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Topic:Infection

Infections in horses encompass a range of diseases caused by various pathogens, including bacteria, viruses, fungi, and parasites. These infections can affect different systems within the horse, such as the respiratory, gastrointestinal, and integumentary systems, leading to a variety of clinical signs depending on the pathogen and the severity of the infection. Common infectious diseases in horses include equine influenza, strangles, and equine herpesvirus. Diagnosis often involves clinical examination, laboratory testing, and sometimes imaging, to identify the causative agent and assess the extent of the disease. Treatment strategies may include antimicrobial therapy, supportive care, and preventive measures such as vaccination and biosecurity practices. This page aggregates peer-reviewed research studies and scholarly articles that explore the pathogenesis, diagnosis, treatment, and prevention of infectious diseases in equine populations.
Specific immune responses are required to control parasitemia in Babesia equi infection.
Infection and immunity    May 1, 1994   Volume 62, Issue 5 1909-1913 doi: 10.1128/iai.62.5.1909-1913.1994
Knowles DP, Kappmeyer LS, Perryman LE.Horses possessing a normal immune system and spleen often control infection caused by Babesia equi. However, splenectomized horses are unable to control B. equi infection and usually succumb to the infection. To investigate the role of the spleen in the control of B. equi infection in the absence of specific immune responses, two 1-month-old foals with severe combined immunodeficiency (SCID) and two age-matched normal foals were inoculated with B. equi. The SCID foals became febrile seven days postinoculation and developed terminal parasitemias of 41 and 29%. The SCID foals had greater than 50...
Influence of estrogen on antibacterial and immunoglobulin secretory activities of uterine fluids from ovariectomized mares.
American journal of veterinary research    May 1, 1994   Volume 55, Issue 5 643-649 
Johnson JU, Oxender WD, Berkhoff HA.Effect of estrogen (E2) and progesterone (P4) on uterine antibacterial activity and immunoglobulin concentrations in mares was studied. In 2 in vitro experiments, 6 mixed-breed mares were ovariectomized, and uterine fluid and blood serum were analyzed. Antibacterial assay methods were used to determine inhibitory effects on Streptococcus zooepidemicus of uterine fluid samples collected on days 3, 5, and 8, and serum obtained on day 8 of treatment. Single radial immunodiffusion methods were used to quantify amounts of IgA and IgG in uterine fluid and serum on days 3, 5, 8, and 14 of treatment. ...
Hydrops amnii in a mare.
Journal of the American Veterinary Medical Association    May 1, 1994   Volume 204, Issue 9 1481-1482 
Sertich PL, Reef VB, Oristaglio-Turner RM, Habecker PL, Maxson AD.A multiparous pregnant Welsh Pony mare was examined because of anorexia, dyspnea, and a large abdomen. Ultrasonography of the uterus revealed an excessive amount of amniotic fluid surrounding the fetus. Transabdominal ultrasonography permitted differentiation of hydrops amnii from hydrops allantois. The mare aborted a 7-month-old fetus with brachygnathia and a large, edematous umbilical cord. Hydrops amnii, an excessive accumulation of amniotic fluid in the amniotic cavity, is most commonly reported in cattle and sheep.
Update on neonatal septicemia.
The Veterinary clinics of North America. Equine practice    April 1, 1994   Volume 10, Issue 1 109-135 doi: 10.1016/s0749-0739(17)30371-1
Paradis MR.Septicemia is the second most commonly diagnosed problem in the equine neonate, superseded only by the problem of inadequate transfer of maternal antibodies. This article reviews the factors that may put a foal at high risk for developing sepsis, the diagnostic tools used to identify these animals, some of the sequelae of sepsis, and the therapeutic modalities available to the clinician.
Fumonisin B2 in cultured Fusarium proliferatum, M-6104, causes equine leukoencephalomalacia. Ross PF, Nelson PE, Owens DL, Rice LG, Nelson HA, Wilson TM.No abstract available
Transmission of some species of internal parasites in horses born in 1990, 1991, and 1992 in the same pasture on a farm in central Kentucky.
Veterinary parasitology    April 1, 1994   Volume 52, Issue 3-4 257-269 doi: 10.1016/0304-4017(94)90117-1
Lyons ET, Tolliver SC, Stamper S, Drudge JH, Granstrom DE, Collins SS.Studies were conducted on transmission of natural infections of several species of internal parasites in horses born and kept on the same pasture on a farm in central Kentucky. Data for the first year (1989) of a 4 year study on this farm have been published recently. The present research represents the second (1990), third (1991), and fourth (1992) years of the investigation. The number of animals (n = 28) examined varied from eight born in 1990 to ten each born in 1991 and 1992. For each year, examination was made of one horse per month, beginning in June of the year of birth and extending t...
Isolation of Pasteurella canis from a foal with polyarthritis.
The Canadian veterinary journal = La revue veterinaire canadienne    April 1, 1994   Volume 35, Issue 4 244-245 
Bourgault A, Bada R, Messier S.No abstract available
Expression of functional protease and subviral particles by vaccinia virus containing equine infectious anaemia virus gag and 5′ pol genes.
The Journal of general virology    April 1, 1994   Volume 75 ( Pt 4) 895-900 doi: 10.1099/0022-1317-75-4-895
McGuire TC, O'Rourke KI, Baszler TV, Leib SR, Brassfield AL, Davis WC.Cells infected with vaccinia viruses expressing the equine infectious anaemia virus (EIAV) gag gene (VGag) or gag plus the 5' pol encoding protease (VGag/PR) were evaluated with monoclonal antibody to a p26 capsid protein linear epitope (QEISKFLTD). Both recombinant viruses expressed Gag precursor protein (55K) whereas only VGag/PR expressed a detectable Gag-Pol fusion protein (82K) with a functional protease, shown by subviral particles containing processed p26. Horses inoculated with VGag/PR produced antibodies reactive with EIAV Gag proteins.
Identification of diagnostic antigens for South American Babesia caballi infections.
International journal for parasitology    April 1, 1994   Volume 24, Issue 2 255-258 doi: 10.1016/0020-7519(94)90034-5
Böse R, Peymann B, Barbosa IP.Sera from 60 horses held in breeding herd in Brazil were examined monthly by ELISA, immunofluorescence antibody test (IFAT) and Western blot. All foals had maternal antibodies detectable by ELISA and IFAT, and sero-conversion took place between the 2nd and 5th month of age. The 48 and 50 kDa antigens were recognized first in the course of infection. Of 79 sera taken after sero-conversion 78 reacted with the 48 kDa antigen, 76 with the 50 kDa, 50 with the 70 kDa, 54 with the 112 kDa, 72 with the 141 kDa antigen. In general, sera from horses older than 1 year reacted with all 5 diagnostic antige...
Detection of African horsesickness virus by reverse transcriptase polymerase chain reaction (RT-PCR) using primers for segment 5 (NS1 gene).
The Journal of veterinary medical science    April 1, 1994   Volume 56, Issue 2 347-352 doi: 10.1292/jvms.56.347
Mizukoshi N, Sakamoto K, Iwata A, Ueda S, Kamada M, Fukusho A.The reverse transcription followed by the polymerase chain reaction (RT-PCR) technique was applied to the detection of African horsesickness virus (AHSV) using primers specific for attenuated AHSV serotype 4 segment 5 (NS1 gene). Total RNA which contains both messenger RNA and genomic dsRNA was extracted by the acid guanidinium-phenol-chloroform method from the AHSV infected Vero cells and was used as templates to optimize the RT-PCR. A pair of primer (NP2-NP32) amplified the product of the expected size from all serotypes of attenuated AHSV when four pairs of primers were tested. Using this p...
Epidemiological investigation of equid herpesvirus-4 (EHV-4) excretion assessed by nasal swabs taken from thoroughbred foals.
Veterinary microbiology    April 1, 1994   Volume 39, Issue 3-4 275-283 doi: 10.1016/0378-1135(94)90164-3
Gilkerson J, Jorm LR, Love DN, Lawrence GL, Whalley JM.Equid herpesvirus-4 (EHV-4) was detected in nasal swabs taken from foals using a PCR based test and this information used to study the epidemiology of EHV-4 disease on three Australian Thoroughbred stud farms in NSW in 1992. There was a very high level of agreement (kappa value of 0.84) between the PCR results and virus isolation using cell culture techniques. There was a strong seasonal distribution of EHV-4 shedding. Twenty-five of 26 positive samples were collected in January and March with the remaining positive sample collected in February. Foals with clinical signs of upper respiratory t...
In vivo replicative status and envelope heterogeneity of equine infectious anemia virus in an inapparent carrier.
Journal of virology    April 1, 1994   Volume 68, Issue 4 2777-2780 doi: 10.1128/JVI.68.4.2777-2780.1994
Kim CH, Casey JW.The distribution and replicative status of equine infectious anemia virus (EIAV) DNA in the tissues of a well-characterized inapparent carrier horse were established by using the PCR technique. The EIAV pol region could be amplified in all of the tissues tested, including the cerebellum and periventricular tissue, at concentrations approximately 10(5)-fold less than in the same tissue from an acutely infected horse. Further analysis of the EIAV genome, with primer pairs diagnostic for sequential stages of reverse transcription, suggests that EIAV DNA in the brain, liver, and lymph nodes was in...
In-situ hybridization for demonstration of equine herpesvirus type 1 DNA in paraffin wax-embedded tissues and its use in horses with disseminated necrotizing myeloencephalitis.
Journal of comparative pathology    April 1, 1994   Volume 110, Issue 3 215-225 doi: 10.1016/s0021-9975(08)80275-7
Schmidt P, Meyer H, Hübert P, Hafner A, Andiel E, Grabner A, Dahme E.The detection of equine herpesvirus type 1 (EHV-1) in infected cell cultures, and in tissues taken at necropsy, by the in-situ hybridization technique is described. A 4.9 kb Bam HI fragment of EHV-1 vaccine strain RacH was used as a probe after labelling with [alpha-32P] thymidine 5'-triphosphate ([32P]TTP) or digoxigenin-deoxyuridine 5'-triphosphate (dUTP). Both probes specifically detected EHV-1 DNA in either cytospin or paraffin wax-embedded preparations of infected cells. The digoxigenin-labelled probe was further used to examine tissue sections of equine fetuses which had been aborted due...
Babesia equi erythrocytic stage continuously cultured in an enriched medium.
The Journal of parasitology    April 1, 1994   Volume 80, Issue 2 232-236 
Holman PJ, Chieves L, Frerichs WM, Olson D, Wagner GG.Babesia equi was continuously cultured through 90 passages in an enriched chemically defined basal medium (HL-1) supplemented with 20% fetal bovine serum and serum replacement factors, including lipid-rich bovine serum albumin, bovine insulin, and human transferrin. Cryopreservation and subsequent recovery of B. equi were easily achieved. Inoculation of a splenectomized and an intact horse with cultured infected erythrocytes resulted in parasitemias and B. equi in vitro reisolation from both animals. In vitro forms of the parasite resembled in vivo forms. After establishment, parasitemias of 1...
Development and evaluation of PCR test for detection of Taylorella equigenitalis.
Journal of clinical microbiology    April 1, 1994   Volume 32, Issue 4 893-896 doi: 10.1128/jcm.32.4.893-896.1994
Bleumink-Pluym NM, Werdler ME, Houwers DJ, Parlevliet JM, Colenbrander B, van der Zeijst BA.A PCR for the detection of Taylorella equigenitalis, the causative agent of contagious equine metritis, was developed and evaluated. A genus-specific primer-probe set was derived from the 16S ribosomal DNA sequences. The PCR was specific and amplified a 585-bp product from all 64 available T. equigenitalis isolates. This PCR product hybridized with a specific probe in a dot spot assay. A variety of microorganisms from the genital tracts of horses or with a close phylogenetic relationship to T. equigenitalis did not yield a visible PCR product and were all negative in the dot spot hybridization...
Toxigenic strains of Stachybotrys atra associated with poisonous straw in Morocco.
Veterinary and human toxicology    April 1, 1994   Volume 36, Issue 2 93-96 
Tantaoui-Elaraki A, Mekouar SL, el Hamidi M, Senhaji M.From 10 moldy straw samples collected in a Moroccan area with an apparent equine stachybotryotoxicosis outbreak in November 1991, 8 isolates of Stachybotrys atra were obtained. They all showed toxigenesis, however they were variable in nature and intensity. While 1 isolate had only mild toxicity when fed to mice as moldy barley, another revealed very high toxicity to Artemia saline larvae, or rat skin, and to mice. The toxicity of the other 6 isolates were between these 2 limits. This study indicates that the November 1991 outbreak was due to toxigenic strains of Stachybotrys atra.
Leishmaniasis disseminated by Leishmania braziliensis in a mare (Equus cabalus) immunotherapy and chemotherapy assays.
Memorias do Instituto Oswaldo Cruz    April 1, 1994   Volume 89, Issue 2 217-220 doi: 10.1590/s0074-02761994000200018
Barbosa-Santos EG, Marzochi MC, Urtado W, Queirós F, Chicarino J, Pacheco RS.Cutaneous disseminated lesions caused by Leishmania sp. were found in a pregnant mare (Equus cabalus) from a rural city in the State of Rio de Janeiro, Brazil. Before delivering, treatment was undertaken by immunotherapy followed by chemotherapy. Histopatology and serology were performed during treatment, as well as the biochemical characterization of the parasite (L. braziliensis) that was isolated from one of the lesions.
Characterization of a red blood cell antigen in donkeys and mules associated with neonatal isoerythrolysis.
Animal genetics    April 1, 1994   Volume 25, Issue 2 119-120 doi: 10.1111/j.1365-2052.1994.tb00091.x
McClure JJ, Koch C, Traub-Dargatz J.A red cell antigen of donkeys and mules was identified using antibodies in serum from a mare which produced a mule foal affected with neonatal isoerythrolysis (NI). Subsequently antibodies with similar activity were identified in the sera of other mares which had produced mule foals and were produced by immunization of horses with blood from donkeys. The antigen detected by these antibodies does not correspond to any recognized horse red cell alloantigen. This may be a xenoantigen since all donkeys (and mules) tested have shared this antigen and all horses tested have lacked the antigen. The r...
Characterisation of proteolytic activity of excretory-secretory products from adult Strongylus vulgaris.
Veterinary parasitology    April 1, 1994   Volume 52, Issue 3-4 285-296 doi: 10.1016/0304-4017(94)90120-1
Caffrey CR, Ryan MF.An excretory-secretory (ES) preparation derived from adult Strongylus vulgaris in vitro was assessed for proteolytic activity using azocasein and synthetic, fluorogenic, peptide substrates. Fractionation was by molecular sieve fast protein liquid chromatography (molecular sieve FPLC) and resolution by gelatin-substrate sodium dodecyl sulphate-polyacrylamide gel electrophoresis (gelatin-substrate SDS-PAGE). The cysteine proteinase activator, dithiothreitol (DTT), enhanced azocaseinolysis and hydrolysis of carbobenzoxy-phenylalanyl-arginine-7-amido-4-methylcoumarin (Z-Phe-Arg-NMec) by the ES pre...
Antigenicity and immunogenicity of equine influenza vaccines containing a Carbomer adjuvant.
Epidemiology and infection    April 1, 1994   Volume 112, Issue 2 421-437 doi: 10.1017/s0950268800057848
Mumford JA, Wilson H, Hannant D, Jessett DM.Equine influenza vaccines containing inactivated whole virus and Carbomer adjuvant stimulated higher levels and longer lasting antibody to haemagglutinin in ponies than vaccines of equivalent antigenic content containing aluminium phosphate adjuvants. Five months after the third dose of vaccine containing Carbomer adjuvant, ponies were protected against clinical disease induced by an aerosol of virulent influenza virus (A/equine/Newmarket/79, H3N8). In contrast ponies which received vaccine containing aluminium phosphate adjuvant were susceptible to infection and disease. There was an inverse ...
Peripartum asphyxia.
The Veterinary clinics of North America. Equine practice    April 1, 1994   Volume 10, Issue 1 187-218 doi: 10.1016/s0749-0739(17)30374-7
Vaala WE.The abysmal survival rates for the first barking foals described more than 60 years ago were probably due to the cumulative effects of asphyxia on multiple organ systems. Successful treatment of asphyxiated foals requires recognition of periparturient conditions associated with the syndrome and appreciation of the spectrum of clinicopathologic complications that can ensue.
Improved sensitivity in the diagnosis of dermatophytosis by fluorescence microscopy with calcafluor white.
The Veterinary record    March 19, 1994   Volume 134, Issue 12 307-308 doi: 10.1136/vr.134.12.307
Sparkes AH, Werrett G, Stokes CR, Gruffydd-Jones TJ.No abstract available
Pneumocystis carinii pneumonia in foals.
Journal of the American Veterinary Medical Association    March 15, 1994   Volume 204, Issue 6 929-933 
Ewing PJ, Cowell RL, Tyler RD, MacAllister CG, Meinkoth JH.Pneumocystis carinii pneumonia was diagnosed in 3 foals. In 2 foals (No. 1 and 2), diagnosis was by histologic evaluation of pulmonary tissue. On retrospective evaluation, P carinii cysts were found on sediment smears of bronchoalveolar lavage fluid in 1 foal (No. 1). A different foal (No. 3) was diagnosed as having pneumocytosis by finding P carinii cysts in bronchoalveolar lavage fluid, and was treated successfully. Definitive diagnosis of pneumocytosis in animals is usually made at necropsy. However, careful cytologic evaluation in bronchoalveolar lavage fluid sediment can provide a diagnos...
Major histocompatibility complex-restricted CD8+ cytotoxic T lymphocytes from horses with equine infectious anemia virus recognize Env and Gag/PR proteins.
Journal of virology    March 1, 1994   Volume 68, Issue 3 1459-1467 doi: 10.1128/JVI.68.3.1459-1467.1994
McGuire TC, Tumas DB, Byrne KM, Hines MT, Leib SR, Brassfield AL, O'Rourke KI, Perryman LE.Cytotoxic T lymphocytes (CTL) can control some viral infections and may be important in the control of lentiviruses, including human immunodeficiency virus type 1. Since there is limited evidence for an in vivo role of CTL in control of lentiviruses, dissection of immune mechanisms in animal lentiviral infections may provide needed information. Horses infected with equine infectious anemia virus (EIAV) a lentivirus, have acute plasma viremia which is terminated in immunocompetent horses. Viremic episodes may recur, but most horses ultimately control infection and become asymptomatic carriers. ...
Studies on oral transmission of Potomac horse fever.
Journal of veterinary internal medicine    March 1, 1994   Volume 8, Issue 2 87-92 doi: 10.1111/j.1939-1676.1994.tb03203.x
Palmer JE, Benson CE.Eight normal ponies placed in direct contact with ponies experimentally infected with Ehrlichia risticii for 30 to 90 days did not develop signs of Potomac horse fever. They also did not seroconvert, and they remained susceptible to IV infection. One of 8 ponies that were force fed fresh feces from infected ponies while in direct contact with ponies experimentally infected with E. risticii developed Potomac horse fever and seroconverted. The other 7 remained asymptomatic, did not seroconvert, and were susceptible to IV infection. Six of 9 ponies inoculated with E. risticii via nasogastric intu...
How important are leptospiral infections as a cause of equine disease?
Equine veterinary journal    March 1, 1994   Volume 26, Issue 2 88 doi: 10.1111/j.2042-3306.1994.tb04340.x
Wood JL.No abstract available
Coccidioides immitis abortion in an Arabian mare.
Veterinary pathology    March 1, 1994   Volume 31, Issue 2 258-259 doi: 10.1177/030098589403100217
Stoltz JH, Johnson BJ, Walker RL, Pappagianis D.No abstract available
Posttranscriptional effector domains in the Rev proteins of feline immunodeficiency virus and equine infectious anemia virus.
Journal of virology    March 1, 1994   Volume 68, Issue 3 1998-2001 doi: 10.1128/JVI.68.3.1998-2001.1994
Mancuso VA, Hope TJ, Zhu L, Derse D, Phillips T, Parslow TG.By systematically dissecting the Rev proteins of feline immunodeficiency virus (FIV) and equine infectious anemia virus (EIAV), we have identified within each a short peptide that is functionally interchangeable with the effector domains found in Rev-like proteins from other retroviruses. The active sequences from FIV and EIAV differ in several respects from other known effectors and may represent a distinct class of effector domain.
The prevalence of latent Equid herpesviruses in the tissues of 40 abattoir horses.
Equine veterinary journal    March 1, 1994   Volume 26, Issue 2 140-142 doi: 10.1111/j.2042-3306.1994.tb04353.x
Edington N, Welch HM, Griffiths L.Equid herpesviruses 1 or 4 (EHV-1 or -4) were isolated by cocultivation from 60% of 40 horses examined at slaughter. The lymph nodes draining the respiratory tract were the most common source of virus. EHV-1 or EHV-4 was never isolated from the trigeminal ganglia (SLG). The polymerase chain reaction (PCR) detected virus in 87.5% of bronchial lymph nodes and a similar level in the trigeminal ganglia that were examined. By both assays approximately one third of the positive animals harboured both viruses. Equid herpesvirus 2 (EHV-2) was isolated from all but one of the horses and from > 75% o...
Scintigraphic measurement of uterine clearance in normal mares and mares with recurrent endometritis.
Equine veterinary journal    March 1, 1994   Volume 26, Issue 2 109-113 doi: 10.1111/j.2042-3306.1994.tb04346.x
LeBlanc MM, Neuwirth L, Asbury AC, Tran T, Mauragis D, Klapstein E.The percentage of Technetium 99m-albumin colloid (99mTc-microAA), a radiocolloid, cleared from the uterine lumen within 4 h of intrauterine infusion, was measured in 15 mares during 2 consecutive cycles, on Day 3 of oestrus and 48 h after ovulation. Four nulliparous (Group 1) and 4 multiparous (Group 2) mares were classified as resistant and the remaining 7 multiparous mares were classified as susceptible (Group 3) to endometritis. Mares in Groups 1 and 2 cleared more 99mTc-microAA from their uteri than did mares in Group 3 during oestrus (P < 0.01) and 48 h after ovulation (P 50% of the c...