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Topic:Serology

Serology in horse research involves the study and analysis of blood serum to detect the presence of antibodies or antigens associated with infectious diseases and other health conditions. It is a diagnostic tool used to identify immune responses to pathogens, vaccination status, and exposure to specific diseases. Serological tests in equine research can include enzyme-linked immunosorbent assays (ELISA), complement fixation tests, and virus neutralization tests. These tests help in understanding the epidemiology of diseases, monitoring herd health, and informing vaccination strategies. This page compiles peer-reviewed research studies and scholarly articles that explore the methodologies, applications, and implications of serological testing in equine medicine.
Biochemical studies on equine infectious anaemia.
Folia veterinaria Latina    July 1, 1976   Volume 6, Issue 3 275-288 
Palomba E, Martone F, Meduri A, Vaccaro A, Damiani N.A description is given of an outbreak of equine infectious anaemia (E.I.A.) in Campania [at Naples and Aversa (Caserta)]; it was diagnosed by clinical, pathological and serological examinations (Coggins test). Using the serum of 45 horses with E.I.A. and 11 healthy horses (controls), numerous investigations were carried out on: enzymes, intrinsic coagulation factors, lipids and other substances. The results obtained were very interesting and show that in this disease there are significant increases in many enzymes (LDH, LAP, gamma-GT, CPK, PK and ALD) and copper. Insignificant increases were f...
[Studies on the flora of the genital- and nasal mucosa of horses, especially of stallions with bacterial pathogens important in horse breeding and with particular reference to klebsiella. III. Serologic studies on klebsiellas].
Berliner und Munchener tierarztliche Wochenschrift    May 15, 1976   Volume 89, Issue 10 193-196 
Weiss R, Böhm KH, Merkt H, Klug E, Heuser H.No abstract available
Serological detection of equid herpesvirus 1 infections of the respiratory tract.
Equine veterinary journal    April 1, 1976   Volume 8, Issue 2 58-65 doi: 10.1111/j.2042-3306.1976.tb03291.x
Thomson GR, Mumford JA, Campbell J, Griffiths L, Clapham P.An investigation was made of 3 serological tests (virus neutralization, complement fixation and indirect immunofluorescence), which are applicable to epidemiological studies of infections by Equid herpesvirus 1 (EHV-1). Sera from gnotobiotic foals inoculated intranasally with various strains of EHV-1 were unable in some cases to neutralize heterologous strains and these results were not consistent with the existence of clearly-defined subtypes of EHV-1, as previously proposed. The cross-reactions in complement-fixation tests paralleled those with neutralization but immunofluorescence tests wer...
Isolation of mycoplasmas from the respiratory tract of horses in Australia.
The Veterinary record    March 20, 1976   Volume 98, Issue 12 235-237 doi: 10.1136/vr.98.12.235
Moorthy AR, Spradbrow PB.Mycoplasmas were isolated from two of 43 nasal swabs taken from live horses, and from one of 28 tracheal swabs taken from slaughtered horses. The slaughtered horse that yielded mycoplasmas had no gross pathological changes in the respiratory tract, but the nasal isolations were made from horses with rhinitis. The three mycoplasmas could be distinguished by cultural characteristics, and probably they represent three different species.
Serologic evidence of equine leptospirosis in the northeast United States.
The Cornell veterinarian    January 1, 1976   Volume 66, Issue 1 105-109 
Smith RE, Williams IA, Kingsbury ET.Serologic testing for leptospiral antibody was conducted with the macroscopic agglutination test on 1,346 equine serum samples. These were collected from clinically normal horses in 123 purebred herds in the Northeast. Sixty-eight samples (5%) from the population tested reacted at significant levels (1:40 or higher) to one or more of the 5 serotype antigens used. These reactors were from 38 (31%) of the herds tested. Reactions to serotype pomona predominated in 25 (72%) of these 38 herds. Smaller numbers of herds had reactors to canicola, icterohemorrhagiae and grippotyphosa. No significant re...
Natural incidence and persistence of complement-fixing antibody to two equine mycoplasmas.
Journal of comparative pathology    January 1, 1976   Volume 86, Issue 1 87-92 doi: 10.1016/0021-9975(76)90032-3
Hooker JM, Butler M.No abstract available
Identification of allergens in extract of horse hair and dandruff by means of crossed radioimmunoelectrophoresis.
International archives of allergy and applied immunology    January 1, 1976   Volume 51, Issue 1 38-47 doi: 10.1159/000231577
Løwenstein H, Markussen B, Weeke B.Sera from 26 patients and 4 normals were examined for specific IgE binding to antigens of extract of horse hair and dandruff by means of CRIE. 22 of the patients were RAST- and intracutaneous-positive to horse extract. 4 more of the patients were RAST-negative to horse allergens, but showed allergies to extract of allergens from sources other than horse. The remaining four sera from controls were RAST-negative to horse and had no history of allergy. Antigens of horse hair and dandruff showed a significantly higher degree of binding to specific IgE in the sera from the first group of patients t...
Evidence of respiratory tract infection induced by equine herpesvirus, type 2, in the horse.
Canadian journal of microbiology    December 1, 1975   Volume 21, Issue 12 1940-1946 doi: 10.1139/m75-281
Blakeslee JR, Olsen RG, McAllister ES, Fassbender J, Dennis R.Five horses were experimentally exposed to equine herpesvirus 2 strain LK. Two young foals developed chronic pharyngitis (98 and 232 days, respectively). Growth characteristics, cytopathic effects (CPE), inclusion body formation, ether sensitivity, and immunofluorescent analysis indicated that the virus recovered from infected animals was a herpesvirus serologically identical with, or at least antigenically related to EHV-2 strain LK. No significant complement-fixing (CF) or virus-neutralizing (VN) antibody responses were observed in adult horses while both foals demonstrated a rise in CF anti...
Coital exanthema in stallions.
Journal of reproduction and fertility. Supplement    October 1, 1975   Issue 23 147-150 
Pascoe RR, Bagust TJ.Equine coital exanthema can be produced experimentally in stallions by inoculation with an equine herpesvirus (strain 65/61) and be transmitted during coitus with an infected mare. Serological responses to this infection include the production of complement-fixing and serum-neutralizing antibodies which reach maximum levels 14 to 21 days after infection. Complement-fixing antibodies decline rapidly and are usually not detectable by 60 days after infection, whereas serum-neutralizing antibody activity is maintained for at least 1 year. This disparity provides a useful method for the diagnosis o...
Identification of multiple equine infectious anemia antigens by immunodiffusion reactions.
Canadian journal of comparative medicine : Revue canadienne de medecine comparee    October 1, 1975   Volume 39, Issue 4 411-415 
Malmquist WA, Becvar CS.Equine infectious anemia (EIA) cell antigens prepared from infected equine spleen, equine leukocyte cultures or a persistently infected equine dermis cell line contained at least two serologically reacting components. For convenience one component was designated as soluble antigen (SA) and the other as cell-associated antigen (CAA). The SA appeared as a single component when it was prepared from EIA virus precipitated from infectious tissue culture fluid with polyethylene glycol and ether treated but it was mixed with CAA when the source was infected cells. Cytolytic or mechanical disruption o...
[Serological studies on Listeriosis in horses].
Berliner und Munchener tierarztliche Wochenschrift    September 15, 1975   Volume 88, Issue 18 345-347 
Mayer H, Seeliger HP, Sickel E, Kinzler M.No abstract available
Leptospiral antibodies in serum from cattle, swine, horses, deer, sheep, and goats: 1973 and 1974.
American journal of veterinary research    September 11, 1975   Volume 36, Issue 9 1367-1370 
Harrington R.During 2 years (fiscal years 1973 and 1974), microscopic agglutination tests were performed on 12,565 serums from cattle, swine, horses, deer, sheep, and goats for the detection of leptospiral antibodies. The most frequent presumptive infecting serogroups were Hebdomadis, Pomona, Autumnalis, Ballum, Australis, and Canicola.
Studies in atypical Streptococcus equi.
Research in veterinary science    September 1, 1975   Volume 19, Issue 2 115-119 
Woolcock JB.An atypical variety of Streptococcus equi is described. It was shown to be deficient in capsular material, to be very virulent for mice and to possess a cell-wall protein similar to the M-like protein of classical Str equi. Antiserum prepared against classical Str equi effectively opsonised the atypical strains, and induced the formation of long chains by these atypical strains. It is possible that this variant of Str equi can be used to overcome many of the current problems associated with the manufacture and use of strangles vaccines.
Investigation of equine infectious anaemia in Queensland using gel diffusion.
Australian veterinary journal    September 1, 1975   Volume 51, Issue 9 440-442 doi: 10.1111/j.1751-0813.1975.tb15795.x
Thomas RJ.An antigen for the gel diffusion test for equine infectious anaemia (EIA) was prepared from the spleen of a horse experimentally infected with the CQ strain of the virus. The antigen produced a single, distinct line of precipitation when tested against a range of known positive serums, and did not react with pre-inoculation and known negative serums. Extracts prepared from uninfected spleens displayed no reaction when similarly tested. Serum from 34 of 451 Queensland horses contained detectable levels of antibody to EIA virus. The positive serums were from horses in widely separated areas of t...
Some serological reactions to “brucella” antigen in the horse.
Equine veterinary journal    July 1, 1975   Volume 7, Issue 3 137-140 doi: 10.1111/j.2042-3306.1975.tb03251.x
Dawson FL, Durrant DS.Seventy-three samples of serum, from 69 horses and one zebra, were subjected to the Rose Bengal Plate, serum tube agglutination, complement fixation, and anti-equine globulin (Coombs') tests for brucellosis. Fifty-one of the samples, from 48 horses, were submitted by practising veterinary surgeons; of these, 22 samples were associated with clinical conditions which might have been due to brucellosis. Fourteen samples were from healthy horses known to have been in contact with infected cattle, and six were from horses which were known not to have been exposed to brucellosis. More reactions at a...
[The agar-gel immunodiffusion test for the demonstration of equine infectious anemia. I. Examination of horse sera in the Federal Republic of Germany].
DTW. Deutsche tierarztliche Wochenschrift    May 5, 1975   Volume 82, Issue 5 184-187 
Böhm HO.No abstract available
Rapid diagnosis of Venezuelan equine encephalomyelitis by fluorescence microscopy.
American journal of veterinary research    February 1, 1975   Volume 36, Issue 2 167-170 
Erickson GA, Maré CJ.Goat Venezuelan equine encephalomyelitis (VEE) antiserum and normal serum were conjugated and evaluated for staining sensitivity and specificity. Cross-staining with either eastern or western equine encephalomyelitis virus-infected cells did not occur. The baby hamster kidney (BHK-21) cell line when combined with highly specific VEE conjugate detected 100 medium suckling mouse intracerebral lethal doses (suckling mouse LD-50/IC) of the 1B subtype of VEE virus per milliliter of equine tissue suspension. Conjugated goat antiserum was assayed for sensitivity for detection of VEE virus-infected eq...
[Contribution to the antigenic study of influenza viruses in animals. I.–Neuraminidase of the equine influenza viruses (author’s transl)].
Annales de recherches veterinaires. Annals of veterinary research    January 1, 1975   Volume 6, Issue 4 397-410 
Fontaine M, Aymard-Henry M.From the Revised Nomenclature of WHO, the fowl influenza virus A/Duck/Ukraine/63 (Hav7 Neq2) has the same neuraminidase as the equine virus A/equi 2/Miami/63 (Heq2 Neq2); the A/Chicken Germany "N"/49 virus has the same neuraminidase as the equine virus A/equi 1/Prague/56. A comparative study of the antigenic specificities confirms that the Neq2 neuraminidases are closely connected, whatever their animal origin, and that the fowl strain Hav7 Neq2 can be used for the titration of anti Neq2 antibodies in the serums of animals immunized with the equine virus Heq2 Neq2. The Neqi neuraminidases of v...
Standardization of a passive haemagglutination test for the assay of antibodies to tetanus.
The Indian journal of medical research    September 1, 1974   Volume 62, Issue 9 1376-1381 
Rao SS, Joshi UM, Raghavan VP.No abstract available
[Production of an antigen and antiserum for the serodiagnosis of equine infectious anemia].
Veterinariia    June 1, 1974   Issue 7 42-43 
Tokarik BI, Nikitin EE, Bondarenko NE, Shlygin AN, Belousov FF.No abstract available
Comparison of SN and HI antibody dose response curves in chickens, rabbits, foals and horses following vaccination with equine influenza vaccine.
Journal of biological standardization    April 1, 1974   Volume 2, Issue 2 129-137 doi: 10.1016/0092-1157(74)90027-4
Stellmann C, Petermann HG.After vaccination of chickens, rabbits, foals and horses, HI and SN antibody dose response curves were compared for A/Equi 1/Prague and A/Equi 2/Paris strains. The two curves are parallel for a given strain and the relationship of HI and SN titres is constant, whatever the animal species. The distribution of HI and SN titres varies for the two strains. This variation, which is independent of animal species, may be related to the number of sites necessary for the antigenic-antibody response in vitro. It is suggested that the testing of equine influenza vaccine be carried out in the ...
Results of serologic examination of domestic animals for leptospirosis in the Mongolian People’s Republic.
Folia parasitologica    January 1, 1974   Volume 21, Issue 1 21-28 
Sebek Z.No abstract available
Occurrence of antibodies to group specific chlamydia antigen in Finnish sheep, cattle and horse sera.
Acta veterinaria Scandinavica    January 1, 1974   Volume 15, Issue 2 256-263 doi: 10.1186/BF03547486
Neuvonen E, Estola T.A serological survey on the occurrence of group-specific chlamydial antibodies in random sera of Finnish sheep, cattle and horses was performed. The whole material consisted of 1347 serum samples, including 432 ovine, 454 bovine and 461 equine sera. The sera were sent to the laboratory for various serological tests during 1968–1972. Of the ovine sera 9.5%, bovine 12.8 % and equine 7.1 % showed a titer ≥ 1:16 in the complement fixation test. No definite geographic differences could be found in the distribution of the herds which showed positive results. The ubiquity of chlamydial infections...
[Standardization of the hemagglutination-inhibition test for two equine influenza viruses]. Bürki F, Sibalin M.No abstract available
Serologic incidence of leptospirosis in Georgia horses. Cole JR, Pursell AR.No abstract available
Lyophilized combination pools of enterovirus equine antisera: preparation and test procedures for the identification of field strains of 42 enteroviruses.
Bulletin of the World Health Organization    January 1, 1973   Volume 48, Issue 3 263-268 
Melnick JL, Rennick V, Hampil B, Schmidt NJ, Ho HH.This paper describes the preparation of 8 dried pools (designated A to H) of sera. Each pool is composed of 10 or 11 of 42 individual enterovirus equine sera and contains 500 antibody units of each serum component per 0.1 ml. Procedures for using the antiserum pools are given, and guidance is provided for interpreting the results of serum neutralization tests in identifying field isolates.
Diagnosis of mixed infections with myxovirus influenzae A equi 2 and herpes virus equi 1 among Danish stud horses.
Acta veterinaria Scandinavica    January 1, 1973   Volume 14, Issue 2 205-218 doi: 10.1186/BF03547437
Jensen K.Examination of nasopharyngeal secretion and organ material from clinical cases of respiratory diseases in horses, using inoculation of embryonated hen eggs and rabbit and horse kidney cell cultures, resulted in the isolation of influenza virus and herpes virus. In 2 cases, both viruses were present in the same specimen. On the basis of the physio-chemical, cytological and serological criteria, the viruses were found to be identical with influenza virus type A equi 2 and herpes virus equi type 1. The methods for serological diagnosis and characterization of the influenza and herpes viruses are ...
[Comparative studies on the occurrence of hemagglutination inhibiting antibodies against influenza virus strains A2-Hongkong-1-68 and A-equi2-Miami-63 in horse sera].
Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B    November 1, 1972   Volume 19, Issue 9 718-727 
Thein P, Bentele B.No abstract available
A study of different equine influenza vaccination schedules in seronegative foals and in horses.
Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B    July 1, 1972   Volume 20, Issue 5 361-366 doi: 10.1111/j.1439-0450.1973.tb01137.x
Petermann HG, Stellmann C, Graveline P.No abstract available
Experimental infection of horses with an attenuated Venezuelan equine encephalomyelitis vaccine (strain TC-83).
Infection and immunity    May 1, 1972   Volume 5, Issue 5 750-756 doi: 10.1128/iai.5.5.750-756.1972
Walton TE, Alvarez O, Buckwalter RM, Johnson KM.Ten horses (Equus caballus) were vaccinated with strain TC-83 Venezuelan equine encephalomyelitis (VEE) virus vaccine. Febrile responses and leukopenia due to a reduction of lymphocytes and neutrophils were observed in all animals. Viremias were demonstrable in eight horses, with a maximum of 10(3.5) median tissue culture infectious dose units per ml of serum in two horses. Clinical illness with depression and anorexia were observed in five horses. Neutralizing (N), hemagglutination-inhibiting, and complement-fixing antibodies to the vaccine virus were demonstrable by 5, 6.5, and 7 days, respe...