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NEISSERIA SPP.

PATHOGEN SAFETY DATA SHEET - INFECTIOUS SUBSTANCES

SECTION I - INFECTIOUS AGENT

NAME: Neisseria spp. (other than N. gonorrhoeae and N. meningitidis)

SYNONYM OR CROSS REFERENCE:

1) The majority of human-associated Neisseria species are non-pathogenic and are normal inhabitants of the upper respiratory tract. Human associated species include: N. gonorrhoeae, N. meningitidis, N. lactamica, N. cinerea, N. polysaccharea, N. mucosa, N. flavescens, N. sicca, N. subflava including the biovars subflava, flava, and perflava, and N. elongata subspecies elongata, glycolytica, and nitroreducens. Only N. gonorrhoeae and N. meningitidis are regarded as pathogens (1, 2).

2) Neisseria species associated with animals include: N. canis, N. weaveri (dogs), N. denitrificans (guinea pigs), N. macacae (rhesus monkey), N. dentiae (cows), and N. iguanae (lizards). (1, 2)

CHARACTERISTICS: Neisseria spp. are gram-negative, non-motile, and non-spore-forming bacteria belonging to the family Neisseriaceae (1, 3). All members of the Neisseria spp., except the three subspecies of N. elongata and N. weaveri, occur as diplococcal bacteria with their adjacent sides flattened, resembling a kidney or coffee bean. The three subspecies of N. elongata and N. weaveri occur as medium to long, plump rods in pairs or short chains. All species are oxidase positive (1, 3), and all species except N. elongata subspecies nitroreducens and N. elongata subspecies elongata are catalase positive (3). Most species grow optimally at temperatures ranging between 35 to 37 °C, and growth is usually stimulated by carbon dioxide and humidity. Species are generally aerobic but some species may demonstrate growth under anaerobic conditions.

SECTION II - HAZARD IDENTIFICATION

PATHOGENICITY/TOXICITY: Neisseria spp. are part of the commensal flora of mucosal membranes of humans and some animals, and are generally considered non-pathogenic except for N. gonorrhoea and N. meningitidis (1). Individuals with underlying medical conditions and/or immune suppression or deficiency may develop serious infections caused by the normally commensal Neisseria species. For example, N. lactamica had been reported to cause bacteramemic pneumonia and septicemia in immunocompromised individuals (4). N. cinerea is commonly isolated from the upper respiratory tract, but has also been isolated from other sites including the cervix, rectum, conjunctivae, blood and cerebrospinal fluid (CSF) (1). It has also been associated with rare cases of peritonitis (5), tonsillitis, lymphadenitis, proctitis, and pulmonary cavitation (6). N. flavescens and N. polysaccharea are found in the upper respiratory tract and the oropharynx (respectively) of humans, and are rarely associated with infectious processes (1). N. subflava, N. flava, N. perflava, N. mucosa, and N. sicca are found in the upper respiratory tract of humans and are occasional isolates from infectious processes, including endocarditis, bacteraemia, meningitis, pneumonia, empyema, pericarditis, peritonitis, septic arthritis, and liver abscess (1, 7-10). N. elongata subspecies are found in the upper respiratory tract of humans and have been isolated from infectious processes, including endocarditis, septicaemia, and osteomyelitis (1, 11-13). N. weaveri is part of the normal canine oral flora and has been isolated from a case of lower respiratory tract infection (14).

EPIDEMIOLOGY: Worldwide; part of the commensal flora of the upper respiratory tract and oropharynx of humans and some animals (1).

HOST RANGE: Humans and some animals (dogs, guinea pigs, rhesus monkeys, cows, and iguanid lizards) (1).

INFECTIOUS DOSE: Unknown.

MODE OF TRANSMISSION: May be transmitted by contact with droplets and discharges from the nose and throat of infected persons; however, transmission is rare due to low virulence. May also be transmitted through bites by infected or colonized dogs (for N. weaveri).

INCUBATION PERIOD: Unknown.

COMMUNICABILITY: Not known to be readily transmitted from person-to-person due to low virulence.

SECTION III - DISSEMINATION

RESERVOIR: Humans and some animals (dogs, guinea pigs, rhesus monkeys, cows, and iguanid lizards) (1).

ZOONOSIS: May be possible for animal pathogens; N. weaveri (found in dogs) has been isolated from wounds sites in humans as a result of dog bites (14).

VECTORS: None.

SECTION IV – STABILITY AND VIABILITY

DRUG SUSCEPTIBILITY: Neisseria spp. are susceptible to cefotaxime, ceftriaxone, and amoxicillin (6, 10, 15). Depending on the strains, some demonstrate intermediate to high resistance to penicillin and amoxicillin (15, 16). N. polysaccharea is resistant to vancomycin (1).

SUSCEPTIBILITY TO DISINFECTANTS: Gram-negative bacteria are generally susceptible to a number of disinfectants, including phenolic compounds, hypochlorites (1% sodium hypochlorite), alcohols (70% ethanol), formaldehyde (18.5 g/L; 5% formalin in water), glutaraldehyde, and iodines (0.075 g/L) (17).

PHYSICAL INACTIVATION: Bacteria are generally sensitive to moist heat (121 °C for at least 15 minutes) and dry heat (160 to 170 °C for at least 1 hour) (18).

SURVIVAL OUTSIDE HOST: Unknown; however, it may be similar to other members of the genus including N. gonorrhoeae and N. meningitis. N. gonorrhoeae is known to survive on different surfaces including toilet seats (brief periods of up to 2 hours) (3, 19), toilet paper (up to 3 hours)(19), slides (up to 17 hours), and towels (up to 24 hours). N. meningitidis does not survive well in the environment, but has been reported to survive on grass and plastic at ambient temperatures for hours to days (20).

SECTION V - FIRST AID / MEDICAL

SURVEILLANCE: Monitor for symptoms. Confirm by CSF or blood culture, or culture of biopsy specimens (6, 21).

Note: All diagnostic methods are not necessarily available in all countries.

FIRST AID/TREATMENT: Wash the exposed area with soap and warm water (omit soap if mucous membrane exposure). Treat with appropriate antibiotic therapy if required.

IMMUNIZATION: None.

PROPHYLAXIS: None.

SECTION VI - LABORATORY HAZARD

LABORATORY-ACQUIRED INFECTIONS: No cases of laboratory-acquired infection have reported up to date.

SOURCES/SPECIMENS: Throat and/or nasopharyngeal swabs and washings (21), pleural-effusion specimens, blood (9, 13), CSF (9), biopsy specimens (6, 10), and wound specimens (14).

PRIMARY HAZARDS: Accidental parenteral inoculation and/or ingestion of contaminated samples, and exposure of mucosal membranes via inhalation of infectious airborne secretions.

SPECIAL HAZARDS: None.

SECTION VII - EXPOSURE CONTROLS / PERSONAL PROTECTION

RISK GROUP CLASSIFICATION: Risk Group 2 (22). This risk group applies to the genus as a whole, and may not apply to every species within the genus.

CONTAINMENT REQUIREMENTS: Containment Level 2 facilities, equipment, and operational practices for work involving infectious or potentially infectious materials, animals, or cultures. These containment requirements apply to the genus as a whole, and may not apply to each species within the genus.

PROTECTIVE CLOTHING: Lab coat. Gloves when direct skin contact with infected materials or animals is unavoidable (23). Eye protection must be used where there is a known or potential risk of exposure to splashes.

OTHER PRECAUTIONS: All procedures that may produce aerosols, or involve high concentrations or large volumes should be conducted in a biological safety cabinet (BSC) (23). The use of needles, syringes, and other sharp objects should be strictly limited. Additional precautions should be considered with work involving animals or large scale activities.

SECTION VIII - HANDLING AND STORAGE

SPILLS: Allow aerosols to settle and, while wearing protective clothing, gently cover spill with absorbent paper towels and apply an appropriate disinfectant, starting at the perimeter and working towards the centre. Allow sufficient contact time before clean up (23).

DISPOSAL: Decontaminate all wastes that contain or have come in contact with the infectious organism by autoclave, chemical disinfection, gamma irradiation, or incineration before disposing (23).

STORAGE: The infectious agent should be stored in leak-proof containers that are appropriately labelled (23).

SECTION IX - REGULATORY AND OTHER INFORMATION

REGULATORY INFORMATION: The import, transport, and use of pathogens in Canada is regulated under many regulatory bodies, including the Public Health Agency of Canada, Health Canada, Canadian Food Inspection Agency, Environment Canada, and Transport Canada. Users are responsible for ensuring they are compliant with all relevant acts, regulations, guidelines, and standards.

UPDATED: September 2011

PREPARED BY: Pathogen Regulation Directorate, Public Health Agency of Canada.

Although the information, opinions and recommendations contained in this Pathogen Safety Data Sheet are compiled from sources believed to be reliable, we accept no responsibility for the accuracy, sufficiency, or reliability or for any loss or injury resulting from the use of the information. Newly discovered hazards are frequent and this information may not be completely up to date.

Copyright ©

Public Health Agency of Canada, 2011

Canada

REFERENCES:

  1. Janda, W. M., & Gaydos, C. A. (2007). Neisseria. In P. R. Murray, E. J. Baron, J. H. Jorgensen, M. L. Landry & M. A. Pfaller (Eds.), Manual of Clinical Microbiology (9th ed., pp. 601-620). Washington, D.C.: ASM Press.

  2. Mietzner, T. A., & Morse, S. A. (2005). Neisseria. In S. P. Borriello, P. R. Murray & G. Funke (Eds.), Topley & Wilson's Microbiology & Microbial Infections (10th ed., pp. 1270-1293). Washington, DC, USA: Edward Arnold Publishers Ltd.

  3. Ryan, K. J. (2004). Neisseria. In K. J. Ryan, & C. G. Ray (Eds.), Sherris Medical Microbiology: An Introduction to Infectious Diseases (4th ed., pp. 327-341). United States: McGraw Hill.

  4. Schifman, R. B., & Ryan, K. J. (1983). Neisseria lactamica septicemia in an immunocompromised patient. Journal of Clinical Microbiology, 17(5), 934-935.

  5. Taegtmeyer, M., Saxena, R., Corkill, J. E., Anijeet, H., & Parry, C. M. (2006). Ciprofloxacin treatment of bacterial peritonitis associated with chronic ambulatory peritoneal dialysis caused by Neisseria cinerea. Journal of Clinical Microbiology, 44(8), 3040-3041. doi:10.1128/JCM.00917-06

  6. Kamar, N., Chabbert, V., Ribes, D., Chabanon, G., Faguer, S., Mari, A., Guitard, J., Durand, D., & Rostaing, L. (2007). Neisseria-cinerea-induced pulmonary cavitation in a renal transplant patient. Nephrology, Dialysis, Transplantation: Official Publication of the European Dialysis and Transplant Association - European Renal Association, 22(7), 2099-2100. doi:10.1093/ndt/gfm040

  7. Chung, H. C., Teng, L. J., & Hsueh, P. R. (2007). Liver abscess due to Neisseria sicca after repeated transcatheter arterial embolization. Journal of Medical Microbiology, 56(Pt 11), 1561-1562. doi:10.1099/jmm.0.47192-0

  8. Shetty, A. K., Nagaraj, S. K., Lorentz, W. B., & Bitzan, M. (2005). Peritonitis due to Neisseria mucosa in an adolescent receiving peritoneal dialysis. Infection, 33(5-6), 390-392. doi:10.1007/s15010-005-5074-4

  9. Sartin, J. S. (2000). Neisseria sicca meningitis in a woman with nascent pernicious anemia. The American Journal of Medicine, 109(2), 175-176.

  10. Roberts, P. J., Gadgil, A., Orendi, J. M., & Brown, M. F. (2003). Infective discitis with Neisseria sicca/subflava in a previously healthy adult. Spinal Cord: The Official Journal of the International Medical Society of Paraplegia, 41(10), 590-591. doi:10.1038/sj.sc.3101497

  11. Haddow, L. J., Mulgrew, C., Ansari, A., Miell, J., Jackson, G., Malnick, H., & Rao, G. G. (2003). Neisseria elongata endocarditis: case report and literature review. Clinical Microbiology and Infection: The Official Publication of the European Society of Clinical Microbiology and Infectious Diseases, 9(5), 426-430.

  12. Picu, C., Mille, C., Popescu, G. A., Bret, L., & Prazuck, T. (2003). Aortic prosthetic endocarditis with Neisseria elongata subspecies nitroreducens. Scandinavian Journal of Infectious Diseases, 35(4), 280-282.

  13. Hsiao, J. F., Lee, M. H., Chia, J. H., Ho, W. J., Chu, J. J., & Chu, P. H. (2008). Neisseria elongata endocarditis complicated by brain embolism and abscess. Journal of Medical Microbiology, 57(Pt 3), 376-381. doi:10.1099/jmm.0.47493-0

  14. Panagea, S., Bijoux, R., Corkill, J. E., Al Rashidi, F., & Hart, C. A. (2002). A case of lower respiratory tract infection caused by Neisseria weaveri and review of the literature. The Journal of Infection, 44(2), 96-98. doi:10.1053/jinf.2001.0965

  15. Arreaza, L., Salcedo, C., Alcala, B., & Vazquez, J. A. (2002). What about antibiotic resistance in Neisseria lactamica? The Journal of Antimicrobial Chemotherapy, 49(3), 545-547.

  16. Handal, T., Olsen, I., Walker, C. B., & Caugant, D. A. (2004). Beta-lactamase production and antimicrobial susceptibility of subgingival bacteria from refractory periodontitis. Oral Microbiology and Immunology, 19(5), 303-308. doi:10.1111/j.1399-302x.2004.00159.x

  17. Disinfection and Sterilization. (1993). Laboratory Biosafety Manual (2nd ed., pp. 60-70). Geneva: WHO.

  18. Joslyn, L. J. (2000). Sterilization by Heat. In S. S. Block (Ed.), Disinfection, Sterilization, and Preservation (5th ed., pp. 695-728). Philadelphia, USA: Lippincott Williams & Wilkins.

  19. Neinstein, L. S., Goldenring, J., & Carpenter, S. (1984). Nonsexual transmission of sexually transmitted diseases: an infrequent occurrence. Pediatrics, 74(1), 67-76.

  20. Swain, C. L., & Martin, D. R. (2007). Survival of meningococci outside of the host: implications for acquisition. Epidemiology & Infection, 135(2), 315-320.

  21. Wang, C. Y., Chuang, Y. M., Teng, L. J., Lee, L. N., Yang, P. C., Kuo, S. H., & Hsueh, P. R. (2006). Bacteraemic pneumonia caused by Neisseria lactamica with reduced susceptibility to penicillin and ciprofloxacin in an adult with liver cirrhosis. Journal of Medical Microbiology, 55(Pt 8), 1151-1152. doi:10.1099/jmm.0.46229-0

  22. Human pathogens and toxins act. S.C. 2009, c. 24, Second Session, Fortieth Parliament, 57-58 Elizabeth II, 2009. (2009).

  23. Public Health Agency of Canada. (2004). In Best B., Graham M. L., Leitner R., Ouellette M. and Ugwu K. (Eds.), Laboratory Biosafety Guidelines (3rd ed.). Canada: Public Health Agency of Canada.