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Literature DB >> 16789270

Increased Efficiency of Group B Coxsackievirus Isolation from Clinical Specimens by Use of BGM Cells.

Abstract

A continuous African green monkey kidney cell line, designated BGM, was compared with primary cynomolgus monkey kidney cells and human embryonic lung cells for efficiency of enterovirus isolation. A selective enhanced sensitivity of BGM cells both in terms of isolation rate and speed of isolation was found for group B coxsackieviruses but could not be demonstrated for a number of other nonpolio enteroviruses.

Entities: Disease Species

Year: 1982 PMID： 16789270 PMCID： PMC272218 DOI： 10.1128/jcm.15.5.945-948.1982

Source DB: PubMed Journal: J Clin Microbiol ISSN： 0095-1137 Impact factor: 5.948

13 in total

1. Comparative susceptibility of kidney cells from different monkey species to enteric viruses (poliomyelitis, Coxsackie, and echo groups).

Authors: G D HSIUNG; J L MELNICK
Journal: J Immunol Date: 1957-02 Impact factor: 5.422

2. Non-polio enterovirus activity in Wisconsin based on a 20-year experience in a diagnostic virology laboratory.

Authors: D Nelson; H Hiemstra; T Minor; D D'Alessio
Journal: Am J Epidemiol Date: 1979-03 Impact factor: 4.897

3. Comparative sensitivity of various cell culture systems for isolation of viruses from wastewater and fecal samples.

Authors: N J Schmidt; H H Ho; J L Riggs; E H Lennette
Journal: Appl Environ Microbiol Date: 1978-09 Impact factor: 4.792

4. BGM, a continuous cell line more sensitive than primary rhesus and African green kidney cells for the recovery of viruses from water.

Authors: D R Dahling; G Berg; D Berman
Journal: Health Lab Sci Date: 1974-10

5. Lyophilized combination pools of enterovirus equine antisera: preparation and test procedures for the identification of field strains of 42 enteroviruses.

Authors: J L Melnick; V Rennick; B Hampil; N J Schmidt; H H Ho
Journal: Bull World Health Organ Date: 1973 Impact factor: 9.408

6. Experience in laboratory diagnosis of enterovirus infections in routine medical practice.

Authors: E C Herrmann; D A Person; T F Smith
Journal: Mayo Clin Proc Date: 1972-08 Impact factor: 7.616

7. A comparison of two cell culture systems for the primary isolation of enteric viruses.

Authors: D A McSwiggan; R George
Journal: Bull World Health Organ Date: 1970 Impact factor: 9.408

8. Comparison of cynomolgus and rhesus monkey kidney cells for recovery of viruses from clinical specimens.

Authors: J Clark; C Schley; K Irvine; K McIntosh
Journal: J Clin Microbiol Date: 1979-04 Impact factor: 5.948

9. Comparison of primary rhesus and cynomolgus monkey kidney cell cultures for viral isolation from clinical specimens.

Authors: G E Hollick; L Reichrath; T F Smith
Journal: Am J Clin Pathol Date: 1977-08 Impact factor: 2.493

10. Enteric virus isolation in different cell cultures.

Authors: L H Lee; C A Phillips; M A South; J L Melnick; M D Yow
Journal: Bull World Health Organ Date: 1965 Impact factor: 9.408

11 in total

1. Engineered BGMK cells for sensitive and rapid detection of enteroviruses.

Authors: Yung T Huang; Paul Yam; Huimin Yan; Yan Sun
Journal: J Clin Microbiol Date: 2002-02 Impact factor: 5.948

2. Use of cell culture-PCR assay based on combination of A549 and BGMK cell lines and molecular identification as a tool to monitor infectious adenoviruses and enteroviruses in river water.

Authors: Cheonghoon Lee; Seung-Hoon Lee; Euiri Han; Sang-Jong Kim
Journal: Appl Environ Microbiol Date: 2004-11 Impact factor: 4.792

Increased Efficiency of Group B Coxsackievirus Isolation from Clinical Specimens by Use of BGM Cells.

1. Comparative susceptibility of kidney cells from different monkey species to enteric viruses (poliomyelitis, Coxsackie, and echo groups).

2. Non-polio enterovirus activity in Wisconsin based on a 20-year experience in a diagnostic virology laboratory.

3. Comparative sensitivity of various cell culture systems for isolation of viruses from wastewater and fecal samples.

4. BGM, a continuous cell line more sensitive than primary rhesus and African green kidney cells for the recovery of viruses from water.

5. Lyophilized combination pools of enterovirus equine antisera: preparation and test procedures for the identification of field strains of 42 enteroviruses.

6. Experience in laboratory diagnosis of enterovirus infections in routine medical practice.

7. A comparison of two cell culture systems for the primary isolation of enteric viruses.

8. Comparison of cynomolgus and rhesus monkey kidney cells for recovery of viruses from clinical specimens.

9. Comparison of primary rhesus and cynomolgus monkey kidney cell cultures for viral isolation from clinical specimens.

10. Enteric virus isolation in different cell cultures.

1. Engineered BGMK cells for sensitive and rapid detection of enteroviruses.

2. Use of cell culture-PCR assay based on combination of A549 and BGMK cell lines and molecular identification as a tool to monitor infectious adenoviruses and enteroviruses in river water.

3. Presumptive identification of enteroviruses with RD, HEp-2, and RMK cell lines.

4. Optimization of the BGM cell line culture and viral assay procedures for monitoring viruses in the environment.

5. A monoclonal antibody specific for the cellular receptor for the group B coxsackieviruses.

6. Removal of enteric viruses from surface water at eight waterworks in The Netherlands.

7. Comparison of cell cultures for rapid isolation of enteroviruses.

8. Purification of a HeLa cell receptor protein for group B coxsackieviruses.

Review 9. Role of the virology laboratory in diagnosis and management of patients with central nervous system disease.

10. Diagnostic virology laboratory within a microbiology setting.