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Chapter 27: Scombrotoxin (Histamine) Formation
Updated:
09/22/07
Scombrotoxin formation as a result of time/temperature abuse of certain
species of fish can cause consumer illness. The illness is most closely linked
to the development of histamine in these fish. In most cases histamine levels in
illness-causing fish have been above 200 ppm, often above 500 ppm. There
are indications that decomposition can result in the production of other toxins
(e.g. biogenic amines, such as putrescine and cadaverine) that have the
potential to cause illness, even in the absence of histamine formation. Such
illnesses have been reported in a number of fish species. FDA has also received
a number of consumer complaints concerning illnesses that are associated with
the consumption of decomposed shrimp (FDA, 2001a; FDA, 2001b).
Scombroid poisonings have primarily been associated with the consumption of
tuna, mahi mahi, and bluefish. However, Table #3-1
lists a number of species that are also capable of developing elevated levels of
histamine when temperature abused (FDA, 2001a).
Certain bacteria produce the enzyme histidine decarboxylase during growth.
This enzyme reacts with free histidine, a naturally occurring chemical that is
present in larger quantities in some fish than in others. The result is the
formation of histamine.
Histamine-forming bacteria are capable of growing and producing histamine
over a wide temperature range. Growth is more rapid, however, at high-abuse
temperatures (e.g. 70°F [21.1°C] ) than at moderate-abuse temperatures (e.g.
45°F [ 7.2°C] ). Growth is particularly rapid at temperatures near 90°F (32.2°C).
Histamine is more commonly the result of high temperature spoilage than of long
term, relatively low temperature spoilage. Nonetheless, there are a number of
opportunities for histamine to form under more moderate abuse temperature
conditions.
Once the enzyme histidine decarboxylase has been formed, it can continue to
produce histamine in the fish even if the bacteria are not active. The enzyme
can be active at or near refrigeration temperatures. The enzyme is likely to
remain stable while in the frozen state and may be reactivated very rapidly
after thawing.
Freezing may inactivate the enzyme-forming bacteria. Both the enzyme and the
bacteria can be inactivated by cooking. However, once histamine is formed, it
cannot be eliminated by heat (including retorting) or freezing. After cooking,
recontamination of the fish with the enzyme-forming bacteria is necessary for
additional histamine to form. For these reasons, histamine development is more
likely in raw, unfrozen fish.
The kinds of bacteria that are associated with histamine development are
commonly present in the salt water environment. They naturally exist on the
gills and in the gut of live, salt water fish, with no harm to the fish. Upon
death, the defense mechanisms of the fish no longer inhibit bacterial growth,
and histamine-forming bacteria start to grow and produce histamine. Evisceration
and removal of the gills in a sanitary manner may reduce, but not eliminate, the
number of histamine-forming bacteria. However, when done under insanitary
conditions, these steps may accelerate the process of histamine development in
the edible portions of the fish by spreading the bacteria to the flesh of the
fish.
With some harvesting practices, such as long lining, death can occur before
the fish is removed from the water. Under the worst conditions histamine
formation can already be underway before the fish is landed on the vessel. This
condition can be aggravated when the fish is allowed to remain on the line for a
period of time after death, a situation that in certain tuna species may cause
its internal temperature to increase to a more favorable growth range for the
enzyme-forming bacteria.
The potential for histamine formation is increased when the flesh of the fish
is directly exposed to the enzyme-forming bacteria. This occurs when the fish
are processed (e.g. butchering or filleting).
At least some of the histamine-forming bacteria are halotolerant
(salt-tolerant) or halophilic (salt-loving). This causes some salted and smoked
fish products produced from scombrotoxin-forming species to continue to be
suspect for histamine development. Further, a number of the histamine-forming
bacteria are facultative anaerobes that can grow in reduced oxygen environments (FDA,
2001a).
Rapid chilling of fish immediately after death is the most important element
in any strategy for preventing the formation of scombrotoxin, especially for
fish that are exposed to warmer waters or air, and for large tuna that generate
heat in the tissues of the fish following death. It is recommended that:
- Generally, fish should be placed in ice or in refrigerated seawater or
brine at 40°F (4.4°C) or less within 12 hours of death, or placed in
refrigerated seawater or brine at 50°F (10°C) or less within 9 hours of
death;
- Fish exposed to air or water temperatures above 83°F (28.3°C), or large
tuna (i.e., above 20 lbs.) that are eviscerated before on-board chilling,
should be placed in ice (including packing the belly cavity of large tuna
with ice) or in refrigerated seawater or brine at 40°F (4.4°C) or less
within 6 hours of death;
- Large tuna (i.e., above 20 lbs.) that are not eviscerated before on-board
chilling should be chilled to an internal temperature of 50°F (10°C) or
less within 6 hours of death.
This will prevent the rapid formation of the enzyme histidine decarboxylase.
Once this enzyme is formed, control of the hazard is unlikely.
Further chilling towards the freezing point is also desirable to safe-guard
against longer-term, low-temperature development of histamine. Additionally, the
shelf-life of the fish is significantly compromised when product temperature is
not rapidly dropped to near freezing.
The time required to lower the internal temperature of fish after capture
will be dependent upon a number of factors, including:
- The harvest method;
- Delays in removing fish from a long line may significantly limit the
amount of time left for chilling and may allow some fish to heat up
after death;
- The quantity of fish landed in a purse seine or on a long line may
exceed a vessel's ability to rapidly chill the product;
- The size of the fish;
- The chilling method;
- Ice alone takes longer to chill fish than does an ice slurry or
recirculated refrigerated sea water or brine, a consequence of reduced
contact area and heat transfer;
- The quantity of ice or ice slurry and the capacity of refrigerated sea
water or brine systems must be suitable for the quantity of catch.
Once chilled, the fish should be maintained as close as possible to the
freezing point (or held frozen) until it is consumed. Exposure to ambient
temperature should be minimized. The allowable exposure time is dependent
primarily upon the speed with which the fish were chilled on-board the harvest
vessel and whether the fish has been previously frozen (e.g. on-board the
harvest vessel).
Unfrozen scombrotoxin-forming fish has a safe shelf-life (days before
elevated levels of histamine are formed) that is dependent upon the harvest
methods, the on-board handling, and the time/temperature exposures throughout
processing, transit, and storage. This safe shelf-life can be as little as 5 to
7 days for product stored at 40°F (4.4°C).
Any exposure time above 40°F (4.4°C) significantly reduces the expected
safe shelf-life. For this reason, fish that have not been previously frozen
should not be exposed to temperatures above 40°F (4.4C) for more than 4 hours,
cumulatively, if any portion of that time is at temperatures above 70°F (21°C);
or the fish should not be exposed to ambient temperatures above 40°F (4.4°C)
for more than 8 hours, cumulatively, as long as no portion of that time is at
temperatures above 70°F (21°C) after chilling on board the harvest vessel. The
safety of these limits is dependent upon proper handling at sea.
Fish that have been previously frozen can safely withstand considerably more
exposure to elevated temperatures during post-harvest handling. Such fish should
not be exposed to temperatures above 40°F (4.4C) for more than 12 hours,
cumulatively, if any portion of that time is at temperatures above 70°F (21°C);
or the fish should not be exposed to ambient temperatures above 40°F (4.4°C)
for more than 24 hours, cumulatively, as long as no portion of that time is at
temperatures above 70°F (21°C), after chilling on board the harvest vessel.
The safety of these limits is again dependent upon proper handling at sea.
Extended frozen storage (e.g. 24 weeks) or cooking minimizes the risk of
additional histamine development by inactivating the enzyme-forming bacteria
and, in the case of cooking, the enzyme itself. As previously mentioned,
recontamination with enzyme-forming bacteria and significant temperature abuse
is necessary for histamine formation under these conditions. Such
recontamination may not be likely if the fish is processed under a conscientious
sanitation program.
Sensory evaluation is generally used to screen fish for spoilage odors that
develop when the fish is exposed to time/temperature abuse. It is an effective
means of detecting fish that have been subjected to a variety of abusive
conditions.
However, odors of decomposition that are typical of relatively low
temperature spoilage may not be present if the fish has undergone high
temperature spoilage. This condition makes sensory examination alone an
ineffective control for scombrotoxin.
Chemical testing is an effective means of detecting the presence of histamine
in fish flesh. However, the validity of such testing is dependent upon the
design of the sampling plan. The amount of sampling required to accommodate such
variability is necessarily quite large. For this reason, chemical testing alone
will not normally provide adequate assurance that the hazard has been
controlled. Because histamine is generally not uniformly distributed in a
decomposed fish, a guidance level of 50 ppm has been set. If 50 ppm is found in
one section, there is the possibility that other sections may exceed 500 ppm.
Observations for the presence of honeycombing in precooked tuna loins
intended for canning is also a valuable means of screening for fish that have
been exposed to the kinds of temperature abuse that can lead to histamine
development. Any fish that demonstrate the trait should be destroyed (FDA,
2001a).
1a. For receipt by primary (first) processor (Harvest Vessel Control Option):
All lots received are
accompanied by harvest vessel records that show:
- Generally, the fish were:
- Placed in ice, or in refrigerated seawater or brine at 40°F (4.4°C)
or less, within 12 hours of death;
OR
- Placed in refrigerated seawater or brine at 50°F (10°C) or less
within 9 hours of death and chilling continued to bring the internal
temperature of the fish to 40°F (4.4°C) or less;
OR
- Fish exposed to air or water temperatures above 83°F (28.3°C), ), or
large tuna (i.e., above 20 lbs.) that are eviscerated before on-board
chilling, should be placed in ice (including packing the belly cavity of
large tuna with ice) or in refrigerated seawater or brine at 40°F (4.4°C)
or less within 6 hours of death;
OR
- Large tuna (i.e., above 20 lbs.) that are not eviscerated before on-board
chilling: The internal temperature of the fish was brought to 50°F (10°C)
or less within 6 hours of death and chilling continued to bring the internal
temperature of the fish to 40°F (4.4°C) or less;
OR
- Other critical limits for on-board handling (e.g. maximum refrigerated
brine or seawater temperature, maximum fish size, maximum fish to
brine/seawater/ice ratio, maximum ambient temperature exposure time before
chilling) necessary to achieve a cooling rate that will prevent development
of histamine in the specific species, as established through a scientific
study;
AND
- For fish held refrigerated (not frozen) on-board the vessel: The fish were
stored at or below 40°F (4.4°C) thereafter;
AND
- Sensory examination of a representative sample of fish shows no more than
2.5% decomposition (persistent and readily perceptible) in the sample. For
example, no more than 3 fish in a sample of 118 fish may show signs of
decomposition;
AND
- For fish held iced or refrigerated (not frozen) on-board the vessel and
delivered 24 or more hours after death: The internal temperature should be
40°F (4.4°C) or below;
OR
- For fish held iced or refrigerated (not frozen) on-board the vessel and
delivered from 12 to less than 24 hours after death: The internal
temperature should be 50°F (10°C) or below;
OR
- For fish held iced or refrigerated (not frozen) on-board the vessel and
delivered in less than 12 hours after death: The internal temperature should
demonstrate that appropriate chilling methods were used onboard the harvest
vessel. Chilling of the fish must begin on the harvest vessel regardless of
the time from death to delivery, unless the environmental conditions (e.g.
air and water temperatures) are consistently below 40°F (4.4°C) from the
time of death to delivery (FDA, 2001a).
1b. For receipt by primary (first) processor Histamine Testing Option):
Analysis of a representative sample of fish shows less than 50 ppm histamine
in all fish in the sample;
AND
- Sensory examination of a representative sample of fish shows no more than
2.5% decomposition (persistent and readily perceptible) in the sample. For
example, no more than 3 fish in a sample of 118 fish may show signs of
decomposition;
AND
- For fish held iced or refrigerated (not frozen) on-board the vessel and
delivered 24 or more hours after death: The internal temperature should be
40°F (4.4°C) or below;
OR
- For fish held iced or refrigerated (not frozen) on-board the vessel and
delivered from 12 to less than 24 hours after death: The internal
temperature should be 50°F (10°C) or below;
OR
- For fish held iced or refrigerated (not frozen) on-board the vessel and
delivered in less than 12 hours after death: The internal temperature should
demonstrate that appropriate chilling methods were used onboard the harvest
vessel. Chilling of the fish must begin on the harvest vessel regardless of
the time from death to delivery, unless the environmental conditions (e.g.
air and water temperatures) are consistently below 40°F (4.4°C) from the
time of death to delivery (FDA, 2001a).
2. For receipt by secondary processor (including warehouse):
- For fish delivered refrigerated (not frozen): All lots received are
accompanied by transportation records that show that the fish were held at
or below 40°F (4.4°C) throughout transit;
OR
- For fish held under ice or chemical cooling media: There is an adequate
quantity of ice or other cooling media at the time of delivery to completely
surround the product (FDA, 2001a).
3. For processing steps:
During processing and refrigerated (not frozen) storage that occurs before
cooking (e.g. canned tuna "precook"): For fish that have not been
previously frozen:
- The fish are not exposed to ambient temperatures above 40°F (4.4°C) for
more than 4 hours, cumulatively, if any portion of that time is at
temperatures above 70°F (21°C);
OR
- The fish are not exposed to ambient temperatures above 40°F (4.4°C) for
more than 8 hours, cumulatively, as long as no portion of that time is at
temperatures above 70°F (21°C);
(Note: Only one of the above two limits may be selected. They may not be
added for a total exposure of 12 hours.)
OR
- For fish that have been previously frozen: The fish are not exposed to
ambient temperatures above 40°F (4.4°C) for more than 12 hours,
cumulatively, if any portion of that time is at temperatures above 70°F (21°C);
OR
- The fish are not exposed to ambient temperatures above 40°F (4.4°C) for
more than 24 hours, cumulatively, as long as no portion of that time is at
temperatures above 70°F (21°C).
(Note: Only one of the above two limits may be selected. They may not be
added for a total exposure of 12 hours.) (FDA, 2001a)
FDA guidelines for
histamine in tuna, mahi mahi, and related fish.
-
Histamine by capillary electrophoresis (Mopper and Sciacchitano,
1993)
-
Histamine in canned fish: High performance liquid chromatography
method (Yen and Hsieh, 1991).
-
Histamine in canned tuna: Fluorometric method (Lerke and
Bell, 1976).
-
Histamine in fish products: Thin layer chromatographic method
(Schutz et al., 1976).
-
Histamine in fish: Enzyme-based screening test (Lerke et
al., 1983).
-
Histamine in fish: Fluorometric method (Taylor et al., 1978).
-
Histamine in fish: Oxygen-sensor-based method (Ohashi et
al., 1994).
-
Histamine in seafood: Automated kinetics-enhanced flow-injection method
(Hungerford et al., 2001)
-
Histamine in seafood: Biological method (AOAC, 1995a).
-
Histamine in seafood: Chemical method (AOAC, 1995b).
-
Histamine in seafood: Flow-injection method (Hungerford et
al., 1990).
-
Histamine in seafood: Fluorometric method (AOAC, 1995c).
-
Histamine in tuna: Copper chelation method (Bateman et al.,
1994).
-
Histamine in unprocessed and canned fish: Guinea pig ileum
method (Geiger, 1944).
-
Inhibitors of histaminase enzymes (Hungerford and Arefyev,
1992)
Commercial test products for histamine.
|
Test |
Analytical Technique |
Approx.
Total Test Time |
Supplier |
ALERT® for Histamine
[Sensitivity: 2.5 ppm] |
ELISA |
35 min |
Neogen Corporation
Contact: Jennifer Baker
620 Lesher Pl.
Lansing, MI 48912
Phone: 800/234-5333; 517/372-9004
E-mail: neogen-info@neogen.com
Web: www.neogen.com |
|
EIA for Histamine in Fish Extract, K1-HTM
[Sensitivity: 2.5 ppm, quantitative 1-50 ppm] |
Enzyme immunoassay |
90 min |
Immuno-Diagnostic Reagents
Contact: Siong Wie
P.O. Box 2659
Vista, CA 92085-2659
Phone: 858/350-9608
E-mail: idr@tiora.net
Web: www.tiora.net/~idr/ |
EIA for Histamine Fishmeal and Bonemeal, K2-HTM
[Sensitivity: 5 ppm, qualitative] |
Enzyme immunoassay |
35 min |
Immuno-Diagnostic Reagents
Contact: Siong Wie
P.O. Box 2659
Vista, CA 92085-2659
Phone: 858/350-9608
E-mail: idr@tiora.net
Web: www.tiora.net/~idr/ |
EIA for Histamine in Raw and Canned fish, K3-HTM
[Sensitivity: 5 ppm, qualitative] |
Enzyme immunoassay |
35 min |
Immuno-Diagnostic Reagents
Contact: Siong Wie
P.O. Box 2659
Vista, CA 92085-2659
Phone: 858/350-9608
E-mail: idr@tiora.net
Web: www.tiora.net/~idr/ |
HISQUICK™ Histamine (BA-20-3000 - 48 Columns)
[Sensitivity: 20 ppm, quantitative] |
Color test |
12 min. |
Rocky Mountain Diagnostics, Inc.
Contact: Tim Folks
703 N. Tejon Suite C.
Colorado Springs, CO 80903
Phone: 877/477-0039
E-mail: tfolks@rmdiagnostics.com
Web: www.rmdiagnostics.com/ |
Histamine EIA Food (BA-10-3100 - 96 Wells)
[Sensitivity: 0.5 ppb, quantitative] |
Enzyme immunoassay |
2 h |
Rocky Mountain Diagnostics, Inc.
Contact: Tim Folks
703 N. Tejon Suite C.
Colorado Springs, CO 80903
Phone: 877/477-0039
E-mail: tfolks@rmdiagnostics.com
Web: www.rmdiagnostics.com/ |
Histamarine Test Kit1
[Sensitivity: 0.5 ppm, quantitative from 1 to 500 ppm] |
Enzyme immunoassay |
1 h |
Immunotech
Contact: Alain Artus
130, av. Delattre de Tassigny
B.P. 177
13276 Marseille Cedex 9
FRANCE
Phone: 33 491 17 27 46
E-mail: artus@immunotech.fr
Web: www.immunotech.fr |
HistaMeter
[Sensitivity: 0-50 ppm, qualitative] |
Enzyme immunoassay |
1 h |
Biomedix
Contact: Claver Bundac
1105 #F North Golden Springs Dr.
Diamond Bar, CA 91765
Phone: 800/674-8648 #4282; 909/396-0244
E-mail: cb4biomedx@aol.com
|
HistaQuant
[Sensitivity: 0-500 ppm, quantitative] |
Enzyme immunoassay |
1-1/2 h |
Biomedix
Contact: Claver Bundac
1105 #F North Golden Springs Dr.
Diamond Bar, CA 91765
Phone: 800/674-8648 #4282; 909/396-0244
E-mail: cb4biomedx@aol.com
|
HistaSure Dipstick Assay
[5ppm Pass/Fail] |
Fluorescence Labeled Optical-Read Immuno Dipstick Assay (F.L.O.R.I.D.A.) |
5 min |
|
RIDASCREEN® Histamin R1602
[Sensitivity: 2.5 ppm; quantitative] |
ELISA |
2-5/6h |
R-Biopharm, Inc.
Contact: Sean Tinkey
7950 US 27 South
Marshall, MI 49068
Phone: 877/789-3033
E-mail: sales@r-biopharm.com
Web: www.r-biopharm.com/food/other/hista.html |
RidaQuick Histamin (R1603-96 Wells)
[Sensitivity 20 ppm; quantitative] |
ELISA |
12 min |
R-Biopharm, Inc.
Contact: Sean Tinkey
7950 US 27 South
Marshall, MI 49068
Phone: 877/789-3033
E-mail: sales@r-biopharm.com
Web: www.r-biopharm.com/quickhistamin.pdf |
|
Transia Tube Histamine |
ELISA |
1 h |
Diffchamb AB
FO Petersons Gata 32
SE-421 31 Västra Frölunda, Sweden
Phone: +46 -31-742 33 50
E-mail: market.dept@diffchamb.se
Web: www.diffchamb.se |
Veratox® for Histamine
[Sensitivity: < 2.5 ppm, quantitative from 0 to 50 ppm] |
ELISA |
35 min |
Neogen Corporation
Contact: Jennifer Baker
620 Lesher Pl.
Lansing, MI 48912
Phone: 800/234-5333; 517/372-9004
E-mail: neogen-info@neogen.com
Web: www.neogen.com |
1AOAC Approved
AOAC. 1995a. Histamine in seafood: Biological method. Sec. 35.1.30, Method 954.04. In Official Methods of Analysis of AOAC International, 16th ed., P.A. Cunniff (Ed.), p.14-15. AOAC International, Gaithersburg, MD.
AOAC. 1995b. Histamine in seafood: Chemical method. Sec. 35.5.31, Method 957.07. In Official Methods of Analysis of AOAC International, 16th ed., P.A. Cunniff (Ed.), p.15-16. AOAC International, Gaithersburg, MD.
AOAC. 1995c. Histamine in seafood: Fluorometric method. Sec. 35.1.32, Method 977.13. In Official Methods of Analysis of AOAC International, 16th ed., P.A. Cunniff (Ed.), p. 6-17. AOAC International, Gaithersburg, MD.
Bateman, R.C., Eldrige, D.B., Wade, S., McCoy, Messer, J., Jester, E.L.E., and Mowdy, D.E. 1994. Copper chelation assay for histamine in tuna. J. Food Sci. 59(3):517-518, 543.
FDA. 2001a. Scombrotoxin (histamine) formation. Ch. 7. In Fish and Fishery Products Hazards and Controls
Guidance. 3rd ed., p. 83-102. Food and Drug Administration, Center for Food Safety and Applied Nutrition, Office of Seafood, Washington, DC.
FDA. 2001b. Other Decomposition-Related Hazards. Ch. 8. In Fish and Fishery Products Hazards and Controls
Guidance. 3rd ed., p. 103-104. Food and Drug Administration, Center for Food Safety and Applied Nutrition, Office of Seafood, Washington, DC.
FDA. 1998c. FDA & EPA Guidance Levels. Appendix 5. In Fish and Fishery Products Hazards and Controls Guide. 2nd ed., p. 245-248. Department of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Food Safety and Applied Nutrition, Office of Seafood, Washington, DC.
Geiger, E. 1944. Histamine content of unprocessed and canned fish. A tentative method for quantitative determination of spoilage. Food Research 9(4):293-297.
Hungerford, J.M. and Arefyev, A.A. 1992. Flow-injection assay of enzyme inhibition using immobilized diamine oxidase.
Anal. Chim. Acta 261(1-2):351-359.
Hungerford, J.M., Hollingworth, T.A., and Wekell, M.M. 2001. Automated kinetics-enhanced flow-injection
method for histamine in regulatory laboratories: rapid screening and suitability requirements,
Anal. Chim. Acta 438(1-2):123-129.
Hungerford, J.M., Walker, K.D., Wekell, M.M., LaRose, J.E., and Throm, H.R. 1990. Selective determination of histamine by flow injection analysis. Anal.
Chem.62(18):1971-1976.
Lerke, P.A., Porcuna, M.N., and Chin, H.B. 1983. Screening test for histamine in fish. J. Food Sci. 48:155-157.
Lerke, P.A. and Bell, L.D. 1976. A rapid fluorometric method for the determination of histamine in canned tuna. J. Food Sci. 41:1282-1284.
Mopper, B. and Sciacchitano, C.J. 1993. Capllary zone electrophoretic determination of histamine in fish. JAOAC 77(4):881-883.
Ohashi, M., Nomura, F., Suzuki, M., Otsuka, M., Adachi, O., and Arakawa, N. 1994. Oxygen-sensor-based simple assay of histamine in fish using purified amine oxidase. J. Food Sci. 59(3):519-522.
Schutz, D.E., Chang, G.W., and Bjeldanes, L.F. 1976. Rapid thin layer chromatographic method for the determination of histamine in fish products. J. AOAC. 59(6):1224-1225.
Taylor, S.L., Lieber, E.R., and Leatherwood, M. 1978. A simplified method for histamine analysis of foods. J. Food Sci. 43:247-250.
Yen G. and Hsieh, C. 1991. Simultaneous analysis of biogenic amines in canned fish by HPLC. J. Food Sci. 56(1):158-160.
Send questions or comments to rjprice@ucdavis.edu
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