Aerosols as a Source of Widespread Mycoplasma Contamination of Tissue Cultures
Author(s) -
Robert C. O'Connell,
Ruth G. Wittler,
John E. Faber
Publication year - 1964
Publication title -
applied microbiology
Language(s) - English
Resource type - Journals
ISSN - 0003-6919
DOI - 10.1128/am.12.4.337-342.1964
Subject(s) - trypsinization , mycoplasma , microbiology and biotechnology , tissue culture , complement fixation test , biology , contamination , mycoplasma hominis , virology , in vitro , immunology , antibody , trypsin , serology , biochemistry , enzyme , ecology
Mycoplasma isolates were cultured from 15 antibiotic-free cell cultures obtained from a single laboratory. Complement-fixation tests showed that these isolates were antigenically related to each other but were unrelated toM. hominis type 1,M. hominis type 2,M. arthritidis, M. laidlawii type B,Mycoplasma sp. H.Ep. #2 (Barile), orM. salivarium . Examination of serum used to feed the infected cell lines revealed noMycoplasma . Infection resulting from cross-contamination by a singleMycoplasma strain from one cell culture to another was investigated. Although the organisms were not found in the air over the work area, aerosols containing these contaminants were produced in tissue culture bottles during the trypsinization of cell monolayers. The minimal infectious dose ofMycoplasma for tissue cultures was measured, and it was determined that one organism was capable of initiating an infection in a tissue culture. The pattern of contamination and the small dose required for infection indicated thatMycoplasma contamination was spread from one tissue culture to another via aerosols. It was demonstrated thatMycoplasma can be transferred from one cell culture to another through the use of a common burette for dispensing medium.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom