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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.
Physical and serologic examinations of foals at 30 and 45 days of age for early diagnosis of Rhodococcus equi infection on endemically infected farms.
Journal of the American Veterinary Medical Association    April 16, 1998   Volume 212, Issue 7 976-981 
Higuchi T, Taharaguchi S, Hashikura S, Hagiwara S, Gojo C, Satoh S, Yoshida M, Takai S.To evaluate results of physical and serologic examinations of foals at 30 and 45 days of age on 3 types of farms with various prevalences of clinical disease (endemic, sporadic, none) caused by Rhodococcus equi and to determine whether evaluations were helpful in early diagnosis and control of the disease. Methods: Prospective cohort study. Methods: 144 foals at 30 and 45 days of age. Methods: During a 2-year period, 36 foals on farms at which R equi infection was endemic, 71 foals on farms at which the disease was sporadically detected, and 37 foals on farms without the disease were examined ...
Antibodies against equine herpesviruses in free-ranging mountain zebras from Namibia.
Journal of wildlife diseases    December 10, 1997   Volume 33, Issue 4 812-817 doi: 10.7589/0090-3558-33.4.812
Borchers K, Frölich K.Twenty-one blood samples of free-ranging mountain zebras (Equus zebra) from Namibia were tested for equine herpesvirus (EHV-1, -2, -3, -4) specific antibodies by immunofluorescence assay (IFA) and neutralization test (NT). Additionally, type-specific nested polymerase chain reactions (nested PCR) were employed for detection of EHV-1, -2 and -4 DNA. Equine herpesvirus-1 antibodies were detected by IFA in all zebras, while only seven serum samples contained EHV-4 IFA antibodies. Sera with high IFA antibodies also were found to neutralize EHV-1 and -4. Furthermore, 20 zebras were EHV-2 seropositi...
Comparison of PCR and culture to the indirect fluorescent-antibody test for diagnosis of Potomac horse fever.
Journal of clinical microbiology    September 1, 1997   Volume 35, Issue 9 2215-2219 doi: 10.1128/jcm.35.9.2215-2219.1997
Mott J, Rikihisa Y, Zhang Y, Reed SM, Yu CY.Potomac horse fever is an acute systemic equine disease caused by Ehrlichia risticii. Currently, serologic methods are widely used to diagnose this disease. However, serologic methods cannot determine whether the horse is presently infected or has been exposed to ehrlichial antigens in the past. The purpose of the present study was to compare the sensitivities of the nested PCR and cell culture with that of the indirect fluorescent-antibody (IFA) test for the diagnosis of Potomac horse fever. Blood and fecal specimens serially collected from a pony experimentally infected with E. risticii Mary...
Comparative performance of four serodiagnostic procedures for detecting bovine and equine vesicular stomatitis virus antibodies. Katz JB, Eernisse KA, Landgraf JG, Schmitt BJ.No abstract available
Borna disease virus infection in animals and humans.
Emerging infectious diseases    July 1, 1997   Volume 3, Issue 3 343-352 doi: 10.3201/eid0303.970311
Richt JA, Pfeuffer I, Christ M, Frese K, Bechter K, Herzog S.The geographic distribution and host range of Borna disease (BD), a fatal neurologic disease of horses and sheep, are larger than previously thought. The etiologic agent, Borna disease virus (BDV), has been identified as an enveloped nonsegmented negative-strand RNA virus with unique properties of replication. Data indicate a high degree of genetic stability of BDV in its natural host, the horse. Studies in the Lewis rat have shown that BDV replication does not directly influence vital functions; rather, the disease is caused by a virus-induced T-cell mediated immune reaction. Because antibodi...
Prevention of Rhodococcus equi pneumonia of foals using two different inactivated vaccines.
Veterinary microbiology    June 16, 1997   Volume 56, Issue 3-4 205-212 doi: 10.1016/s0378-1135(97)00089-8
Varga J, Fodor L, Rusvai M, Soós I, Makrai L.Two different, inactivated, aluminium salt adsorbed vaccines, one containing a R. equi strain (serotype 1, 10(9) CFU/ml and equine herpesvirus 2 (EHV-2) (1.5 x 10(7) PFU/ml) and another containing R. equi only were used on three studfarms to determine whether the disease can be prevented by vaccination of both pregnant mares and their foals. Pregnant mares received two 3 ml doses of vaccine intramuscularly 6 and 2 weeks before parturition and their foals were vaccinated on two or three occasions at 3, 5 or 7 weeks of age. The efficacy of the vaccines was evaluated on the basis of the clinical ...
Experimental exposure of pregnant mares to the asinine-94 strain of equine arteritis virus.
Journal of the South African Veterinary Association    June 1, 1997   Volume 68, Issue 2 49-54 doi: 10.4102/jsava.v68i2.869
Paweska JT, Henton MM, van der Lugt JJ.Clinical, virological and serological responses were evaluated in 10 pregnant mares after different challenge exposures to the asinine-94 strain of equine arteritis virus (EAV). The outcome of maternal infection on the progeny was also investigated. Mares were inoculated intranasally (n = 4), intramuscularly (n = 2), intravenously (n = 1), or contract-exposed (n = 3). All inoculated mares developed pyrexia, 5 showed mild clinical signs related to EAV infection and 2 remained asymptomatic. Viraemia was detected in all the inoculated animals and shedding of virus from the respiratory tract occur...
Effect of the South African asinine-94 strain of equine arteritis virus (EAV) in pregnant donkey mares and duration of maternal immunity in foals.
The Onderstepoort journal of veterinary research    June 1, 1997   Volume 64, Issue 2 147-152 
Paweska JT.Clinical, virological and serological responses were investigated in five pregnant donkey mares after experimental exposure to the South African asinine-94 strain of equine arteritis virus (EAV), and the duration of maternal immunity to EAV was studied in their foals. In four intranasally inoculated mares, fever with maximum rectal temperatures of 39.1-40.7 degrees C was recorded 2-11 d after challenge. All the inoculated mares developed mild depression, and a serous ocular and nasal discharge; in three mares mild conjuctivitis was observed. The virus was recovered from the nasopharynx and fro...
Equine arteritis virus.
Theriogenology    April 15, 1997   Volume 47, Issue 6 1275-1295 doi: 10.1016/s0093-691x(97)00107-6
Glaser AL, Chirnside ED, Horzinek MC, de Vries AA.Equine arteritis virus (EAV) is a small, enveloped, positive-stranded RNA virus, in the family Arteriviridae , W.H.ich can infect both horses and donkeys. While the majority of EAV infections are asymptomatic, acutely infected animals may develop a wide range of clinical signs, including pyrexia, limb and ventral edema, depression, rhinitis, and conjunctivitis. The virus may cause abortion and has caused mortality in neonates. After natural EAV infection, most horses develop a solid, long-term immunity to the disease. Marzz and geldings eliminate the virus within 60 days, but 30 to 60% of acut...
Seroprevalence of antibodies to Sarcocystis neurona in horses residing in a county of southeastern Pennsylvania.
Journal of the American Veterinary Medical Association    February 15, 1997   Volume 210, Issue 4 517-518 
Bentz BG, Granstrom DE, Stamper S.To determine seroprevalence of Sarcocystis neurona-specific antibodies in a population of horses residing in Chester County, Pa. Methods: Prevalence survey. Methods: 117 serum samples from selected members of a population of 580 Thoroughbred horses. Methods: Serum was analyzed for antibodies to Sarcocystic neurona, using a western blot. Information regarding age, sex, and housing of horse was obtained by questionnaire. Data were analyzed, using multivariable logistic regression. Results: Seroprevalence was 45.3% (95% CI, 36.3 to 54.3%). A relationship was not found between seroprevalence and s...
Case report: field-acquired subclinical Babesia equi infection confirmed by in vitro culture.
Journal of clinical microbiology    February 1, 1997   Volume 35, Issue 2 474-476 doi: 10.1128/jcm.35.2.474-476.1997
Holman PJ, Hietala SK, Kayashima LR, Olson D, Waghela SD, Wagner GG.A horse with no prior clinical history of equine piroplasmosis tested negative for Babesia caballi and Babesia equi in the complement fixation test before importation into the United States from France. After 5 years in residence in the United States, the animal tested serologically positive for B. equi by the complement fixation test, the immunofluorescent antibody test, and Western blot analysis. The carrier status of the horse was confirmed by culture of B. equi parasites. In vitro culture offers an efficient and comparatively inexpensive method to determine the carrier status of horses sus...
Fatal encephalitis due to novel paramyxovirus transmitted from horses.
Lancet (London, England)    January 11, 1997   Volume 349, Issue 9045 93-95 doi: 10.1016/s0140-6736(96)06162-4
O'Sullivan JD, Allworth AM, Paterson DL, Snow TM, Boots R, Gleeson LJ, Gould AR, Hyatt AD, Bradfield J.In September, 1994, an outbreak of severe respiratory disease affected 18 horses, their trainer, and a stablehand in Queensland, Australia. Fourteen horses and one human being died. A novel virus was isolated from those affected and named equine morbillivirus (EMV). We report a case of encephalitis caused by this virus. Results: A 35-year-old man from Queensland had a brief aseptic meningitic illness in August, 1994, shortly after caring for two horses that died from EMV infection and then assisting at their necropsies. He then suffered severe encephalitis 13 months later, characterised by unc...
Serologic diagnosis of canine and equine borreliosis: use of recombinant antigens in enzyme-linked immunosorbent assays.
Journal of clinical microbiology    January 1, 1997   Volume 35, Issue 1 169-173 doi: 10.1128/jcm.35.1.169-173.1997
Magnarelli LA, Flavell RA, Padula SJ, Anderson JF, Fikrig E.Serum samples from dogs and equids suspected of having canine or equine borreliosis, respectively, were analyzed in polyvalent enzyme-linked immunosorbent assays (ELISAs) with whole-cell or recombinant antigens of Borrelia burgdorferi sensu stricto. Purified preparations of recombinant antigens included outer surface protein A (OspA), OspB, OspC, OspE, OspF, and p41-G (a fragment of flagellin). Of the 36 dog sera that reacted positively to whole-cell antigen, 32 (88.9%) contained antibodies to one or more recombinant antigens. Reactivities to OspF (88.9% positive) and p41-G (75% positive) were...
Infectious agents in acute respiratory disease in horses in Ontario. Carman S, Rosendal S, Huber L, Gyles C, McKee S, Willoughby RA, Dubovi E, Thorsen J, Lein D.A study of acute respiratory disease in horses in Ontario was undertaken to determine the identity of current causative infectious agents. A nasopharyngeal swab was designed and utilized to maximize isolation of viruses, mycoplasma, and pathogenic bacteria. Serum samples were collected for parallel determination of antibody titers to equine influenza virus type A subtype 1 (H7N7) and subtype 2 (H3N8), equine rhinovirus types 1 and 2, equine herpesvirus type 1, Mycoplasma equirhinius, and Mycoplasma felis. Equine rhinovirus type 2 was recovered from 28/92 horses tested, and equine influenza vir...
Application of equine infectious anemia virus core proteins produced in a baculovirus expression system to serological diagnosis.
Microbiology and immunology    January 1, 1997   Volume 41, Issue 12 975-980 doi: 10.1111/j.1348-0421.1997.tb01957.x
Kong XG, Pang H, Sugiura T, Sentsui H, Onodera T, Matsumoto Y, Akashi H.Equine infectious anemia virus (EIAV) core proteins were obtained from a baculovirus expression system. Recombinant baculoviruses (rBVs) highly expressed the Gag precursor and p26 antigens in an rBV-infected Sf21 cell culture supernatant. Enzyme-linked immunosorbent assay (ELISA) and agar gel immunodiffusion (AGID) were conducted using the expressed proteins to detect antibodies from experimentally infected horses. The expressed antigens showed low background levels, high specificity and sensitivity in ELISA and AGID. The results of the serological tests using the expressed antigens were ident...
Correlation of antigen specific IgG and IgG(T) responses with Anoplocephala perfoliata infection intensity in the horse.
Parasite immunology    October 1, 1996   Volume 18, Issue 10 499-506 doi: 10.1046/j.1365-3024.1996.d01-18.x
Proudman CJ, Trees AJ.There is increasing interest in the application of serological methods to macro-parasite infections to indicate infection intensity, which in turn is related to pathogenicity. Colic is the single most important cause of mortality in horses and there is evidence that a proportion of colic cases are associated with infection with the intestinal cestode Anoplocephala perfoliata. In order to develop better tools to investigate this association, the correlation between antigen-specific equine IgG and IgG(T) and infection intensity of A. perfoliata was investigated. Affinity purification of a 12/13 ...
Serum antibody responses of foals to virulence-associated 15- to 17-kilodalton antigens of Rhodococcus equi.
Veterinary microbiology    September 1, 1996   Volume 52, Issue 1-2 63-71 doi: 10.1016/0378-1135(96)00042-9
Tákai S, Hidaka D, Fujii M, Shindoh Y, Murata T, Nakanishi S, Sasaki Y, Tsubaki S, Kamada M.Humoral immune responses in 16 foals to virulence-associated 15- to 17-kDa antigens of Rhodococcus equi were studied during the first fourteen weeks of life on two horse-breeding farms with a persistent incidence of R. equi infection. Serum antibody levels specific for 15- to 17-kDa antigens were measured by enzyme-linked immunosorbent assay and Western immunoblotting. Immunoglobulin G (IgG) antibodies specific to 15- to 17-kDa antigens were detected by all the foals. R. equi was found in the feces of foals during week 1 of life, and the number of fecal R. equi rapidly increased to the highest...
Negative findings from serological studies of equine morbillivirus in the Queensland horse population.
Australian veterinary journal    September 1, 1996   Volume 74, Issue 3 241-243 doi: 10.1111/j.1751-0813.1996.tb15412.x
Ward MP, Black PF, Childs AJ, Baldock FC, Webster WR, Rodwell BJ, Brouwer SL.No abstract available
Use of a virulence-associated protein based enzyme-linked immunosorbent assay for Rhodococcus equi serology in horses.
Equine veterinary journal    September 1, 1996   Volume 28, Issue 5 344-349 doi: 10.1111/j.2042-3306.1996.tb03103.x
Prescott JF, Fernandez AS, Nicholson VM, Patterson MC, Yager JA, Viel L, Perkins G.An enzyme-linked immunosorbent assay (ELISA) was developed against Rhodococcus equi using Triton X-114 detergent extracted whole cell material, in which the virulence associated protein (VapA) predominated. Enzymelinked immunosorbent assay titres corresponded to antibody reacting with VapA on Western blots. There was considerable variation in antibody titres of nonimmunised mares and in the time when the colostrally derived antibody of their foals had declined to low or undetectable titres. In general, antibodies in foals declined to their lowest levels at age 4-8 weeks. Seroconversion occurre...
Corynebacterium pseudotuberculosis infection in horses: 538 cases (1982-1993).
Journal of the American Veterinary Medical Association    August 15, 1996   Volume 209, Issue 4 804-809 
Aleman M, Spier SJ, Wilson WD, Doherr M.To describe clinical manifestations of Corynebacterium pseudotuberculosis infection in horses and to evaluate diagnostic methods for identification of this disease. Methods: Retrospective case series. Methods: 538 horses with a diagnosis of C pseudotuberculosis infection. Results: Median age of horses with external abscesses was similar to that in horses with internal abscesses. Breed and sex did not appear to be associated with infection. Cases were detected during all 12 months; however, the disease was most common in the fall and early winter, with the highest incidence in September, Octobe...
Serologic responses to Rhodococcus equi in individuals with and without human immunodeficiency virus infection. Vullo V, Mastroianni CM, Lichtner M, Mengoni F, Chiappini E, D'Agostino C, Delia S.Thirty healthy blood donors, 15 workers from horse-breeding farms, 69 human immunodeficiency virus (HIV)-negative persons at risk for HIV infection, 125 HIV-infected subjects without Rhodococcus equi infection, and nine HIV-infected patients with Rhodococcus equi pneumonia were evaluated in order to detect serum antibodies to Rhodococcus equi precipitate-soluble antigen by an enzyme immunoassay (EIA). Whereas EIA values for healthy donors, horse farm workers, individuals at risk for HIV infection, and HIV-positive subjects without Rhodococcus equi infection were comparable, HIV-infected patien...
Clinical and pathological features of Nigerian equine encephalitis.
The Veterinary record    April 6, 1996   Volume 138, Issue 14 323-326 doi: 10.1136/vr.138.14.323
Adeyefa CA, Tomori O, Akpavie SO, Awoseyi OA.Thirteen cases of a disease with a low morbidity and very high mortality in horses in Nigeria are described; the disease is characterised by fever (rectal temperature > or = 40 degrees C), generalised muscle spasms, ataxia, increased respiratory and heart rates and terminal lateral recumbency. The illness generally lasts three to five days but durations of 12 to 30 hours have been observed. Laboratory investigations, including histopathology and serology suggest a viral aetiology, possibly an alphavirus of the equine encephalitis group.
Methods for the Detection of Trichinellosis in Horses.
Journal of food protection    April 1, 1996   Volume 59, Issue 4 420-425 doi: 10.4315/0362-028X-59.4.420
Gamble HR, Gajadhar AA, Solomon MB.Twelve horses were infected with various doses of Trichinella spiralis and then tested for infection using direct (artificial digestion) and indirect (enzyme immunoassay) methods. Horses became infected in a dose-dependent manner. Larvae accumulated preferentially in the tongue, followed by the masseter, neck, supraspinatus, trapezius, and diaphragm. At lower infection levels, the tongue harbored several times more parasites than were found in other tissues. The sensitivity of artificial digestion methods for detecting infections was directly related to sample size. One-gram samples were not r...
Equine piroplasmosis an update on diagnosis, treatment and prevention.
The British veterinary journal    March 1, 1996   Volume 152, Issue 2 139-151 doi: 10.1016/s0007-1935(96)80070-4
Brüning A.Two haemoprotozoan parasites, Babesia caballi and Babesia equi, can cause equine piroplasmosis. Due to the presence of potential tick vectors in areas so far unaffected by equine babesias, import and export regulations often require the serum testing of animals for evidence of infection. Although the complement fixation test (CFT) has been recommended for detecting the presence of antibodies to Babesia spp., it has been demonstrated to have several disadvantages, including false-positive results and low sensitivity for detecting latent infections. An enzyme-linked immunosorbent assay (ELISA) m...
Lack of virulence of the murine fibroblast adapted strain, Kentucky A (KyA), of equine herpesvirus type 1 (EHV-1) in young horses.
Veterinary microbiology    February 1, 1996   Volume 48, Issue 3-4 353-365 doi: 10.1016/0378-1135(09)59999-3
Matsumura T, O'Callaghan DJ, Kondo T, Kamada M.The virulence of the cell culture adapted KyA strain of equine herpesvirus type 1 (EHV-1), which lacks at least six genes by deletions in its genome, was assessed by intranasal inoculation of six young horses that were serologically negative for EHV-1. No horses showed clinical signs, and a neutralizing antibody response against EHV-1 was detected in two horses which had antibodies against EHV-4 prior to the inoculation. A challenge experiment using a highly virulent strain of EHV-1 conducted 4 weeks later against 4 of the 6 horses inoculated intranasally with the KyA strain and 2 control hors...
[Outbreaks of equine trypanosomiasis caused by Trypanosoma evansi in Formosa Province, Argentina].
Revue scientifique et technique (International Office of Epizootics)    September 1, 1995   Volume 14, Issue 3 747-752 
Monzón CM, Hoyos CB, Jara GA.Tests on 257 blood samples from 21 herds of horses in Formosa Province of Argentina, using the technique of centrifuging microhaematocrit capillary tubes, revealed Trypanosoma evansi in 90 of 137 animals in eight herds. Application of the direct agglutination test to serum samples from the same animals revealed antibodies to T. evansi in 107 horses. Antibody was also detected in nine horses from two herds where the parasite was not detected. Outbreaks of 'mal de caderas' occurred in the humid (eastern) and sub-humid (central) zones of Formosa. More than 95% of the equine population of the prov...
Demonstration of Borna disease virus RNA in peripheral blood mononuclear cells from healthy horses in Japan.
Vaccine    August 1, 1995   Volume 13, Issue 12 1076-1079 doi: 10.1016/0264-410x(95)00050-b
Nakamura Y, Kishi M, Nakaya T, Asahi S, Tanaka H, Sentsui H, Ikeda K, Ikuta K.Borna disease (BD) is a progressive poliomeningoencephalomyelitis which occurs naturally in horses and sheep. Here, peripheral blood mononuclear cells (PBMC) derived from 57 healthy horses in Japan were examined by a nested reverse transcription-polymerase chain reaction to determine the prevalence of BD virus (BDV) infection. Seventeen (29.8%) of the samples were positive by this examination and the specificity of the amplified product was confirmed by hybridization with authentic oligomer probes. About 60% of the BDV RNA-positive individuals also showed seropositivity by Western blotting. Th...
Seroepidemiological and molecular evidence for the presence of two H3N8 equine influenza viruses in China in 1993-94.
The Journal of general virology    August 1, 1995   Volume 76 ( Pt 8) 2009-2014 doi: 10.1099/0022-1317-76-8-2009
Guo Y, Wang M, Zheng GS, Li WK, Kawaoka Y, Webster RG.In May 1993, a severe epidemic of respiratory disease began in horses in Inner Mongolia and spread throughout horses in China. The disease affected mules and donkeys as well as horses but did not spread to other species, including humans. The severity of the disease raised the question of whether the outbreak might have been caused by the new avian-like influenza viruses detected in horses in China in 1989 or by current variants ofA/equine/Miami/1/63 (H3N8) (equine-2) or by a reassortant between these viruses. Antigenic and sequence analysis established that all gene segments of the influenza ...
The relationship between single radial hemolysis, hemagglutination inhibition, and virus neutralization assays used to detect antibodies specific for equine influenza viruses.
Veterinary microbiology    June 1, 1995   Volume 45, Issue 1 81-92 doi: 10.1016/0378-1135(94)00105-6
Morley PS, Hanson LK, Bogdan JR, Townsend HG, Appleton JA, Haines DM.Antibodies specific for equine influenza viruses are usually quantified using single radial hemolysis (SRH), hemagglutination inhibition (HI) or virus neutralization (VN). Neutralizing antibodies are thought to provide optimum protection to challenged animals. The purpose of this study was to determine the extent to which SRH and HI assays detect antibodies which neutralize equine influenza viruses. Acute and convalescent sera from 41 horses were analyzed using VN, SRH, and HI assays. These horses were present in a population of Thoroughbred racehorses during an epidemic of upper respiratory t...
Serological study of equine viral arteritis in standard-breds in the UK.
The Veterinary record    May 13, 1995   Volume 136, Issue 19 499 doi: 10.1136/vr.136.19.499-a
Wood JL, Newton JR.No abstract available
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