guidelines for the microbiological assessment of water
TRANSCRIPT
Contents
INTRODUCTION 1
MORE INFORMATION 2
ACRONYMS 2
AQUATIC FACILITIES 3
Swimming Pools 3
Spas 4
Hydrotherapy pools 5
Floatation Tanks 6
BIOSOLIDS 7
DRINKING WATER 8
FOOD BUSINESS WATER SUPPLY 9
NATURAL WATERS 10
POULTRY PROCESSING WATER 12
RECYCLED WATERS 13
General 13
Wash down facilities 15
SHELLFISH HARVESTING WATERS 16
WASTEWATER 17
LEGIONNAIRES DISEASE 19
Cooling towers and Air Conditioners 19
General 19
OTHER SAMPLE TYPES 21
HUMAN SAMPLES 21
MOORE SWABS 21
STANDARDS REFERENCE LIST 22
GUIDELINES REFERENCE LIST 23
APPENDICES 24
Appendix A – PathWest Waters examination laboratory request form 25
Page 1
INTRODUCTION These guidelines collate and standardise PathWest’s microbiological analysis methods as part of the sampling, testing and analysis agreement between Western Australian Local Governments and the Department of Health. This document is not intended for public release.
The samples covered by this document include and are limited to:
Aquatic Facilities
Biosolids
Drinking Water
Food business water supply
Natural Waters
Poultry Processing Water
Recycled Water
Shellfish Harvesting Waters
Wastewater
Legionnaires’ disease
Other sample types
o Human Samples
o Moore Swabs
All samples are to be submitted to PathWest with the ‘PathWest Waters Examination Laboratory (WEL) Request Form’ (shown in Appendix A). How to fill out the WEL Request Form for each sample type to ensure correct testing and analysis is discussed in each section.
This document relates to and should be read in conjunction with:
Site Code Identification System for Water and Allied Samples (Department of
Health, 2015)
Standard drinking water sampling procedure – microbiological (Department of
Health, 2015a)
Recycled Water Sampling Technique (Department of Health, 2013a)
Page 2
MORE INFORMATION More information is available from:
Water Unit Environmental Health Directorate Department of Health PO Box 8172 PERTH BUSINESS CENTRE WA 684 Telephone: (08) 9388 4999 Facsimile: (08) 9388 4955
ACRONYMS
Abbreviation Definition
ADWG Australian Drinking Water Guidelines
APHA American Public Health Association
AS Australian Standard
AS/NZS Australian and New Zealand Standard
AWQC Australian Water Quality Centre
CFU Colony Forming Units
DoH Western Australian Department of Health
mL millilitre
MPN Most Probable Number
NATA National Association of Testing Authorities
NHMRC National Health and Medical Research Council
PFU Plaque Forming Units
WEL Waters Examination Laboratory
WHO World Health Organization
Page 3
AQUATIC FACILITIES Testing required has been determined from the Code of practice for the design, construction, operations, management and maintenance of aquatic facilities (Department of Health, 2013). The code of practice is informed by AS 2610.1-2007 Spa Pools Part 1: Public Spas (Standards Australia, 2007) and AS 3979-2006 Hydrotherapy Pools (Standards Australia, 2006).
The testing category for all aquatic facilities on the WEL Request Form is ‘Pools, Spas, Hydros, Float tanks (Aquatic Amenities)’.
Swimming Pools
A swimming pool is defined as a man-made structure capable of being filled with water, and intended to be used for swimming, diving, wading or paddling, that cannot be emptied by a simple overturning of the structure. The definition does not include individual therapeutic tubs or baths used for cleaning of the body (Department of Health, 2013).
The Swimming Pool testing suite is shown in Table 1. For testing to be done as a pool, the category on the WEL Request Form is ‘Pools, Spas, Hydros, Float tanks’ and the sample description must include the word ‘Pool’. If the water temperature at the time of testing is greater than or equal to 32°C, the sample will be tested as a spa rather than a pool.
TABLE 1 TESTING REQUIREMENTS FOR POOLS (TEMPERATURE LESS THAN 32°C.)
Organism
Guideline Value Code Of Practice (DoH 2013)
PathWest Testing Method
Testing Standard
Units Minimum sample volume
Limit of Detection
Escherichia coli
<1 CFU/100 mL Membrane Filtration
AS/NZS 4276.7(2007)
CFU/100 mL 100mL <1 CFU/100 mL
Thermophilic Amoebae
Not Detected Culture/ Microscopy
AWQC South Australia (1992)
/250 mL
250 mL (total) requires separate bottle
Detected/ Not Detected/ 250 mL
Thermophilic Naegleria
Not Detected Culture/ Microscopy
AWQC South Australia (1992)
/250 mL As above Detected/ Not Detected/ 250 mL
Naegleria fowleri
Not Detected PCR In –House (NATA accredited)
/sample As above Detected/ Not Detected
Note: If Acanthamoeba is observed microscopically a comment is added stating ‘Acanthamoeba spp. Detected’.
Page 4
Spas
A spa is defined as a man-made pool or other water-retaining structure designed for human use, which has a capacity of not less than 680 litres, which may or may not be heated. It incorporates, or is connected to, equipment for heating the water contained in it and injecting air bubbles or jets of water under pressure, so as to cause general turbulence in the water (Department of Health, 2013).
The Spa testing suite is shown in Table 2. For testing to be done as a spa, the category on the WEL Request Form is ‘Pools, Spas, Hydros, Float tanks’ and the sample description must include the word ‘Spa’.
It should be noted that any sample with the sample description containing the word ‘Spa’ will be tested as a spa regardless of temperature; in addition, if the sample description contains the word ‘Pool’ but the water temperature is greater than or equal to 32°C then the sample will be tested as a spa.
TABLE 2 TESTING REQUIREMENTS FOR SPAS
Organism
Guideline Value Code Of Practice (DoH 2013)
PathWest Testing Method
Testing Standard
Units Minimum sample volume
Limit of Detection
Escherichia coli < 1 CFU/100 mL Membrane Filtration
AS/NZS 4276.7 (2007)
CFU/100 mL 100 mL <1 CFU/100 mL
Presumptive Pseudomonas aeruginosa
Not detected in 100 mL of pool water
Membrane Filtration
AS/NZS 4276.13 (2008)
CFU/100 mL 100 mL <1 CFU/100 mL
Thermophilic Amoebae
Not Detected Culture /Microscopy
AWQC South Australia (1992)
/250 mL
250 mL (total) Requires Separate bottle
Detected/ Not Detected/ 250 mL
Thermophilic Naegleria
Not Detected Culture /Microscopy
AWQC South Australia (1992)
/250 mL As above Detected/ Not Detected/ 250 mL
Naegleria fowleri
Not Detected PCR In-House (NATA accredited)
/sample As above Detected/ Not Detected
Note: If Acanthamoeba is observed microscopically a comment is added stating ‘Acanthamoeba spp. Detected’
Page 5
Hydrotherapy pools
A hydrotherapy pool is defined as a pool containing heated water, designed to meet the therapeutic needs of persons of any age with impairments due to illness, injury, disease, intellectual handicap, congenital defects, or for fitness exercising, recreational and educational purposes (Department of Health, 2013).
The Hydrotherapy testing suite is shown in Table 3. For testing to be done as a Hydrotherapy Pool, the category on the WEL Request Form is ‘Pools, Spas, Hydros, Float Tanks’ and the sample description must include the word ‘Hydro’.
TABLE 3 TESTING REQUIREMENTS FOR HYDROTHERAPY POOLS
Organism
Guideline Value Code Of Practice (DoH 2013)
PathWest Testing Method
Testing Standard
Units Minimum sample volume
Limit of Detection
Escherichia coli < 1 CFU/100 mL Membrane Filtration
AS/NZS 4276.7 (2007)
CFU/100 mL 100 mL <1 CFU/100 mL
Presumptive Pseudomonas aeruginosa
Not detected in 100 mL of pool water
Membrane Filtration
AS/NZS 4276.13 (2008)
CFU/100 mL 100 mL <1 CFU/100 mL
Heterotrophic Plate Count
<100 CFU / mL 22°C ±2°C and 36°C±2°C
AS/NZS 4276.3.1 (2007).
CFU/mL 50 mL <1 CFU / mL
Thermophilic Amoebae
Not Detected Culture /Microscopy
AWQC South Australia (1992)
/250 mL
250 mL (total) Requires Separate bottle
Detected/ Not Detected/ 250 mL
Thermophilic Naegleria
Not Detected Culture/ Microscopy
AWQC South Australia (1992)
/250 mL As above Detected/ Not Detected/ 250 mL
Naegleria fowleri
Not Detected PCR In-House (NATA accredited)
/sample As above Detected/ Not Detected
Note: If Acanthamoeba is observed microscopically a comment is added stating ‘Acanthamoeba spp. Detected’
Page 6
Floatation Tanks
Floatation tanks, sometimes referred to as sensory deprivation tanks are small clamshell enclosed pods that contain roughly 1000L of water, contain very high concentrations of Epsom salts (Magnesium Sulfate) at around 30-40% by weight, and are usually heated to around 30°C - 35°C. The tanks are designed to be used by one person at a time, are often marketed as providing a sensation of floating and possible health benefits from the magnesium salt, and are becoming popular in Western Australia.
Testing requirements are summarised in Table 4. For testing to be done as a Floatation Tank, the category on the WEL Request Form is ‘Pools, Spas, Hydros, Float tanks’ and the sample description must include the word ‘Float tank’.
TABLE 4 TESTING REQUIREMENTS FOR FLOATATION TANKS
Organism Guideline Value
PathWest Analytical Method
Standard Units Minimum sample volume
Limit of Detection
Escherichia coli N/A Membrane Filtration
AS/NZS 4276.7 (2007)
CFU/100mL 100 mL < 1 CFU/100 mL
Presumptive Pseudomonas aeruginosa
N/A Membrane Filtration
AS/NZS 4276.13 (2008)
CFU/100 mL 100 mL <1 CFU/100 mL
Enterococci N/A
Defined Substrate Technology (MPN)
APHA (2012) MPN/100 mL 100 mL <10 MPN/100 mL
Heterotrophic Plate Count
N/A 22°C ±2°C and 36°C±2°C
AS/NZS 4276.3.1 (2007).
CFU/mL 50 mL <1 CFU / mL
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BIOSOLIDS Testing required has been determined from the Western Australian Guidelines for Biosolids Management (Department of Environment and Conservation, 2012)
Biosolids are graded one of four pathogen grades: P1, P2, P3 and P4. All sludges are assumed to be pathogen Grade P4 unless proven otherwise. The biosolids testing suite is shown in Table 5; testing is done on final dry biosolids. For testing to be done as a Biosolid, the category on the WEL Request Form is ‘Other – Biosolids’.
TABLE 5 TESTING REQUIREMENTS FOR BIOSOLIDS
Organism
Guideline Value Guidelines for Biosolids Management (2012) PathWest
Testing Method
Testing standard
Units Minimum sample volume
Limit of Detection
Grade P1 Grade P2 Grade P3 Grade P4
Escherichia coli
<100 counts / gram <1,000 counts / gram
<2,000,000 counts / gram
>2,000,000 counts / gram
MPN AS/NZS 4276.6 (2007)
MPN/gram 100 gram <3 MPN/gram
Somatic Coliphages
<10 PFU/ 10 grams NR NR NR Single Agar Layer Method
APHA 22nd
Edition 9244E(2012)
PFU/100grams 100 gram <1 PFU/100 grams
Strongyloides & Hookworm
<1 viable ova / 50 grams
<1 viable ova / 50 grams
<1 viable ova / 50 grams
NR
Isolation and Microscopic Identification
WHO Geneva (1991)
Strongyloides & Hookworm (Larvae and Ova)
100 gram <1/100 grams
Helminth <1 ova/ 10 grams <1 ova/ 10 grams <1 ova/ 10 grams NR
Isolation and Microscopic Identification
WHO Geneva (1991)
Strongyloides & Hookworm (Larvae and Ova)
100 gram <1/100 grams
Note: Testing for Helminths - Strongyloides & Hookworm (viable ova) only required for biosolids north of the 26th parallel
Counts /gram are counts per gram of dry biosolids
NR: Not required
Page 8
DRINKING WATER Drinking water testing requirements are informed by the Australian Drinking Water Guidelines Paper 6 (NHMRC, 2011). The drinking water testing suite is shown in Table 6. For testing to be done as drinking water, the category on the WEL Request Form is ‘Drinking Water (source to Consumer)’.
TABLE 6 TESTING REQUIREMENTS FOR DRINKING WATER
Organism Guideline Value ADWG (2011)
PathWest Analytical Method
Standard Units Minimum sample volume
Limit of Detection
Escherichia coli
<1 CFU/100 mL Membrane Filtration
AS/NZS 4276.7 (2007)
CFU/100 mL 100 mL <1 CFU/100 mL
Thermophilic Amoebae
Not Detected Culture /Microscopy
AWQC South Australia (1992)
/250 mL
250 mL (total) requires separate bottle
Detected/ Not Detected/ 250 mL
Thermophilic Naegleria
Not Detected Culture /Microscopy
AWQC South Australia (1992)
/250 mL As above Detected/ Not Detected/ 250 mL
Naegleria fowleri
Not Detected PCR In-House (NATA accredited)
/sample As above Detected/ Not Detected
Note: If Acanthamoeba is observed microscopically a comment is added stating ‘Acanthamoeba spp. Detected’.
Page 9
FOOD BUSINESS WATER SUPPLY Food businesses need to use potable drinking water in their production. If testing is being done on the water supply outside the food business then the testing requirements are the same as the drinking water section. Testing within the food business does not fall within these guidelines. It is the responsibility of the business owner to complete the correct testing as required by the Food Act to ensure compliance.
For testing to be done as Food business water supply, the category on the WEL Request Form is ‘Drinking Water (source to Consumer) with additional sample comments ‘Food Business’.
Page 10
NATURAL WATERS This section deals with samples from naturally occurring bodies of water that may be used for boating, wading and swimming and include oceans, rivers, lakes, drains and farm dams. Natural waters that are used as source water are dealt within the drinking water section.
The guidelines that inform testing are the Guidelines for Managing Risks in Recreational Water (NHMRC, 2008). In addition the DoH has its own additional testing requirements depending on the type of water (summary shown Table 7).
The Natural Waters testing suite is shown in Table 8. For fresh to brackish and estuarine waters the category on the WEL Request Form is ‘Natural Waters (Fresh). For Marine water environments the category on the WEL Request Form is ‘Natural Waters (Marine).
TABLE 7 NATURAL WATER MICROBIOLOGICAL TESTING REQUIREMENTS BASED ON WATER TYPES (DEPARTMENT OF HEALTH TESTING REQUIREMENTS)
Fresh to Brackish Water Environments
Estuarine Water Environments Marine Water Environments
Enterococci Enterococci Enterococci
Escherichia coli Escherichia coli
Thermophilic Amoebae
Thermophilic Naegleria
Page 11
TABLE 8 TESTING REQUIREMENTS FOR NATURAL WATERS
Organism
Guideline Value Trigger Values
PathWest Testing Method
Testing standard
Units Minimum sample volume
Limit of Detection NHMRC (2008) DoH
Category A Category B Category C Category D Primary Contact Secondary Contact
Enterococci ≤40 organisms/ 100mL
41-200 organisms/ 100mL
201-500 organisms/ 100mL
>500 organisms/ 100mL
≥ 700 (any 1 sample) > 100 & < 700 (2 consecutive samples)
≥ 7000 (any 1 sample) > 1000 & < 7000 (2 consecutive samples)
Defined Substrate Technology (MPN)
APHA (2012) MPN/100 mL 100 mL <10 MPN/100 mL
Escherichia coli No guideline value ≥ 550/100mL Membrane Filtration
AS/NZS 4276.7 (2007)
CFU/100 mL 100 mL <10 CFU/100 mL
Thermophilic Amoebae
No guideline value Detected Culture /Microscopy
AWQC South Australia (1992)
/250 mL
250 mL (total) requires separate bottle
Detected/ Not Detected/ 250 mL
Thermophilic Naegleria
No guideline value Detected Culture/ Microscopy
AWQC South Australia (1992)
/250 mL As above Detected/ Not Detected/ 250 mL
Naegleria fowleri
No guideline value Detected PCR In-House (NATA accredited)
/sample As above Detected/ Not Detected
Page 12
POULTRY PROCESSING WATER These samples include discharge waters used during the factory production of Poultry. Depending on where the sample is taken, the analyte tested for changes. The microbiological testing suite is shown in Table 9. For testing to be done as Poultry Processing Water, the category on the WEL Request Form is ‘Other – Poultry Processing Water.’ The sample description must contain the water type.
Whole birds are tested for Salmonellae and Campylobacter spp; however this testing falls outside the scope of this document.
TABLE 9 TESTING REQUIREMENTS FOR POULTRY PROCESSING WATER
Analyte Water Type PathWest Testing Method
Testing standard
Unit Minimum Sample Volume
Limit of Detection
Escherichia coli
Spin Chiller Water Tub
Membrane Filtration
AS/NZS 4276.7 (2007)
CFU/100mL 100 mL <10 CFU/ 100mL
Salmonellae
Spin chiller Wash tub Post evisceration drain
Culture AS 4276.14 (2014)
/100mL 100 mL Detected/ Not Detected/ 100mL
Note: Samples are tested at up to 3 dilutions to determine a reliable endpoint.
Page 13
RECYCLED WATERS
General
Testing for recycled water is described in the Guidelines for the Non-potable uses of recycled water in Western Australia (Department of Health, 2011). Water use has been classified into four exposure risk levels: High, Medium, Low and Extra Low. The details of what types of end-uses these exposure risk levels relate to are described below.
High
Multi-unit dwellings, internal use and external surface irrigation
Agricultural irrigation - unprocessed foods (e.g. salad crops)
Urban irrigation with unrestricted access and application
Communal use – flushing toilets and designated cold tap washing machines
Medium
Urban irrigation with some restricted access and application
Fire fighting
Fountains and water features
Industrial use with potential human exposure
Dust suppression
Low
Communal sub-surface irrigation
Urban irrigation with enhanced restricted access and application
Agricultural irrigation; non-edible crops
Extra Low
Note: no monitoring is required for the extra low risk category
Woodlots
Sub-surface irrigation (non-food crops)
The recycled water testing suite is shown in Table 10. For testing to be done as RecycledWater, the category on the WEL Request Form is ‘Recycled Water.’ When Helminth testing is required it will need to be noted on the testing request form in the section ‘Specify non routine tests required.’
Page 14
TABLE 10 TESTING REQUIREMENTS FOR RECYCLED WATER
Microbiology
Guideline Values
PathWest Testing Method
Testing standard Units Minimum sample volume
Limit of Detection Exposure Risk Level
High Medium Low
Escherichia coli < 1 MPN/100 mL < 10 MPN /100 mL < 1000 MPN/100 mL Defined Substrate Technology (MPN)
AS/NZS 4276.21 (2005)
MPN/100 mL 100 mL <1 MPN/100mL
Somatic Coliphages
< 1 PFU/100 mL Not required Not required Single Agar Layer Method
APHA 22nd
Edition 9244E (2012)
PFU/100 mL 100 mL <1 PFU/100 mL
Clostridium < 1 Spores/100 mL Not required Not required Membrane Filtration
AS/NZS 4276.17.1 (2000)
Spores/100 mL 100 mL <1 Spores/100mL
Helminths <1 ova/larvae/100mL <1 ova/larvae/100mL <1 ova/larvae/100mL Isolation and Microscopic Identification
WHO Geneva (1991)
Strongyloides &
Hookworm (Larvae and Ova)
100 mL <1 /100 mL
Note: Helminth control is necessary in the following locations:
north of the 20th parallel to irrigate public open spaces (parks, sports fields and municipal areas) or
where the recycled water is used to irrigate pasture and fodder for beef cattle; or
where the recycled water is used to irrigate pasture and fodder for dairy animals; or
where the recycled water is used for drinking water for stock (except pigs) or
where the recycled water is used as wash down water for dairies.
Page 15
Wash down facilities
Washdown facilities washing water testing requirements are informed by the Guidance note for wash down facilities using recycled water (Department of Health & WorkSafe, 2011).
The washing water testing suite is shown in Table 11. For testing to be done as washing water, the category on the WEL Request Form is ‘Recycled Water’. The sample description must include Wash down facility.
TABLE 11 TESTING REQUIREMENTS FOR WASHING WATERS
Organism Guideline Values PathWest Testing Method
Testing Standard
Units Minimum sample volume
Limit of Detection
Escherichia coli
< 10 CFU/100 mL Membrane Filtration
AS/NZS 4276.7(2007)
CFU/100 mL 100 mL <1 CFU/100 mL
Page 16
SHELLFISH HARVESTING WATERS The guideline that informs testing is the Western Australian Shellfish Quality Assurance Program (WASQAP) Operations Manual (Department of Health, 2015b). This manual is intended to apply to the WA aquaculture industry that currently produces clams, mussels and edible oysters for the domestic and export markets.
This section only relates to the Harvesting waters testing requirements. Any testing of flesh falls outside the scope of this document.
The shellfish harvesting waters testing suite is shown in Table 12. For testing to be done as Shellfish harvesting waters, the category on the WEL Request Form is ‘Other – Shellfish Harvesting Waters’.
TABLE 12 TESTING REQUIREMENTS FOR SHELLFISH HARVESTING WATERS
Organism Guideline Value
PathWest Testing Method
Testing Standard
Units Minimum sample volume
Limit of Detection
Total coliforms 70 CFU/ 100 mL Membrane Filtration
AS/NZS 4276.5 (2007)
CFU/100 mL 100 mL <1 CFU/100 mL
Escherichia coli 14 CFU/ 100 mL Membrane Filtration
AS/NZS 4276.7 (2007)
CFU/100 mL 100 mL <1 CFU/100 mL
Page 17
WASTEWATER
General
In times of drying climate and limited water supply wastewater is starting to be seen as a water source. This section relates to in stream wastewater (generally Pre-treatment) to determine the treatment requirements for the water’s intended future use. An example of a location where sampling may occur is a potential sewer mining location.
Wastewater testing requirements are shown in Table 13. For testing to be done as wastewater, the category on the WEL Request Form is ‘Sewage/Wastewater.’
Note: This section does not relate to post treatment effectiveness.
TABLE 13 TESTING REQUIREMENTS FOR WASTEWATER
Organism Guideline Values
PathWest Testing Method
Testing Standard
Units Minimum sample volume
Limit of Detection
Escherichia coli
N/A
Defined Substrate technology Colilert
AS/NZS 4276.21 (2005)
/100 mL 100 mL <10 MPN/100 mL
Page 18
Wastewater Spills
There are no guidelines to inform wastewater spill testing requirements. The DOH requires testing to be done as shown Table 14.
To ensure the correct testing suites occurs, the category on the WEL Request Form is ‘Sewage/Wastewater;’ with additional sample comments “Wastewater Spill.”
TABLE 14 TESTING REQUIREMENTS FOR WASTEWATER SPILLS
Organism Guideline Values
PathWest Testing Method
Testing Standard Units Minimum sample volume
Limit of Detection
Escherichia coli
N/A Membrane Filtration
AS/NZS 4276.7 (2007)
CFU/100 mL 100 mL
<10 CFU/100 mL (initial stages of spill)
<1 CFU/100 mL (as spill clears)
Enterococci N/A
Defined Substrate Technology (MPN)
APHA (2012) MPN/100 mL 100 mL <10 MPN/100 mL
Page 19
LEGIONNAIRES’ DISEASE Legionnaires’ Disease is caused by bacteria belonging to the genus Legionella. The guideline to inform testing is the Code of practice for the prevention and control of Legionnaires’ disease (Commission for occupational safety and health, 2010).
Cooling towers and Air Conditioners
Cooling tower water and Air Conditioners testing requirements are informed by the Code of Practice and AS/NZS 3666.6:2011 Air-handling and water system of buildings – Microbial control Part 3: performance-based maintenance of cooling systems (Standards Australia, 2011).
The testing regime for Cooling towers and Air Conditioners is shown in Table 15. For testing to be done as cooling tower or Air Conditioner water, the category on the WEL Request Form is ‘Air-conditioning/Cooling Towers.’
TABLE 15 TESTING REQUIREMENTS FOR COOLING TOWERS AND AIR CONDITIONERS
Organism Guideline Values AS/NZS 3666.6 (2011)
Testing Standard Units Minimum sample volume
Limit of Detection
Legionella Not Detected (< 10 CFU/mL)
AS/NZS 3896 (2008) CFU/mL 100 mL (requires separate bottle)
< 10 CFU/mL
Heterotrophic Plate Count
< 100,000 CFU/mL AS/NZS 4276.3.2 (2008)
CFU/mL 100 mL < 100 CFU/mL
General
Legionella has also been known to accumulate in:
• evaporative condensers;
• hot and cold water systems;
• spas;
• humidifiers or foggers and water misting systems;
• coolant in industrial milling machines;
• high pressure cooling and cleansing processes;
• potable water aerosols, such as shower heads;
• nebulisers; and
• other domestic and industrial-based water systems.
Page 20
Should testing for Legionella be required for any of the above water types the testing requirements are the same as for cooling towers and air conditioners above.’ For Legionella testing to be done a note in the additional sample comments of Legionella suite needs to written on the WEL Request Form.
Note: Testing of Spas is only recommended if there has been an infectious disease notification from the DoH.
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OTHER SAMPLE TYPES
HUMAN SAMPLES
These include predominantly human corneal/eye scrapings from patients with ocular keratitis or cerebrospinal fluid from cases of suspected amoebic meningoencephalitis.
The testing requirements are shown in Table 16. For testing to be done as Human Samples , the category on the WEL Request Form is ‘Other – Human Samples.’
TABLE 16 TESTING REQUIREMENTS FOR HUMAN SAMPLES
Organism Guideline Value
PathWest Testing Method
Testing Standard
Units Minimum sample volume
Limit of Detection
Acanthamoeba N/A Culture/ Microscopy
AWQC South Australia (1992)
/sample 1 Sample Detected/ Not Detected/ Sample
Thermophilic Amoebae
N/A Culture/ Microscopy
AWQC South Australia (1992)
/sample 1 Sample Detected/ Not Detected/ Sample
Thermophilic Naegleria
N/A Culture/ Microscopy
AWQC South Australia (1992)
/sample As above Detected/ Not Detected/ Sample
Naegleria fowleri
N/A PCR In-House (NATA accredited)
/sample As above Detected/ Not Detected
MOORE SWABS
Moore swabs are used by the Department of Health to monitor effluents from smallgoods production plants for the presence of Salmonella spp. The testing requirements are shown in Table 17. For testing to be done as a Moore Swab, the category on the WEL Request Form is ‘Other – Moore Swab.’
TABLE 17 TESTING REQUIREMENTS FOR MOORE SWABS
Organism DoH requirement
PathWest Testing Method
Testing Standard
Units Minimum sample volume
Limit of Detection
Salmonellae Should not be detected
Culture AS 4276.14 (2014)
/Swab 1 swab Detected/ Not Detected
Page 22
STANDARDS REFERENCE LIST The testing and analysis standards cited in this document are summarised below.
Test Reference
AS 4276.14 Standards Australia. (2014). AS 4276.14:2014 Water microbiology Method 14: Detection of
Salmonella spp. (ISO 19250:2010, MOD). Sydney, NSW, Australia
AS 4276.21 Standards Australia. (2005). AS 4276.21-2005 Water Microbiology - Examination for coliforms
and Escherichia coli - Determination of most probable number (MPN) using enzyme hydrolysable substrates. Sydney, NSW, Australia
AS/NZS 3896 Standards Australia. (2008). AS/NZS 3896:2008 Waters - Examination for Legionella spp.
including Legionella pneumophila. Sydney, NSW, Australia.
AS/NZS 4276.13 Standards Australia. (2008a). AS/NZS 4276.13:2008 Water microbiology Method 13:
Pseudomonas aeruginosa - Membrane filtration method. Sydney, NSW, Australia.
AS/NZS 4276.3.1 Standards Australia. (2007). AS/NZS 4276.3.1:2007 Water Microbiology Method 3.1:
Heterotrophic colony count methods - Pour plate method using yeast extract agar. Sydney, NSW, Australia.
AS/NZS 4276.3.2 Standards Australia. (2003). AS/NZS 4276.3.2:2003 Water Microbiology Method 3.2:
Heterotrophic colony count methods - Plate count of water containing biocides. Sydney, NSW, Australia.
AS/NZS 4276.5 Standards Australia. (2007a). AS/NZS 4276.5:2007 Water Microbiology Method 5: Coliforms -
Membrane filtration method. Sydney, NSW, Australia.
AS/NZS 4276.6 Standards Australia. (2007b). AS/NZS 4276.6:2007 Water microbiology - Coliforms, Escherichia
coli and thermotolerant coliforms - Determination of most probably number (MPN). Sydney, NSW, Australia.
AS/NZS 4276.7 Standards Australia. (2007c). AS/NZS 4276.7: 2007 Water microbiology Method 7: Escherichia
coli and thermotolerant coliforms - Membrane filtration method. Sydney, NSW, Australia.
AS/NZS 4276.9 Standards Australia. (2007d). AS/NZS 4276.9:2007 Water microbiology Method 9: Enterococci -
Membrane filtration method (ISO 7899-2:2000, MOD). Sydney, NSW, Australia.
AWQC South Australia
Robinson B.et al (1992) Analytical Methods Manual Protozoology Australian Water Quality Centre South Australia. AWQC Report No 39.
APHA 22nd
Edition 9244E
American Public Health Association American Water Works Association and Water Environment Federation. 2012. In: EW Rice, RB Baird, AD Eaton, LS Clesceri (eds.) Standard Methods for the Examination of Water and Wastewater, 22
nd Ed. P.9-101 to 9-102.
American Public Health Association, Washington DC.
APHA (2012)
American Public Health Association, American Water Works Association and Water Environment Federation. 2012. In: EW Rice, RB Baird, AD Eaton, LS Clesceri (Eds.) Standard Methods for the Examination of Water and Wastewater, 22
nd Ed. P.9-110 to 9-
116. American Public Health Association, Washington DC.
WHO Geneva (1991)
Basic Laboratory Methods in Medical Parasitology, World Health Organization, Geneva (1991)
Page 23
GUIDELINES REFERENCE LIST The guidelines cited in this document are summarised below:
Commission for occupational safety and health. (2010). Code of practice: Prevention and control of
Legionnaires' disease. Perth: Department of Commerce and Department of Mines and Petroleum,
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© Department of Health 2015
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