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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.
Experimental transmission of eastern equine encephalitis virus by strains of Aedes albopictus and A. taeniorhynchus (Diptera: Culicidae).
Journal of medical entomology    March 1, 1994   Volume 31, Issue 2 287-290 doi: 10.1093/jmedent/31.2.287
Turell MJ, Beaman JR, Neely GW.The vector competence of Aedes taeniorhynchus (Wiedemann) and four strains of Aedes albopictus (Skuse) was assessed for eastern equine encephalitis (EEE) virus isolated from Ae. albopictus collected in Polk County, Florida. Both species became infected with and transmitted EEE virus by bite after feeding on 1-d-old chicks that had been inoculated with EEE virus (viremia = 10(10.1) plaque-forming units [PFU] per ml of blood). However, when fed on an older chick with a lower viremia (viremia = 10(6.1) PFU per ml of blood), Ae. albopictus was significantly more susceptible to infection (90%, n = ...
Detection of African horse sickness virus by reverse transcription-PCR.
Journal of clinical microbiology    March 1, 1994   Volume 32, Issue 3 697-700 doi: 10.1128/jcm.32.3.697-700.1994
Stone-Marschat M, Carville A, Skowronek A, Laegreid WW.Reverse transcription-PCR (RT-PCR) was used to detect African horse sickness virus (AHSV). A single primer pair which amplified a 423-bp fragment of the S8 gene which encodes the NS2 protein of AHSV was identified. Amplification of this fragment from all nine serotypes of AHSV was achieved with these primers. Between 10(1) and 10(2) copies of AHSV genomic double-stranded RNA could be detected by RT-PCR followed by agarose gel electrophoresis and ethidium bromide staining. Application of RT-PCR to blood samples from AHSV-infected horses resulted in earlier detection of viremia than virus isolat...
Tetanus in the horse: a review of 20 cases (1970 to 1990).
Journal of veterinary internal medicine    March 1, 1994   Volume 8, Issue 2 128-132 doi: 10.1111/j.1939-1676.1994.tb03210.x
Green SL, Little CB, Baird JD, Tremblay RR, Smith-Maxie LL.The case records of 20 horses with tetanus referred to the Ontario Veterinary College-Veterinary Teaching Hospital between 1970 and 1990 were reviewed. The fatality rate was 75%. There was a strong association with previous vaccination and survival (P = .03). Most of the animals had been injured an average of 9 days (range 2 to 21 days) prior to development of clinical signs. Hyperesthesia and prolapse of the third eyelid were the most common clinical signs. Treatment regimens varied during hospitalization; however, all horses received parenteral penicillin, tranquilizers, tetanus toxoid, and ...
[The isolation of hyperimmune horse serum to the Ebola virus].
Voprosy virusologii    March 1, 1994   Volume 39, Issue 2 91-92 
Krasnianskiĭ VP, Mikhaĭlov VV, Borisevich IV, Gradoboev VN, Evseev AA, Pshenichnov VA.Immunization of horses with Ebola virus resulted in the production of specific virus-neutralizing antibody with maximum titres at 28-42 days. Repeated cycles of immunization led to a rise in antibody titres to 1:4096.
Horses and MRLs.
The Veterinary record    February 26, 1994   Volume 134, Issue 9 224 doi: 10.1136/vr.134.9.224-a
Cole MJ.No abstract available
Further studies on the efficacy of an inactivated African horse sickness serotype 4 vaccine.
Vaccine    February 1, 1994   Volume 12, Issue 2 142-144 doi: 10.1016/0264-410x(94)90052-3
House JA, Lombard M, Dubourget P, House C, Mebus CA.The immunity induced by two inoculations of a commercial inactivated African horse sickness (AHS) serotype 4 (AHSV-4) vaccine was studied. No adverse reaction was observed in five horses following vaccination. Following challenge-inoculation, no clinical signs attributable to AHS, no viraemia indicating infection, and no anamnestic response was observed in the vaccinated ponies. Two control ponies developed clinical signs typical of AHS, high levels of viraemia, and died 7 and 8 days postchallenge-inoculation. The quality of immunity induced by the two-dose regimen was compared with a one-dose...
Echinococcus granulosus (Taeniidae) and autochthonous echinococcosis in a North American horse.
The Journal of parasitology    February 1, 1994   Volume 80, Issue 1 141-144 
Hoberg EP, Miller S, Brown MA.We report the first documented case of autochthonous echinococcosis in a horse of North American origin. Three fully mature and viable unilocular hydatid cysts of Echinococcus granulosus (Batsch, 1786) were an incidental finding at necropsy in the liver of a 14-yr-old gelding thoroughbred that had been foaled in Virginia and raised in Maryland. Protoscolices were armed with 2 rows of 28-37 rostellar hooks; small hooks measured 23-30 microns; large hooks measured 26-33 microns. Morphologically, these were compatible with rostellar armature considered typical for the equine strain of E. granulos...
Characterization of A/eq-1 virus isolated during the equine influenza epidemic in India.
Acta virologica    February 1, 1994   Volume 38, Issue 1 25-26 
Singh G.The equine influenza virus, Ludhiana/5/87, isolated from the clinical material during the epidemic of equine influenza in India in 1987 was inhibited in haemagglutination-inhibition test by the antiserum against the prototype A/eq/Prague/1/56 (H7N7) virus and by post-epidemic horse sera. In haemagglutinin and neuraminidase analysis, the A/eq/Ludhiana/5/87 isolate appeared similar to the prototype A/eq/Prague/1/56 virus and was characterized as the H7N7 subtype.
The equine herpesvirus type 1 glycoprotein homologous to herpes simplex virus type 1 glycoprotein M is a major constituent of the virus particle.
The Journal of general virology    February 1, 1994   Volume 75 ( Pt 2) 439-442 doi: 10.1099/0022-1317-75-2-439
Pilling A, Davison AJ, Telford EA, Meredith DM.Glycoprotein 45 is a major envelope glycoprotein of equine herpesvirus type 1. The gene encoding this protein is located between map units 0.615 and 0.636 on the virus genome and evidence has suggested that it is encoded by gene 52, one of four genes within this region. Using PCR we have amplified gene 52 and subsequently cloned it into a mammalian expression vector under the control of the human cytomegalovirus immediate early gene promoter. The gene was expressed in COS-7 cells and its product was detected by immunofluorescence and Western blotting. The results indicate that glycoprotein 45 ...
[Detection of mycoplasmas in horses with respiratory diseases and their biochemical and serologic characterization].
Berliner und Munchener tierarztliche Wochenschrift    February 1, 1994   Volume 107, Issue 2 52-55 
Shams Eldin HE, Kirchhoff H.Tracheal swabs were taken from 25 horses with respiratory diseases and investigated for mycoplasmas using three different media. Mycoplasmas could be isolated from 5 horses. The isolates were characterized by serological and biochemical methods. Four isolates could be identified as Mycoplasma equirhinis. The fifth isolate could not be typed. It did not react with antisera against mycoplasmas found in the respiratory tract of horses and its biochemical characteristics were different from the mycoplasmas described so far. It may represent a new species.
Diagnosis of the African horse sickness virus serotype 4 by a one-tube, one manipulation RT-PCR reaction from infected organs.
Journal of virological methods    February 1, 1994   Volume 46, Issue 2 179-188 doi: 10.1016/0166-0934(94)90102-3
Zientara S, Sailleau C, Moulay S, Cruciere C.A single tube reverse transcription-polymerase chain reaction (RT-PCR) method for detection of African horse sickness virus (AHSV) in splenic tissues from infected horses is described. Double stranded RNA was extracted from infected organs of horses and used to produce complementary DNA (cDNA) with the two primers selected for the PCR. The 1179 bp amplified product (the segment 7 which encodes for VP 7), detected by electrophoresis on agarose gel and ethidium bromide staining, was hydrolysed with eight restriction endonucleases for characterization of the AHSV. The sensitivity of this method i...
Detection of Borna disease virus RNA in naturally infected animals by a nested polymerase chain reaction.
Journal of virological methods    February 1, 1994   Volume 46, Issue 2 133-143 doi: 10.1016/0166-0934(94)90098-1
Zimmermann W, Dürrwald R, Ludwig H.Borna disease virus in naturally infected horses, a donkey and sheep was detected for the first time by amplification of viral RNA using PCR. In contrast to a control group of healthy horses, brain tissue was positive by this assay in all animals with neurological symptoms. The use of a second round of PCR with nested primers following Southern hybridization confirmed the specificity and increased the sensitivity of the test. Comparison with conventional methods recommends this technique for monitoring of BDV infections at a molecular level.
Update on equine influenza.
The Veterinary record    January 15, 1994   Volume 134, Issue 3 71 doi: 10.1136/vr.134.3.71-b
Mumford JA.No abstract available
[An outbreak of equine arteritis virus infection in a riding school].
Tijdschrift voor diergeneeskunde    January 15, 1994   Volume 119, Issue 2 30-32 
van Gorkom LP, van Wessum R, van den Hoven R.A major part of the residing horses and ponies of a riding school in Noord-Holland became affected by a febrile disorder that included anorexia, depression, conjunctivitis, urticaria, edema of the legs and laborious locomotion. All remaining horses fell ill within one week. Based on the clinical symptoms the disorder was diagnosed as vasculitis. With serology the causative agent of the disorder appeared to be equine arteritis virus.
Export of stallions vaccinated against equine viral arteritis.
The Veterinary record    January 1, 1994   Volume 134, Issue 1 23 doi: 10.1136/vr.134.1.23-a
Bell RA.No abstract available
Rhodococcus equi vertebral osteomyelitis in 3 quarter horse colts.
Equine veterinary journal    January 1, 1994   Volume 26, Issue 1 74-77 doi: 10.1111/j.2042-3306.1994.tb04336.x
Giguère S, Lavoie JP.No abstract available
Estimation of the size of the genome of Taylorella equigenitalis by crossed-field gel electrophoresis.
Veterinary research communications    January 1, 1994   Volume 18, Issue 2 99-102 doi: 10.1007/BF01839226
Matsuda M, Asami Y, Miyazawa T, Sugawara T, Kumano M, Isayama Y, Honda M.No abstract available
Parasitic protozoa of horses: a subject of burgeoning concern.
Equine veterinary journal    January 1, 1994   Volume 26, Issue 1 4-5 doi: 10.1111/j.2042-3306.1994.tb04318.x
Taylor MA.No abstract available
[Trichinellosis in slaughtered and wild animals in Switzerland using a digestion method and a serologic method (E/S-ELISA)].
Schweizer Archiv fur Tierheilkunde    January 1, 1994   Volume 136, Issue 9 298-308 
Jakob HP, Eckert J, Jemmi T, Gottstein B.For many decades trichinellosis has not been reported among Swiss domestic pigs. Considering the fact that Trichinella occurs in a sylvatic cycle in Switzerland, a study was designed to reevaluate the present epidemiologic situation by investigating 10,904 fattening pigs, 218 pigs with free access to pasturage or being kept on an alp, 104 domestic boars, 106 horses, 44 wild boars and 538 foxes using a direct and an indirect diagnostic technique (digestion method and serology with ELISA and an excretory/secretory antigen, respectively). The digestion method was performed according to EC-guideli...
Vertebral body osteomyelitis due to Rhodococcus equi in two Arabian foals.
Equine veterinary journal    January 1, 1994   Volume 26, Issue 1 79-82 doi: 10.1111/j.2042-3306.1994.tb04338.x
Olchowy TW.No abstract available
Development of the Coggins test.
The Cornell veterinarian    January 1, 1994   Volume 84, Issue 1 3-5 
Coggins L.No abstract available
[Vaccination against Rhinopneumonia].
Tijdschrift voor diergeneeskunde    January 1, 1994   Volume 119, Issue 1 20 
Binkhorst GJ.No abstract available
Cystic adenomatous hyperplasia of the equine allantois: a report of eight cases. Shivaprasad HL, Sundberg JP, McEntee K, Gordon L, Johnstone AC, Lombardo de Barros CS, Hoffman RL.No abstract available
Streptococcus pneumoniae and equine disease.
Equine veterinary journal    January 1, 1994   Volume 26, Issue 1 5-6 doi: 10.1111/j.2042-3306.1994.tb04319.x
Chanter N.No abstract available
Evolution of alphaviruses in the eastern equine encephalomyelitis complex.
Journal of virology    January 1, 1994   Volume 68, Issue 1 158-169 doi: 10.1128/JVI.68.1.158-169.1994
Weaver SC, Hagenbaugh A, Bellew LA, Gousset L, Mallampalli V, Holland JJ, Scott TW.Evolution of viruses in the eastern equine encephalomyelitis (EEE) complex was studied by analyzing RNA sequences and oligonucleotide fingerprints from isolates representing the North and South American antigenic varieties. By using homologous sequences of Venezuelan equine encephalomyelitis virus as an outgroup, phylogenetic trees revealed three main EEE virus monophyletic groups. A North American variety group included all isolates from North America and the Caribbean. One South American variety group included isolates from the Amazon basin in Brazil and Peru, while the other included strain...
The development of Babesia (Theileria) equi (Laveran, 1901) in the gut and the haemolymph of the vector ticks, Hyalomma species.
Parasitology research    January 1, 1994   Volume 80, Issue 4 297-302 doi: 10.1007/BF02351869
Zapf F, Schein E.The development of the piroplasm Babesia equi was studied by light microscopy in the gut and the haemolymph of three different Hyalomma species during and after the nymphs had engorged on parasitaemic horses. The stock of B. equi used was isolated from a horse imported from Turkmenistan (CIS) in 1991. The existence of gamogony was identified by the occurrence of gamonts and gametes in the gut contents of the nymphs at between 3 and 4 days after infestation of the nymphs, before the ticks dropped off the experimentally infected horses. Zygotes and kinetes were observed in the intestinal cells f...
Trichinellosis in Greece (1992-1993).
Wiadomosci parazytologiczne    January 1, 1994   Volume 40, Issue 4 396 
Feidas S.No abstract available
Review of equine Cryptosporidium infection.
Equine veterinary journal    January 1, 1994   Volume 26, Issue 1 9-13 doi: 10.1111/j.2042-3306.1994.tb04322.x
Xiao L, Herd RP.Diarrhoea is one of the most important diseases of foals and 7040% are affected within the first 6 months of life (Palmer 1985). Although the cause is multifactorial and changes in the physiology and nutrition of foals are sometimes responsible, diarrhoea is frequently the result of infection by enteropathogens such as bacteria, viruses and nematodes (Palmer 1985; Tzipori 1985). There is increasing evidence that Cryptosporidium infection can also cause diarrhoea in foals (Austin et a/. 1990; Kim 1990). Cryptosporidiosis in horses is caused by Cryptosporidium parvum, a coccidial paras...
Cloning and sequencing of horse interferon-gamma cDNA.
Immunogenetics    January 1, 1994   Volume 39, Issue 6 448-449 doi: 10.1007/BF00176167
Grünig G, Himmler A, Antczak DF.No abstract available
Proteolytic enzymes in equine joints with infectious arthritis.
Equine veterinary journal    January 1, 1994   Volume 26, Issue 1 48-50 doi: 10.1111/j.2042-3306.1994.tb04330.x
Spiers S, May SA, Harrison LJ, Bennett D, Edwards GB.Significant amounts of collagenase and caseinase activity were detected in infected synovial fluid samples. Partial characterisation of the enzymes by gel filtration suggested that synovial fluid from cases of infectious arthritis may contain enzymes from both the synovial cells and neutrophils. This finding was also supported by analysis of sequential synovial fluid samples from 4 infected joints. In 3 joints the concentration of caseinase and in 1 joint collagenase paralleled the decline in total nucleated cell count. However, in 3 joints the concentration of collagenase remained high after ...