J strains were intermediate. The Km values for C57BL/6J and A/J are 2.29 +/- 0.10 and 1.01 +/- 0.02 microM, respectively. The F1 values in both directions were intermediate, which argues against X-linkage of this trait. F2 values show scattered high-intermediate-low values compatible with assay variation superimposed on the segregation of codominant alleles. When assayed for both testicular and liver steroid sulfatase, nine recombinant inbred lines between A/J and C57BL/6J segregate to near the parental strain values. Thus, this activity variation for steroid sulfatase appears to be determined by a single gene, which is not X-linked. Sex and steroidal hormone differences in liver steroid sulfatase activity were not present in the A/J strain, but females of the C57BL/6J and some recombinant inbred lines had higher levels. Electrophoretic studies only disclosed a variant in the SM/J strain, which seems to be secondary to the well-known neuraminidase variation in SM/J.

Animals↗

Non-gastrointestinal Bacillus cereus infections: an analysis of exotoxin production by strains isolated over a two-year period.

Isolates of Bacillus cereus from 118 cases, and two maternity unit outbreaks, of non-gastrointestinal infection were grouped on the basis of their estimated probable involvement in the infections from which they were isolated: (i) high probability--48 strains; (ii) intermediate--16 strains; (iii) low--7 strains; (iv) very low ("irrelevant")--49 strains. Rabbit skin test, haemolysin and phospholipase assays were used to determine exotoxin activities of strains within each group. The results suggest a significant relation between the virulence of an isolate as reflected in the degree to which it appeared responsible for the signs and symptoms of an infection, and its toxigenicity in the skin test. This is attributed to the ability of B cereus strains to synthesise, in varying degrees, a necrotic enterotoxin, possibly in conjunction with the primary haemolysin (cereolysin). The cases analysed in this study support the contention that B cereus, when isolated from an infection, may not be an inconsequential contaminant and should not be too readily dismissed as such.

Bacillus cereus↗

Comparisons of the complete sequences of two collagen genes from Caenorhabditis elegans.

Several collagen genes have been isolated from the nematode Caenorhabditis elegans. The complete nucleotide sequences of two of these genes, col-1 and col-2, have been determined. These collagen genes differ from vertebrate collagen genes in that they contain only one or two introns, their triplehelical regions are interrupted by nonhelical amino acid sequences and they are smaller. A high degree of nucleotide and amino acid homology exists between col-1 and col-2. In particular, the regions around cysteines and lysines are most highly conserved. The C. elegans genome contains 50 or more collagen genes, the majority of which probably encode cuticle collagens; col-1 and col-2 apparently are members of this large family of cuticle collagen genes.

Amino Acid Sequence↗

Analysis of stage-specific protein synthesis during spermatogenesis of the mouse by two-dimensional gel electrophoresis.

Cells were labelled by intratesticular injection of [35S]methionine. After 14-16 h the relative rates of incorporation of label in spermatocytes, early spermatids and late spermatids were 10:2:1 respectively. Approximately 15% of the soluble (100 000 g supernatant) and 20% of the particulate proteins solubilized by NP-40 (from the 100 000 g pellet) that were detectable on two-dimensional gels showed stage-specific synthesis. A large number of proteins were detectable only in post-meiotic cells and may be valuable for studying the control of gene expression in haploid cells.

Animals↗