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Biomedical subjects

R L Heberling

Publications and source records attributed to R L Heberling.

At least 37 records · Page 2Linked to original sources

Infection of baboons ("Papio cynocephalus") with rotavirus (SA11).

A recent survey of nonhuman primate sera indicated that antibody to a rotavirus (SA11) was prevalent among a wide spectrum of animals. Both New and Old World species were found with antibody, many with surprisingly high titers (1:320). Whether or not infection per se was due to SA11 or an antigenically closely related agent could not be determined by that study; however, it is apparent from this study as well as from a survey of the literature that natural as well as experimental infection of nonhuman primates occurs. Recognizing that there is a need for an animal model for the study of viruses associated with human diarrhea, a preliminary investigation attempting to ascertain the susceptibility of the baboon (Papio cynocephalus) to a rotavirus was undertaken. Inoculation of four newborn baboons with SA11 resulted in diarrhea within 24 to 48 hours in all animals. One animal died 10 days postinoculation following severe diarrhea and dehydration. Virus was isolated as well as seen by electron microscopy in the stools of all four animals.

Animals↗

Coronavirus-like particles in nonhuman primate feces.

Coronavirus-like particles were detected by electron microscopy in normal and diarrhea stool specimens from baboons, chimpanzees, macaques, and marmosets. There was a high prevalence of particles in both normal and diarrhea stools of older animals, whereas stools from nonweaned animals rarely contained these coronavirus-like particles.

Aging↗

Chemical inhibition of foamyvirus in primary baboon (Papio cynocephalus) kidney cells.

This report describes the conditions for the use of aluminum chloride (AlCl3) in growth and maintenance media for the suppression or inhibition of simian foamyviruses (SFV) in primary baboon kidney (BAK) and rabbit kidney (RK) cell cultures. When RK cells were planted in medium containing AlCl3, infected with SFV, and passaged, the growth of SFV was suppressed or inhibited by the presence of AlCl3. With this method, BAK cells yielded higher viral titers after infection with various viruses, thus making these cells more suitable for virological applications.

Aluminum↗

A comparison of neutralization tests for the detection of antibodies to Herpesvirus simiae (monkey B virus).

Neutralization tests used in one laboratory in the USA and one laboratory in England to detect antibodies to Herpesvirus simiae have been compared. Complete concordance in results was obtained with 53 (90%) of 59 monkey sera. The remaining six sera all had titers no greater than 1:3. Four were positive only in the American test, and two were positive only in the British test. The importance of using complement if maximum sensitivity is to be achieved in detecting antibodies to this virus has been confirmed.

Animals↗

The differential diagnosis of herpesvirus infections in man and animals.

The precise number of human and nonhuman herpesviruses is unknown. It is recognized, however, that the complex antigenic components of this group of viruses and their group interrelationships make specific differentiation of certain herpesviruses extremely difficult with routine serologic procedures. The question of differentiating herpes simplex (H. hominis) infection from B virus (H. simiae) infection frequently requires resolution. When SA8, another primate herpesvirus (principally of African primates) is also involved, differentiation becomes more difficult. The serum neutralization (SN) test, currently the procedure of choice for serologic diagnosis, is not without error. A number of factors control its specificity and variability. Neither EIA, RIA nor FA improves the specificity. Polyarcylamide electrophoresis of the highly lethal B virus indicates the presence of antigens (polypeptides and glycoproteins) distinct from those in other herpesviruses, which may aid in the specific diagnosis, particularly when these antigens are used for the production of monoclonal antibody. DNA fragments have been identified in B virus by restriction endonuclease analysis that appear to be unique for this agent in comparison to human herpesviruses types 1 and 2.

Animals↗

AXC rat prostatic adenocarcinoma: characterization of cells in culture.

We have described the establishment of AXC rat prostatic cancer cells in continuous culture. When injected into isogeneic male rats, these cells produce prostatic adenocarcinomas. The response of androgen and prolactin receptors and ODC in LSC-AXC prostatic cancer cells and tumors to androgen ablation is indistinguishable from that of ventral prostate. In addition, LSC-AXC prostatic tumors retain levels of secretory acid phosphatase comparable to those of ventral prostate of aged AXC rats. These data demonstrate that LSC-AXC prostatic cancer cells and tumors retain a high degree of differentiation, androgen regulated function. The LSC-AXC prostatic cancer cells and tumors appear to represent a unique model system for combined in vivo and in vitro studies of androgen regulation of prostate cancer cell function.

Acid Phosphatase↗

[Experimentally induced herpesvirus SA 8-pneumonia (bronchopneumonia) in Kenya baboons (papio cynocephalus) (author's transl)].

Captive baboons of three age groups were experimentally infected with Herpesvirus SA 8-strain 0430. Intravenous inoculation of the virus induced minor, transient, interstitial pneumonia of a nonspecific type in newborn baboons. Intratracheal inoculation, in contrast, invariably produced multifocal or diffuse necrotizing inclusion body bronchopneumonia within two days in newborn, two months and one year old baboons. Differences in the outcome of the experimental intratracheal infections were noticed, depending on the animals age. All the newborns either died from the extensive pulmonary damage or had to be sacrificed because of serious illness. Older animals, in contrast, survived the initial impact with only minor clinical symptoms and repair of the necrotic and inflammatory lesions. The healing stages were characterized by interstitial fibrosis and transient tumorlike bronchial and bronchiolar epithelial proliferations, which lasted for approximately two months. Intranuclear inclusion bodies in ganglionic cells, ganglioneuritis and neuritis in different parts of the pulmonary plexus in intratracheally infected animals suggested the viral invasion of the pulmonary autonomous nervous system.

Age Factors↗

Distribution of Legionella pneumophilia antibody among primate species.

Sera representing 16 different primate species were surveyed by indirect immunofluorescence for evidence of antibody to Legionella pneumophila. The presence of antibody in Old and New World monkeys and in apes supports previous observations of the ubiquity of Legionella pneumophila.

Animals↗

A x C rat prostate adenocarcinoma: initial characterization of testosterone regulation of hormone receptors of cultured cancer cells and derived tumors.

A x C rat prostate cancer cells were established in continuous culture. The polygonal epithelial cells had granular cytoplasm and well-defined cell margins, contained round to oval nuclei with prominent nucleoli, and were tumorigenic when inoculated into A x C male rats. The tumors produced by the injected prostate cancer cells grew as well-vascularized, solid, cribriform adenocarcinomas. The rat prostate cancer cells and derived tumors contained cytoplasmic and nuclear androgen receptors and prolactin receptors. Androgen regulation of prolactin receptor content and androgen receptor distribution in A x C rat prostate cancer cells were comparable to those of the normal ventral prostate gland. These studies suggest that the A x C rat prostate cancer cells and tumors may represent a unique model for studies of hormonal regulation of prostate cancer cell behavior.

Adenocarcinoma↗

Chemically defined serum-free media for the cultivation of primary cells and their susceptibility to viruses.

Chemically defined media SFRE-199-1 for the growth and SFRE-199-2 for the maintenance of primary baboon kidney (Bak) cell cultures were formulated by supplementing medium M199 with insulin, sodium pyruvate, zinc sulfate, and increasing arginine-HCl, cysteine, cystine, L-glutamine, L-glutamatic acid, glycine, histidine, tyrosine, and glucose to maximally active nontoxic concentrations. For prolonged maintenance of the cells, physiological pH control, and blocking of excessive lactic acid accumulation in the spent medium of the cell cultures, it is necessary to supplement the medium containing Earle's balanced salts with D-(+)galactose. The cells grew and were maintained equally well on glass or polystyrene surfaces. Selenium, when added to growth medium or substituted for insulin and zinc sulfate, did not stimulate cell growth. Electron microscopy showed that numerous dense particles, approximately 250 to 400 A in diameter, with the appearance of glycogen, were found throughout the cytoplasm in the cells grown in SFRE-199-1 and maintained in SFRE-199-2. Echovirus types 1 to 3, poliovirus types 1 to 3, coxsackievirus types B2, B4, B5, Herpes-virus hominis type 1, simian herpesvirus H. simiae and SA8, and simian adenovirus SV34 when titrated in primary Bak cells and grown and maintained in SFRE-199-1 and 2, respectively, developed titers comparable to those obtained in conventionally grown and maintained cells.

Amino Acids↗

Simian virus nomenclature, 1980.

Approximately 75 simian viruses, counterparts of other animal viruses, are recognized. Nomenclature of these isolates, in general, consists of an SV (simian virus) or SA (simian agent) numerical series with no attempt to group them according to virus families. The biologic characteristics of these viruses indicate they may be classified into recognized families and groups. A simple sequential numerical designation is recommended as a nomenclature within virus families and groups. Finalization of nomenclature would follow approval by the Study Groups of the International Committee on Taxonomy of Viruses.

Adenoviruses, Simian↗

Detection of primate herpesvirus antibodies including Herpesvirus simiae by enzyme immunoassay.

An enzyme immunoassay (EIA) was used for the detection of antibodies to Herpesvirus hominis type 1 and 2 (HVH-1 and HVH-2), SA8 and Herpesvirus simiae (HVB) in human and nonhuman primate sera. Optimal assay conditions were approximately the same for HVH-1, HVH-2, and SA8 but different for HVB. The recognized lethality of HVB required studies to determine whether or not inactivated HVB could be used in the EIA outside a biohazard safety cabinet. Ten percent buffered formalin destroyed infectivity of antigen coated discs after 5 minutes while retaining activity in the EIA. Antibody titers to HVB determined by serum neutralization were up to eightfold higher in the EIA. Using EIA to survey sera for antibodies to herpesviruses, it was determined that most humans reacted to HVH-1 (88%), HVH-2 (81%) and SA8 (94%), and 38% to HVB. Whereas baboons reacted almost exclusively to their indigenous herpesvirus SA8 (44%), rhesus monkeys demonstrated a high positive rate to HVH-1 (63%), SA8 (94%), and HVB (50%). These data indicate that EIA is rapid, sensitive, reproducible, and useful in the detection of antibodies to human and nonhuman primate herpesviruses but does not, at this point, resolve problems related to cross-reactivity among these viruses.

Animals↗