Luminometry: A novel bioluminescent immunoassay enhances the quantitation of mucosal and systemic antibody responses

被引:33
作者
Jackson, RJ
Fujihashi, K
Kiyono, H
McGhee, JR
机构
[1] UNIV ALABAMA,MED CTR,DEPT MICROBIOL,MUCOSAL IMMUNIZAT RES GRP,BIRMINGHAM,AL 35294
[2] UNIV ALABAMA,MED CTR,DEPT ORAL BIOL,MUCOSAL IMMUNIZAT RES GRP,BIRMINGHAM,AL 35294
[3] OSAKA UNIV,MICROBIAL DIS RES INST,DEPT MUCOSAL IMMUNOL,SUITA,OSAKA 565,JAPAN
关键词
luminometry; mucosal immunoassay; aequorin; AquaLite(R);
D O I
10.1016/0022-1759(95)00276-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We have directly compared enzyme-linked immunoassays (ELISAs) with bioluminescent immunoassays employing derivatives of the bioluminescent molecule aequorin, and have shown that detection of mucosal and serum antibodies is considerably more sensitive when detected by luminometry. Luminometry is based upon counting photons of light via phototubes and is generally similar to scintillation spectrometry. Current commercial luminometric technology employs a phototube which is most efficient for light emission in the 400-420 nm wavelength range. For this reason, we have chosen the bioluminescent molecule, aequorin, which upon the addition of Ca2+ undergoes a conformational change resulting in the emission of blue light at 469 nm, The high quantum yield is reflected by the fact that addition of Ca2+ to 1 ng of recombinant streptaequorin, a covalent conjugate of streptavidin and aequorin, resulted in the production of 7 x 10(8) relative light units, In this study, we show the superior sensitivity of biotin-streptaequorin when directly compared with biotin-streptavidin linked horseradish peroxidase commonly used for ELISA. For example, mice orally immunized once with cholera toxin (CT) did not exhibit detectable fecal IgA antibodies as determined by ELISA, whereas use of streptaequorin and the bioluminescent immunoassay revealed fecal IgA anti-CT-B subunit antibody titers of 1:24 500. In addition, no detectable anti-CT-B antibodies were noted in saliva samples by ELISA 7 days following oral immunization with CT, while IgA endpoint titers could be extrapolated to 1:393 000. The 21 day fecal IgA anti-CT-B titers were 1:512 by ELISA, whereas titers determined by luminometry reached 1:10(7) when Neutralite avidin and biotinylated aequorin were employed. In general, the bioluminescent immunoassay was > 10(4)-fold more sensitive when compared with ELISA for detection of mucosal and serum antigen- and isotype-specific antibody responses, Thus, the bioluminescent immunoassay is a more sensitive assay for detection of antibodies in dilute external secretions.
引用
收藏
页码:189 / 197
页数:9
相关论文
共 15 条
  • [1] CAMPBELL AK, 1993, FLUORESCENT LUMINESC, P58
  • [2] THE ENZYMOLOGY AND MOLECULAR-BIOLOGY OF THE CA-2+-ACTIVATED PHOTOPROTEIN, AEQUORIN
    CORMIER, MJ
    PRASHER, DC
    LONGIARU, M
    MCCANN, RO
    [J]. PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1989, 49 (04) : 509 - 512
  • [3] A SOLID-PHASE ENZYME-LINKED IMMUNOSPOT (ELISPOT) ASSAY FOR ENUMERATION OF SPECIFIC ANTIBODY-SECRETING CELLS
    CZERKINSKY, CC
    NILSSON, LA
    NYGREN, H
    OUCHTERLONY, O
    TARKOWSKI, A
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 1983, 65 (1-2) : 109 - 121
  • [4] A LAVAGE TECHNIQUE ALLOWING REPEATED MEASUREMENT OF IGA ANTIBODY IN MOUSE INTESTINAL SECRETIONS
    ELSON, CO
    EALDING, W
    LEFKOWITZ, J
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 1984, 67 (01) : 101 - 108
  • [5] GREEN NM, 1963, BIOCHEM J, V89, P593
  • [6] HART RC, 1993, BIOLUMINESCENCE CHEM, P320
  • [7] CLONING AND SEQUENCE-ANALYSIS OF CDNA FOR THE LUMINESCENT PROTEIN AEQUORIN
    INOUYE, S
    NOGUCHI, M
    SAKAKI, Y
    TAKAGI, Y
    MIYATA, T
    IWANAGA, S
    MIYATA, T
    TSUJI, FI
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (10) : 3154 - 3158
  • [8] OPTIMIZING ORAL VACCINES - INDUCTION OF SYSTEMIC AND MUCOSAL B-CELL AND ANTIBODY-RESPONSES TO TETANUS TOXOID BY USE OF CHOLERA-TOXIN AS AN ADJUVANT
    JACKSON, RJ
    FUJIHASHI, K
    XUAMANO, JC
    KIYONO, H
    ELSON, CO
    MCGHEE, JR
    [J]. INFECTION AND IMMUNITY, 1993, 61 (10) : 4272 - 4279
  • [9] SCHAAP AP, 1989, CLIN CHEM, V35, P1863
  • [10] A SOLID-PHASE IMMUNOENZYMATIC TECHNIQUE FOR THE ENUMERATION OF SPECIFIC ANTIBODY-SECRETING CELLS
    SEDGWICK, JD
    HOLT, PG
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 1983, 57 (1-3) : 301 - 309