Suppression of chromosome segregation defects of Escherichia coli muk mutants by mutations in topoisomerase I
- 31 January 2000
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 97 (4) , 1671-1676
- https://doi.org/10.1073/pnas.030528397
Abstract
One hundred thirty specimens from 108 consecutive patients with a history of recurrent genital ulcerations were used in a study comparing herpes simplex virus (HSV) isolation with a direct fluorescent-antibody (DFA) technique using mouse monoclonal antibodies. HSV was isolated from 70% of vesicular lesions, 67% of pustular lesions, 32% of ulcerative lesions, and 17% of crusted lesions, whereas the DFA technique detected HSV antigen in 87, 67, 30, and 10% of lesions in similar stages, respectively. When both methods were used, HSV was identified in 97, 79, 45, and 17% of vesicles, pustules, ulcers, and crusted lesions, respectively. The overall sensitivity and specificity of the DFA technique in comparison with virus isolation (VI) were 74 and 85%, respectively. Of the 17 patients from whom DFA-positive, VI-negative samples were obtained, HSV was subsequently isolated from a genital lesion in 14, suggesting that they were not DFA false-positives. Similarly, of the 46 patients whose initial lesion samples were DFA and VI negative, 37 (80%) had HSV identified from subsequent genital lesions during follow-up. Thus, a single sample for VI or DFA testing from a recurrent genital lesion had a sensitivity of only 53 and 51%, respectively. Combining the DFA technique and VI increased the sensitivity of laboratory diagnosis of a single recurrent episode of genital HSV; however, repetitive laboratory testing was often required to confirm the diagnosis of recurrent genital HSV infection.Keywords
This publication has 54 references indexed in Scilit:
- 13S Condensin Actively Reconfigures DNA by Introducing Global Positive WritheCell, 1999
- The Symmetrical Structure of Structural Maintenance of Chromosomes (SMC) and MukB Proteins: Long, Antiparallel Coiled Coils, Folded at a Flexible HingeThe Journal of cell biology, 1998
- Cell Cycle–Dependent Duplication and Bidirectional Migration of SeqA-Associated DNA–Protein Complexes inMolecular Cell, 1998
- The effect of ionic conditions on the conformations of supercoiled DNA. II. equilibrium catenationJournal of Molecular Biology, 1997
- The SMC family: from chromosome condensation to dosage compensationCurrent Opinion in Cell Biology, 1995
- Two mutant alleles ofmukB, a gene essential for chromosome partition inEscherichia coliFEMS Microbiology Letters, 1994
- Bacterial chromosome segregation: Evidence for DNA gyrase involvement in decatenationCell, 1984
- Facile transition of poly[d(TG)·d(CA)] into a left-handed helix in physiological conditionsNature, 1983
- Escherichia coli DNA topoisomerase I mutants have compensatory mutations in DNA gyrase genesCell, 1982
- Transposition of the lac region of Escherichia coliJournal of Molecular Biology, 1966