scholarly journals Comparison of Antibody Titers against Borrelial Strains Isolated in Japan by the Microcapsule Agglutination Test for Serological Studies of Early Lyme Disease

1994 ◽  
Vol 38 (4) ◽  
pp. 269-272 ◽  
Author(s):  
Yoshiko Arimitsu ◽  
Masaaki Seki ◽  
Minoru Nakao ◽  
Kenji Miyamoto
1991 ◽  
Vol 163 (3) ◽  
pp. 682-683 ◽  
Author(s):  
Y. Arimitsu ◽  
I. Takashima ◽  
Z. Yoshii ◽  
Y. Higashi ◽  
S. Kameyama ◽  
...  

2001 ◽  
Vol 8 (3) ◽  
pp. 624-627 ◽  
Author(s):  
Takuo Sawada ◽  
Raafat Hassanein ◽  
Tohru Yamamoto ◽  
Takaharu Yoshida

ABSTRACT Serum samples collected from 854 cattle in nine prefectures of Japan, from Hokkaido to Okinawa, between 1988 and 1992 were examined for presence of antibodies against Erysipelothrix rhusiopathiae by growth agglutination test. Most of the sera showed positive reactions, and the antibody titers ranged from below 4 to above 128. Seventy-six percent of the sera showed titers of 32 or above, and 34% showed titers of 128 or above. The titers had a tendency to be higher in the south and lower in the north and were clearly low in sera from areas with no swine industry. These results indicated that Japanese cattle had been infected with E. rhusiopathiae and that clinical cases of the disease were possible.


2021 ◽  
Vol 17 (9) ◽  
pp. e1009436
Author(s):  
Siyu Chen ◽  
Jennifer A. Flegg ◽  
Lisa J. White ◽  
Ricardo Aguas

Accurate knowledge of prior population exposure has critical ramifications for preparedness plans for future SARS-CoV-2 epidemic waves and vaccine prioritization strategies. Serological studies can be used to estimate levels of past exposure and thus position populations in their epidemic timeline. To circumvent biases introduced by the decay in antibody titers over time, methods for estimating population exposure should account for seroreversion, to reflect that changes in seroprevalence measures over time are the net effect of increases due to recent transmission and decreases due to antibody waning. Here, we present a new method that combines multiple datasets (serology, mortality, and virus positivity ratios) to estimate seroreversion time and infection fatality ratios (IFR) and simultaneously infer population exposure levels. The results indicate that the average time to seroreversion is around six months, IFR is 0.54% to 1.3%, and true exposure may be more than double the current seroprevalence levels reported for several regions of England.


2000 ◽  
Vol 182 (12) ◽  
pp. 3597-3601 ◽  
Author(s):  
Fang Ting Liang ◽  
Jena M. Nowling ◽  
Mario T. Philipp

ABSTRACT Borrelia burgdorferi, the Lyme disease spirochete, possesses a surface protein, VlsE, which undergoes antigenic variation. VlsE contains two invariable domains and a variable one that includes six variable and six invariable regions (IRs). Five of the IRs are conserved among strains and genospecies of B. burgdorferisensu lato. IR6 is conserved, immunodominant, and exposed at the VlsE surface but not at the spirochete surface, as assessed in vitro. In the present study, the remaining conserved IRs (IR2 to IR5) were investigated. Antisera to synthetic peptides based on each of the IR2 to IR5 sequences were produced in rabbits. Antipeptide antibody titers were similarly high in all antisera. Native VlsE was immunoprecipitable with antibodies to IR2, IR4, and IR5 but not to IR3, indicating that the first three sequences were exposed at the VlsE surface. However, negative surface immunofluorescence and in vitro antibody-mediated killing results indicated that none of the IRs were accessible to antibody at the spirochetal surface in vitro.


Author(s):  
S. Babyuk ◽  
O. Piskun ◽  
V. Ukhovskyi ◽  
A. Piskun ◽  
L. Korniienko ◽  
...  

Leptospirosis – common to humans and animals is a dangerous infectious disease that is caused by microbes - leptospires. The disease is accompanied by fever, kidney damage, liver, cardiovascular and nervous system. Leptospirosis in dogs is considered one of the most common diseases. Particularly difficult is the breed with a faulty type of body structure, such as: Neapolitan Mastino, Bulmastiff, English Bulldog, French Bulldog, Boxer, Bologna, Bloodhound, Basset Hound. The disease is most often diagnosed in dogs of hunting breeds, as a result of frequent contact with standing water, as well as in courtyard and stray dogs. Young animals and puppies get sick more often, as they do not have a stable immunity, the hemorrhagic form is more often diagnosed in older dogs. The subject was to study the distribution of leptospirosis among dogs, to establish the seropositivity level and to determine the seroprevalence of the most common of Leptospira serotypes that circulate among this species of animals. For research, an extensive diagnostic series of L. interrogans which includes 20 serovars, and blood serum from dogs that were selected in veterinary clinics in the city of Kyiv, were used as antigen and were transferred to the laboratory of leptospirosis in agricultural animals from the Museum of Microorganisms of the Institute of Veterinary Medicine of the National Academy of Sciences of Ukraine. Studies of blood serum were performed by the microagglutination test (MAT) followed by dark-field microscopy. PMA was placed in 4 dilutions: 1:50, 1: 100, 1: 500 and 1: 2500. According to numerous publications of scientists from different countries of the world, the seroprevalence level of leptospirosis infection among the dogs varies from 39% to 95%. A total of 1831 samples of blood serum were studied in the microscopic agglutination test. As a result of the serological study, 873 animals reacted positively, which is 47.7% of the total number of investigated ones. Analyzing the registered antibody titers, which is most often found titer 1: 100, which is 50.4% of the total number of positive reactions. This indicates the presence of a disease in dogs. Serrogroup Icterohaemorrhagiae is recorded in almost 50% of all positive reactions to leptospirosis and plays a major role in the etiology of the disease. It can be assumed that these dogs had contact with rats or their urine. In turn, the leading for these animals serogroup Canicola was detected in only a third of cases. Other serological groups played a minor role in the etiological structure. Summing up the aforesaid, according to the results of our work, serological prevalence of the pathogenesis of leptospirosis among dogs was determined to be 47.7%. Was detected the circulation of Leptospira`s antibodies in blood serum of these animals. The analysis of the etiological structure of leptospirosis showed that the dominant serogroups were Icterohaemorrhagiae and Canicola. Seven serogroups (Pomona, Sejroe, Grippotyphosa, Australis, Autumnalis, Celledoni, Ballum) were recorded in the range of 1% to 4%. Other serogroups do not have a significant effect on the morbidity of dogs. Keywords: leptospirosis, dogs, etiological structure, serological monitoring, antibody, microscopic agglutination test.


1976 ◽  
Vol 4 (1) ◽  
pp. 22-27
Author(s):  
G S Bowen ◽  
C H Calisher

During the 1971 epidemic of Venezuelan equine encephalomyelitis (VEE) in south Texas, 203 suspect VEE cases were evaluated by the Center for Disease Control. Sixty-seven were confirmed as cases of VEE. Laboratory confirmation was accomplished by isolation of VEE virus from a serum specimen taken during the acute illness in 50 (75%) of the confirmed cases. Serological confirmation was obtained in 17 cases (25%). Virus isolations were most often obtained from sera collected during the first 3 days of illness. Peak serum virus titers (algebraic mean, 10(5-7) suckling mouse intracranial 50% lethal doses [SMICLD50] per ml) occurred on day 2 of illness. One-half of the sera from which virus was isolated contained at least 10(5) SMICLD50/ml, which has been shown to be sufficient to infect some vector mosquitoes. Blood from 13 virus-positive VEE cases was obtained 1 and 11 months after illness. Hemagglutination-inhibiting, complement-fixing, and neutralizing antibodies were formed by all 13 patients 1 month after illness. Hemagglutination-inhibiting antibody titers were essentially unchanged 11 months after illness. Complement-fixing antibody was undetectable 11 months after illness in 23% of cases and was detectable at dilutions of 1:8 or 1:6 in 77%. Neutralizing antibody (measured by log neutralization index) was not detectable 1 year after illness in one person (8%); titers had declined from 1.0 to 2.0 in 46%, were unchanged in 39%, and were not tested in one person (8%). No evidence of intrafamilial spread of VEE virus was obtained in either of two illness and antibody surveys. A randomized household illness and antibody survey of 681 Port Isabel residents revealed an inapparent infection ratio of 1:11 and an overall antibody prevalence of 3.2%.


2010 ◽  
Vol 18 (2) ◽  
pp. 346-348 ◽  
Author(s):  
Kamlesh Gidwani ◽  
Albert Picado ◽  
Bart Ostyn ◽  
Shri Prakash Singh ◽  
Rajiv Kumar ◽  
...  

ABSTRACTThe persistence of anti-Leishmania donovaniantibodies in past visceral leishmaniasis (VL) cases was retrospectively assessed by means of the direct agglutination test (DAT) and the rK39 enzyme-linked immunosorbent assay (ELISA). Antibody titers remained high for an extended period of time in past cases of VL. These results highlight the need to carefully elicit the history of patients with VL symptoms.


2008 ◽  
Vol 32 (2) ◽  
pp. 137-146
Author(s):  
Hussein A. S.

Sera from1722 cattle of different age (3 months to 8 years) wereexamined by the Rose Bengal and tube agglutination test: 134 cow givepositive result and the overal Brucella seroprevalence was (8%) milksamples zeropositive milking cattle were cultured on Brucella selecativemedia.Seropositive cattle (102) were treated for the first time with long actingoxytetracyclin at the dose of 20 mg/kg of body weight administeredintramuscularly (i.m) every 2 days for 30 days and streptomycin at 25mg/kg (i.m) every 2 days for 16 days.The regimen was found to be effective in eliminating the shedding ofBrucella organisms by cattle in milk.Moreover all treated cattle became zeronegative within 16 months aftertreatment…zeronegative cattle (1588)were vaccinated for the first timewith the Br.Melitensis as follows1. 362 young cattle(aged three months to one year)were each inoculatedsubcutaneously with a full dose(1×106)viable organisms in 1 ml, Brucellaantibody titers were detected 2-4 weeks post vaccination then decreasedgradually until the animals became zeronegative 8 months aftervaccination.2. 1226cattle aged more than one year were each inoculatedsubcutaneously with reduced dose (1×103 viable organism in 1ml)antibody titers measured 2-4 weeks post vaccination then decreasedgradually until the animals became zeronegative 3 months postvaccination.No Brucella organisms were seen from repeated udeersecretion samples from all vaccinated milking cattle, and no abortionswere recorded among pregnant vaccinated cattle.


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