scholarly journals A localized outbreak of dengue fever in Kuala Lumpur: serological aspects

1957 ◽  
Vol 55 (2) ◽  
pp. 207-223 ◽  
Author(s):  
C. E. Gordon Smith

1. Sera from an outbreak of about forty cases of dengue fever due to dengue-1 virus have been studied using the neutralization, haemagglutinin-inhibition, and complement-fixation tests.2. The neutralization test was the most specific and the complement-fixation test the least so.3. The neutralization test is essential for clear identification of the causal virus by serological means, and serial serum specimens from each patient must be examined.4. The haemagglutinin-inhibition test can be used to screen patients in outbreaks where some cases have been fully identified by neutralization tests.5. Homologous neutralizing antibodies persist in high titre for at least 30 weeks after infection, while heterologous antibodies have disappeared by that time.6. Both haemagglutinin-inhibiting and complement-fixing antibodies to homologous and heterologous viruses usually persist for at least 30 weeks, although the homologous titres tend to be highest.7. The implications of these findings in serological surveys are discussed.8. Some evidence suggesting the occurrence of inapparent infections during the epidemic is presented.I am greatly indebted to my staff for help with this work: especially to my senior technician, Che Ali bin Mohamed Amin, and to Che Mohamed bin Omar who drew the figures.

1952 ◽  
Vol 50 (2) ◽  
pp. 265-274 ◽  
Author(s):  
Forrest Fulton ◽  
J. E. Friend

A method of titrating influenza virus-neutralizing antibodies is described. This method is based on the technique for cultivating virus in fragments of chick chorio-allantoic membrane using a special plastic tray with cups for 100 replicates. The neutralization test cannot be made directly by adding the antiserum to the cups in which the virus is growing in the membrane fragments because there is a significant non-specific inhibitory effect. Therefore, use is made of the observation that virus added to the cups is rapidly fixed by the membrane so that, after a short time, the membrane may be washed and transferred to a fresh cup which will later be found to contain the new virus released from the membrane.In the neutralization test the membrane fragments are exposed to virus-serum mixtures for 18 hr. and then transferred to other cups without serum to determine which pieces have become infected. The titre of neutralizing antibodies is defined as the serum dilution which will protect from infection with 100 ID 50 of virus, half of a large number of replicate pieces of membrane.The neutralization technique has been applied to the antigenic comparison of six strains of influenza virus. The results support the relationships disclosed between the six strains by a complement-fixation technique. It is suggested, however, that the neutralization technique, because of its greater specificity, and because of its dependence on the infectivity of the strain, is not as satisfactory as the complement-fixation test for strain comparisons. Apart from its use for titrating neutralizing antibodies, the technique may also be of value for proving the virtual identity of two virus strains and in the selection of strains for a vaccine.It is a pleasure to acknowledge the help given by Dr Isaacs of the WHO Influenza Centre. Not only did he provide many of the virus strains and antisera, but he also undertook the purification of the WS strain.


1970 ◽  
Vol 68 (2) ◽  
pp. 211-219 ◽  
Author(s):  
P. K. Uppal

SUMMARYThe direct complement fixation test was performed to follow the antibody response in chickens infected with avian infectious bronchitis virus. Concentrated allantoic fluid (4 units) was used as an antigen and allowed to react with serially diluted antiserum in the presence of two complete units of guinea-pig complement for 3 hr. at 4°C. and ½ hr. at 37°C. before the addition of sensitized cells. Serum was unheated and used either fresh or within one month of storage at −30°C. Individual birds showed a rise and fall of complement-fixing antibody both after primary and secondary inoculations. The complement-fixing antibody was detected as early as the seventh day after primary inoculation. The highest complement fixation titre (1/32 to 1/64) was recorded from 14 to 21 days after inoculation with a subsequent gradual decline.The results of the direct complement fixation tests have been correlated with the serum neutralization test. The neutralizing antibodies usually appeared by the 14th day but were not detected at a significant titre until the 21st day after primary inoculation. Serum neutralizing antibodies were still present at high titres even after 7 weeks of infection but the complement-fixing antibodies had disappeared by that time.


1969 ◽  
Vol 67 (2) ◽  
pp. 193-208 ◽  
Author(s):  
R. F. W. Goodwin ◽  
Ruth G. Hodgson ◽  
P. Whittlestone ◽  
Rosemary L. Woodhams

SUMMARYHysterectomy-produced, colostrum-deprived pigs, reared in special isolation accommodation, were infected with enzootic pneumonia and later challenged with the same strain of the disease. Both the original infections and the subsequent challenges were made with intranasal inoculations of suspensions of ground pneumonic lung, but there was no evidence to suggest that any mycoplasma other than the J strain of Mycoplasma suipneumoniae was involved.Pigs that had recovered from the disease were strongly immune to challenge, in that they developed virtually no lung lesions when inoculated with lung suspensions that produced extensive lesions of enzootic pneumonia in control animals. This was the case, even when the pigs were as young as 16 days old when first infected and were not challenged until up to 60 weeks later.Sera from these pigs taken before infection, about 2–3 weeks after infection, at various times after natural recovery, and before and after challenge were examined using the metabolic-inhibition test, the indirect-haemagglutination test and the complement-fixation test.The metabolic-inhibition test proved of little value, because non-specific inhibitory substances were present in the sera of some pigs both before and after infection: these substances inhibited the growth of Mycoplasma hyorhinis, Mycoplasma pneumoniae and Mycoplasma gallisepticum as effectively as M. suipneumoniae. Sometimes the non-specific inhibition was reduced by heating the sera at 56° C. for 30 min., but at other times it was not, which suggests that at least two types of non-specific inhibitors were present.Apart from one pig, all the sera that were expected to be negative for antibodies against M. suipneumoniae proved to be so by the indirect-haemagglutination test. Titres of less than 1/5 were obtained in this test using the sera from pigs killed 12–22 days after infection, but high titres were obtained 16–60 weeks after infection. It was not possible to say whether these titres correlated with immunity.All the pre-infection sera when examined by the complement-fixation test had titres of less than 1/10, but by 12–22 days after infection over half the serum samples had titres of 1/40 or more, and titres of 1/80–1/640 were obtained at 4 and 9 months after infection. There was some evidence to show that these titres declined more rapidly than the titres obtained in the indirect-haemagglutination test; for they were very low at 60 weeks after infection, at which time the indirect-haemagglutination titres were still high.It seemed, therefore, that these two serological tests were measuring different aspects of the post-infection response. Also, because the complement-fixation titres were very low in two pigs that were shown to be powerfully immune, these titres did not appear to correlate with immunity.Our work with the metabolic-inhibition test and the complement-fixation test has benefited from discussions with Dr D. Taylor-Robinson and Mr A. S. Wallis, respectively. We are grateful to Drs H. P. Chu, R. H. Leach and D. Taylor-Robinson for the reference sera and the culture mentioned in the text. Most of the expenses of this work, including the salary of two of the authors (R. G.H. and R.L.W.), were met by a grant from the Agricultural Research Council.


1961 ◽  
Vol 59 (4) ◽  
pp. 401-412 ◽  
Author(s):  
Ruth M. Lemcke

By means of a complement-fixation test of the sera of laboratory rats and mice, the immunological response of these animals to both naturally occurring and induced PPLO infections was determined, and the presence and extent of infection in the animals determined by culture.PPLO antibodies specific for the infecting strain were demonstrable in rats and mice from which PPLO were isolated.The amount of serum antibody rises with the extent and severity of the infection. Thus, young rats with PPLO infections confined to the nasopharynx had little or no antibody whereas the oldest rats with consolidated lungs had the highest titres. In mice too, the sera of those with pneumonia had the highest titres.The comparatively low titres found in rat bronchiectasis together with the failure to isolate PPLO from the spleen and other organs, suggest that the chronic form of the disease remains localized. This is in contrast to infections with rat polyarthritis and related PPLO in which the organisms can be isolated from the lymph nodes and other organs and in which antibody is present in high titre.In view of the high degree of correlation between the presence of antibodies to PPLO in the blood and the presence of PPLO in the tissue of rats and mice, it is suggested that specific antibody found in man is a significant indicator of PPLO infection.


1982 ◽  
Vol 35 (3) ◽  
pp. 343 ◽  
Author(s):  
DH Cybinski ◽  
TD St George

Between 1974 and 1980, 424 viruses were isolated at the Long Pocket Laboratories of the Division of Animal Health, CSIRO, either from insects or from the blood of sentinel cattle, and of these, 165 cross-reacted with D'Aguilar virus (an Australian Palyam group virus) in a complement fixation test. Neutralization tests were used to classify these viruses into four serotypes with the isolates D'Aguilar B8112, CSIRO 11, CSIRO 58 and CSIRO 82 as the type strains. The latter three were new to Australia. Like other orbiviruses, these four serotypes were partially sensitive to treatment with ether or chloroform. Neutralizing antibodies against D' Aguilar, CSIRO 11 and CSIRO 58 viruses were detected in sera from cattle, buffalo, deer and sheep but not in sera from humans, horses, pigs or marsupials. Antibodies against CSIRO 82 virus were detected in 85 % of 26 buffalo, and O� 4 % of 495 cattle sera tested. The antibody distribution in Australia for D' Aguilar, CSIRO 11 and CSIRO 58 viruses fell within the distribution limits of Culicoides brevitarsis, the insect from which these viruses were most commonly recovered. The antibody distribution for CSIRO 82 virus, which was isolated from a pool containing C. schultze; and C. peregrinus, fell within the much more restricted distribution limits of these species. None of these viruses has been associated with disease.


1941 ◽  
Vol 74 (5) ◽  
pp. 409-426 ◽  
Author(s):  
J. Casals ◽  
R. Palacios

A specific complement fixation test can be obtained in various central nervous system virus infections by using as antigens emulsions of infected brain tissue, freezing and thawing the brain emulsion, and then centrifuging it in an angle head centrifuge at 3500 R.P.M. for 1 hour. The method has proved reliable in the case of rabies, St. Louis encephalitis, Japanese B encephalitis, lymphocytic choriomeningitis, Eastern equine encephalomyelitis, Western equine encephalomyelitis, louping ill, and spontaneous encephalomyelitis of mice (Theiler's disease). The specificity of the reaction, regardless of the virus involved, requires different temperatures of inactivation of the sera according to animal species: 56°C. for guinea pig, 60°C. for mouse, and 65°C. for rabbit and dog sera, all heated for 20 minutes. For human sera a temperature of inactivation of 60°C. also for 20 minutes has been adopted; at this temperature the reaction is in general specific. Complement-fixing antibodies in high titre were found in the sera of rabbits, guinea pigs, mice, and dogs immunized with rabies virus. Complement-fixing antibodies were present in high titre in sera drawn from two persons 8 years after an attack of louping ill, from five persons 2½ years after an attack of Eastern equine encephalomyelitis, and from two persons 2½ years after Western equine encephalomyelitis. In cases of St. Louis encephalitis and lymphocytic choriomeningitis, complement-fixing antibodies have been found shortly following infection but not after long periods.


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