Laboratory Biosafety Plan

Similar documents
UNIVERSITY OF NEVADA LAS VEGAS BSL-2 LABORATORY STANDARD OPERATING PROCEDURES (SOPS)

Minimum Safety Equipment. Standard microbiological practices Sink Required

Biosafety Level 2 Criteria Based on Biosafety in Microbiological and Biomedical Laboratories (BMBL) 5th Edition

Lab Biosafety Self-Audit Form (Applies to all microbial work.)

December 2009 CDC-NIH

BIOSAFETY LEVEL LABORATORIES

VIII. Biosafety Laboratory Practices and Equipment

Animal Facility Biosafety Level 3 Checklist (date: April 16, 1998)

You are responsible for reading and understanding the content from the section Basic Microbiology Laboratory Safety.

Amherst College. Health and Safety Manual for the Use of Recombinant DNA and Biological Agents Current as of May 14, 2010

PI s Name Date Bldg./Rm#

Biosafety Training. WVU Shared Research Facilities 2012

Vertebrate Animal Biosafety Level 2 Criteria

Biosafety Level 2 (BSL-2) Laboratory Guidelines

Inspection Checklist for BSL-3 Laboratories Non-Smile Resource

Lab Safety, Biological Safety and Bloodborne Pathogen Training

BIOSAFETY LEVEL 2 PROTOCOLS BIOPROCESS OPTIMIZATION LABORATORY - POULIOT BUILDING, ROOM 1541 ALAIN GARNIER JUNE 2007, LAVAL UNIVERSITY

Biosafety Primer. An introduction to the world of biosafety

Health, Safety & Environment Technical Guideline

Texas A&M University Commerce April 11, 2014

Biosafety Checklist. 07-BiosafetyChecklist-LTC-SOP-v2.0-17Feb of 6

Departmental Exposure Control Plan

Laboratory Safety Inspection BSL-2 Laboratories

SOP #: Title: Recombinant or Synthetic Nucleic Acid Incident Spill Response and Reporting SOP

Please refer to The University of Chicago Biosafety Manual for supplementary information about the concepts presented in this training module.

To the Principal Investigator:

DUQUESNE UNIVERSITY. Biosafety Guidelines

DUQUESNE UNIVERSITY. Biosafety Guidelines

To the Principal Investigator:

Inspection Checklist for NIH BL3 Laboratories (7 CFR 331; 9 CFR 121; 42 CFR 73; NIH Guidelines)

ENHANCED CONTAINMENT CL2 + (Level 3 practices in a Level 2 lab)

Biosafety Manual 2016

Biosafety Protocol. Biodesign Swette Center for Environmental Biotechnology Standard Operating Procedures

I. BIOLOGICAL SAFETY. A. Biological Risk Assessment. Risk assessment is a process used to identify the hazardous characteristics of a known

UW LOCAL RISK ASSESSMENT WORKSHEET FOR WORK WITH BIOLOGICAL MATERIALS

7. BIOLOGICAL HAZARDS AND CONTROL

BIOSAFETY MANUAL 2014

Bloodborne Pathogens Exposure Control Plan

XIV. Animal Research Safety

Standard Operating Procedure Title: Good laboratory practices (GLP) for microbiology and chemistry laboratories

SAFETY MANUAL OF GOOD LABORATORY

Pathogen Safety Sheet

BIOSAFETY LABORATORY AUDIT Department of Biological Safety University of Kentucky

Personal Protective Equipment Guidelines. Chemical

IBC Requirements for Laboratory Operating Practices, Physical Containment, and Training for Research Involving Biological Agents

Rice University Biosafety Manual

Animal cell and tissue culture. Lab 1

RESEARCH LABORATORY SAFETY

LABORATORY BIOLOGICAL SAFETY (BSL-1) MANUAL

THE UNIVERSITY OF NEWCASTLE- SCHOOL of BIOMEDICAL SCIENCES

Yeo Soh Bee / Zhou Lei A/Prof Dan Yock Young 29/9/2017 Prepared by Approved By Issue Date

Standard Microbiological Practices

Dartmouth College. Institutional Biosafety Committee. Biohazardous Waste Disposal Guide IBC Approved: 4/5/17

Dartmouth College. Institutional Biosafety Committee. Biohazardous Waste Disposal Guide IBC Approved: 10/3/18

BIOLOGICAL SAFETY BSL- 2 LABORATORY PROCEDURES

96-well Genomic DNA Extraction Kit. Protocol Book. (Deep Well) Ver RBP96B-2

An Overview: Laboratory Safety and work Practices in Infectious Disease Research

Laboratory Close-Out Guidelines

MICROBIOLOGICAL SAFETY RULES

BIOSAFETY GUIDELINES BACKGROUND ON BIOSAFETY

Introduction to Syracuse University s Microbiological Safety Program

BIOSAFETY LABORATORY AUDIT Department of Biological Safety University of Kentucky

Working in PC-1 and PC-2 Tissue Culture Facilities Description: This procedure is applied when working in PC-1 and PC-2 tissue culture labs

Biology Lab Safety. Document No Audit Title Biology Lab Safety Inspection. Conducted on 9/28/16, 1:43 PM

Environment, Health and Safety

THE UNIVERSITY OF NEWCASTLE- DISCIPLINE OF MEDICAL BIOCHEMISTRY. STANDARD OPERATING PROCEDURE PROCEDURE NO: GLP 104 MOD: 1st Issue Page: 1 of 8

BIOSAFETY INSPECTIONS. What to ask and what to look for

Biological Safety Training. October 1, 2014

Safety and Health Policy and Procedure Manual. Biological Safety Manual Section 280

Biological Safety Program. For. Otterbein University

Standard Operating Procedure for Fluorouracil in Animals

Dr. M. Tariq Javed. Biohazard Biosafety in Biomedical Laboratories. Biosafety definition. Biorisk definition

SOP for Recombinant Viral Work in Animal Facilities

CONTACTS. Environmental Health and Safety. Regulated Materials Management Center

FACULTY OF HEALTH AND MEDICAL SCIENCES HEALTH AND SAFETY PROCEDURES PART 3 BIOSAFETY AND BIOSECURITY

Biosafety at Ryerson. 4. Standard Operating Procedures

EliGene MTB Isolation Kit

Standard Operating Procedure Safe Autoclave Operations

Laboratory Biosafety Manual

Activities Involving the Use of External Fermentors

Laboratory Research Conduct & Safety: Biohazards and Biosafety. Environmental Health & Safety

Welcome to Courses facilities in building 301 at Department of Systems Biology

THE UNIVERSITY OF NEWCASTLE- DISCIPLINE OF MEDICAL BIOCHEMISTRY. STANDARD OPERATING PROCEDURE PROCEDURE NO: GLP 107 MOD: 1st Issue Page: 1 of 8

SV GUIDELINES Decontamination / Spill cleaning

Laboratory Research Conduct & Safety: Biohazards and Biosafety. Environmental Health & Safety

General Guidelines on Research Projects Involving Lentivirus

BIO-SAFETY IN MICROBIOLOGIC AND BIOMEDICAL LABORATORIES. Dr. K. P. Narkhede

Registration Document For Biohazards

Institutional Biosafety Committee Policy: BIOSAFETY BEST PRACTICES FOR RESEARCH USE OF BIOLOGICAL TOXINS & VENOMS

Biological Safety Level 2 (BSL2)

Laboratory Research Ethics, Conduct and Safety

Skidmore College Institutional Biosafety Committee (IBC) Protocol Registration Form

Scott & White Healthcare Institutional Biosafety Committee (IBC) IBC Initial Application

BIOLOGICAL SAFETY MANUAL

Biosafety Practices This resource developed by LabCentral for the Pagliuca Harvard Life Lab Revision 2, Effective Mar 17,2017

BGSU s Biosafety and Infectious Waste Safety Procedures. Environmental Health & Safety 1851 N. Research Drive Bowling Green, OH

Urine DNA Isolation Maxi Kit (Slurry Format) Product # 50100

ENVIRONMENTAL HEALTH & SAFETY

6/19/2015. This lecture provides an overview of some of the safety precautions you can practice in order to create a safe lab environment.

University of Pittsburgh Bloodborne Pathogen Exposure Control Plan

Transcription:

DUKE NEUROBIOLOGY SCHOOL OF MEDICINE Laboratory Biosafety Plan Laboratory of Boris Kantor Laboratory Biohazards: Biosafety Level 1 Recombinant DNA cloning in E. coli K-12 and derivatives Adeno-Associated Vectors Biosafety Level 2 o o Lentivirus (replication-defective, derived from human immunodeficiency virus and pseudotyped with vesicular stomatitis virus glycoprotein) Rabies Viruses (replication-defective) Biosafety Level 1: 1) Gloves should be worn if the skin on the hands is broken or if a rash is present. Lab personnel must wash their hands after they handle viable materials, after removing gloves, and before leaving the laboratory. 2) Eating, drinking, smoking, handling contact lenses, applying cosmetics, and storing food for human use are not permitted in the work areas. Persons who wear contact lenses in laboratories should also wear goggles or a face shield. Food is stored outside the work area in cabinets or refrigerators designated and used for this purpose only. 3) Mouth pipetting is prohibited; mechanical pipetting devices are used. 4) A high degree of precaution must always be taken with any contaminated sharp items, including needles and syringes, slides, pipettes, capillary tubes, and scalpels.

5) All procedures are performed carefully to minimize the creation of splashes or aerosols. Protective eyewear should be worn for conduct of procedures in which splashes of microorganisms or other hazardous materials is anticipated. 6) Work surfaces where bacteria containing recombinant DNA have been used must be decontaminated at least once each day and after any spill of viable material. Appropriate disinfectants include 1% bleach (500 ppm) and 70% ethanol. 7) All bacterial cultures, culture plates and other contaminated items must be decontaminated before disposal by autoclaving or other approved methods. a) Materials to be autoclaved are to be placed in a durable, leakproof container and closed for transport from the laboratory. b) Reusable items such as centrifuge tubes or culture flasks should be decontaminated by soaking in 10% bleach (5000 ppm) or 70% ethanol or 1% Lysol concentrate (500 ppm) for at least 20 minutes and rinsed before standard laboratory washing. c) Liquid waste should be treated with Lysol concentrate at a final concentration of at least 1% (add an approximately equal volume of 2.5%) for at least 10 minutes before disposal. Biosafety Level 2 * : 1) When work with infectious agents is in progress access to the laboratory is limited to personnel with appropriate Biosafety Level 2 training. 2) Protective laboratory coats, gowns, smocks, or uniforms designated for lab use must be worn while working with BSL2 agents. Open-toed shoes are not permitted. This protective clothing must be removed and left in the laboratory before leaving for non-laboratory areas. All protective clothing is either disposed of in the laboratory or laundered by the institution; it should never be taken home by personnel. 3) Gloves are worn when hands may contact potentially infectious materials, contaminated surfaces or equipment. Wearing two pairs of gloves may be appropriate. Gloves are disposed of when overtly contaminated, and removed when work with infectious materials is completed or when the integrity of the glove is compromised. Disposable gloves are not washed, reused, or used for touching "clean" surfaces (keyboards, telephones, etc.), and they should not be worn outside the lab. Gloves used for BSL-2 work must be treated as contaminated and discarded with other contaminated material. Hands are washed following removal of gloves. 4) Eating, drinking, smoking, handling contact lenses, and applying cosmetics are not permitted in the work areas. Food is stored outside the work area in cabinets or refrigerators designated for this purpose only. 5) Mouth pipetting is prohibited; mechanical pipetting devices are used. 6) The biological safety cabinet must be used whenever possible, including procedures with a potential for creating infectious aerosols or splashes are conducted. Such procedures include opening containers of infectious materials and all cell culture work with BSL2 agents and cell lines. Such materials may be centrifuged or otherwise manipulated in the open laboratory if * These procedures apply only to non-animal work involving BSL2 agents. Additional precautions and procedures apply to work involving administration of BSL2 agents to animals.

sealed centrifuge tubes, sealed rotor heads or other sealed vessels are used, and if these containers are opened only in a biological safety cabinet. 7) Culture flasks and dishes containing high-titer virus should be labeled as a biohazard during incubation or manipulation outside of the biological safety cabinet. 8) All procedures are performed carefully to minimize the creation of splashes or aerosols. Face protection (goggles, mask, face shield or other splatter guard) must be used for anticipated splashes or sprays of infectious or other hazardous materials to the face when the microorganisms must be manipulated outside the biological safety cabinet. 9) A high degree of precaution must always be taken with any contaminated sharp items, including needles and syringes, slides, pipettes, capillary tubes, and scalpels. BSL2 agents should never loaded into syringes with needles. Plasticware should be substituted for glassware whenever possible. 10) Broken glassware must not be handled directly by hand, but must be removed by mechanical means such as a brush and dustpan, tongs, or forceps. Containers of contaminated needles, sharp equipment, and broken glass are decontaminated before disposal. 11) Laboratory equipment and work surfaces should be decontaminated with an effective disinfectant (1% bleach [500 ppm] or 70% ethanol) on a routine basis, after work with infectious materials is finished. Overt spills, splashes, or other contamination by infectious materials should be flooded with 10% bleach (5000 ppm) or 70% ethanol before removal. Contaminated equipment must be decontaminated before it is sent for repair or maintenance or packaged for transport. 12) All cultures, stocks, and materials contaminated with BSL2 agents must be decontaminated before disposal by an approved decontamination method such as autoclaving. Materials to be decontaminated outside of the immediate laboratory are placed in a durable, leakproof container and closed for transport from the laboratory. a) All disposables contaminated with high concentrations of BSL-2 agents should be rinsed with 10% bleach or 70% ethanol after use and before autoclaving. b) All materials to be autoclaved should be placed in a container with a cover that prevents leakage during collection, handling, processing, storage, transport, or shipping. c) Reusable items such as centrifuge tubes or bottles should be decontaminated by soaking in 10% bleach or 70% ethanol for at least 20 minutes and rinsed before standard laboratory washing. d) Liquid waste should be treated with bleach at a final concentration of 10% for at least 20 minutes before disposal. Perform this treatment in the chemical fume hood. 13) Spills and accidents that result in overt exposures to infectious materials are immediately reported to the laboratory director. Medical evaluation, surveillance, and treatment are provided as appropriate and written records are maintained. Disinfectants Lysol (Lysol Brand Concentrate, Original Scent): Prepare a 1:40 (2.5%) dilution in deionized water. The active ingredient is o-benzyl-p-chlorophenol, present at 5-6% in the concentrate. A

final concentration of 1% (500-600 ppm) is effective against bacteria and most enveloped viruses. Ethanol (or isopropanol): When used at a final concentration of 70-85% it is effective against bacteria and enveloped viruses. Lysol brand II Disinfectant Spray contains 79% ethanol, so it is also effective. Note that these alcohols are flammable, so should not be used near a flame. Sodium hypochlorite (household bleach): Sold as a solution containing 5.25% free chlorine. Used at a 1:10 dilution (10% bleach, 5000 ppm), it is useful for disinfecting spilled suspensions of bacteria or viruses and to disinfect liquid waste. Note that treatment of liquid waste must be performed in a chemical fume hood because of the generation of chlorine gas. Used at a dilution of 1:100 (1% bleach, 500 ppm), it is useful for routine surface decontamination, although it should not be used for disinfection of biological safety cabinets because of reaction with stainless steel.

Virus Transport Protocol 1. Virus samples are prepared and stored in capped 0.5- to 2.0-ml plastic microfuge tubes. Storage is at -80 C. 2. For transport to other institutional laboratories, tubes containing virus samples must be placed in clean 50-ml plastic centrifuge tubes (or other clean, sealable containers) and caps closed tightly. Samples should be placed on ice or dry ice for transport. 3. Laboratory personnel must wear gloves while placing samples into carrier tubes or containers these gloves must be discarded into the biohazard waste before leaving the laboratory. Clean gloves should be worn during sample transport. 4. The Principal Investigator of the recipient laboratory assumes all responsibility for safe transport and use of the viruses once the samples leave the Viral Vector Laboratory. DUKE UNIVERSITY DURHAM, NORTH CAROLINA 27701 919.684.0044 FAX 919.613.6750 AN AFFIRMATIVE ACTION / EQUAL OPPORTUNITY INSTITUTION