This review describes the foundations, methodology, applications, advantages, and disadvantages of immunohistochemistry used for the diagnosis of swine infectious disease. Immunohistochemistry (IHC) relies on the binding of immunoglobulins to antigens present in tissues. Numerous proteins from infectious agents (viruses, bacteria, parasites, fungi) can be detected with this technique. The antigen-antibody reaction is revealed by an enzymatic reaction or the color emission of a fluorochrome. Due to the specificity and sensitivity of this reaction, IHC is an excellent alternative to more complex, expensive, and time-consuming laboratory procedures such as virus isolation or microbiological culture.
Keywords: swine, diagnosis, immunohistochemistry, infectious disease
Received: April 6, 1998
Accepted: November 15, 1998
Many factors--history, gross and microscopic findings, availability of certain techniques, cost, sensitivity, specificity, and speed--determine which diagnostic test practitioners and diagnosticians should use. Immunohistochemistry (IHC) is used increasingly frequently because it is relatively inexpensive, fast, and sensitive, and is less laborious than traditional microbiologic procedures. Immunohistochemistry uses immunologic techniques to detect specific proteins to identify an infectious agent. This paper describes the scientific basis of IHC, as well as its methodology, advantages, disadvantages, and application in the diagnosis of swine infectious disease.
Immunohistochemical techniques detect antigens in tissues or cells. Many compounds--mainly proteins, but also carbohydrates, nucleic acids, lipids, and other compounds--can act as antigens that will be recognized by antibodies.
Two types of antibodies are used in immunohistochemistry:
Polyclonal antibodies are produced by immunizing rabbits or another species with the antigen to be detected. Polyclonal antibodies are multivalent, meaning that they contain antibodies for several regions of the antigen molecule, providing a strong detection capacity. However, polyclonal antibodies can cross-react with antigens from different organisms (e.g., polyclonal antibodies raised against bacterial lipopolysaccharide might also recognize different species of Gram-negative bacteria).
Monoclonal antibodies are produced in mice and are the result of fusing immunoglobulin-producing B cells with myeloma (plasma cell tumor) cells. This fusion results in hybrid cells, which continue to grow and divide in culture and which also produce antibodies. Monoclonal antibodies have the advantage of being highly specific for a single sequence or "epitope" of the antigen molecule. However, because monoclonal antibodies will bind only to one site (epitope) of the antigen molecule, fewer antibody molecules will bind to the antigen and be subsequently detected by the labeling method. Fixation may modify that particular binding site, making the antibody unable to recognize (bind to) the antigen; and thus fail to detect it. Deciding whether to use polyclonal or monoclonal antibodies, therefore, depends on the availability of reagents and how they perform in tissue sections. There is no rule of thumb--usually, it is necessary to try different antibodies to determine which one performs better under standard fixation and tissue processing methods. In theory, prolonged fixation will be more damaging to monoclonal antibodies than to polyclonal antibodies.
Most of the antibodies (immunoglobulins) used in IHC are of the immunoglobulin G (IgG) class (Figure 1). An IgG molecule consists of four polypeptide chains: two heavy chains and two light chains. At one end of the heavy chains is the constant fragment (Fc) of a particular species; at the other end of the heavy chains and the two light chains are the variable regions of immunoglobulins (two variable regions per immunoglobulin). The variable region of the immunoglobulin is the binding site for antigens (antigen-binding fragment or F[ab]). Each immunoglobulin will recognize only one antigen through its variable regions. Infectious organisms are made of multiple proteins and other antigenic molecules. Ideally, IHC will detect a single protein, or a component thereof, that is specific to a given specific infectious agent.
Immunohistochemistry is usually conducted on formalinized tissues. Immunohistochemical techniques that can be used on frozen samples are available but they are not widely used in field situations. It is critical that the time lapse between the death of the animal and the collection of tissues for IHC be as brief as possible. Postmortem decomposition can cause both false positive and false negative results.
Factors that influence tissue quality for IHC include:
Unfortunately, antigens are not always evenly distributed through a lesion or organ and, on occasion, the severity of lesions does not correlate with the localization of the infectious agent.
For practical purposes, the sooner the samples are placed in formalin, the better. Samples should include both the severely affected areas and the adjacent "normal looking" area, a sampling approach that should be used for any type of pathological examination. If a combined bacterial and viral infection is suspected (e.g., pneumonia), take different samples of the organ, including severely affected and less affected regions.
Fixation can preserve both the antigenicity of proteins and the morphology of tissues; ideally, it preserves tissues as they were. The routine fixative used in histopathology is 10% neutral buffered formalin and it is also the standard fixative for IHC.
One additional advantage of formalin-fixed and paraffin-embedded tissues is that retrospective studies can be done using tissues stored for many years. Therefore, diseases not detectable several decades ago can now be retrospectively diagnosed with IHC on formalin-fixed, paraffin-embedded tissues.
In general, the sensitivity of a reaction depends on how many signal-generating molecules (e.g., peroxidase) are bound to an antigen-immunoglobulin complex in the tissue section. Formalin cross links proteins that can limit access of antibodies to antigenic sites and therefore may cause false negative results even in the presence of large amounts of antigen. Therefore, it is important to limit the time the sample spends in the fixative. This interval should be limited to no more than 2 days, although response to fixation might be different depending on the type of antigen examined.
Since it may not always be possible to limit the duration of fixation to less than 2 days, laboratories use a variety of antigen unmasking techniques (such as enzymes and/or heat) to recover antigen expression. Samples to be fixed should not be thicker than 0.5 cm and ideally the ratio of fixative to sample should be 10:1 (v:v). If you collect samples of good quality (fresh, of the right size, and representative of the lesion) and place them in formalin immediately, you have preserved the specimen indefinitely. If for any reason fresh tissues do not arrive at the diagnostic laboratory in good condition, making isolation or fluorescent antibody procedures impossible, IHC can still be used to detect pathogens on fixed tissues.
Once tissue samples are fixed, they are embedded in paraffin or resins, sectioned in a microtome and mounted on glass slides. Immunohistochemical procedures are then performed on these unstained tissue sections.
There are several steps in an immunohistochemical reaction. In general, it is necessary to use procedures that allow antigens in formalin-fixed tissues to be recognized by antisera. These methods are generically referred to as antigen unmasking or antigen retrieval. Sometimes it is also necessary to reduce nonspecific reactions (background) before starting the immunohistochemical reaction.
There are several systems to retrieve antigens:
A major advance in immunohistochemistry was the discovery in the early 1990s that some previously nonreactive antigens in formalin-fixed, paraffin-embedded tissues, even after enzymatic treatment, could be "retrieved" by heating sections in a buffer solution. Microwave ovens, pressure cookers, and steamers have all been successfully used as sources of heat. It has been hypothesized that heating provides the energy not only to rupture the hydroxyl bonds formed by the fixative with the protein antigen, freeing some antigens, but also releases tissue-bound calcium ions that contribute to tighter bonds with the fixative. Heat-based retrieval systems not only permit some antigens to be detected that otherwise go undetected, but also increase the sensitivity of some methods, allowing the antibody to be further diluted. However, every antigen has to be tested to find the best retrieval conditions to optimize results.
The use of blocking agents for endogenous enzyme activity (e.g., peroxidase, alkaline phosphatase, etc.) are also necessary when using enzyme-based methods. A similar problem may exist with avidin-biotin methods due to the presence of endogenous biotin activity in many tissues.
Visualization of the antigen-antibody reaction site depends on a signal-generating system which is conjugated to the antibody, or other molecules such as avidin. There are three types of signal-generating systems:
The primary goal of an IHC test is to be sensitive enough to demonstrate a specific antigen-antibody binding in tissue sections. Since Coons first described an in situ immunocytochemical technique, new methods have been developed that dramatically increase sensitivity while maintaining the specificity of the reaction.
Immunohistochemistry can use a direct, indirect, or multiple layer method:
With the PAP method (Figure 9), two first layers of antibodies are similar to the indirect method but are not labeled. The third layer consists of immunoglobulins that recognize (bind) the peroxidase molecules (PAP complex) and they are raised in the same species as for the first antibody layer. Therefore, the second antibody layer will act as a "bridge" between the first and the third layer of antibodies. This method is 100-1000 times more sensitive than the indirect method (due to the increased number of signal-generating molecules per molecule of antigen) without loss of specificity.
The avidin-biotin complex (ABC) method (Figure 10) is a multiple-layer method that relies on the extremely high affinity between avidin, a glycoprotein from egg white, and biotin, a vitamin. In this method, the second antibody is biotinylated and the third layer is a complex of avidin mixed with biotin that is labeled with a marker (enzyme, fluorochrome, etc.).
Immunohistochemistry is intended to help in diagnosing the etiologic agent of an infectious process. The presence of a colored reaction (provided that it is specific according to the controls used) indicates the presence of components of the infectious agent tested for. Whether the appearance of a specific color is significant or not in the context of the case is open to interpretation by the diagnostician. A careful assessment of the clinical history, lesions, and all test results should be made before attempting to formulate a definitive diagnosis. Conversely, a negative result by immunohistochemistry does not completely rule out the presence of a particular infectious agent or its potential significance to the case. Results by immunohistochemistry, like those obtained by other diagnostic methods, must be supported by clinicopathologic data.
Table 1 lists porcine infectious agents that can be detected by IHC. Because not every laboratory has the resources to detect all of these or other infectious agents by immunohistochemistry, it is advisable to contact your local diagnostic laboratory to know what tests are available in your area.
Immunohistochemistry is a valuable technique for diagnosing infectious diseases of pigs. It is sensitive, specific, fairly inexpensive, and easy to perform. Although in most diagnostic laboratories it is not considered the "gold standard," it is as specific as bacterial and virus isolation, provided adequate controls are used.
1. Beesley JE. Immunocytochemistry. A practical approach. Oxford, United Kingdom: Oxford University Press. 1993.
2. Polak JM, Van Noorden S. Introduction to Immunocytochemistry. 2nd edition. New York: Springer Verlag. 1997.
3. Haines DM, Chelack BJ. Technical considerations for developing enzyme immunohistochemical staining procedures on formalin-fixed paraffin-embedded tissues for diagnostic pathology. J Vet Diagn Invest. 1991;3:101-112.
4. Werner M, von Wasielewski R, Komminoth P. Antigen retrieval, signal amplification and intensification in immunohistochemistry. Histochem Cell Biol. 1996;105:253-260.
5. White AK, Hansen-Lardy L, Broderssen BW, et al. Enhanced immunohistochemical detection of infectious agents in formalin-fixed, paraffin-embedded tissues following heat-mediated antigen retrieval. J Vet Diagn Invest. 1998;10:214-217.
6. Shi S-R, Key ME, Kalra KL. Antigen retrieval in formalin-fixed, paraffin-embedded tissues: an enhancement method for immunocytochemical staining staining based on microwave oven heating of tissue sections. J. Histochem. Cytochem. 1991;39:741-748.
7. Morgan JM, Navabi H, Schmid KW, et al. Possible role of tissue-bond calcium ions in citrate-mediated high-temperature antigen retrieval. J Pathol. 1994;174:301-307.
8. Cattoretti G, Suurjmeijer AJH. Antigen unmasking on formalin-fixed paraffin embedded tissues using microwaves: A review. Adv Anat Pathol. 1995;2:2-9.
9. Cuevas EC, Bateman AC, Wilking BS, et al. Microwave antigen retrieval in immunohistochemistry: a study of 80 antibodies. J Clin Pathol. 1994;47:448-452.
10. Shi S-R, Cote RJ, Taylor CR. Antigen retrieval immunohistochemistry: Past, present, and future. J Histochem Cytochem. 1997;45:327-343.
11. Taylor CR, Shi S-R, Cote RJ. Antigen retrieval for immunohistochemistry: Status and need for greater standardization. Appl Immunohistochem. 1996;4:144-166.
12. Speel EJM, Ramaekers FCS, Hopman AHN. Cytochemical detection systems for in situ hybridization, and the combination with immunocytochemistry. Who is still afraid of red, green and blue? Histochem J. 1995;27:833-858.
13. Lackie PM. Immunogold silver staining for light microscopy. Histochem Cell Biol. 1996;106:9-17.
14. Holgate CS, Jackson P, Lauder I, et al. Surface membrane staining of immunoglobulins in paraffin sections of non-Hodgkin's lymphoma using immunogold-silver staining technique. J Clin Pathol. 1983;36:742-746.
15. Coons AH, Kaplan MH. Localization of antigen in tissue cells. J Exp Med. 1950;91:1-13.
16. Haines DM, Clark EG. Enzyme immunohistochemical staining of formalin-fixed tissues for diagnosis in veterinary pathology. Can Vet J. 1991;32:295-302.
17. Chu RM, Li N-J, Glock RD et al. Applications of peroxidase-antiperoxidase staining technique for detection of transmissible gastroenteritis virus in pigs. Am J Vet Res. 1982;43:77-81.
18. Larochelle R, Magar R. The application of immunogold silver staining (IGSS) for the detection of the transmissible gastroenteritis virus in fixed tissue. J Vet Diagn Invest. 1993;5:16-20.
19. Shoup DI, Swayne DE, Jackwood DJ et al. Immunohistochemistry of transmissible gastroenteritis virus antigens in fixed paraffin-embedded tissues. J Vet Diagn Invest. 1996;8:161-167.
20. Belak K, Funa K, Kelly R et al. Rapid diagnosis of Aujeszky's disease in pigs by improved in situ hybridization using biotinylated probes on paraffin-embedded tissue sections. J Vet Med. 1989;36:10-20.
21. Ducatelle R, Coussement W, Hoorens J. Immunoperoxidase study of Aujeszky's disease in pigs. Res Vet Sci. 1982;32:294-302.
22. Grieco V, Gelmetti D, Finazzi G et al. Immunohistologic diagnosis of pseudorabies (Aujeszky's disease) using monoclonal antibodies. J Vet Diagn Invest. 1997;9:326-328.
23. Segalés J, Balasch M, Domingo M et al. Immunohistochemical demonstration of the spread of pneumotropic strain 4892 of Aujeszky's disease virus in conventional pigs. J Comp Path. 1997;116:387-395.
24. Larochelle R, Magar R. Comparison of immunogold silver staining (IGSS) with two immunoperoxidase staining systems for the detection of porcine reproductive and respiratory syndrome virus (PRRSV) antigens in formalin-fixed tissues. J Vet Diagn Invest. 1995;7:540-543.
25. Larochelle R, Magar R. Detection of porcine reproductive and respiratory syndrome virus in paraffin-embedded tissues: comparison of immunohistochemistry and in situ hybridization. J Virol Meth. 1997;63:227-235.
26. Brown IH, Done SH, Spencer YI et al. Pathogenicity of a swine influenza H1N1 virus antigenically distinguishable from classical and European strains. Vet Rec. 1993;132:598-602.
27. Vincent LL, Janke BH, Paul PS et al. A monoclonal-antibody-based immunohistochemical method for the detection of swine influenza virus in formalin-fixed, paraffin-embedded tissues. J. Vet. Diagn. Invest. 1997;9:191-195.
28. Ahn K, Chae C, Kweon CH. Immunohistochemical identification of porcine respiratory coronavirus antigen in the lung of conventional pigs. Vet. Pathol. 1997;34:167-169.
29. O'Toole D, Broewn I, Bridges A et al. Pathogenicity of experimental infection with "pneumotropic" porcine coronavirus. Res Vet Sci. 1989;47:23-29.
30. Fernández A, Perez J, Carrasco L et al. Detection of African swine fever viral antigens in paraffin-embedded tissues by use of immunohistologic methods and polyclonal antibodies. Am J Vet Res. 1992;53:1462-1467.
31. Gelberg HB, Hall WF, Woode GN et al. Multinucleate enterocytes associated with experimental group A porcine rotavirus infection. Vet Pathol. 1990;27:453-454.
32. Magar R, Larochelle R. Immunohistochemical detection of porcine rotavirus using immunogold silver staining (IGSS). J Vet Diagn Invest. 1992;4:3-7.
33. Sueyoshi M, Tsuda T, Yamazaki K et al. An immunohistochemical investigation of porcine epidemic diarrhoea. J Comp Path. 1995;113:59-67.
34. de las Mulas JM, Ruiz-Villamor E, Donoso S et al. Immunohistochemical detection of hog cholera viral glycoprotein 55 in paraffin-embedded tissues. J Vet Diagn Invest. 1997;9:10-16.
35. Mulder WAM, van Poelwijk F, Moormann RJM et al. Detection of early infection of swine vesicular disease virus in porcine cells and skin sections. A comparison of immunohistochemistry and in-situ hybridization. J Virol Meth. 1997;68:169-175.
36. Agungpriyono DR, Nakagawa M, Morozumi T et al. Pathology of naturally occurring porcine adenovirus type 4 infection in Japan. Res. Bull. Obihiro Univ. 1997;20:113-122.
37. Allan GM, McNeilly F, Walker I et al. A sequential study of experimental porcine paramyxovirus (LPMV) infection of pigs: immunostaining of crysotat sections and virus isolation. J. Vet. Diagn. Invest. 1996;8:405-413.
38. Kawashima K, Yamada S, Kobayashi H et al. Detection of porcine reproductive and respiratory syndrome virus and Mycoplasma hyorhinis antigens in pulmonary lesions of pigs suffering from respiratory distress. J. Comp. Pathol. 1996;114:315-323.
39. Segalés J, Domingo M, Solano GI et al. Immunohistochemical detection of Haemophilus parasuis serovar 5 in formalin-fixed, paraffin-embedded tissues of experimentally infected swine. J Vet Diagn Invest. 1997;9:237-243.
40. Ajito T, Haga Y, Homma S et al. Immunohistological evaluation on respiratory lesions of pigs intranasally inoculated with Actinobacillus pleuropneumoniae serotype I. J. Vet. Med. Sci. 1996;58:297-303.
41. Scanziani E, Treves E, Giusti AM et al. Identificazione immunohistochimica di Streptococcus suis tipo 2 in tonsille di suino. Obiettivi e Documenti Vet. 1993;14:51-54.
42. Morita T, Fukuda H, Awakura T et al. Demonstration of Mycoplasma hyorhinis as a possible primary pathogen for porcine otitis media. Vet Pathol. 1995;32:107-111.
43. Dee SA. Apparent prevention of Mycoplasma hyopneumoniae infection in growing pigs with a low-cost modified medicated-early-weaning program. Swine Health Prod. 1994;2:7-12.
44. Pospischil A, Wood RL, Anderson TD. Peroxidase-antiperoxidase and immunogold labeling of Salmonella typhimurium and Salmonella choleraesuis var kunzendorf in tissues of experimentally infected swine. Am J Vet Res. 1990;51:619-624.
45. Ackerman MR, Cheville NF, Gallagher JE. Colonization of the pharyngeal tonsil and respiratory tract of the gnotobiotic pig by a toxigenic strain of Pasteurella multocida type D. Vet. Pathol. 1991;28:267-274.
46. Webb DL, Duhamel GE, Mathiesen MR et al. Cecal spirochetosis associated with Serpulina pilosicoli in captive juvenile ring-necked pheasants. Avian Dis. 1997;41:997-1002.
47. Wada Y, Nakaoka Y, Kondo H et al. Dual infection with attaching and effacing Escherichia coli and enterotoxigenic Escherichia coli in post-weaning pigs. J Comp Path. 1996;114:93-99.
48. Szeredi L, Schiller I, Sydler T et al. Intestinal Chlamydia in finishing pigs. Vet Pathol. 1996;33:369-374.
49. Chappel RJ, Prime RW, Millar BD, et al. Comparison of diagnostic procedures for porcine leptospirosis. Vet Microbiol. 1992;30:151-163.
50. Oh KS, Lee CS. Pathological studies on exudative epidermitis in experimentally infected pigs. II. Immunohistochemistry and electron microscopy. Korean J. Vet. Res. 1995;35:553-562.
51. Franz B, Davies ME, Horner A. Localization of viable bacteria and bacterial antigens in arthritic joints of Erysipelothrix rhusiopathiae-infected pigs. FEMS Immunol. Med. Microbiol. 1995;12:137-142.
52. Griglio B, Sattanino G, Grivetto V et al. Sulla epidemiologia e diagnosi della tuberculosi suina in Piemonte. Nuovo Progr. Vet. 1992;47:467-471.
53. Dubey JP, Beasttie CP. Toxoplasmosis of Animals and Man. Boca Raton, Florida: CRC Press, Inc. 1988.
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