Pei W. Chang

Isolation of a viral agent causing hematopoietic neoplasia in the soft-shell clam, Mya arenaria☆

Abstract A virus from neoplastic soft-shell clams, Mya arenaria, has been isolated. Its morphological and physical properties are similar to those of B-type retroviruses. It is enveloped, pleomorphic, averaging 120 nm in size with an eccentric nucleoid. Possible A-type particles have also been observed. The bouyant density of the particle ranged from 1.17 to 1.18 g/cm3 and the ultraviolet absorption 260 280 - nm ratio was 1.23. The virus has been shown to cause a hematopoietic neoplasm in Mya. Purified virus from neoplastic clams was innoculated into nonneoplastic clams. Most of these clams developed tumors within 2 months. Virus isolated from inoculated clams which developed neoplasia was inoculated into nonneoplastic clams. Most of these clams also developed neoplasia thus completing Kochs postulates.

The course and mortality of a hematopoietic neoplasm in the soft-shell clam, Mya arenaria

Abstract Results from two experiments containing approximately 280 Mya arenaria indicated that significantly higher (P The prevalence of the neoplasm in clams collected from an epizootic area followed a biphasic seasonal pattern. The highest prevalences occurred in October, November, and in May. The hematopoietic neoplasm in M. arenaria was also age and species specific.

5-Bromodeoxyuridine induction of hematopoietic neoplasia and retrovirus activation in the soft-shell clam, Mya arenaria☆

Abstract Hematopoietic neoplasia and virus replication were induced in shoft-shell clams, Mya arenaria, by 5-bromodeoxyuridine (5-BrdUrd). Eighty clams were found to be nonneoplastic by the in vivo bleeding method. These clams were randomly distributed into four aquaria and maintained in seawater at 1°C. 5-BrdUrd was added to aquaria in the following concentrations: 0, 20, 100, and 200 μg/ml. After 4 days of treatment, the aquaria were drained, rinsed, and fresh sea water without 5-BrdUrd was added. Sea water was changed on a weekly basis thereafter. The clams were diagnosed for neoplasia by the in vivo method at days 4, 9, 16, and 23 of the experiment. Results showed that on day 23, neoplasia was not found in the aquarium without 5-BrdUrd, but in the aquaria containing 20, 100, and 200 μg/ml of 5-BrdUrd the incidences of neoplasia were 37, 79, and 35%, respectively. 5-BrdUrd-induced neoplastic tissue was homogenized and subjected to differential ultracentrifugation. Retrovirus-like particles resembling ones previously shown to induce neoplasia were isolated from neoplastic clams which were induced by 5-BrdUrd. When these particles were inoculated into healthy clams, the clams developed neoplasia. Neoplastic hemocytes, cultured in sea water containing 50 μg/ml of 5-BrdUrd, formed pseudopodia after 4 days. Pseudopod formation is a trait of normal hemocytes. This indicates that differentiation of neoplastic hemocytes may be induced by the drug.

An Enzyme-Linked Immunosorbent Assay for Detection of Antibodies to Avian Adenovirus and Avian Adenovirus-Associated Virus in Chickens

An enzyme-linked immunosorbent assay system (ELISA) was adapted for the detection of antibodies to avian adenovirus (AV) and avian adenovirus-associated virus (A-AV). Both before and after exposure, sera from chickens undergoing natural and experimental infections were assayed by ELISA, virus neutralization (VN), and immunodiffusion (ID) for antibody to both CELO virus and A-AV. The ELISA system was found to be comparable to VN for determining antibody concentrations to CELO virus and A-AV. In many cases, ELISA was found to be more sensitive than ID.

Use of egg yolk in serological tests (ELISA and HI) to detect antibody to Newcastle disease, infectious bronchitis, and Mycoplasma gallisepticum.

Serum and yolks from commercial flocks and from hens exposed to Newcastle disease virus (NDV), infectious bronchitis virus (IBV), and Mycoplasma gallisepticum (MG) were tested for immunoglobulin G antibody by the enzyme-linked immunosorbent assay (ELISA) and the hemagglutination-inhibition (HI) test. Yolks prepared by chloroform extraction and low-speed centrifugation performed well in the serological tests used and were a suitable alternative to serum for antibody determination by the ELISA for NDV, IBV, and MG and by HI test for NDV.

Accuracy of blood cytological screening techniques for the diagnosis of a possible hematopoietic neoplasm in the bivalve mollusc, Mya arenaria☆

Abstract The two in vivo bleeding techniques currently in use in our laboratory to diagnose a hematopoietic neoplasm in Mya arenaria are: (1) phase-contrast microscopy with fresh unstained hemocytes, and (2) bright-field microscopy with Giemsa-stained hemocytes. All in vivo diagnoses were checked by histopathological studies on tissues of the same mollusc. For both methods the correct diagnosis (true + or true −) was made in 94 out of 100 clams examined. A gradation of tissue involvement was observed in the diseased clams and the accuracy of the in vivo diagnosis is related to the disease severity. There is a positive correlation between the degree of tissue involvement and the number of circulating neoplastic cells. For this reason the more extensive the neoplasm the better is the ability to diagnose the neoplasm by the in vivo bleeding techniques. Depending on the percentage of neoplastic cells present in the hemolymph, the neoplasm was graded from level 1 to 5, with 5 being the most severe. In general, at level 1, the accuracy of a single in vivo diagnosis varied from 66 to 71% and at level 2, the accuracy of diagnosis varied from 76 to 93%, while at all other levels the accuracy was 100%. The percentage of diseased clams detected by the in vivo bleeding technique was 89–91% and the percentage of nondiseased clams detected was 95%. These values can be further improved by combining the two tests and/or through multiple bleedings. Between the two types of in vivo tests, the Giemsa-stained hemocytes provided better precision of diagnosis than the fresh unstained cells, although the differences were slight.

Some observations of the propagation of infectious laryngotracheitis virus in tissue culture.

HE virus of infectious laryngotracheitis (LT) produced cytopathogenic effect (CPE) and plaques in chick-embryo fibroblast and respiratory epithelium.1 However, Buthala, et a.3 was unable to find CPE with LT virus in chick-embryo kidney cells, although the virus proliferated in the cell culture. The present study had three objectives: 1. to study the effect of LT virus in chick-embryo kidney cells and its ability to produce CPE and plaques, 2. to attempt the isolation of the virus by plaque method from chickens artificially or naturally infected with LT virus, 3. to study the differences between plaques formed by LT virus, chick-embryo-lethalorphan (CELO) virus and Newcastle disease (ND) virus.

Neutralizing antibodies to CELO and avian adenovirus-associated viruses in the albumen of chicken eggs.

Neutralizing antibodies to CELO virus and to avian adenovirus-associated virus (A-AV) were detected in the albumen of eggs from four hens inoculated with these viruses. The antibody concentrations of serum, yolk, and albumen were determined before inoculation and at various times postinoculation (PI) by enzyme-linked immunosorbent assay (ELISA) and virus-neutralization (VN) tests. The antibody concentration in albumen was 0.3% to 1.0% of that detected in serum and yolk. Uninoculated hens showed no detectable antibody in serum, yolk, or albumen. It is suggested that the presence of antibody in the egg albumen may play a role in egg-transmission of viruses.

Use of Egg Yolk to Determine Antibody Levels in Chickens Inoculated with a Hemagglutinating Duck Adenovirus (Adenovirus 127-Like)

Chickens were experimentally infected with a duck adenovirus that has been shown to be serologically indistinguishable from Adenovirus 127. Sera and eggs were collected at intervals after exposure for antibody determination by the hemagglutination-inhibition (HI) test, the enzyme-linked immunosorbent assay (ELISA), and the immunodiffusion (ID) test. Egg yolks were processed for use in the serological tests by (a) dilution in phosphate-buffered saline (PBS), (b) extraction of the water-soluble fraction with chloroform, or (c) freezing and thawing PBS-diluted yolks and testing the supernatant fluid. HI antibody titers from serum and extracted yolk were similar except during the initial 2 weeks, when yolk antibody levels were low or absent. Chloroform-extracted yolks were suitable material for the HI, ELISA, and ID tests. Heat inactivation of the chloroform-extracted yolk had no effect on titers.

The Effect of Incubation Temperature on the Propagation of Duck Adenovirus (Virus 127-like) in Duck and Chicken Cells

Duck adenovirus (Cornell strain) was propagated in duck and chicken embryo cells at 37.5 C and at 40 C. In duck cells, virus levels, as indicated by HA titers, peaked earlier at 40 C than at 37.5 C. High titers were eventually observed in duck cells at both temperatures. In chicken embryo fibroblasts, no titers were observed at 37.5 C, whereas low titers were observed at 40 C. Evidence of virus propagation was not detected in chicken embryo liver and kidney cells.