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Biohazard Levels

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Last Update: September 19, 2022.

Definition/Introduction

Biohazard levels, more commonly referred to as “biological safety levels” or “biosafety levels,” are classifications of safety precautions necessary to be applied in the clinical microbiology laboratory depending on specific pathogens handled when performing laboratory procedures. Developed by the Centers for Disease Control and Prevention (CDC), this principle provides a way for medical laboratory scientists and other lab personnel to identify and limit any biological hazards and further reducing the risk in the laboratory. Biohazard levels, on the other hand, also support the principle of biosecurity, which aims at preventing the use of microorganisms as harmful biological agents.

Four classifications of biosafety levels (BSLs) exist. Each level contains specific recommendations for a clinical microbiology laboratory with a focus on laboratory practices, safety equipment, and facility construction. As each level progresses, it includes additional biosafety considerations from the previous level. For example, BSL-2 has kept the components of BSL-1 with further requirements, and the same applies to BSL-3 (BSL-2 with additional requirements) and BSL-4 (BSL-3 with additional requirements). The complexity of each level aligns with infectivity, disease severity, the microorganisms’ ability for transmission (including exposure routes), and the nature of the laboratory work to be performed.

Implementation of biosafety and biosecurity in the laboratory can initially present as an additional burden to laboratory staff and managers. However, they should not ignore the relevance of applying biosafety principles at the workplace.[1]

Issues of Concern

Laboratory associated infections continue to become sources of diseases to the laboratory workforce; this is because of the failure in implementing fundamental control measures in the laboratory which stems from the most effective control which is "elimination", followed by "substitution", "engineering controls", "administrative", and "personal protective equipment" (e.g., respirator use) as the least effective.[2][3]

Biosafety level 1 (BSL-1) controls microorganisms unusually known to cause disease with "minimal hazards" to the laboratory and the community. A recent study involves the selection of a BSL-1 bacteriophage surrogate to assess the efficacy of a chlorine-based surface disinfectant for Ebola outbreaks. This study recommends the collaboration of BSL-4 and non-BSL-4 facilities to assist in the selection and research of better surrogates, which can be more effective in BSL-4 conditions.[4]

Biosafety level 2 (BSL-2) controls microorganisms generating "moderate hazards" to the laboratory and the community. In other parts of the world, there are still no available guidelines for the validation and certification of biosafety laboratories[2]. The year 2017 saw the identification and analysis of issues regarding biosafety implementation in BSL-2 and BSL-3. There is a need to make clear distinctions between certification and validation of clinical and microbiological laboratories. The need for careful implementation must be first recognized.[5]

Biosafety level 3 (BSL-3) includes the control of infectious agents, which can cause both "serious hazards" and can cause a potentially lethal condition to laboratory and community via the respiratory transmission of the organism. A typical example of an organism under this classification is the Mycobacterium tuberculosis, the bacterial agent responsible for tuberculosis. There have been challenges for program and tuberculosis (TB) laboratory managers in implementing the specific considerations for this level, particularly in resource-limited and TB, high-burden settings because there is insufficient biosafety expertise available to conduct individualized risk assessments for TB laboratories. The application of the biosafety level classification in BSL-3 requirements may not practically and adequately match the specific precautions relevant to the laboratories performing TB-related tests and procedures. To solve this problem, TB laboratories adopted a risk-assessment approach instead of applying the concept of BSL-3 (which is a risk-group approach). Any TB laboratory (a clinical, medical, or public health laboratory carrying out TB diagnostic tests) can classify as low risk, moderate risk, or a high TB risk based on the amount of aerosol generated during the conduct of a particular laboratory procedure. Countries where TB is still a significant public health concern, have already adopted these guidelines.[6][7][8]

Biosafety level 4 (BSL-4) is the highest and "most complex" biohazard level, involving a relatively few clinical microbiology laboratories. There is a high transmission via aerosol, making the pathogens more dangerous for the laboratory workforce and the surrounding community. Marburg and Ebola viruses fall into this risk group. Stakeholders and international experts attended conferences in the past in Europe to revisit the issues that emerged for BSL-4 implementation. They seek opportunities for the use of BSL-4 in public health, diagnostics, and research in terms of its sustainability, improvement of existing training designs and curricula, and strong collaboration to address biosafety and biosecurity. An integrated partnership of human, veterinary, and military laboratories with BSL-4 facilities is necessary to unify its approach to the development of laboratory biosafety standards. The participation of BSL-4 in outbreaks can be substantial to attain a more effective outbreak management.[9]

Clinical Significance

Risk-group classification of required biosafety precautions is ideally a logical approach to minimize laboratory-acquired infections. However, while each laboratory can easily identify and meet the special considerations required, the practicality of the actual day-to-day situation of the laboratory workflow is still more important. Strict adherence to these biohazard levels can be useful and beneficial for some facilities with the capability to comply. In a similar case previously described for TB laboratories, a risk-based approach is more applicable so that safety precautions can "tailor-fit" to the activities of each clinical laboratory. Further studies are still essential to make this a reality on a global scale.[10][8]

Biohazard Level and Significance 

  • Biohazard Level 1 usually includes viruses and bacteria like Escherichia coli and chickenpox and many non-infectious bacteria. The level of precaution at this level is minimal and usually involves wearing a face mask and no close contact.
  • Biohazard Level 2 usually involves microorganisms that are responsible for mild infections in humans and are often difficult to contract via aerosolized particles, like hepatitis A, B, and C, Lyme disease, Salmonella, measles, mumps, HIV, and dengue. Laboratory personnel can carry out diagnostic tests on the specimens but need to wear gloves, facial protection, and a gown. Additionally, standard precautions at this level should be applied when handling clinical samples from the current outbreak investigations of acute respiratory distress syndrome (ARDS) caused by the Coronavirus Disease 2019 (COVID-19).
  • Biohazard Level 3 includes microorganisms that can be fatal to humans but for which vaccines and other treatments are available. Aside from Mycobacterium tuberculosis, this grouping also includes anthrax, many types of viral encephalitis, hantavirus, Rift valley fever, malaria, Rocky Mountain spotted fever, and yellow fever.
  • Biohazard Level 4 usually includes dangerous viruses like Ebola, Marburg virus, Lassa fever, Bolivian hemorrhagic fever, and many other hemorrhagic viruses found in the tropics. Only specific persons can work with these viruses, and it requires them to wear a positive pressure personnel suit, with a segregated air supply. There is no treatment available for these viruses, and extreme isolation precautions are mandatory. The CDC has many recommendations on how to manage these viruses. There are no bacteria in this group.

Knowledge of biohazard levels must not be limited to laboratory professionals. All healthcare workers (clinicians, nurses, pharmacists, etc.) need to be aware of the categories of biohazard levels because they have the potential to impact every patient. For instance, signs and symbols should always be posted on medical and nursing floors when dealing with a high-level biohazard.

Review Questions

References

1.
Coelho AC, García Díez J. Biological Risks and Laboratory-Acquired Infections: A Reality That Cannot be Ignored in Health Biotechnology. Front Bioeng Biotechnol. 2015;3:56. [PMC free article: PMC4412124] [PubMed: 25973418]
2.
Mourya DT, Yadav PD, Majumdar TD, Chauhan DS, Katoch VM. Establishment of Biosafety Level-3 (BSL-3) laboratory: important criteria to consider while designing, constructing, commissioning & operating the facility in Indian setting. Indian J Med Res. 2014 Aug;140(2):171-83. [PMC free article: PMC4216491] [PubMed: 25297350]
3.
Callaway E. Biosafety concerns for labs in the developing world. Nature. 2012 May 22;485(7399):425. [PubMed: 22622543]
4.
Gallandat K, Lantagne D. Selection of a Biosafety Level 1 (BSL-1) surrogate to evaluate surface disinfection efficacy in Ebola outbreaks: Comparison of four bacteriophages. PLoS One. 2017;12(5):e0177943. [PMC free article: PMC5439676] [PubMed: 28531182]
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Mourya DT, Yadav PD, Khare A, Khan AH. Certification & validation of biosafety level-2 & biosafety level-3 laboratories in Indian settings & common issues. Indian J Med Res. 2017 Oct;146(4):459-467. [PMC free article: PMC5819027] [PubMed: 29434059]
6.
Tuberculosis Laboratory Biosafety Manual. World Health Organization; Geneva: 2012. [PubMed: 24404640]
7.
Parsons LM, Somoskövi A, Gutierrez C, Lee E, Paramasivan CN, Abimiku A, Spector S, Roscigno G, Nkengasong J. Laboratory diagnosis of tuberculosis in resource-poor countries: challenges and opportunities. Clin Microbiol Rev. 2011 Apr;24(2):314-50. [PMC free article: PMC3122496] [PubMed: 21482728]
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van Soolingen D, Wisselink HJ, Lumb R, Anthony R, van der Zanden A, Gilpin C. Practical biosafety in the tuberculosis laboratory: containment at the source is what truly counts. Int J Tuberc Lung Dis. 2014 Aug;18(8):885-9. [PubMed: 25199000]
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Nisii C, Castilletti C, Raoul H, Hewson R, Brown D, Gopal R, Eickmann M, Gunther S, Mirazimi A, Koivula T, Feldmann H, Di Caro A, Capobianchi MR, Ippolito G. Biosafety Level-4 laboratories in Europe: opportunities for public health, diagnostics, and research. PLoS Pathog. 2013 Jan;9(1):e1003105. [PMC free article: PMC3547859] [PubMed: 23349630]
10.
Kojima K, Booth CM, Summermatter K, Bennett A, Heisz M, Blacksell SD, McKinney M. Risk-based reboot for global lab biosafety. Science. 2018 Apr 20;360(6386):260-262. [PubMed: 29674576]

Disclosure: Marlon Bayot declares no relevant financial relationships with ineligible companies.

Disclosure: Kevin King declares no relevant financial relationships with ineligible companies.

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Bookshelf ID: NBK535351PMID: 30570972

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