Evaluation of ethyl alcohol for use in a minimally invasive technique for equine proximal interphalangeal joint arthrodesis

Objective: To determine whether intra‐articular 70% ethyl alcohol alone (IAEA) or in combination with 2 percutaneously placed transarticular lag screws (EA‐TLS) would result in arthrodesis of the equine proximal interphalangeal (PIP) joint. Study Design: Experimental. Animals: Healthy horses (n=6), aged 1.5–3 years, free of lameness, diagonally paired front and hind PIP joints. Methods: Six milliliters 70% ethyl alcohol was injected into randomly selected diagonally paired front and hind PIP joints. Thirty days later, 2 parallel 5.5 mm cortical screws were inserted in lag fashion across the hind PIP joints and the limbs were cast. Horses were confined for 60 days after surgery before free exercise was permitted. Serial lameness examinations were performed at 1, 6, and 10 months. Radiographs of the PIP joints were obtained before injection with alcohol (front, hind PIP joints), at 6 and 10 months (front PIP joints) and 1, 3, 6, and 10 months (hind PIP joints). At 10 months, horses were euthanatized and gross and histopathologic examination of the treated joints was performed. Results: Horses had variable cartilage thinning (more severe in hind PIP joints) and dorsal bone proliferation. One front and 1 hind PIP joint were fused 10 months after alcohol injection. Conclusions: Ethyl alcohol injected alone or in combination with percutaneously placed transarticular lag screws failed to reliably produce fusion of the PIP joint.     

Evaluation of the testosterone response to hCG and the identification of a presumed anorchid dog

A two-year-old dog was presented with no scrotal testes. There was no history of castration but at laparotomy no testes were found. To confirm that the dog was truly anorchid a human chorionic gonadotrophin stimulation test was performed. This was then validated in normal entire and castrated dogs.     

Polymerase chain reaction detection of Mycobacterium tuberculosis complex and Mycobacterium avium organisms in formalin-fixed tissues from culture-negative ruminants

In the US eradication program for bovine tuberculosis, a definitive diagnosis depends on the isolation of Mycobacterium bovis. However, in some cases bacterial culture is unsuccessful, even though the tissue is considered suspicious by histopathology because granulomatous lesions and acid-fast organisms are present. The purpose of this study was to determine if polymerase chain reaction (PCR) tests on formalin-fixed tissue would successfully identify the organisms observed in suspect lesions from culture-negative animals. Diagnostic laboratory records were used to select paraffin blocks of tissue from 102 ruminants that had suspect microscopic lesions but no bacterial isolation. Sections from these blocks were examined with PCR primers for IS6110 to detect Mycobacterium tuberculosis complex infection, or with 16S ribosomal RNA and IS900 primers for detection of Mycobacterium avium. The PCR tests successfully identified a mycobacterial infection in 58 of 102 tissues, including 41 M. tuberculosis complex and 17 M. avium (11 subspecies paratuberculosis). These results demonstrate that PCR testing of formalin-fixed tissue, in combination with bacterial culture, may increase the effectiveness of laboratory diagnostic efforts to detect and identify the most common mycobacterial diseases of ruminants.     

Experimental transmission of Hepatozoon americanum to rodents

Laboratory-raised cotton rats (Sigmodon hispidus), outbred white mice (Mus musculus), and C57BL/6J-Lystbg-J/J mice (M. musculus) that were administered approximately 50 sporulated oocysts of Hepatozoon americanum (AF176836) by gavage developed inflammatory lesions containing parasitic cystozoites in cardiac and skeletal muscle, kidney, and lung. Sprague-Dawley rats (Rattus norvegicus) similarly exposed showed no evidence of infection. Cystozoites were first detected by histopathologic examination four weeks after exposure to oocysts. Globular, PAS-positive material accumulated around the cystozoites as the duration of infection lengthened. Nested PCR analysis of tissues collected 16 weeks post-exposure was positive for the 18S rRNA Hepatozoon sp. gene and the DNA sequence of the fragment amplified was 99.6% and 99.8% identical to H. americanum sequences previously reported from naturally-infected dogs (AF176836 and AY864676, respectively). Merogonous and gamontogonous stages of the parasite were not detected in any of the cystozoite-infected rodents.     

Forage systems for production of stocker steers in the upper south

The southern states produce large numbers of beef calves that are generally weaned and sold in autumn. Keeping calves in this region beyond weaning to graze high-quality forages through a stocker cattle phase could improve profitability. Autumn-weaned Angus crossbred steers were allocated by breeding and weight to four forage systems that began in mid-November and continued through mid-October as follows: System 1, tall fescue (Festuca arundinacea Schreb.) and Kentucky bluegrass (Poa pratensis L.)-white clover (Trifolium repens L.); System 2, tall fescue, caucasian bluestem (Bothriochloa caucasica [Trin.] C. E. Hubbard) and tall fescue-red clover (Trifolium pratense L.); System 3, orchardgrass-alfalfa and bluegrass-white clover; and System 4, rye (Secale cereale L.), soybeans (Glycine max)-foxtail millet (Setaria italica), and bluegrass-white clover. All steers were supplemented with hay or silage previously cut from their respective systems when forage for grazing was limited. System 2 which used stockpiled tall fescue for winter grazing and caucasian bluestem for summer forage plus fescuered clover for hay and grazing in a three-paddock system, resulted in greater (P < .01) gain per hectare and per steer, more grazing days, and reduced stored forage requirements and produced more surplus feed than the other systems tested. Gains per hectare for Systems 1 through 4 were 454, 554, 472, and 487 kg (SE = 18), respectively. Harvested forage from Systems 1, 2, and 3 met needs for stored forages but System 4 required additional "purchased" hay. Stored forage was fed for 61, 38, 112, or 104 d for Systems 1 through 4, respectively. Within the physio-climatic region of this experiment, a simple three-paddock system based on cool- and warm-season perennial forages could improve beef production per unit of land area while reducing inputs of labor and equipment.