Hemagglutinin of Haemophilus paragallinarum serotype 1 organisms.
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Biomedical subjects
Publications and source records attributed to K Kume.
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Dermonecrotic toxin (DNT) produced by serotype D strains of Pasteurella multocida, isolated from pigs, was characterized and compared with DNT produced by Bordetella bronchiseptica. The DNT prepared by sonication from P multocida or B bronchiseptica had dermonecrotic activity and lethal toxicity for guinea pigs and mice, and also induced marked atrophy of spleens in the mice. Toxicity of P multocida or B bronchiseptica DNT was completely inactivated by heating at 70 C for 30 minutes, and was reduced by treatment with trypsin, formalin, or glutaraldehyde, indicating that the DNT may be a protein. Although biologic and toxic properties of P multocida DNT were similar to those of B bronchiseptica DNT, cross-neutralization tests between P multocida and B bronchiseptica indicated that DNT from the 2 bacterial species were serologically distinct.
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Antigens, prepared from 17 strains of Haemophilus paragallinarum by treatment with potassium thiocyanate followed by sonication, uniformly agglutinated glutaraldehyde-fixed chicken erythrocytes and formed specific hemagglutination inhibition antibodies in rabbits. Attempts were made to classify the strains into serotypes by a combination of cross-hemagglutination inhibition and cross-absorption tests, using the hemagglutinating antigens, designated as HA-L hemagglutinin, and their antisera. The cross-hemagglutination inhibition tests showed the existence of three distinct groups among the 17 strains. Further cross-absorption studies indicated that two of the three groups could be subdivided into three serotypes each, forming a total of seven serotypes, designated HA-1 through HA-7. Classification based on the serotype-specific HA-L system was found to be superior in its wider and more clearly defined specificities to other previous classifications, which are based on the agglutination test. There appeared to be a correlation between serotypes and geographic origins of the strains.
Relationships between morphological or serological properties and virulence were investigated in seven Haemophilus paragallinarum variants. The variants, originated from five serotype 1 strains, were classified into seven types on the basis of colony morphology and iridescence and the presence of variant-specific antigens. Smooth (S) and encapsulated organisms having variant-specific antigens and forming highly iridescent (ir+) colonies were highly virulent in vivo; slightly encapsulated organisms having variant-specific antigens and forming slightly iridescent (ir +/-) colonies were moderately virulent; and nonencapsulated or slightly encapsulated organisms with or without variant-specific antigens and forming noniridescent (ir-) or ir +/- colonies were avirulent. Virulence was well correlated with the amount of capsule substance containing hyaluronic acid. The evidence suggests that the presence of variant-specific agglutinogen L and hemagglutinin HA-L seem to be responsible for adherence or colonization, but not for virulence, of the organisms in chickens.
A case of verrucous squamous cell carcinoma of the oesophagus treated with bleomycin is reported. Bleomycin brought prompt reduction of the tumour and relief of symptoms. There have been no previous reports on experience with anti-cancer agents for verrucous carcinoma of the oesophagus. Administration of bleomycin might be an effective treatment for verrucous carcinoma of the oesophagus.
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Production and characterization of Haemophilus pleuropneumoniae hemolysin were investigated by using 5 serotype 2 strains. The hemolysin was produced in chicken meat-infusion broth medium both in stationary and in shaking cultures. In stationary culture, hemolytic activity against horse RBC reached maximum at postincubation day 5 (at the late stage of stationary phase), and the activity was maintained at the same level for 2 days thereafter. The hemolytic activity of shaking culture reached a maximum at postincubation hour 9 (at the early stage of logarithmic-growth phase), gradually decreased, and disappeared at postincubation day 2. The hemolysin was shown to be an extracellular product of the bacterial cells. The RBC of horses, rabbits, and sheep were highly susceptible to the hemolysin, and those of pigs and guinea pigs were less susceptible, whereas RBC of 60-day-old chicks were not susceptible. The hemolysin was not inactivated by autoclaving at 121 C for 2 hours, and by treatments with formalin, trypsin, or pronase. The presence of calcium or magnesium ions did not change the activity, whereas iodoacetic acid significantly reduced the activity.
Hemagglutinating properties of Haemophilus paragallinarum serotype 2 and serotype C against freshly collected and glutaraldehyde (GA)- fixed chicken RBC were investigated. Different from serotype 1, the nontreated organisms of serotype 2 and serotype C lacked hemagglutinating activity. However, when the organisms were treated with potassium thiocyanate (KSCN) and/or sonication, activity occurred not only against GA-fixed chicken RBC, but also against GA-fixed RBC of various animal species. The maximum hemagglutination titer (1:64 to 1:256) was obtained against GA-fixed RBC with the KSCN-treated organisms that were also sonicated. The activity was inactivated by heating at 100 C or by treatments with formalin or trypsin, but not by treatments with hyaluronidase or neuraminidase. By using KSCN-treated and sonicated organisms and GA-fixed chicken RBC, a detection of hemagglutination-inhibition (HI) antibody was possible. The HI tests showed that serotype 2 hemagglutinin was immunologically distinct from serotype 1 and that the HI antibody correlated to protective activity against challenge exposure with serotype 2 and serotype C. Chicks having HI antibody greater than 1:5 were protected against challenge exposure with homologous type, but were not protected with serotype 1. Applicability of the HI test was also shown for evaluating protective potency in the serotype 2 vaccine, as well as in the serotype 1 vaccine.
Development of a model in experimental small animals will facilitate research on the mechanisms of nasal turbinate atrophy of swine. Atrophy of the nasal turbinate with Bordetella bronchiseptica phase I organisms of pig origin was induced by intranasal inoculation in 5-day-old or younger mice. Inoculations of phase I organisms into 10-day-old or older mice and of avirulent phase III organisms into 5-day-old or younger mice did not induce lesions of the disease, however. The lesions appeared in 40% of the susceptible-age mice which were examined at 2 weeks after inoculation and were present in 80% of the susceptible-age mice by 3 weeks. The lesions observed in young mice were similar to those reported for swine.
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