Simultaneous measurement of specific serum IgG responses to five select agents

被引:19
作者
Biagini, RE
Sammons, DL
Smith, JP
MacKenzie, BA
Striley, CAF
Robertson, SA
Snawder, JE
Quinn, CP
机构
[1] NIOSH, Biomonitoring & Hlth Assessment Branch, Div Appl Res & Technol, Ctr Dis Control & Prevent, Cincinnati, OH 45226 USA
[2] Ctr Dis Control & Prevent, Microbial Pathogenesis & Immune Response Lab, Natl Inst Infect Dis, Atlanta, GA 30333 USA
关键词
anthrax; tularemia; plague; staphylococcal enterotoxin B; ricin;
D O I
10.1007/s00216-005-3204-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Select Agents are defined by CDC and the USDA Animal and Plant Health Inspection Service (APHIS) as biological agents or toxins deemed a threat to public, animal, or plant health, or to animal or plant products. They are classified on the basis of their ease of dissemination, mortality/morbidity rate, and potential for social disruption. A subset of these agents includes Bacillus anthracis, Yersinia pestis, Francisella tularensis, ricin toxin (RT), and staphylococcal enterotoxin B (SEB). Infection or intoxication with these agents has been shown to elicit an antigen-specific serum IgG response. We describe a fluorescent covalent microsphere immunoassay (FCMIA) for measurement of specific IgG antibodies to seven different antigens from five different select agents; B. anthracis [protective antigen (PA) and lethal factor (LF)], Y. pestis (F1 and V antigens), F. tularensis, RT and SEB simultaneously in human B. anthracisvaccinee sera (containing anti-PA and anti-LF IgG) which had been spiked with animal specific IgG antibodies to the other select agents. Inter-assay and intra-assay coefficients of variation were 6.5 and 13.4%, respectively (N=4). There were no significant differences (P > 0.70) between assay responses when the assays were performed individually or multiplexed. When the observed versus expected interpolated concentrations were compared, highly linear relationships were observed (r(2) values from 0.981 to 0.999, P < 0.001). Minimum detectable concentrations (MDC) ranged from 0.3 ng mL(-1) (Y. pestis F1) to 300 ng mL(-1) (RT). Finally, the curves showed responses were linear for most analytes from their MDC to 125 (SEB) to 1,300 (Y. pestis F1)xtheir MDC. These data indicate that multiplexed FCMIA is a sensitive and accurate method for simultaneous measurement of specific IgG in serum to CDC select agents and may be of value in screening either decontamination workers or the general population for exposure to/infection with these agents.
引用
收藏
页码:1027 / 1034
页数:8
相关论文
共 37 条
[1]   Serodiagnosis of infectious diseases with antigen microarrays [J].
Bacarese-Hamilton, T ;
Mezzasoma, L ;
Ardizzoni, A ;
Bistoni, F ;
Crisanti, A .
JOURNAL OF APPLIED MICROBIOLOGY, 2004, 96 (01) :10-17
[2]   RIBOSOME-INACTIVATING PROTEINS FROM PLANTS [J].
BARBIERI, L ;
BATTELLI, MG ;
STIRPE, F .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1154 (3-4) :237-282
[3]   Comparison of a multiplexed fluorescent covalent microsphere immunoassay and an enzyme-linked immunosorbent assay for measurement of human immunoglobulin G antibodies to anthrax toxins [J].
Biagini, RE ;
Sammons, DL ;
Smith, JP ;
MacKenzie, BA ;
Striley, CAF ;
Semenova, V ;
Steward-Clark, E ;
Stamey, K ;
Freeman, AE ;
Quinn, CP ;
Snawder, JE .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2004, 11 (01) :50-55
[4]   Determination of serum IgG antibodies to Bacillus anthracis protective antigen in environmental sampling workers using a fluorescent covalent microsphere immunoassay [J].
Biagini, RE ;
Sammons, DL ;
Smith, JP ;
Page, EH ;
Snawder, JE ;
Striley, CAF ;
MacKenzie, BA .
OCCUPATIONAL AND ENVIRONMENTAL MEDICINE, 2004, 61 (08) :703-708
[5]   Development of a sensitivity enhanced multiplexed fluorescence covalent microbead immunosorbent assay (FCMIA) for the measurement of glyphosate, atrazine and metolachlor mercapturate in water and urine [J].
Biagini, RE ;
Smith, JP ;
Sammons, DL ;
MacKenzie, BA ;
Striley, CAF ;
Robertson, SK ;
Snawder, JE .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2004, 379 (03) :368-374
[6]   Method for simultaneous measurement of antibodies to 23 pneumococcal capsular polysaccharides [J].
Biagini, RE ;
Schlottmann, SA ;
Sammons, DL ;
Smith, JP ;
Snawder, JC ;
Striley, CAF ;
MacKenzie, BA ;
Weissman, DN .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2003, 10 (05) :744-750
[7]   Production of antibodies to staphylococcal superantigens in atopic dermatitis [J].
Campbell, DE ;
Kemp, AS .
ARCHIVES OF DISEASE IN CHILDHOOD, 1998, 79 (05) :400-404
[8]   Production and purification of a recombinant staphylococcal enterotoxin B vaccine candidate expressed in Escherichia coli [J].
Coffman, JD ;
Zhu, JW ;
Roach, JM ;
Bavari, S ;
Ulrich, RG ;
Giardina, SL .
PROTEIN EXPRESSION AND PURIFICATION, 2002, 24 (02) :302-312
[9]   Tularemia as a biological weapon - Medical and public health management [J].
Dennis, DT ;
Inglesby, TV ;
Henderson, DA ;
Bartlett, JG ;
Ascher, MS ;
Eitzen, E ;
Fine, AD ;
Friedlander, AM ;
Hauer, J ;
Layton, M ;
Lillibridge, SR ;
McDade, JE ;
Osterholm, MT ;
O'Toole, T ;
Parker, G ;
Perl, TM ;
Russell, PK ;
Tonat, K .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (21) :2763-2773
[10]  
*DHHS, 2002, FED REGISTER, V240, P76866