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Topic:Infectious Disease

Infectious diseases in horses encompass a range of illnesses caused by bacteria, viruses, fungi, or parasites. These diseases can affect various systems within the equine body, leading to symptoms that range from mild discomfort to severe systemic illness. Common infectious diseases in horses include equine influenza, strangles, equine herpesvirus, and West Nile virus. These diseases can be transmitted through direct contact with infected animals, contaminated surfaces, or vectors such as insects. Understanding the mechanisms of transmission, pathogenesis, and immune response is essential for effective prevention and control. This page compiles peer-reviewed research studies and scholarly articles that explore the epidemiology, diagnosis, treatment, and management of infectious diseases in horses.
Physical and functional characterization of transcriptional control elements in the equine infectious anemia virus promoter.
Journal of virology    April 1, 1993   Volume 67, Issue 4 2064-2074 doi: 10.1128/JVI.67.4.2064-2074.1993
Carvalho M, Derse D.Equine infectious anemia virus (EIAV) is a lentivirus that causes a chronic disease of horses characterized by cyclic episodes of fever, anemia, and viremia. Although the genome and promoter of EIAV are much less complex than those of its relatives the primate immunodeficiency viruses, the cellular proteins that activate and regulate transcription of EIAV have not yet been identified. In this report, we show by electrophoretic mobility shift assays and DNase I footprinting that the EIAV promoter contains multiple binding sites for ubiquitous, cell type-specific, and inducible cellular proteins...
Intermittent antimicrobial infusion for management of a septic distal interphalangeal joint in a horse.
Journal of the American Veterinary Medical Association    March 15, 1993   Volume 202, Issue 6 973-975 
McClure SR, Hooper RN, Watkins JP.A 13-month-old Quarter Horse colt sustained a puncture wound to the frog region of the foot, which penetrated the navicular bursa and distal interphalangeal joint, 7 days prior to examination. A street-nail procedure was performed to debride the tract and provide drainage of the navicular bursa and distal interphalangeal joint. An indwelling lavage system was placed through the dorsal aspect of the joint and antimicrobials were infused intermittently to supply a high local concentration of drug and to frequently lavage the distal interphalangeal joint and navicular bursa.
Immunodeficiency and serious pneumonia in foals: the plot thickens.
Equine veterinary journal    March 1, 1993   Volume 25, Issue 2 88-89 doi: 10.1111/j.2042-3306.1993.tb02913.x
Prescott JF.No abstract available
Culture confirmation of the carrier status of Babesia caballi-infected horses.
Journal of clinical microbiology    March 1, 1993   Volume 31, Issue 3 698-701 doi: 10.1128/jcm.31.3.698-701.1993
Holman PJ, Frerichs WM, Chieves L, Wagner GG.Culture of horse blood for Babesia caballi identified four carrier horses among nine previously infected horses. Three of the carriers had no detectable parasitemias on stained blood smears, and sera from two carrier horses were complement fixation test negative. Three cultures were continuously cultivated. Cryopreserved fourth-passage B. caballi was successfully reestablished in vitro. Blood from a 10th horse previously subinoculated with blood from a suspected carrier was cultured, with negative results.
Cutaneous pythiosis in horses from Brazil.
Mycoses    March 1, 1993   Volume 36, Issue 3-4 139-142 doi: 10.1111/j.1439-0507.1993.tb00702.x
Meireles MC, Riet-Correa F, Fischman O, Zambrano AF, Zambrano MS, Ribeiro GA.Equine pythiosis was studied in five animals from two farms located in a swampy region of southern Brazil (Rio Grande do Sul State). Granulomatous lesions exuding necrotic material and containing a central yellow and firm tissue core, the 'kunker', were observed on the top of the nose of one horse, on the abdomen of two horses and on the hind limbs of two other animals. Direct microscopic preparations, histopathological examination of lesion material, and macroscopic and microscopic characteristics of the isolates confirmed the diagnosis of pythiosis. Surgical intervention of the inflammatory ...
‘Frozen’ evolution of equine influenza viruses?
Equine veterinary journal    March 1, 1993   Volume 25, Issue 2 87 doi: 10.1111/j.2042-3306.1993.tb02912.x
Wood JM.No abstract available
Characterisation of equine influenza isolates from the 1987 epizootic in India by nucleotide sequencing of the HA1 gene.
Equine veterinary journal    March 1, 1993   Volume 25, Issue 2 99-102 doi: 10.1111/j.2042-3306.1993.tb02916.x
Gupta AK, Yadav MP, Uppal PK, Mumford JA, Binns MM.Two A/Equi-2 (H3N8) isolates were obtained during the 1987 Indian equine influenza epizootic. The sequence of the Ludhiana/87 HA1 gene revealed that this isolate was very similar to recent European and North American isolates of equine influenza. In contrast, the Bhiwani/87 HA1 gene was nearly identical to the Miami/63 prototype H3 sequence. These results support the antigenic analysis previously carried out on these isolates using monoclonal antibodies. However, the finding that Bhiwani/87 is so similar to Miami/63, coupled with the finding that equine H3N8 influenza viruses have previously b...
Serological diagnosis of Trypanosoma evansi (Steel, 1885) in horses using a direct agglutination test.
Veterinary parasitology    March 1, 1993   Volume 47, Issue 1-2 25-35 doi: 10.1016/0304-4017(93)90173-k
Monzón CM.A direct agglutination test is described to diagnose 'Mal de Caderas' caused by Trypanosoma evansi. The antigen used was a suspension of trypsin-treated parasites stabilized with formalin. The test was evaluated in horses with both natural and experimental infections. Test sensitivity and specificity were 94 and 97%, respectively. Treatment of serum with 2-mercaptoethanol before testing permitted the differentiation of IgM and IgG antibodies, and possible differentiation of current infection from past exposure to the parasite. The antigen was stable over a 6-month evaluation period and also sh...
Replication of equid herpesvirus-1 in the vaginal tunics of colts following local inoculation.
Research in veterinary science    March 1, 1993   Volume 54, Issue 2 249-251 doi: 10.1016/0034-5288(93)90066-o
Smith KC, Tearle JP, Boyle MS, Gower SM, Mumford JA.Equid herpesvirus-1 (EHV-1; Ab4 isolate) was inoculated unilaterally into the cavum vaginale of four pony colts under general anaesthesia. The animals were monitored daily for evidence of scrotal or testicular swelling and euthanased electively on days 3, 4, 6 and 12 after infection. Detailed pathological examination of the male genital tract was carried out. In animals examined at days 3 and 4 after infection, replication of EHV-1 was detected bilaterally in mesothelial and endothelial cells of the parietal and visceral vaginal tunics. The mesothelial infection had resolved by day 12 after in...
Report of the Thirteenth Meeting of the OIE Ad hoc Group on Non Tsetse-Transmitted Animal Trypanosomoses.
Revue scientifique et technique (International Office of Epizootics)    March 1, 1993   Volume 12, Issue 1 237-272 
Touratier L.There is increasing interest in many parts of the world in trypanosomoses other than those transmitted by tsetse flies, as shown by numerous research projects and field studies. The refinement of techniques for studying the behaviour of trypanosomes (techniques of molecular biology) in axenic culture or in the parasitised host has led to progress in diagnosis and immunology, and a rational approach to chemotherapy and chemoprophylaxis of these infections. Field trials of enzyme-linked immunosorbent assays in Africa, Asia and South America have shown that these tests may now be regarded as reli...
Equine influenza in Hong Kong.
The Veterinary record    February 6, 1993   Volume 132, Issue 6 144 doi: 10.1136/vr.132.6.144-a
Watkins KL, Shortridge KF, Powell DG.No abstract available
In situ hybridisation of equine sarcoids with bovine papilloma virus.
The Veterinary record    February 6, 1993   Volume 132, Issue 6 132-133 doi: 10.1136/vr.132.6.132
Lory S, von Tscharner C, Marti E, Bestetti G, Grimm S, Waldvogel A.No abstract available
Structural features of the trans-activation response RNA element of equine infectious anemia virus.
Biochemistry    February 2, 1993   Volume 32, Issue 4 1096-1104 doi: 10.1021/bi00055a015
Hoffman DW, Colvin RA, Garcia-Blanco MA, White SW.A 25-nucleotide RNA with the sequence of the trans-activation response (TAR) element of equine infectious anemia virus (EIAV) was analyzed by biochemical methods and by one- and two-dimensional NMR spectroscopy. NMR, nuclease probing, and polyacrylamide gel migration rates show that the RNA consists of an A-helical stem capped by two non-Watson-Crick U-G base pairs and a compact four-nucleotide loop. The loop is stabilized by base stacking, with loop nucleotides C12 and C15 stacked upon U11 and G16, respectively. Near the 5' end of the molecule, the stem contains a bulge at nucleotide C2, most...
Detection of antibodies against equine herpesvirus types 1 and 4 by using recombinant protein derived from an immunodominant region of glycoprotein B.
Journal of clinical microbiology    February 1, 1993   Volume 31, Issue 2 265-271 doi: 10.1128/jcm.31.2.265-271.1993
Sinclair R, Binns MM, Chirnside ED, Mumford JA.The N-terminal fragment comprising residues +1 to +50 (gB1-50) of equine herpesvirus type 1 (EHV-1) glycoprotein B was expressed as a glutathione S-transferase fusion protein in Escherichia coli. Recombinant gB1-50 (rgB1-50) was recognized in immunoblots by sera from rabbits immunized with EHV-1 and by convalescent-phase sera from horses with natural EHV-1 infections. An enzyme-linked immunosorbent assay (ELISA) for monitoring antibody levels against EHV-1 was developed by using rgB1-50, and its specificity was assessed with a panel of reference antisera against other equine viruses. A specifi...
Trypanosomiasis of domestic animals in China.
Parasitology today (Personal ed.)    February 1, 1993   Volume 9, Issue 2 41-45 doi: 10.1016/0169-4758(93)90029-f
Lun ZR, Fang Y, Wang CJ, Brun R.Trypanosomiasis caused by Trypanosoma evansi (surra) is a problem of great economic importance in livestock in China because it affects important working animals: buffaloes in the south and east, and horses and cattle in the north and west. In addition, buffaloes are an important source of meat and leather for the Chinese population. In the north and west, T. evansi is found mainly in camels, whereas in the east, the south and the southwest, it is primarily buffaloes, cattle and horses that are affected by this parasitic flagellate. Although trypanosomiasis is one of the most important parasit...
The genome of equine herpesvirus type 2 harbors an interleukin 10 (IL10)-like gene.
Virus genes    February 1, 1993   Volume 7, Issue 1 111-116 doi: 10.1007/BF01702353
Rode HJ, Janssen W, Rösen-Wolff A, Bugert JJ, Thein P, Becker Y, Darai G.A gene was identified within the DNA sequences of the EcoRI DNA fragment N (4.3 kbp) of the genome of equine herpesvirus type 2 (EHV-2) coding for a protein (179 amino acid residues) homologous to the cytokine synthesis inhibitory factor (CSIF; interleukin 10) of the human and mouse, and to the Epstein-Barr virus (EBV) protein BCRF1. This finding is further significant evidence that the interleukin 10 (IL-10) and/or IL-10-like gene can indeed be present in the genomes of members of the herpesviral family.
Inhibitory effects of horse serum on immunoassay of horse ferritin.
The Journal of veterinary medical science    February 1, 1993   Volume 55, Issue 1 45-49 doi: 10.1292/jvms.55.45
Orino K, Saji M, Ozaki Y, Ohya T, Yamamoto S, Watanabe K.The effects of horse serum on the immunoassay of horse ferritin were investigated using two sandwich enzyme-linked immunosorbent assay (ELISA) systems. In System A, affinity-purified antibody to horse spleen ferritin and its conjugate with alkaline phosphatase were used as the first and second antibodies, respectively. In System B, whole antiserum and its conjugate with the enzyme were used. The recoveries of horse spleen ferritin added to horse sera were very low in either system (50-71% in System A; 42-79% in System B). However, heat treatment of the sera at 75 degrees C for 15 min improved ...
Protein characterization of Babesia equi piroplasms isolated from infected horse erythrocytes.
Parasitology research    January 1, 1993   Volume 79, Issue 8 639-643 doi: 10.1007/BF00932505
Ali S, Sugimoto C, Matsuda M, Sugiura T, Kanemaru T, Onuma M, Kamada M.Proteins of Babesia equi piroplasms were characterized. The piroplasms of B. equi were purified by lysis of infected horse erythrocytes with N2 gas cavitation followed by separation in Percoll density-gradient centrifugation. The relative molecular weights (Mr) of major proteins separated by two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis were 18, 28, 30, 41, 43, 54, 66.5, and 96 kDa. Immunoblot analysis using serum from an experimentally infected horse revealed six immunodominant proteins of 15, 18, 28, 30, 41, and 96 kDa. Two immunodominant proteins of 18 and 28 kDa...
A review of techniques for the serologic diagnosis of equine infectious anemia. Issel CJ, Cook RF.No abstract available
Current status of the diagnosis and control of African horse sickness.
Veterinary research    January 1, 1993   Volume 24, Issue 2 189-197 
Rodriguez M, Hooghuis H, Castaño M.African horse sickness (AHS) is an infectious, non-contagious, highly fatal viral disease of Equidae, transmitted by arthropod vectors of the genus Culicoides, and endemic in Africa south and east of the Sahara. The disease is caused by a virus of the Reoviridae family, genus Orbivirus, and 9 serotypes have been recognized. Recent outbreaks of AHS in the Iberian peninsula and Northern Africa emphasize the need for accurate diagnosis and rapid implementation of control measures. In this paper, the epizootiological factors, clinical signs and necropsy findings of AHS are discussed, and an update...
Did vaccinia virus come from a horse?
Equine veterinary journal    January 1, 1993   Volume 25, Issue 1 8-10 doi: 10.1111/j.2042-3306.1993.tb02892.x
Taylor CE.No abstract available
A comparison of ELISA, FAST-ELISA and gel diffusion tests for detecting antibody to equine infectious anaemia virus.
Veterinary microbiology    January 1, 1993   Volume 34, Issue 1 1-5 doi: 10.1016/0378-1135(93)90002-o
Lew AM, Thomas LM, Huntington PJ.Sera of sixteen horses with clinical signs of EIA from six different outbreaks and sera of 100 uninfected horses were used to validate an ELISA for EIA diagnosis. The antigen used was a recombinant protein derived from the amino-terminal portion of the transmembrane envelope protein of EIA (gp45). Reactivity between positive and negative sera could be clearly distinguished. Comparison with the traditional agar gel immunodiffusion test (commonly called the Coggins test) showed that the ELISA was superior in sensitivity. Comparison of this ELISA with the FAST-ELISA system showed that the latter ...
Epizootic of equine influenza in 1969 in Poland.
Archivum veterinarium Polonicum    January 1, 1993   Volume 33, Issue 3-4 139-145 
Kita J.Epidemiological observations on the course and spread of equine influenza in Poland during the 1969 epizootic were carried out. The dynamics of the spread of the disease in the country are shown graphically by voivodship. The disease incidence and mortality rates for the entire country are also shown. The highest incidence of disease and mortality rates were found to be in November 1969. A/equi-2/Warsaw/69 was identified as the causal virus. It caused the largest epizootic in the country since 1954.
Poliomyelomalacia and ganglioneuritis in a horse with paralytic rabies. O'Toole D, Mills K, Ellis J, Welch V, Fillerup M.No abstract available
Unravelling the ecology of influenza A virus.
History and philosophy of the life sciences    January 1, 1993   Volume 15, Issue 1 23-32 
Beveridge WI.For 20 years after the influenza A virus was discovered in the early 1930s, it was believed to be almost exclusively a human virus. But in the 1950s closely related viruses were discovered in diseases of horses, pigs and birds. Subsequently influenza A viruses were found to occur frequently in many species of birds, particularly ducks, usually without causing disease. Researchers showed that human and animal strains can hybridise thus producing new strains. Such hybrids may be the cause of pandemics in man. Most pandemics have started in China or eastern Russia where many people are in intimat...
WHO/OIE meeting: consultation on newly emerging strains of equine influenza. 18-19 May 1992, Animal Health Trust, Newmarket, Suffolk, UK.
Vaccine    January 1, 1993   Volume 11, Issue 11 1172-1175 doi: 10.1016/0264-410x(93)90092-c
Mumford J, Wood J.No abstract available
Detection of humoral antigen and antibody by enzyme-linked immunosorbent assay in horses with experimentally induced Ehrlichia equi infection. Corstvet RE, Gaunt SD, Karns PA, McBride JW, Battistini RA, Mauterer LA, Austin FW.An enzyme-linked immunosorbent assay (ELISA) was used to detect antigen in plasma and antibody in serum of 3 horses inoculated with Ehrlichia equi. Clinical signs, including rectal temperature, were correlated with the antigen and antibody detection. ELISA was very efficient in detection of serum antibody. Antigen detection using monoclonal antibodies to E. equi and ELISA should be considered as a diagnostic method.
High prevalence of serum antibodies to equine infectious anemia virus reverse transcriptase.
AIDS research and human retroviruses    January 1, 1993   Volume 9, Issue 1 7-11 doi: 10.1089/aid.1993.9.7
DeVico AL, Issel CJ, Le Grice SF, Payne SL, Montelaro RC, Sarngadharan MG.The immunogenicity of the equine infectious anemia virus (EIAV) reverse transcriptase (RT) was examined by immunoblot assay with recombinant EIAV RT. All of the 19 sera from EIAV-infected horses tested contained antibodies that recognized EIAV RT and directly inhibited the polymerase activity of the enzyme. An examination of sera obtained sequentially from two experimentally infected animals revealed that anti-RT antibodies arise early in infection and increase in level. The appearance of the antibodies correlated with progression toward the asymptomatic period of infection.
[The occurrence and significance of enterotoxin-producing Clostridium perfringens strains in the intestinal tract of horses].
Berliner und Munchener tierarztliche Wochenschrift    January 1, 1993   Volume 106, Issue 1 1-6 
Gautsch S, Beckmann G, Amtsberg G, Dieckmann M, Deegen E.100 faecal samples from clinically healthy horses of different age groups and feeding habits, 50 samples of faeces from horses suffering from enteropathy accompanied by diarrhoea and small and/or large intestine from 25 horses that had died after an intestinal disease were examined for the presence of Clostridium (Cl.) perfringens. The frequency with which Cl. perfringens was detected was 22% in clinically healthy horses, 32% in horses with diarrhoea and 52% in the dead horses. In two faecal samples from the horses with diarrhoea the microbial count of Cl. perfringens was ca. 10(6) cfu/g faece...
African horse sickness: transmission and epidemiology.
Veterinary research    January 1, 1993   Volume 24, Issue 2 199-212 
Mellor PS.African horse sickness (AHS) virus causes a non-contagious, infectious, arthropod-borne disease of equines and occasionally of dogs. The virus is widely distributed across sub-Saharan African where it is transmitted between susceptible vertebrate hosts by the vectors. These are usually considered to be species of Culicoides biting midges but mosquitoes and/or ticks may also be involved to a greater or lesser extent. Periodically the virus makes excursions beyond its sub-Saharan enzootic zones but until recently does not appear to have been able to maintain itself outside these areas for more t...