Legionella

Legionella is a genus of pathogenic Gram-negative bacteria that includes the species L. pneumophila, causing legionellosis[3] (all illnesses caused by Legionella) including a pneumonia-type illness called Legionnaires' disease and a mild flu-like illness called Pontiac fever.[3]

Legionella
Legionella sp. under UV light
Scientific classification
Domain: Bacteria
Phylum: Proteobacteria
Class: Gammaproteobacteria
Order: Legionellales
Family: Legionellaceae
Genus: Legionella
Brenner et al. 1979
Species

Legionella adelaidensis[1]
Legionella anisa[1]
Legionella beliardensis[1]
Legionella birminghamensis[1]
Legionella bozemanae[1]
Legionella brunensis[1]
Legionella busanensis[1]
Legionella cardiaca[1]
Legionella cherrii[1]
Legionella cincinnatiensis[1]
Legionella clemsonensis[2]
Legionella donaldsonii[1]
Legionella drancourtii[1]
Legionella dresdenensis[1]
Legionella drozanskii[1]
Legionella dumoffii[1]
Legionella erythra[1]
Legionella fairfieldensis[1]
Legionella fallonii[1]
Legionella feeleii[1]
Legionella geestiana[1]
Legionella genomospecies 1
Legionella gormanii[1]
Legionella gratiana[1]
Legionella gresilensis[1]
Legionella hackeliae[1]
Legionella impletisoli[1]
Legionella israelensis[1]
Legionella jamestowniensis[1]
Candidatus Legionella jeonii
 Legionella jordanis[1]
Legionella lansingensis[1]
Legionella londiniensis[1]
Legionella longbeachae[1]
Legionella lytica[1]
Legionella maceachernii[1]
Legionella massiliensis[1]
Legionella micdadei[1]
Legionella monrovica[1]
Legionella moravica[1]
Legionella nagasakiensis[1]
Legionella nautarum[1]
Legionella norrlandica[1]
Legionella oakridgensis[1]
Legionella parisiensis[1]
Legionella pittsburghensis[1]
Legionella pneumophila[1]
Legionella quateirensis[1]
Legionella quinlivanii[1]
Legionella rowbothamii[1]
Legionella rubrilucens[1]
Legionella sainthelensi[1]
Legionella santicrucis[1]
Legionella shakespearei[1]
Legionella spiritensis[1]
Legionella steelei[1]
Legionella steigerwaltii[1]
Legionella saoudiensis[1]
Legionella taurinensis[1]
Legionella thermalis[1]
Legionella tucsonensis[1]
Legionella tunisiensis[1]
Legionella wadsworthii[1]
Legionella waltersii[1]
Legionella worsleiensis[1]
Legionella yabuuchiae[1]

Legionella may be visualized with a silver stain or cultured in cysteine-containing media such as buffered charcoal yeast extract agar. It is common in many environments, including soil and aquatic systems, with at least 50 species and 70 serogroups identified. These bacteria, however, are not transmissible from person to person;[4] furthermore, most people exposed to the bacteria do not become ill.[5] Most outbreaks are traced to poorly maintained cooling towers.

The side chains of the cell wall carry the bases responsible for the somatic antigen specificity of these organisms. The chemical composition of these side chains both with respect to components and arrangement of the different sugars determines the nature of the somatic or O antigen determinants, which are essential means of serologically classifying many Gram-negative bacteria.

Legionella acquired its name after an outbreak of a then-unknown "mystery disease" sickened 221 persons, causing 34 deaths. The outbreak was first noticed among people attending a convention of the American Legion—an association of U.S. military veterans. The convention occurred in Philadelphia during the U.S. Bicentennial year in July 21–24, 1976. This epidemic among U.S. war veterans, occurring in the same city as—and within days of the 200th anniversary of—the signing of the Declaration of Independence, was widely publicized and caused great concern in the United States.[6] On January 18, 1977, the causative agent was identified as a previously unknown bacterium subsequently named Legionella.

Detection

Legionella is traditionally detected by culture on buffered charcoal yeast extract agar. Legionella requires the presence of cysteine and iron to grow, so does not grow on common blood agar media used for laboratory-based total viable counts or on-site dipslides. Common laboratory procedures for the detection of Legionella in water[7] concentrate the bacteria (by centrifugation and/or filtration through 0.2-μm filters) before inoculation onto a charcoal yeast extract agar containing selective agents (e.g. glycine, vancomycin, polymixin, cyclohexamide, GVPC) to suppress other flora in the sample. Heat or acid treatment are also used to reduce interference from other microbes in the sample.

After incubation for up to 10 days, suspect colonies are confirmed as Legionella if they grow on buffered charcoal yeast extract agar containing cysteine, but not on agar without cysteine added. Immunological techniques are then commonly used to determine the species and/or serogroups of bacteria present in the sample.

Although the plating method is quite specific for most species of Legionella, one study has shown that a coculture method that accounts for the close relationship with amoebae may be more sensitive since it can detect the presence of the bacteria even when masked by their presence inside the amoeba.[8] Consequently, the clinical and environmental prevalence of the bacteria is likely to be underestimated due to the current lab methodology.

Many hospitals use the Legionella urinary antigen test for initial detection when Legionella pneumonia is suspected. Some of the advantages offered by this test are that the results can be obtained in hours rather than the several days required for culture, and that a urine specimen is generally more easily obtained than a sputum specimen. Disadvantages are that the urine antigen test only detects antigen of Legionella pneumophila serogroup 1 (LP1); only a culture will detect infection by non-LP1 strains or other Legionella species and that isolates of Legionella are not obtained, which impairs public health investigations of outbreaks.[9]

New techniques for the rapid detection of Legionella in water samples have been developed, including the use of polymerase chain reaction and rapid immunological assays. These technologies can typically provide much faster results.

Government public health surveillance has demonstrated increasing proportions of drinking water–associated outbreaks, specifically in healthcare settings.[10]

Pathogenesis
A Legionella pneumophila bacterium (green) caught by a Vermamoeba vermiformis amoeba (orange)

In the natural environment, Legionella lives within amoebae such as Acanthamoeba spp., Naegleria spp., and Vermamoeba vermiformis, or other protozoa such as Tetrahymena pyriformis.[11]

Upon inhalation, the bacteria can infect alveolar macrophages, where the bacteria can replicate. This results in Legionnaires' disease and the less severe illness Pontiac fever. Legionella transmission is via inhalation of water droplets from a contaminated source that has allowed the organism to grow and spread (e.g., cooling towers). Transmission also occurs less commonly via aspiration of drinking water from an infected source. Person-to-person transmission has not been demonstrated;[4] though, it could be possible in rare cases.[12]

Once inside a host, the incubation period may be up to two weeks. Prodromal symptoms are flu-like, including fever, chills, and dry cough. Advanced stages of the disease cause problems with the gastrointestinal tract and the nervous system and lead to diarrhea and nausea. Other advanced symptoms of pneumonia may also present. However, the disease is generally not a threat to most healthy individuals, and tends to lead to severe symptoms more often in immunocompromised hosts and the elderly. Consequently, the water systems of hospitals and nursing homes should be periodically monitored. The Texas Department of State Health services provides recommendations for hospitals to detect and prevent the spread of hospital-acquired disease due to Legionella infection.[13] According to Infection Control and Hospital Epidemiology, hospital-acquired Legionella pneumonia has a fatality rate of 28%, and the source is the water distribution system.[14]

Legionella species typically exist in nature at low concentrations, in groundwater, lakes, and streams. They reproduce after entering man-made equipment, given the right environmental conditions. In the United States, the disease affects between 8,000 and 18,000 individuals a year.[15]

Sources of Legionella

Documented sources include cooling towers,[16] swimming pools (especially in Scandinavian countries), domestic water systems and showers, ice-making machines,[17] refrigerated cabinets, whirlpool spas,[18][19] hot springs,[20] fountains,[21] dental equipment,[22] soil,[23] automobile windshield washer fluid,[24] industrial coolant,[25] and waste water treatment plants.

Airborne transmission from cooling towers

The largest[26] and most common source of Legionnaires' disease outbreaks are cooling towers (heat rejection equipment used in air conditioning and industrial cooling water systems) primarily because of the risk for widespread circulation. Many governmental agencies, cooling tower manufacturers, and industrial trade organisations have developed design and maintenance guidelines for controlling the growth and proliferation of Legionella within cooling towers.

Research in the Journal of Infectious Diseases (2006) provided evidence that L. pneumophila, the causative agent of Legionnaires' disease, can travel at least 6 km from its source by airborne spread. It was previously believed that transmission of the bacterium was restricted to much shorter distances. A team of French scientists reviewed the details of an epidemic of Legionnaires' disease that took place in Pas-de-Calais, northern France, in 2003–2004. Of 86 confirmed cases during the outbreak, 18 resulted in death. The source of infection was identified as a cooling tower in a petrochemical plant, and an analysis of those affected in the outbreak revealed that some infected people lived as far as 6–7 km from the plant.[27]

Vaccine research

No vaccine is available for legionellosis. Vaccination studies using heat-killed or acetone-killed cells have been carried out in guinea pigs, which were then given Legionella intraperitoneally or by aerosol. Both vaccines were shown to give moderately high levels of protection. Protection was dose-dependent and correlated with antibody levels as measured by enzyme-linked immunosorbent assay to an outer membrane antigen and by indirect immunofluorescence to heat-killed cells. However, a licensed vaccine for people in the US is most probably still many years away.

Molecular biology

Legionella has been discovered to be a genetically diverse species with 7-11% of genes strain-specific. The molecular function of some of the proven virulence factors of Legionella have been discovered.[28]

Legionella control

Control of Legionella growth can occur through chemical, thermal or ultraviolet treatment methods.

Heat

The more expensive option is temperature control—i.e., keeping all cold water below 25 °C (77 °F) and all hot water above 51 °C (124 °F). The high cost incurred with this method arises from the extensive retrofitting required for existing complex distribution systems in large facilities and the energy cost of chilling or heating the water and maintaining the required temperatures at all times and at all distal points within the system.

Temperature affects the survival of Legionella as follows:[3]

  • Above 70 °C (158 °F) – Legionella dies almost instantly
  • At 60 °C (140 °F) – 90% die in 2 minutes (Decimal reduction time (D) = 2 minutes)
  • At 50 °C (122 °F) – 90% die in 80–124 minutes, depending on strain (D = 80–124 minutes)
  • 48 to 50 °C (118 to 122 °F) – can survive but do not multiply
  • 32 to 42 °C (90 to 108 °F) – ideal growth range
  • 25 to 45 °C (77 to 113 °F) – growth range
  • Below 20 °C (68 °F) – can survive, even below freezing, but are dormant

Other temperature sensitivity[29][30]

  • 60 to 70 °C (140 to 158 °F) to 80 °C (176 °F) – Disinfection range
  • 66 °C (151 °F) – Legionella dies within 2 minutes
  • 60 °C (140 °F) – Legionella dies within 32 minutes
  • 55 °C (131 °F) – Legionella dies within 5 to 6 hours

Water can be monitored in real-time with sensors.

Chlorine

A very effective chemical treatment is chlorine. For systems with marginal issues, chlorine provides effective results at 0.5 ppm residual in the hot water system. For systems with significant Legionella problems, temporary shock chlorination—where levels are raised to higher than 2 ppm for a period of 24 hours or more and then returned to 0.5 ppm—may be effective. Hyperchlorination can also be used where the water system is taken out of service and the chlorine residual is raised to 50 ppm or higher at all distal points for 24 hours or more. The system is then flushed and returned to 0.5 ppm chlorine prior to being placed back into service. These high levels of chlorine penetrate biofilm, killing both the Legionella bacteria and the host organisms. Annual hyperchlorination can be an effective part of a comprehensive Legionella preventive action plan.[31]

Copper-silver ionization

Industrial-sized copper-silver ionization is recognized by the U.S. Environmental Protection Agency and WHO for Legionella control and prevention. Copper and silver ion concentrations must be maintained at optimal levels, taking into account both water flow and overall water usage, to control Legionella. The disinfection function within all of a facility's water distribution network occurs within 30 to 45 days. Key engineering features such as 10 amps per ion chamber cell and automated variable voltage outputs having no less than 100 VDC are but a few of the required features for proper Legionella control and prevention, using a specific, nonreferenced copper-silver system. Swimming pool ion generators are not designed for potable water treatment.

Questions remain whether the silver and copper ion concentrations required for effective control of symbiotic hosts could exceed those allowed under the U.S. Safe Drinking Water Act's Lead and Copper Rule. In any case, any facility or public water system using copper-silver for disinfection should monitor its copper and silver ion concentrations to ensure they are within intended levels – both minimum and maximum. Further, no current standards for silver in the EU and other regions allow use of this technology.

Copper-silver ionization is an effective process to control Legionella in potable water distribution systems found in health facilities, hotels, nursing homes, and most large buildings. However, it is not intended for cooling towers because of pH levels greater than 8.6, that cause ionic copper to precipitate. Furthermore, tolytriazole, a common additive in cooling water treatment, could bind the copper making it ineffective. Ionization became the first such hospital disinfection process to have fulfilled a proposed four-step modality evaluation; by then, it had been adopted by over 100 hospitals.[32] Additional studies indicate ionization is superior to thermal eradication.[33]

Chlorine dioxide

Chlorine dioxide has been approved by the U.S. Environmental Protection Agency as a primary disinfectant of potable water since 1945. Chlorine dioxide does not produce any carcinogenic byproducts like chlorine when used in the purification of drinking water that contains natural organic compounds such as humic and fulvic acids; chlorine tends to form halogenated disinfection byproducts such as trihalomethanes. Drinking water containing such disinfection byproducts has been shown to increase the risk of cancer. ClO2 works differently from chlorine; its action is one of pure oxidation rather than halogenation, so these halogenated byproducts are not formed.[34] Chlorine dioxide is not a restricted heavy metal like copper. It has proven excellent control of Legionella in cold and hot water systems and its ability as a biocide is not affected by pH, or any water corrosion inhibitors such as silica or phosphate. However, it is 'quenched' by metal oxides, especially manganese and iron. Metal oxide concentrations above 0.5 mg/l may inhibit its activity. Monochloramine is an alternative. Like chlorine and chlorine dioxide, monochloramine is approved by the Environmental Protection Agency as a primary potable water disinfectant. Environmental Protection Agency registration requires a biocide label which lists toxicity and other data required for all registered biocides. If the product is being sold as a biocide, then the manufacturer is legally required to supply a biocide label, and the purchaser is legally required to apply the biocide per the biocide label. When first applied to a system, chlorine dioxide can be added at disinfection levels of 2 ppm for 6 hours to clean up a system. This will not remove all biofilm, but will effectively remediate the system of Legionella.

Moist heat sterilization

Moist heat sterilization (superheating to 140 °F (60 °C) and flushing) is a nonchemical treatment that typically must be repeated every 3–5 weeks.

Ultraviolet

Ultraviolet light, in the range of 200 to 300 nm, can inactivate Legionella. According to a review by the US EPA,[35] three-log (99.9%) inactivation can be achieved with a dose of less than 7 mJ/cm2.

European standards

Several European countries established the European Working Group for Legionella Infections[36] to share knowledge and experience about monitoring potential sources of Legionella. The working group has published guidelines about the actions to be taken to limit the number of colony-forming units (that is, live bacteria that are able to multiply) of Legionella per litre:

Legionella bacteria CFU/litreAction required (35 samples per facility are required, including 20 water and 10 swabs)
1000 or lessSystem under control
more than 1000
up to 10,000		Review program operation: The count should be confirmed by immediate resampling. If a similar count is found again, a review of the control measures and risk assessment should be carried out to identify any remedial actions.
more than 10,000Implement corrective action: The system should immediately be resampled. It should then be "shot dosed" with an appropriate biocide, as a precaution. The risk assessment and control measures should be reviewed to identify remedial actions. (150+ CFU/ml in healthcare facilities or nursing homes require immediate action.)

Monitoring guidelines are stated in Approved Code of Practice L8 in the UK. These are not mandatory, but are widely regarded as so. An employer or property owner must follow an Approved Code of Practice, or achieve the same result. Failure to show monitoring records to at least this standard has resulted in several high-profile prosecutions, e.g. Nalco + Bulmers – neither could prove a sufficient scheme to be in place whilst investigating an outbreak, therefore both were fined about £300,000GBP. Important case law in this area is R v Trustees of the Science Museum 3 All ER 853, (1993) 1 WLR 1171[37]

Employers and those responsible for premises within the UK are required under Control of Substances Hazardous to Health to undertake an assessment of the risks arising from Legionella. This risk assessment may be very simple for low risk premises, however for larger or higher risk properties may include a narrative of the site, asset register, simplified schematic drawings, recommendations on compliance, and a proposed monitoring scheme.[38]

The L8 Approved Code of Practice recommends that the risk assessment should be reviewed at least every 2 years and whenever a reason exists to suspect it is no longer valid, such as water systems have been amended or modified, or if the use of the water system has changed, or if there is reason to suspect that Legionella control measures are no longer working.

Weaponization

Legionella could be used as a weapon, and indeed genetic modification of L. pneumophila has been shown where the mortality rate in infected animals can be increased to nearly 100%.[39][40][41] A former Soviet bioengineer, Sergei Popov, stated in 2000 that his team experimented with genetically enhanced bioweapons, including Legionella.[41] Popov worked as a lead researcher at the Vector Institute from 1976 to 1986, then at Obolensk until 1992, when he defected to the West. He later divulged much of the Soviet biological weapons program and settled in the United States.

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See also

References
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