Legionella

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Legionella
Legionella Plate 01.png
Legionella sp. under UV light
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Bacteria
Phylum: Pseudomonadota
Class: Gammaproteobacteria
Order: Legionellales
Family: Legionellaceae
Brenner et al. 1979
Genus: Legionella
Brenner et al. 1979
Species

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]

Contents

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 in 1976 of a then-unknown "mystery disease" made 221 people sick and caused 34 deaths. The outbreak was first noticed among attendees at a convention of the American Legion—an association of U.S. military veterans. The convention occurred in Philadelphia during the U.S. Bicentennial year on 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. It 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. [8]

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. [4]

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 amoebae. [9] Consequently, the clinical and environmental prevalences of the bacteria are likely to be underestimated due to the current laboratory methodology.[ citation needed ]

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. [10]

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. [11]

Government public-health surveillance has demonstrated increasing proportions of drinking water–associated outbreaks, specifically in healthcare settings. [12]

Analyses of genome sequences from Legionellales have identified 24 conserved signature indels (CSIs) in diverse proteins including 30S ribosomal protein S8, periplasmic serine endoprotease DegP precursor, DNA polymerase I, and ABC transporter permease, etc. that are specifically present in different species from the genus Legionella. [13] These molecular signatures provide novel and reliable means for distinguishing members of the genus Legionella from all other bacteria and for their diagnostics.[ citation needed ]

Pathogenesis

A Legionella pneumophila bacterium (green) caught by a Vermamoeba vermiformis amoeba (orange) Harmannella entrapping Legionella.png
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., Vermamoeba spp., or other protozoa such as Tetrahymena pyriformis . [14]

Upon inhalation, the bacteria can infect alveolar macrophages, where they 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. [15]

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. [16] 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. [17]

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. [18] In the United States, the disease affects between 8,000 and 18,000 individuals a year. [19]

Sources

Documented sources include cooling towers, [20] swimming pools (especially in Scandinavian countries), domestic water systems and showers, ice-making machines, [21] refrigerated cabinets, whirlpool spas, [22] [23] hot springs, [24] fountains, [25] dental equipment, [26] soil, [27] automobile windshield washer fluid, [28] industrial coolant, [29] and waste water treatment plants.

Airborne transmission

The largest [30] and one of the 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. [31] [32]

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. [33]

Because of these risks, a UK legal mandate requires owners to notify the local authorities of any cooling towers a company operates. [34]

Recreational exposure

As outlined above, cooling towers are well established as sources of Legionella that may have an effect on community exposure to the bacterium and Legionnaires' disease epidemics. [35] In addition to cooling towers, use of swimming pools, spa pools, and other recreational water bodies has also been shown to increase risk of exposure to Legionella, though this differs by species of Legionella. [36] In a review of disease caused by recreational exposure to Legionella, most exposures occurred in spas or pools used by the public (hotels or recreational centers) or in natural settings (hot springs or thermal water). [36]

Hotels and other tourist destinations have contributed to Legionella exposure. [37] Relative danger at commonly used facilities with heating and cooling water systems depends on several factors, such as the water source, how much Legionella is present (if there is any), if and how the water system is treated, how people are interacting with this water, and other factors that make the water systems so dynamic. [37]

In addition to tourists and other recreators, gardeners may be at increased risk for exposure to Legionella. [38] In some countries (like Australia), Legionella lives in soil and compost. [38] Warmer temperatures and increased rainfall in some regions of the world due to climate change may impact Legionella in soil, gardeners seasonal exposure to contaminated soil, and complex water systems used by the public. [38]

Not only are Legionella spp. present in man-made water systems and infrastructure, but this bacteria also lives in natural bodies of water, such as lakes and rivers. [36] Weather patterns and other environmental factors may increase risk of Legionella outbreaks; a study in Minnesota, USA, using outbreak information from 2011 to 2018 showed precipitation as having the greatest effect of increasing risk of Legionella exposure when taking into account other environmental factors (temperature, relative humidity, land use and age of infected person). [39] Weather patterns heavily relate to the established infrastructure and water sources, especially in urban settings. In the US, most cases of Legionella infection have occurred in the summertime, though they were likely more associated with rainfall and humidity than summer temperatures. [38] Severe rain patterns can increase risk of water source contamination through flooding and unseasonable rains; therefore, natural disasters, especially those associated with climate change, may increase risk of exposure to Legionella. [38]

Vaccine research

No vaccine is available for legionellosis. [40] [41] 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. [42]

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. [43]

Legionella control

A biomonitoring solution exists in a Legionella-specific aptamer-based assay. Control of Legionella growth can occur through chemical, thermal or ultraviolet treatment methods. [44]

Heat

One option is temperature control—i.e., keeping all cold water below 25 °C (77 °F) and all hot water above 51 °C (124 °F). [3]

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

Other temperature sensitivity [45] [46]

Water temperature can be monitored in real-time with sensors. [47]

Chlorine

A very effective chemical treatment is chlorine. For systems with marginal issues, chlorine provides effective results at >0.5 ppm [48] 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. [49] 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. [50]

Copper-silver ionization

Copper-silver ionization is recognized by the U.S. Environmental Protection Agency and WHO for Legionella control and prevention. [51] [52] 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.[ citation needed ] 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.[ citation needed ]

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.[ citation needed ]

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, tolyltriazole, 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. [53] Additional studies indicate ionization is superior to thermal eradication. [54]

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. [55] 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.[ citation needed ] Monochloramine is an alternative. Like chlorine and chlorine dioxide, monochloramine is approved by the U.S. Environmental Protection Agency as a primary potable water disinfectant. [56] 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.[ citation needed ]

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.[ citation needed ]

Ultraviolet

Ultraviolet light, in the range of 200 to 300 nm, can inactivate Legionella. According to a review by the US EPA, three-log (99.9%) inactivation can be achieved with a dose of less than 7 mJ/cm2. [56]

Biomonitoring

A Legionella-specific aptamer has been discovered [57] and in 2022 was developed into an assay for detecting to a limit of 104.3 cells/mL with no processing steps. [58]

European standards

Several European countries established the European Working Group for Legionella Infections [59] 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 while 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 [60]

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. [61]

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.[ citation needed ]

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%. [62] [63] [64] A former Soviet bioengineer, Sergei Popov, stated in 2000 that his team experimented with genetically enhanced bioweapons, including Legionella. [64] 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.[ citation needed ]

See also

Related Research Articles

Pontiac fever is an acute, nonfatal respiratory disease caused by various species of Gram-negative bacteria in the genus Legionella. It causes a mild upper respiratory infection that resembles acute influenza. Pontiac fever resolves spontaneously and often goes undiagnosed. Both Pontiac fever and the more severe Legionnaire's disease may be caused by the same bacteria, but Pontiac fever does not include pneumonia.

<span class="mw-page-title-main">Chlorine dioxide</span> Chemical compound

Chlorine dioxide is a chemical compound with the formula ClO2 that exists as yellowish-green gas above 11 °C, a reddish-brown liquid between 11 °C and −59 °C, and as bright orange crystals below −59 °C. It is usually handled as an aqueous solution. It is commonly used as a bleach. More recent developments have extended its applications in food processing and as a disinfectant.

<span class="mw-page-title-main">Disinfectant</span> Antimicrobial agent that inactivates or destroys microbes

A disinfectant is a chemical substance or compound used to inactivate or destroy microorganisms on inert surfaces. Disinfection does not necessarily kill all microorganisms, especially resistant bacterial spores; it is less effective than sterilization, which is an extreme physical or chemical process that kills all types of life. Disinfectants are generally distinguished from other antimicrobial agents such as antibiotics, which destroy microorganisms within the body, and antiseptics, which destroy microorganisms on living tissue. Disinfectants are also different from biocides—the latter are intended to destroy all forms of life, not just microorganisms. Disinfectants work by destroying the cell wall of microbes or interfering with their metabolism. It is also a form of decontamination, and can be defined as the process whereby physical or chemical methods are used to reduce the amount of pathogenic microorganisms on a surface.

<span class="mw-page-title-main">Cooling tower</span> Device which rejects waste heat to the atmosphere through the cooling of a water stream

A cooling tower is a device that rejects waste heat to the atmosphere through the cooling of a coolant stream, usually a water stream, to a lower temperature. Cooling towers may either use the evaporation of water to remove heat and cool the working fluid to near the wet-bulb air temperature or, in the case of dry cooling towers, rely solely on air to cool the working fluid to near the dry-bulb air temperature using radiators.

An antimicrobial is an agent that kills microorganisms (microbicide) or stops their growth. Antimicrobial medicines can be grouped according to the microorganisms they act primarily against. For example, antibiotics are used against bacteria, and antifungals are used against fungi. They can also be classified according to their function. The use of antimicrobial medicines to treat infection is known as antimicrobial chemotherapy, while the use of antimicrobial medicines to prevent infection is known as antimicrobial prophylaxis.

<i>Legionella pneumophila</i> Species of bacterium

Legionella pneumophila is an aerobic, pleomorphic, flagellated, non-spore-forming, Gram-negative bacterium of the genus Legionella. L. pneumophila is the primary human pathogenic bacterium in this group. In nature, L. pneumophila infects freshwater and soil amoebae of the genera Acanthamoeba and Naegleria. This pathogen is found commonly near freshwater environments and will then invade the amoebae found in these environments, using them to carry out metabolic functions.

Legionella longbeachae is one species of the family Legionellaceae. It was first isolated from a patient in Long Beach, California. It is found predominantly in potting soil and compost. Human infection from L. longbeachae is particularly common in Australia, but cases have been documented in other countries including the United States, Japan, Greece and the UK.

Infection prevention and control is the discipline concerned with preventing healthcare-associated infections; a practical rather than academic sub-discipline of epidemiology. In Northern Europe, infection prevention and control is expanded from healthcare into a component in public health, known as "infection protection". It is an essential part of the infrastructure of health care. Infection control and hospital epidemiology are akin to public health practice, practiced within the confines of a particular health-care delivery system rather than directed at society as a whole.

<span class="mw-page-title-main">Copper-silver ionization</span>

Copper-silver ionization is a disinfection process, primarily used to control Legionella, the bacteria responsible for Legionnaires' disease. There is strong evidence that treating water supplies in hospitals with this technique decreases the risk.

<span class="mw-page-title-main">1976 Philadelphia Legionnaires' disease outbreak</span> First occasion of a cluster of a pneumonia cases later identified as Legionnaires disease

The 1976 Legionnaires' disease outbreak, occurring in the late summer in Philadelphia, Pennsylvania, United States was the first occasion in which a cluster of a particular type of pneumonia cases were determined to be caused by the Legionella pneumophila bacteria. Previous outbreaks were retroactively diagnosed as being most probably caused by Legionella bacteria.

<span class="mw-page-title-main">1999 Bovenkarspel legionellosis outbreak</span> Outbreak of legionellosis in Bovenkarspel, the Netherlands

The Bovenkarspel legionellosis outbreak began on 25 February 1999 in Bovenkarspel, the Netherlands, and was one of the largest outbreaks of legionellosis in history. With at least 32 dead and 206 severe infections, it was the deadliest legionellosis outbreak since the original 1976 outbreak in Philadelphia, United States.

Legionella anisa is a Gram-negative bacterium, one of more than 40 species in the family Legionellaceae. After Legionella pneumophila, this species has been isolated most frequently from water samples. This species is also one of the several pathogenic forms of Legionella having been associated with rare clinical cases of illness including Pontiac fever and Legionnaires' disease.

Legionella cherrii is an aerobic, flagellated, Gram-negative bacterium from the genus Legionella. It was isolated from a heated water sample in Minnesota. L. cherrii is similar to another Legionella species, L. pneumophila, and is believed to cause major respiratory problems.

Legionella jordanis is a Gram-negative bacterium from the genus Legionella which was isolated from the Jordan River in Bloomington, Indiana and from the sewage in DeKalb County, Georgia. L. jordanis is a rare human pathogen and can cause respiratory tract infections.

<span class="mw-page-title-main">Legionnaires' disease</span> Form of atypical pneumonia

Legionnaires' disease is a form of atypical pneumonia caused by any species of Legionella bacteria, quite often Legionella pneumophila. Signs and symptoms include cough, shortness of breath, high fever, muscle pains, and headaches. Nausea, vomiting, and diarrhea may also occur. This often begins 2–10 days after exposure.

<span class="mw-page-title-main">2015 Bronx Legionnaires' disease outbreaks</span> Disease outbreaks in New York City, United States

In 2015, there were two outbreaks of Legionnaires' disease in the Bronx, New York City, United States. Between January and August 2015, one hundred and thirty people in New York City were infected with Legionnaires', but the majority of them were in the Bronx.

Legionella clemsonensis was isolated in 2006, but was described in 2016 by Clemson University researchers. It is a Gram-negative bacterium.

<span class="mw-page-title-main">2022 Tucumán legionellosis outbreak</span> Disease outbreak in Argentina

The 2022 Tucumán legionellosis outbreak refers to an epidemic that originated in San Miguel de Tucumán, Argentina. It was first identified on Saturday, 20 August 2022, when 7 people arrived at the Tucumán Hospital with fever, malaise, shortness of breath, and headache.

<span class="mw-page-title-main">Symbiosis in Amoebozoa</span>

Amoebozoa of the free living genus Acanthamoeba and the social amoeba genus Dictyostelium are single celled eukaryotic organisms that feed on bacteria, fungi, and algae through phagocytosis, with digestion occurring in phagolysosomes. Amoebozoa are present in most terrestrial ecosystems including soil and freshwater. Amoebozoa contain a vast array of symbionts that range from transient to permanent infections, confer a range of effects from mutualistic to pathogenic, and can act as environmental reservoirs for animal pathogenic bacteria. As single celled phagocytic organisms, amoebas simulate the function and environment of immune cells like macrophages, and as such their interactions with bacteria and other microbes are of great importance in understanding functions of the human immune system, as well as understanding how microbiomes can originate in eukaryotic organisms.

References

  1. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 Parte, A.C. "Legionella". LPSN .
  2. Palmer, Allison; Painter, Joseph; Hassler, Hayley; Richards, Vincent P.; Bruce, Terri; Morrison, Shatavia; Brown, Ellen; Kozak-Muiznieks, Natalia A.; Lucas, Claressa; McNealy, Tamara L. (1 October 2016). "Legionella clemsonensis sp. nov.: a green fluorescing Legionella strain from a patient with pneumonia". Microbiol Immunol. 60 (10): 694–701. doi: 10.1111/1348-0421.12439 . PMID   27619817. S2CID   3331351.
  3. 1 2 3 4 Legionella and the prevention of legionellosis (PDF). World Health Organization. 2007. ISBN   978-9241562973.
  4. 1 2 3 Winn, Washington C. (1996). "Chapter 40: Legionella". In Baron, Samuel (ed.). Medical Microbiology (4th ed.). University of Texas Medical Branch at Galveston. ISBN   0-9631172-1-1.
  5. Kutty, Preeta K. (October 26, 2015). "What Everyone Needs to Know About Legionnaires Disease". Medscape .
  6. Lawrence K. Altman (August 1, 2006). "In Philadelphia 30 Years Ago, an Eruption of Illness and Fear". New York Times.
  7. ISO 11731-2:2004 Water quality – Detection and enumeration of Legionella – Part 2: Direct membrane filtration method for waters with low bacterial counts
  8. Rech, Melanie M.; Swalla, Brian M.; Dobranic, Jason K. (2018-10-01). "Evaluation of Legiolert for Quantification of Legionella pneumophila from Non-potable Water". Current Microbiology. 75 (10): 1282–1289. doi:10.1007/s00284-018-1522-0. ISSN   1432-0991. PMC   6132855 . PMID   29980812.
  9. La Scola B, Mezi L, Weiller PJ, Raoult D (January 2001). "Isolation of Legionella anisa using an amoebic coculture procedure". Journal of Clinical Microbiology. 39 (1): 365–6. doi:10.1128/JCM.39.1.365-366.2001. PMC   87733 . PMID   11136802.
  10. Benin AL, Benson RF, Besser RE (November 2002). "Trends in legionnaires disease, 1980-1998: declining mortality and new patterns of diagnosis". Clinical Infectious Diseases. 35 (9): 1039–46. doi: 10.1086/342903 . PMID   12384836.
  11. "Legionnaires Disease Diagnosis, Treatment, and Prevention". CDC. 2021-03-25. Retrieved 2023-12-04.
  12. Beer, Karlyn D.; Gargano, Julia W.; Roberts, Virginia A.; Hill, Vincent R.; Garrison, Laurel E.; Kutty, Preeta K.; Hilborn, Elizabeth D.; Wade, Timothy J.; Fullerton, Kathleen E.; Yoder, Jonathan S. (August 14, 2015). "Surveillance for Waterborne Disease Outbreaks Associated with Drinking Water — United States, 2011–2012". Morbidity and Mortality Weekly Report. 64 (31): 842–848. doi:10.15585/mmwr.mm6431a2. JSTOR   24856648. PMC   4584589 . PMID   26270059.
  13. Saini, Navneet; Gupta, Radhey S. (July 2021). "A robust phylogenetic framework for members of the order Legionellales and its main genera (Legionella, Aquicella, Coxiella and Rickettsiella) based on phylogenomic analyses and identification of molecular markers demarcating different clades". Antonie van Leeuwenhoek. 114 (7): 957–982. doi:10.1007/s10482-021-01569-9. PMID   33881638. S2CID   233326323.
  14. Swanson MS, Hammer BK (2000). "Legionella pneumophila pathogesesis: a fateful journey from amoebae to macrophages". Annual Review of Microbiology. 54: 567–613. doi:10.1146/annurev.micro.54.1.567. PMID   11018138. S2CID   19944003.
  15. "Legionella - Causes and Transmission - Legionnaires". CDC. 2018-04-30.
  16. "Legionellosis (Legionnaires' Disease) Task Force Recommendations". Texas DSHS. Retrieved 2023-12-04.
  17. Stout JE, Muder RR, Mietzner S, et al. (July 2007). "Role of environmental surveillance in determining the risk of hospital-acquired legionellosis: a national surveillance study with clinical correlations". Infection Control and Hospital Epidemiology. 28 (7): 818–24. doi:10.1086/518754. PMID   17564984. S2CID   13774784.
  18. Oliva, Giulia; Sahr, Tobias; Buchrieser, Carmen (2018-01-19). "The Life Cycle of L. pneumophila: Cellular Differentiation Is Linked to Virulence and Metabolism". Frontiers in Cellular and Infection Microbiology. 8: 3. doi: 10.3389/fcimb.2018.00003 . ISSN   2235-2988. PMC   5780407 . PMID   29404281.
  19. "Legionella (Legionnaires' Disease and Pontiac Fever)". CDC. June 1, 2017. Retrieved June 16, 2017.
  20. Osawa K, Shigemura K, Abe Y, et al. (January 2014). "A case of nosocomial Legionella pneumonia associated with a contaminated hospital cooling tower". Journal of Infection and Chemotherapy. 20 (1): 68–70. doi:10.1016/j.jiac.2013.07.007. PMID   24462430.
  21. Graman PS, Quinlan GA, Rank JA (September 1997). "Nosocomial legionellosis traced to a contaminated ice machine". Infection Control and Hospital Epidemiology. 18 (9): 637–40. doi:10.2307/30141491. JSTOR   30141491. PMID   9309436. S2CID   32896608.
  22. Coetzee N, Duggal H, Hawker J, et al. (2012). "An outbreak of Legionnaires' disease associated with a display spa pool in retail premises, Stoke-on-Trent, United Kingdom, July 2012". Euro Surveillance. 17 (37). doi: 10.2807/ese.17.37.20271-en . PMID   22995431.
  23. Campese C, Roche D, Clément C, et al. (July 2010). "Cluster of Legionnaires' disease associated with a public whirlpool spa, France, April-May 2010". Euro Surveillance. 15 (26). doi: 10.2807/ese.15.26.19602-en . PMID   20619131.
  24. Kurosawa H, Fujita M, Kobatake S, et al. (January 2010). "A case of Legionella pneumonia linked to a hot spring facility in Gunma Prefecture, Japan". Japanese Journal of Infectious Diseases. 63 (1): 78–9. doi: 10.7883/yoken.63.78 . PMID   20093771. S2CID   43919158.
  25. Palmore TN, Stock F, White M, et al. (August 2009). "A cluster of cases of nosocomial legionnaires disease linked to a contaminated hospital decorative water fountain". Infection Control and Hospital Epidemiology. 30 (8): 764–8. doi:10.1086/598855. PMC   2886954 . PMID   19580436.
  26. Kadaifciler DG, Cotuk A (June 2014). "Microbial contamination of dental unit waterlines and effect on quality of indoor air". Environmental Monitoring and Assessment. 186 (6): 3431–44. Bibcode:2014EMnAs.186.3431K. doi:10.1007/s10661-014-3628-6. PMID   24469014. S2CID   207135938.
  27. Infection Due to Legionella Species Other Than L. pneumophila Barry S. Fields*, Robert F. Benson, and Richard E. Besser https://academic.oup.com/cid/article/35/8/990/330989
  28. American Society for Microbiology, Windshield washer fluid a source of Legionnaires: Found in most school buses
  29. RR910 - Survival of Legionella pneumophila in metalworking fluids https://www.hse.gov.uk/research/rrhtm/rr910.htm
  30. García-Fulgueiras, Ana; Navarro, Carmen; Fenoll, Daniel; et al. (August 2003). "Legionnaires' Disease Outbreak in Murcia, Spain". Emerging Infectious Diseases. 9 (8): 915–921. doi:10.3201/eid0908.030337. PMC   3020623 . PMID   12967487.
  31. Geary, David F. (2001). "American Society of Heating, Refrigerating and Air-conditioning Engineers Guideline 12-2000: Minimizing the Risk of Legionellosis Associated with Building Water Systems". In Marre, Reinhard; Abu Kwaik, Yousef; Bartlett, Christopher; Cianciotto, Nicholas P.; Fields, Barry S.; Frosch, Matthias; Hacker, Jörg; Lück, Paul Christian (eds.). Legionella. pp. 376–384. doi:10.1128/9781555817985.ch77. ISBN   9781683672357.
  32. "Controlling Legionella in Cooling Towers". CDC. 2021-02-03. Retrieved 2023-12-04.
  33. Nguyen TM, Ilef D, Jarraud S, et al. (January 2006). "A community-wide outbreak of legionnaires disease linked to industrial cooling towers--how far can contaminated aerosols spread?". The Journal of Infectious Diseases. 193 (1): 102–11. doi: 10.1086/498575 . PMID   16323138.
  34. Cooling Tower Notification
  35. García-Fulgueiras, Ana; Navarro, Carmen; Fenoll, Daniel; García, José; González-Diego, Paulino; Jiménez-Buñuales, Teresa; Rodriguez, Miguel; Lopez, Rosa; Pacheco, Francisco; Ruiz, Joaquín; Segovia, Manuel (August 2003). "Legionnaires' Disease Outbreak in Murcia, Spain". Emerging Infectious Diseases. 9 (8): 915–921. doi:10.3201/eid0908.030337. PMC   3020623 . PMID   12967487.
  36. 1 2 3 Leoni, Erica; Catalani, Federica; Marini, Sofia; Dallolio, Laura (2018-07-30). "Legionellosis Associated with Recreational Waters: A Systematic Review of Cases and Outbreaks in Swimming Pools, Spa Pools, and Similar Environments". International Journal of Environmental Research and Public Health. 15 (8): 1612. doi: 10.3390/ijerph15081612 . PMC   6121464 . PMID   30061526.
  37. 1 2 De Giglio, Osvalda; Napoli, Christian; Diella, Giusy; Fasano, Fabrizio; Lopuzzo, Marco; Apollonio, Francesca; D'Ambrosio, Marilena; Campanale, Carmen; Triggiano, Francesco; Caggiano, Giuseppina; Montagna, Maria Teresa (November 2021). "Integrated approach for legionellosis risk analysis in touristic-recreational facilities". Environmental Research. 202: 111649. Bibcode:2021ER....202k1649D. doi: 10.1016/j.envres.2021.111649 . hdl: 11573/1561995 . PMID   34252427.
  38. 1 2 3 4 5 Walker, Jt (September 2018). "The influence of climate change on waterborne disease and Legionella: a review". Perspectives in Public Health. 138 (5): 282–286. doi:10.1177/1757913918791198. PMID   30156484. S2CID   52115812.
  39. Passer, J. K.; Danila, R. N.; Laine, E. S.; Como-Sabetti, K. J.; Tang, W.; Searle, K. M. (2020). "The association between sporadic Legionnaires' disease and weather and environmental factors, Minnesota, 2011–2018". Epidemiology and Infection. 148: e156. doi:10.1017/S0950268820001417. PMC   7378963 . PMID   32594925.
  40. "Legionellosis". WHO. 2022-09-06. Retrieved 2023-12-04.
  41. Khan, Md Tahsin; Mahmud, Araf; Hasan, Mahmudul; Azim, Kazi Faizul; Begum, Musammat Kulsuma; Rolin, Mohimenul Haque; Akter, Arzuba; Mondal, Shakhinur Islam (2022-08-31). Faucher, Sébastien P. (ed.). "Proteome Exploration of Legionella pneumophila To Identify Novel Therapeutics: a Hierarchical Subtractive Genomics and Reverse Vaccinology Approach". Microbiology Spectrum. 10 (4): e0037322. doi:10.1128/spectrum.00373-22. ISSN   2165-0497. PMC   9430848 . PMID   35863001.
  42. Eisenstein, T. K.; Tamada, R.; Meissler, J.; Flesher, A.; Oels, H. C. (1984). "Vaccination against Legionella pneumophila: serum antibody correlates with protection induced by heat-killed or acetone-killed cells against intraperitoneal but not aerosol infection in guinea pigs". Infection and Immunity. 45 (3): 685–691. doi:10.1128/iai.45.3.685-691.1984. ISSN   0019-9567. PMC   263350 . PMID   6469355.
  43. Raychaudhury S, Farelli JD, Montminy TP, et al. (April 2009). "Structure and function of interacting IcmR-IcmQ domains from a type IVb secretion system in Legionella pneumophila". Structure. 17 (4): 590–601. doi:10.1016/j.str.2009.02.011. PMC   2693034 . PMID   19368892.
  44. National Academies of Sciences, Engineering, and Medicine (2019). "Strategies for Legionella Control and Their Application in Building Water Systems". Management of Legionella in Water Systems. Washington DC, US: National Academies Press. ISBN   978-0-309-49947-7.
  45. "Safe Hot Water Temperature" (PDF). Chartered Institute of Plumbing and Heating Engineering. Archived from the original (PDF) on 2011-06-26.
  46. "Employers Guide to the control of Legionella" (PDF). Health and Safety Executive. Archived from the original (PDF) on 11 June 2008. Retrieved 14 July 2019.
  47. Whiley, Harriet; Hinds, Jason; Xi, James; Bentham, Richard (2019). "Real-Time Continuous Surveillance of Temperature and Flow Events Presents a Novel Monitoring Approach for Hospital and Healthcare Water Distribution Systems". International Journal of Environmental Research and Public Health. 16 (8): 1332. doi: 10.3390/ijerph16081332 . ISSN   1661-7827. PMC   6518245 . PMID   31013887.
  48. "HSG274 Part 1 Legionnaires' disease: Technical guidance" (PDF). legionellacontrol.com. Health and Safety Executive - UK. 2013. Retrieved 2023-02-06.
  49. "Guidelines for Environmental Infection Control in Health-Care Facilities". CDC. 2003. Retrieved 2023-12-04.
  50. Reiff, Fred (22 January 2010). "Legionella Control in Institutional Water Systems". Water Quality and Health Council. Retrieved 18 January 2017.
  51. Fewtrell, Lorna; Bevan, Ruth (2018). Silver as a drinking-water disinfectant (PDF). World Health Organization. ISBN   978-92-4-151369-2 . Retrieved 2023-12-04.
  52. Office of Water (2001). "Legionella: Drinking Water Health Advisory" (PDF). US Environmental Protection Agency. EPA-822-B-01-005. Retrieved 2023-12-04.
  53. Stout, Janet E.; Yu, Victor L. (August 2003). "Experiences of the First 16 Hospitals Using Copper-Silver Ionization for Legionella Control: Implications for the Evaluation of Other Disinfection Modalities". Infection Control & Hospital Epidemiology. 24 (8): 563–568. doi:10.1086/502251. PMID   12940575. (1) Demonstrated efficacy of Legionella eradication in vitro using laboratory assays, (2) anecdotal experiences in preventing legionnaires' disease in individual hospitals, (3) controlled studies in individual hospitals, and (4) validation in confirmatory reports from multiple hospitals during a prolonged time.
  54. Block, Seymour Stanton (2001). Disinfection, Sterilization, and Preservation (5th ed.). Lippincott Williams & Wilkins. pp. 423–424. ISBN   978-0-683-30740-5 . Retrieved 2009-03-02.
  55. . Chlorine dioxide residues of health concern in potable water are chlorates and chlorites. Regulatory authorities recommend routine monitoring of chlorate and chlorite residuals in potable water systems <World Health Organisation, Drinking Water Quality Guidelines>. Legionella Control With Chlorine Dioxide. Retrieved from https://feedwater.co.uk/legionella-control-services/
  56. 1 2 "Technologies for Legionella Control in Premise Plumbing Systems: Scientific Literature Review" (PDF). EPA. 2016. p. 60.
  57. Saad, Mariam; Chinerman, Deanna; Tabrizian, Maryam; Faucher, Sebastien (2020). "Identification of two aptamers binding to Legionella pneumophila with high affinity and specificity". Scientific Reports. 10 (1): 9145. Bibcode:2020NatSR..10.9145S. doi:10.1038/s41598-020-65973-3. PMC   7272621 . PMID   32499557.
  58. Saad, Mariam; Castiello, F. Rafael; Sebastien, Faucher; Tabrizian, Maryam (15 January 2022). "Introducing an SPRi-based titration assay using aptamers for the detection of Legionella pneumophila". Sensors and Actuators B: Chemical. 351: 130933. doi:10.1016/j.snb.2021.130933. S2CID   244584437 . Retrieved 2 July 2022.
  59. "European Working Group for Legionella Infections". Archived from the original on 2012-12-25. Retrieved 2006-07-07.
  60. Whittaker, Howard. "The Law & Legionella (& HSE's Enforcement strategy)" (PDF).
  61. "Legionnaires' disease - What you must do". Health and Safety Executive. Retrieved 2023-05-17.
  62. Bhargava, Pushpa M. (December 1, 2008). "The Growing Planetary Threat From Biological Weapons and Terrorism". aina.org. Assyrian International News Agency. Retrieved June 16, 2017.
  63. Gilsdorf JR, Zilinskas RA (April 2005). "New considerations in infectious disease outbreaks: the threat of genetically modified microbes". Clinical Infectious Diseases. 40 (8): 1160–5. doi: 10.1086/428843 . JSTOR   4463254. PMID   15791517.
  64. 1 2 "Interview—Serguei Popov". November 1, 2000. Archived from the original on September 27, 2011. Retrieved June 16, 2017.