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G A Quinlan

Publications and source records attributed to G A Quinlan.

4 recordsLinked to original sources

Nosocomial legionellosis traced to a contaminated ice machine.

OBJECTIVE: To investigate a case of nosocomial legionellosis, identify pathways of transmission, and effect control of the environmental source. DESIGN: Case investigation and environmental culture surveillance. SETTING: A 720-bed university teaching hospital. CASE PATIENT: A ventilator-dependent 66-year-old male developed nosocomial pneumonia due to Legionella pneumophila serogroup 6 after 3 months in an intensive-care unit (ICU). The patient had no intake of potable water except for ice chips from an ice machine in the ICU. RESULTS: Cultures revealed L pneumophila serogroup 6 in the ice (4.3 colony-forming units/mL) and ice machine cold water (too numerous to count). Cultures from adjacent hot and cold taps, plus taps located near the patient, all were negative; ice machines and cold water on seven other patient units also were negative. Only sterile water had been used for tube feedings, mouth care, suctioning, and ventilator humidification. Hospital hot water previously had been colonized with L pneumophila serogroup 6, but all surveillance water cultures had been negative since chlorination of the hot-water system began the previous year; cold-water cultures had never before grown Legionella. The ice machine was disinfected with a 2-hour flush of 2.625% sodium hypochlorite. The supply line to the ice machine was replaced, and the cold-water pipe from the floor below was treated with 83 ppm sodium hypochlorite for 48 hours. All follow-up surveillance cultures of the ice machine remained negative through mid-1996. No additional cases of nosocomial legionellosis occurred. CONCLUSIONS: Ice machines may be reservoirs of L pneumophila in hospitals. Both ice and water dispensed from these machines may be contaminated, and nosocomial transmission may occur. Successful long-term decontamination and control can be accomplished with shock chlorination.

Aged

Neuroectodermal fate of epiblast cells in the distal region of the mouse egg cylinder: implication for body plan organization during early embryogenesis.

The developmental fate of cells in the distal region (distal cap) of the epiblast was analysed by fate mapping studies. The displacement and differentiation of cells labelled in situ with carbocyanine dyes and lacZ-expressing cells grafted to the distal cap were studied over a 48-hour period of in vitro development. The distal cap epiblast differentiates predominantly into neurectodermal cells. Cells at the anterior site of the distal cap colonise the fore-, mid- and hindbrain and contribute to non-neural ectoderm cells of the amnion and craniofacial surface ectoderm. Those cells in the most distal region of the epiblast contribute to all three brain compartments as well as the spinal cord and the posterior neuropore. Cells at the posterior site of the distal cap are mainly localised to the caudal parts of the neural tube. A minor contribution to the embryonic (paraxial and lateral) and extraembryonic (allantoic and yolk sac) mesoderm is also found. Epiblast cells located outside the distal cap give rise to surface ectoderm and other non-ectodermal derivatives, with only a minor contribution to the neuroectoderm. Results of this study provide compelling evidence that the precursor population of the neural tube is contained in the distal cap epiblast of the early-primitive-streak-stage embryo. Furthermore, the regionalisation of cell fate within this small population suggest that a preliminary craniocaudal patterning may have occurred in the neural primordium before neurulation.

Animals