scholarly journals Changes in Agglutinin Titer against Pasteurella piscicida in Cultured Yellowtail during the Epizootics of Pseudotuberculosis in 1993 and 1994.

1995 ◽  
Vol 30 (4) ◽  
pp. 291-292 ◽  
Author(s):  
Koh-ichi Satoh ◽  
Yutaka Fukuda ◽  
Shinya Nakano
Keyword(s):  

2012 ◽  
Vol 35 (2) ◽  
pp. 53-58 ◽  
Author(s):  
ABM Shahidul Alam ◽  
Fahim Ahmed Rupam ◽  
Farhana Chaiti

Background & objectives: The clinical diagnosis of typhoid fever is difficult, as the presenting symptoms are often diverse and similar to those observed with other febrile illnesses. The definitive diagnosis of typhoid fever requires the isolation of Salmonella typhi or paratyphi from the patient concerned. Since patients often receive antibiotics prior to a confirmatory diagnosis, there is uncertainty that bacteria can be isolated from the blood cultures. Besides this, the facilities for blood culture are not always available or feasible. All these limitations have made Widal test the most utilized diagnostic test for typhoid fever. Many studies have produced data which had cast serious doubts on the value of the Widal Test and thus reappraisal of the role of a single Widal test is needed.Methods & materials: This study was carried out to determine the changes in clinical pattern of enteric fever. A total of 153 children, aged 0 to 14 years, diagnosed as typhoid fever (either positive blood culture for Salmonella typhi or paratyphi) were induced in the study. Of them, 86 children were with a definitive diagnosis of typhoid or paratyphoid fever as indicated by the isolation of S. typhi or S. paratyphi from the blood and 17 had negative blood culture but were clinically suspected of having typhoid fever. The control group was comprised of 50 children with non-typhoidal fevers The Widal test was carried out using rapid slide agglutination method and its accuracy was assessed by comparing the findings with that obtained through blood culture.Result: The mean age of the patients was 5.2 ± 2.8 years and the youngest and oldest patients were 0.7 and 14 years respectively and male to female ratio was roughly 1:1. Nearly one-quarter (24.6%) of the patients had been suffering from the disease for >10 days and the mean duration of illness was 8.2 ± 3.3 days. Widal Test result showed that an ‘O’ agglutinin titer of cut-off value e”1:40 gave a sensitivity of 87.2%, a specificity of 47.1%, a positive predictive value (PPV) of 89.2% and a negative predictive value (NPV) of 42.1%. The sensitivity and NPV decreased with the increase in titer levels and were 56.9% and 31.5% at cut-off value of e” 1:320, while the specificity and PPV increased with the increase in titer levels from 47.1% and 89.2% respectively at a titer of e”1:40 to 100% at a titer of e” 1:320. The ‘titer behaved in the same way as did the ‘O’ agglutinin titer. Similarly when H’ agglutinin was used the sensitivity and NPV decreased from 65% and 31.7% at a titer of e”1:40 to only 25% and 20% respectively at a titer of > 1:320, while specificity and PPV increased from 76.4% and 81.1% at >1:40 to 94.1% and 95.6% respectively at e” 1:320. When either ‘O’ or ‘H’ antibody titer of e”1:160 was used, a good sensitivity (71%), specificity (70.6%) and PPV (92.4%) resulted, though NPV decreased to 32.4%.Conclusion: The Widal test can be of diagnostic value when blood cultures are not available nor practically feasible.DOI: http://dx.doi.org/10.3329/bjch.v35i2.10377  Bangladesh J Child Health 2011; Vol 35 (2): 53-58



1957 ◽  
Vol 105 (6) ◽  
pp. 623-634 ◽  
Author(s):  
Rolf Freter ◽  

Studies of the relative combining capacities of different antisera to Vibrio cholerae and Shigella flexneri were carried out using the Talmage test. In this test the absorption of an I131 labelled antibody preparation by antigen is blocked by the addition of unlabelled unknown serum. Sera from rabbits in the early stages of immunization ("early antisera") had a high agglutinin titer, but low combining capacity. Sera from hyperimmune rabbits ("late antisera") had higher combining capacities than early antisera, but similar or lower agglutinin titers. More antigen was needed to absorb the agglutinins from late antisera than from early ones of the same agglutinin titer, indicating that late antisera contained relatively more antibody. At high concentrations, sera from hyperimmune rabbits agglutinated the homologous antigen more rapidly than did early antisera, even though early sera had similar or higher agglutinin titers. Sera drawn after the anamnestic response to bacterial antigen had the characteristics of late sera; i.e., their combining capacities were high. The possible significance of these findings for the in vitro estimation of protective antibody is discussed.



PEDIATRICS ◽  
1950 ◽  
Vol 5 (3) ◽  
pp. 443-447
Author(s):  
HATTIE E. ALEXANDER ◽  
CATHERINE MACPHERSON ◽  
WINIFRED REDMAN

A quantitative chemical method which determines the agglutinin nitrogen content has been shown to be applicable to H. pertussis therapeutic antisera. The two human H. pertussis antisera available for therapeutic purposes contain approximately the same agglutinin nitrogen content per vial, about 1 mg. A vial of the two rabbit antisera analyzed contains approximately 20 mg. of agglutinin nitrogen. A simple slide agglutination test is offered as a procedure for determining the degree of antibody excess in the sera of patients after serum therapy. The greater the content of agglutinin nitrogen in the therapeutic antiserum administered, the higher the relative agglutinin titer in the patient's serum.



Blood ◽  
1950 ◽  
Vol 5 (2) ◽  
pp. 107-122 ◽  
Author(s):  
SAMUEL PENNELL

Abstract 1. A method is described for the treatment of patients with erythroblastosis fetalis by the transfusion of compatible sedimented red cells from bank blood. 2. The case histories of 28 patients with erythroblastosis fetalis, treated by this method, have been analyzed. Three, or 10.7 per cent, of the patients died. This mortality rate compares favorably with other reports in which exchange transfusion was the therapeutic procedure. 3. The transfusion of sedimented red cells in 50-60 cc. amounts is sufficient to cause an adequate rise in the hemoglobin values with a minimum of load on the infant’s circulation. 4. This method, in contrast to that of exchange transfusion, has the advantage of reducing the administration of plasma to a minimum, thereby preventing further hemolysis of the infant’s red cells by enhancing the agglutinin titer. In addition, excessive amounts of extraneous substances such as sodium citrate are not given.



2008 ◽  
Vol 12 ◽  
pp. e463-e464
Author(s):  
H. Kamano ◽  
T. Mori ◽  
H. Maeta ◽  
N. Kishimoto ◽  
T. Katami ◽  
...  


1937 ◽  
Vol 65 (4) ◽  
pp. 587-594 ◽  
Author(s):  
Johannes K. Moen

1. Plasmas from guinea pigs, chronically infected with group C hemolytic streptococci, neutralize the components of bacterial extract which exert a marked toxic action on hypersensitive cells in vitro. 2. The neutralizing capacity of these immune plasmas is relatively specific for the bacterial extract, and is not due to a variable nonspecific effect on normal or hypersensitive tissue cells. 3. A rough correlation between the agglutinin titer and the relative neutralizing capacity of immune plasma suggests that the latter may be a manifestation of antibody action. 4. The tolerance by guinea pigs of chronic hemolytic streptococcal lymphadenitis is explainable, at least in part, by the neutralizing capacity of their plasmas, since such soluble bacterial products as may be absorbed from infectious foci would probably be neutralized before they could exert a deleterious influence on the hypersensitive cells of the animals.



1922 ◽  
Vol 36 (6) ◽  
pp. 697-709 ◽  
Author(s):  
William A. Hagan

1. The infectivity of Bacillus abortus for guinea pigs is extremely great. It is computed that somewhat less than 100 organisms are required to infect most animals. 2. Occasional animals are encountered having much more resistance to Bacillus abortus infection than is possessed by the average. The most resistant animal encountered was infected by a number of organisms computed to be less than 10,000. 3. The principal effect on the character of the Bacillus abortus disease, caused by varying the size of the infecting dose, is a change in the time relations. Very small doses produce an infection of slower course than do larger doses, but the eventual results are practically the same. 4. Judging by the agglutination curves, guinea pigs inoculated with large or medium sized doses of Bacillus abortus generally begin to gain mastery over the disease about the 10th week after inoculation. At this time the agglutination curve begins to decline. As was first shown by Smillie, the numbers of bacteria in the body organs begin to decline at about the 4th week but the change is rather slow until about the 10th or 12th week when a rapid decline begins, coincidently with the fall in the agglutinin titer. When the inoculating dose is small the course of the disease may be much prolonged. The defensive forces of the body would appear to be quite inactive until a certain stage in the disease is reached. 5. The virulence of Bacillus abortus cultures for guinea pigs may be raised or lowered by appropriate passage through these animals. 6. Normal guinea pig blood will not agglutinate Bacillus abortus in a dilution of 1:10. Immune agglutinins are easily produced by inoculations with dead or living organisms. Agglutinins for Bacillus abortus are capable of passing the placental filter. 7. There appears to be little or no danger of normal guinea pigs becoming infected by association with diseased animals of their own sex. One instance is reported, however, of the infection of a male animal that had cohabited with infected females. 8. The susceptibility of guinea pigs to infection through ingestion of Bacillus abortus is relatively slight.



1955 ◽  
Vol 31 (8) ◽  
pp. 555-557 ◽  
Author(s):  
Tanemoto FURUHATA ◽  
Masamoto EGUCHI
Keyword(s):  


PEDIATRICS ◽  
1950 ◽  
Vol 5 (1) ◽  
pp. 38-44
Author(s):  
JOHN P. MCGOVERN

A passive mouse protection test and its use in testing sera from infants given a course of phase I pertussis vaccine is described. Infants 3 to 6 months of age consistently developed mouse protective antibodies following immunization with a phase I H. pertussis vaccine. Agglutinating antibodies did not develop consistently in these infants and the agglutinin titer did not closely parallel the values obtained by the mouse protection test.



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