EHV-1 gene63 is not essential for in vivo replication in horses and mice, nor does it affect reactivation in the horse: short communication

The aim of this study was to investigate the role of immediate early gene (gene63) in the pathogenesis of equine herpesvirus 1 (EHV-1) acute and latent infections in equine and murine models. EHV-1 gene63 mutant virus (g63mut) along with EHV-1 (Ab4) was used for intracerebral and intranasal infection of 3 and 17-day-old mice. Both viruses were recovered at the same frequency from tissues after infection. Two Welsh ponies were infected via the intranasal route with each of the viruses. Acute infection was monitored by virus isolation from nasal swabs and peripheral blood leukocytes. Six weeks post infection, peripheral blood leukocytes were taken from ponies and in vitro reactivation was positive for both viruses. At autopsy, both viruses were isolated by co-cultivation from bronchial and submandibular lymph nodes. These findings indicate that the mutation of EHV-1 gene63 does not play a role in the establishment and reactivation from latency.     

Renal adenocarcinoma, hepatocellular carcinoma, and pancreatic islet cell carcinoma in a binturong (Arctictis binturong).

A 19-yr-old binturong (Arctictis binturong) with acute upper respiratory disease was euthanized. Postmortem findings included hepatocellular carcinoma, pancreatic islet cell carcinoma, and renal adenocarcinoma with metastasis to the spleen, pleura, and pericardium. A link between primary hepatic and renal neoplasms has been noted in older humans.     

Relationship of toxoplasma infections to other diseases in dogs

Toxoplasma infection as detected by the immunofluorescent antibody (IFA) test was found in 13.2% of 448 dogs examined at the Purdue University Small Animal Clinic. Only titres of 1/64 and above were considered positive, but lesser titers were encountered more frequently. The highest titer observed was 1/1024 in 2 dogs one of which had idiopathic epilepsy and the other had dirofilariasis as well as hip dysplasia. The incidence of positive sera from male and female dogs were 11.7 and 14.5%, respectively. The highest frequency of infection occurred in young dogs up to 4 years of age and the lowest was in older animals. The presence of the high toxoplasmosis IFA titers in the sera of dogs seems to be associated with other disease conditions. Stress such as joint dislocations, fractures, helminth parasitism, and concomitant bacterial and viral infections, etc., was observed in 62.7% of the positive cases. Presence of tumors and renal disease conditions were associated with 28.8 and 5.2%, respectively, of the positive sera.     

Non-suture intestinal anastomosis by invagination

Intestinal anastomoses were performed on seventeen mongrel dogs by non-suture invagination technique and by the conventional method. A comparative evaluation revealed the non-suture technique to be easier and less time-consuming. Also the tissue reaction was minimal. Encouraging results suggest further investigation prior to clinical trial of this relatively new technique. Résumé. Des anastomoses intestinales sur dix-sept chiens métis par l'invagination technique pas de suture et la méthode de convention. Une évaluation comparative a révélé que la technique pas de suture était plus facile et moins de temps était perdu. Aussi la réaction du tissu était minimum. Les résultats encourageants proposent un surcro***ît d'investigation antérieurement a l'expérience clinique de cette technique relativement plus nouvelle. Zusammenfassung. Die Darmanastomosen von siebzehn Mischhunden durch die Intussuscep-tiontecknik keiner Naht und die verabredete Methode. Eine vergleichende Abschatzung zeigte, daß die Tecknik keiner Naht leichter ist, und wenigere Zeitverschwendung hat. Auch war die Reaktion des Gewebes minderst. Die ermutigenden Ergebnisse suggerieren eine Forderung der Erforschung vor klinischem Versuch dieser Tecknik, die verhältnismäßig neuere ist.     

Penetration of malathion into locusts

Topically applied dilute solutions of malathion in kerosene extract ‘bottoms’ are more toxic and rapid in action than concentrated ones. Dilute solutions spread farther, penetrate more rapidly and consequently their rate of activation into the more toxic malaoxon is higher. With a single dose of 2·5% malathion the rate of penetration and activation varies according to the loci of topical application, presumably reflecting differences in sclerotisation of the cuticle. There are also inherent differences in the susceptibility of various body regions associated perhaps with the differential vulnerability of some vital internal organ (e.g. the central nervous system). Very rapid hydrolytic degradation of malathion occurs through its conversion into malaoxon; locusts survive the lethal action of malathion by way of such degradation only where activation into malaoxon takes place in areas away from the sensitive head region, or where the rate of activation is slow, or where the circulatory system delays its arrival at such sensitive sites. The higher rate of activation observable in immature adults of Schistocerca gregaria compared with mature adults is, however, counterbalanced by a higher rate of hydrolysis in the former.     

The detection of the meq gene in chicken infected with Marek's disease virus serotype 1

In the genome of strains of very virulent Marek's disease virus serotype 1(vvMDV1), such as Md5 and RB1B, the meq open reading frame (ORF) encoding a 339-amino-acid bZIP protein, is present, while a slightly longer meq ORF, termed as L-meq, in which a 180-bp sequence is inserted into the meq ORF is found in other strains of MDV1, such as CV1988/R6 and attenuated JM. When chickens were infected with vvMDV1 strains and the meq gene was amplified by nested polymerase chain reaction (PCR), the meq gene was detected throughout the experimental period for 7 weeks post inoculation (pi). However, the L-meq gene was also detected at 3 to 5 weeks and 3 to 4 weeks pi. in Md5-infected and RB1B-infected chickens, respectively. In the case of chickens infected with an attenuated MDV1, the JM strain, the L-meq gene was detected at 2 to 7 weeks pi., and the meq gene was also detected at 2 to 6 weeks pi. Both L-meq and meq genes were detected in chickens infected with an attenuated nononcogenic vaccine strain of MDV1 (CVI988/R6), throughout the experimental period. Though quantitative PCR was not performed, a larger amount of the PCR products corresponding to the L-meq than the meq gene was amplified from chickens infected with JM or CVI988/R6. These results suggest that a dynamic population shift between the MDV subpopulations displaying meq and L-meq genes occurs in chickens during the course of MDV infection. Since the MDV subpopulation that displays the L-meq gene only displays it during the latent phase, the L-meq and its gene product, if any, might contribute to the maintenance of the MDV latency.