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Original research
Peer reviewed
Analysis of Lightning and BioClean tests for assessment of
sanitation levels in pork production facilities
Jason A. Kelly; Sandra F. Amass, DVM, PhD, Dipl ABVP; Darryl
Ragland, DVM, PhD; Pat M. Spicer PhD; Roberta M. Alvarez, DVM
JAK, SFA, DR, RMA: Department of Veterinary Clinical Sciences,
Purdue University School of Veterinary Medicine, 1248 Lynn Hall,
West Lafayette, Indiana 47907-1248; PMS: Department of Natural
Resources and Environment, Box 3100 Bendigo Delivery Centre, Bendigo,
Victoria, Australia, 3554
Kelly JA, Amass SF, Ragland D, et al. Analysis of Lightning
and BioClean tests for assessment of sanitation levels in pork
production facilities. J Swine Health Prod. 2001;9(5):207-213.
Also available as a PDF
Summary
Objectives: To determine the test sensitivity and specificity
of Lightning (BioControl Systems, Inc, Bellevue, Washington) and
BioClean (BioVet, St Anthony, Minnesota) testing systems in determining
whether various surfaces in pork production facilities have met
the standards for disinfection; and to identify factors in pork
production units which may interfere with the test sensitivity
and specificity of Lightning or BioClean test results.
Methods: Swab samples were collected from feeders, flooring,
and walls in a wean-finish room and a nursery room of a 1600-sow,
farrow-to-finish commercial operation. In both facilities, three
adjacent swab samples of a 6.16 cm2 (0.955 in2)
area were collected at each sampling site and analyzed using Lightning,
BioClean, and cultural examination for bacteria. The test sensitivity
and specificity of Lightning and BioClean tests were calculated
for each surface using cultural examination as the "gold
standard" for classifying a sample as clean or contaminated.
Factors such as feed, manure, and disinfectant residues were tested
to determine if they interfered with the test sensitivity and
specificity of Lightning or BioClean tests.
Results: Lightning tests were generally highly sensitive
but had low specificity. BioClean tests were generally highly
specific but had low sensitivity.
Implications: Lightning and BioClean testing systems
are not recommended for use in evaluating sanitation levels on
swine farms without prior, independent, on-farm validation. Caution
should be exercised when transferring technologies from other
industries to pork production.
Keywords: swine, Lightning,
BioClean, sanitation, disinfectants
Received: October 31, 2000
Accepted: May 9, 2001
All in-all out management of swine confinement
units is strongly recommended to maintain herd health and increase
profitability. An essential step for implementation of all in-all
out pig flow is the cleaning and disinfection of rooms between
pig groups to prevent exposureto pathogens shed by the previous
groups.1,2,3,4 Recommendations include pressure washing
the room and its equipment with hot water and a detergent to remove
organic matter, and then disinfecting with a suitable product.5,67
Consequently, in most cases, an outbreak of neonatal scours or
other costly disease must occur before producers and veterinarians
reevaluate cleaning methods and disinfectants used. Currently,
producers do not have an objective, rapid, proactive method to
evaluatethe final cleanliness of the room or the disinfectant's
efficacy in inactivating pathogens enzootic to the farm.
Rapid tests to evaluate sanitation levels have not been developed
specifically for use on farms. However, two testing systems, Lightning
(BioControl Systems, Inc, Bellevue, Washington) and BioClean (BioVet,
St Anthony, Minnesota) were developedfor monitoring food safety
in processing plants.8,9 The Lightning system has recently
been used without validation for assessing cleanliness of swine
transport vehicles.10,11
The Lightning test method quantifies residualadenosine triphosphate
(ATP) on surfaces using a luminometer and a swab sample.12
Adenosine triphosphate is found in most food residues and
bacteria. Lightning theoretically correlates increased levels
of ATP with increased contamination of surfaces. The Lightning
test displays a score 11 seconds after the surface sample is obtained.
Each test costs approximately US $2.78 after the initial capital
outlay for the luminometer.
BioClean is a swab test that uses a color- changing reaction
to quantitate protein levels on surfaces as an indicator of food
residue. Increasing amounts of protein yield a more intense color
change.8 Theoretically, surfaces with a high level
of bacterial contamination have a greater protein content. The
BioClean test can be prepared in approximately 1 minute and results
are obtained within 20 minutes after sampling. Each BioClean test
costs approximately US $2.16.
The overall objective of the study was to determine if Lightning
or BioClean tests were valid, rapid test methods to assess the
efficacy of disinfection in pork production facilities. The specific
objectives were to evaluate the test sensitivity and specificity
of Lightning and BioClean testing systems in determining whether
various surfaces in pork production facilities have met the standards
for disinfection,1 and to identify factors in pork
production units which may interfere with the test sensitivity
and specificity of Lightning or BioClean test results.
Our working hypothesis was that the test sensitivity and specificity
of these tests would vary according to the sampled surface.
Materials and methods
Experiment One: Determination of sensitivity and specficity
of Lightning and BioClean tests on surfaces in
swine facilities
Study Design
Swab samples were collected from feeders, flooring, and walls
in a wean-finish room and a nursery room of a 1600-sow, farrow-to-finish
commercial operation. A 26-pen wean-finish room was emptied of
pigs, cleaned, disinfected with a phenolic disinfectant(Triphenol-R/256;
ID Russell Company Laboratories, Longmont, Colorado), and allowed
to dry for 1 day. Each pen in the facility was sampled on three
surfaces: stainless steel feeder trough (Farmweld, Teutopolis,
Illinois), concrete slat, and concrete wall approximately 30 cm
up from the floor. Pigs were also emptiedfrom a 16-pen nursery
room. The room was cleaned and disinfected with Triphenol-R/256
and allowed to dry for 2 days. Samples were taken in each pen
from the stainless steel feeder trough (Farmweld, Teutopolis,
Illinois), plastic mesh flooring (MIK flooring, MIK Heinrich Michel,
Marienhausen, Germany), and PVC plastic-covered wall (AP Livestock,
Assumption, Illinois) approximately 30 cm up from the floor. A
sterile metal washer with an internal surface area of 6.16-cm2
was used to standardize the sampled surface area. In both facilities,
three adjacent swab samples of a 6.16-cm2 area were
collected at each sampling site and analyzed using Lightning,
BioClean, and cultural examination for aerobic bacteria.
Background contamination control samples
Sterile washers were exposed to facility airspacefor approximately
5 seconds at five different locations in each room to quantitate
background aerosol contamination of washers that might occur during
sampling. The inner surface of each washer was swabbed and analyzed
using Lightning, BioClean, and cultural examination for bacteria
as described below. Additionally, metal washers autoclaved in
the same batch as those used for on-farm sampling were culturally
examined under aseptic conditions to confirm sterility.
Bacterial plating analysis
Each surface was sampled with sterile, cotton-tipped swabs
which were placed into 1-mLaliquots of 0.9% saline stored on ice
packs. Original samples and serial dilutions were plated onto
trypticase soy agar with 5% sheep blood (BBL Stacker Plate,
Beckton Dickenson Microbiology Systems, Cockeysville, Maryland)
within 5 hours of collection and incubated aerobically at 37 degrees
C for 18 hours. Colonies were counted on each plate and converted
to colony forming units (CFUs) per cm2 of surface sampled.
The average bacterial count for the five background contamination
control samples for the room was subtracted from each sample swab
count. A surface was classified as either clean (<=1 CFU per
cm2) or contaminated (>1 CFU per cm2).1
Plates indicating more than 487 CFUs per cm2 surface
area were considered "too numerousto count" (TNTC) and
classified as contaminated. Samples that detected less than the
mean background contamination level were classified as sterile
(0 CFUs per cm2).
Lightning analysis
The Lightning system was used according to test instructions.
Briefly, each surface was sampled with a Lightning swab that consists
of three basic parts. A swab, attachedto an ampule containing
buffer solutionat the top, is enclosed in a sheath containing
a luciferin-luciferase pellet. Buffer contained in the ampule
is used to rinse the sample from the swab and mix with the luciferin-luciferase
pellet to activatethe reaction. Residual ATP present on surfaces
reacts with the luciferin-luciferase pellet to yield light. The
Lightning luminometer measures the light output and calculates
a score. Each sample was classified by the standard Lightning
cut-off as either clean (score <=2.5) or contaminated (score
>2.5). Alternative cut-off values (3.0, 3.5, 4.0) were applied
to determine their effects on test sensitivity and specificity.
BioClean analysis
Sample tubes were prepared according to test instructions by
adding 1 drop of reagent B to the tube containing reagent A. Each
surface was sampled with a sterile cotton swab provided with the
BioClean kit. Protein contaminants react with copper ions to form
a complex with the biuret reagent that causes a color-changing
reaction. The sample swab was allowed to react for 20 minutes
in the tube containing the reagent mixture. The surface was classified
as clean (no color change after 20 minutes) or contaminated (any
color change after 20 minutes).
Data analysis
The sensitivity, specificity, positive
predictive value (PPV), and negative predictive value (NPV) of
Lightning and BioClean tests were calculated (Table 1) for each
surface, using cultural examination as the "gold standard"
for classifying a sample as truly clean or contaminated. Sensitivity
was defined as the ability of the test to detect a contaminated
surface when the surface was truly contaminated. Specificity was
defined as the ability of the test to detect a clean surface when
the surface was truly clean. The PPV was defined as the probability
of a contaminated test result corresponding to a truly contaminated
surface. The NPV was defined as the probability of a clean test
result corresponding to a truly clean surface.
Experiment Two: Factors in pork production units that may
interfere with sensitivity and specificity of Lightning or BioClean
tests
Effect of manure residue on test results
Five manure samples were collected from a growing-finishing
facility housing pigs weighing approximately 45 kg. Manure samples
were diluted with sterile 0.22-µm-filtered water to a final
dilution of 0.001 g manure per mL water. Each sample was divided
into two equal aliquots. One aliquot was autoclaved for 20 minutes
at 121 degrees C and the other remained nonautoclaved. A negative
control consistedof a sterile, 0.22-µm-filtered watersample.
The nonautoclaved manure samples, the autoclaved manure samples,
and a negative control were analyzed using cultural examination
for bacteria, Lightning, and BioClean methods.
Effect of feed residue on test results
Five grow-finish feed samples were collected. Feed samples
were diluted with sterile0.22-µm-filtered water to a final
dilution of 0.083 g feed per mL water. Each sample was divided
into two equal aliquots. One aliquot was autoclaved for 20 minutes
at 121 degrees C and the other remained nonautoclaved. A negative
control consisted of a sterile, 0.22-µm-filtered water sample.
The nonautoclaved feed samples, the autoclaved feed samples, and
a negative control were analyzed using cultural examination for
bacteria, Lightning, and BioClean tests.
Effect of disinfectant residue on test results
Disinfectant sampling was performed undercontrolled laboratory
conditions to determine if disinfectant residue affected Lightning
or BioClean test results. Representatives of six classes of disinfectants
were used (Table 2). Clean glass slides (Esco 3"x 1"
microscope slides, Erie Scientific Company, Portsmouth, New Hampshire)
were submerged in disinfectant solution prepared according to
label instructions in sterile, 0.22-µm-filtered water. Slides
were dried in a sterile, HEPA-filtered biosafety cabinet. Dry
slides were sampled using each of the three testing methods. The
top one third of the slide was culturally examined for bacteria,
the middle one third was sampled for the Lightning test, and the
bottom one third was sampled for the BioClean test. Five replicates
were performed for each disinfectant. Five control slides were
submerged in sterile, 0.22-µm-filtered water and tested
as above.

Effects of disinfected manure and feed on test results
Five manure samples were collected from a continuous-flow finishing
facility housing pigs weighing approximately 68 kg. Manure samples
were diluted in sterile, 0.22-µm-filtered water to a concentration
of 0.01 g manure per mL water. Five samples of an SEW diet containing
carbadox were collected and diluted in sterile, 0.22-µm-filtered
water to a concentration of 0.01 g feed per mL water. To simulate
contamination with organic matter and bacteria, seven slides were
submerged in each sample of manure and seven slides were submerged
in each sample of feed. All slides were allowedto dry in a sterile,
HEPA-filtered biosafety cabinet. Then, for both the manure-coated
slides and the feed-coated slides, six of the seven inoculated
slides were each submerged in one of the six disinfectants (Table
2) for 5 seconds and dried a second time. The seventh slide was
used as a positive control that was dried but not disinfected.
Five replicates were performed for each disinfectant and positive
control. A negative control slide was submerged in sterile 0.22-µm-filtered
water and allowed to dry in the biosafety cabinet to confirm sterility
of the water and the biosafety cabinet. All slides were evaluated
using cultural examination for bacteria, Lightning, and BioClean
tests. The top one third of the slide was culturally examined
for bacteria, the middle one third was sampled for the Lightning
test, and the bottom one third was sampled for the BioClean test.
Results
Experiment One: Determination of sensitivity and specificity
of Lightning and BioClean tests on surfaces in swine facilities
Variation existed among cultural examination for bacteria,
Lightning, and BioClean tests with respect to classification of
surfaces as clean or contaminated (Table 3). Lightning was highly
sensitive but had low specificity on stainless steel wean-finish
feeders, stainless steel nursery feeders, concrete slats, plastic
flooring, and concrete walls. However, sensitivity was low and
specificity was high on PVC plastic-covered walls using the standard
cut-off score of 2.5 to distinguish between clean and contaminated
surfaces (Table 4). Incrementally increasingthe Lightning cut-off
score did not improve the accuracy of test results on surfaces
(Table 5). BioClean had high specificity and low sensitivity on
stainless steel wean-finish feeders, stainless steel nursery feeders,
concrete slats, concrete walls, and PVC plastic-covered walls.
BioClean sensitivity on plastic flooring was low but exceeded
specificity (Table 4).



Experiment Two: Factors in pork production units that may
interfere with sensitivity and specificity of Lightning or BioClean
tests
Effect of manure residue on test results
Negative control: A sterile water negative control was classified
as clean using all three tests.
Nonautoclaved manure: All nonautoclaved manure samples grew
bacteria in numbers TNTC on cultural examination and were classified
as contaminated. Lightning (cut-off score 2.5) correctly classified
four of five samples (80%) as contaminated and incorrectly classified
one of five samples (20%) as clean. BioClean incorrectly classified
five of five samples (100%) as clean.
Autoclaved manure: All autoclaved manure samples were sterile
on cultural examination and classified as clean. Lightning (cut-off
score 2.5) correctly classified three of five samples (60%) as
clean and incorrectly classified two of five samples (40%) as
contaminated. BioClean correctly classified all autoclaved manure
samples as clean.
Effect of feed residue on test results
Negative control: A sterile water negative control was classified
as clean using all three tests.
Nonautoclaved feed: All nonautoclaved feed samples grew bacteria
in numbers TNTC on cultural examination and were classified as
contaminated. Both Lightning (cut-off score 2.5) and BioClean
tests correctly classified all samples as contaminated.
Autoclaved feed: All autoclaved feed samples were sterile on
cultural examination and classified as clean. Both Lightning (cut-off
score 2.5) and BioClean tests incorrectlyclassified five of five
autoclaved feed samples (100%) as contaminated.
Effect of disinfectant residue on test results
Thirty-five of 35 slides (100%) were sterile on cultural examination.
Lightning (cut-off score 2.5) correctly classified all disinfected
slides and control slides as clean. BioClean correctly classified
all control slides and all slides coated with Clorox Bleach, Nolvasan
solution, 1-Stroke Environ, Roccal D-Plus, and Virkon
S as clean. However, BioClean incorrectly classified all
slides coated with Cidex Activated Dialdehyde solution as contaminated.
Effect of disinfected manure on test results
Negative control: A negative control slide coated with sterile
water was classified as clean using all three tests.
Disinfected manure: Twenty-five of 25 disinfected manure samples
(100%) were sterileon cultural examination and classified as clean.
Lightning (cut-off score 2.5) correctly classified as clean three
of five (60%) manure-coated slides disinfected with Cidex Activated
Dialdehyde solution and incorrectly classified two of five (40%)
as contaminated. Lightning (cut-off score 2.5) correctly classified
one of five (20%) manure-coated slides disinfected with Clorox
Bleach as clean and incorrectly classified four of five (80%)
as contaminated. Lightning (cut-off score 2.5) correctly classified
four of five (80%) manure-coated slides disinfected with Nolvasan
solution as clean and incorrectly classified one of five (20%)
as contaminated. Lightning (cut-off score 2.5) correctly classified
one of five (20%) manure-coated slides disinfected with 1-Stroke
Environ as clean and incorrectly classified four of five (80%)
as contaminated. Lightning (cut-off score 2.5) correctly classified
two of five (40%) manure-coated slides disinfected with Roccal
D-Plus as clean and incorrectly classified three of five
(60%) as contaminated. BioClean correctly classified all disinfectedmanure
samples as clean.
Effect of disinfected feed on test results
Negative controls: A control slide coated with sterile water
was classified as clean using all three tests.
Disinfected feed: Twenty-five of 25 disinfected feed samples
(100%) were sterile on cultural examination and classified as
clean. Lightning (cut-off score 2.5) correctly classified all
feed-coated slides disinfected with Cidex Activated Dialdehyde
solution or Clorox Bleach as clean. Lightning (cut-off score 2.5)
correctly classified two of five (40%) feed-coated slides disinfected
with Nolvasan solution as clean and incorrectly classified three
of five (60%) as contaminated. Lightning (cut-off score 2.5) correctly
classified three of five (60%) of feed-coated slides disinfected
with 1-Stroke Environ or Roccal D-Plus as clean and
incorrectlyclassified two of five (40%) as contaminated. BioClean
correctly classified all disinfected feed samples as clean.
Discussion
An ideal test for assessing sanitation on pork production facilities
would be inexpensive, rapid, 100% sensitive, and 100% specific.
Lightning and BioClean testing systems were not designed for use
in pork production facilities. Lightning and BioClean technology
were transferred to swine production because of the need by the
industry to quickly and objectively evaluate sanitation protocols.
Unfortunately, Lightning tests were recommended and implemented
without prior validation for on-farm use.10,11
To compensate for the greater contamination of swine facilities
compared to food processing plants, some have recommended using
a higher Lightning cut-off score for classifying a surface as
clean. In our study, incremental increases in cut-off scores improvedspecificity,
but decreased sensitivity of Lightning for all surfaces except
PVC plastic-covered walls. Therefore, altering cut-off scores
did not improve overall test accuracy.
Further evaluation of Lightning under experimental conditions
demonstrated that sterile organic material such as autoclaved
or disinfected feed and manure residues were sometimes classified
as contaminated according to the Lightning tests. Feed is composed
primarily of plant products. Living cells present in the ground
seed coats may contain sufficient ATP to cause false- positive
Lightning results. Sterile manure residue could cause false-positive
results because of ATP in fibrous seed coats, which pass through
the digestive tract of the pig with little degradation. An additional
source of ATP in manure could be epithelial cells sloughed from
the digestive tract. Pure disinfectant residues did not affect
Lightning results.
BioClean tests were recently made available for commercial
use and have not been widely implemented in the pork industry.
Under the conditions of this study, BioClean tests were generally
highly specific for all surfaces except plastic flooring, but
sensitivity was low. Both sensitivity and specificity were low
for plastic flooring. Low overall BioClean sensitivity might result
from inability of reagents in the kit to adequately detect small
quantities of protein. An alternative explanation is that residual
protein is not a good indicator of bacterial contamination. A
second disadvantage of the BioClean test is cross-reaction with
Cidex Activated Dialdehyde solution,an aldehyde disinfectant,
resulting in the classification of sterile solutions of pure disinfectant
as contaminated. However, false classification did not occur when
Cidex Activated Dialdehyde solution was used to disinfect
feed or manure samples. One explanation is that the organic material
bound to or reacted with the residue in Cidex that caused false-positive
reactions. Other classes of disinfectants tested did not affect
BioClean test results.
In conclusion, the low test specificity of Lightning and the
low test sensitivity of BioClean tests resulted in an inability
to accurately assess the efficacy of disinfection in swine production
facilities under the conditions of this study. This experiment
took place in two rooms of a single commercial pork production
facility. The walls, equipment, and flooring of this facility
may not represent those on other swine farms. The investigators
encourage practitioners and producers to validate Lightning and
BioClean testing systems in their own facilities before implementing
biosecurity programs utilizing these testing methods. Future research
should focus on validating additional rapid testing systems used
by other industries to determine whether they are applicable to
the pork industry. Development of rapid testing systems designed
for use in the pork industry should be considered if technology
transfer from other industries is not possible.
Implications
- Lightning and BioClean testing systems are not recommended
for use in evaluating sanitation on swine farms unless prior,
independent, on-farmvalidation is performed.
- Caution should be exercised when transferring technologies
from other industries to pork production.
- When evaluated on three different surface types in a wean-finish
building and a nursery, under the conditions of this study, Lightning
tests were generally highly sensitive but specificity was low
when used on stainless steel feeders, concrete slats, and plastic
flooring, and Lightning tests were highly specific but had low
sensitivity when used on PVC plastic-covered walls.
- When evaluated on three different surface types in a wean-finish
building and a nursery, under the conditions of this study, BioClean
tests were highly specific, but sensitivity was low.
- Under the conditions of this study, Lightning tests classified
sterile organic material such as autoclaved or disinfected feed
and manure residues as contaminated, and BioClean tests cross-reacted
with an aldehyde disinfectant resulting in false classification
of sterile disinfectant solutions as contaminated.
Acknowledgements
Support for this research was provided by the National Pork
Producers Council.
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References -- non refereed
6. Thompson, R. Transportation cleaning and disinfection. Swine
Health Fact Sheet. Jan. 2000; 2(2).
8. BioClean qualitative control of surface cleanliness: Your
surfaces are clean or Bioclean? (Biovet, St Anthony, Minnesota)
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IDEXX Laboratories, Inc; 35.
10. Faust, C. The determination of surface levels of ATP as
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