Heterologous expression, purification, and immunological reactivity of a recombinant HSP60 from Paracoccidioides brasiliensis

被引:35
作者
Cunha, DA
Zancopé-Oliveira, RM
Felipe, MSS
Salem-Izacc, SM
Deepe, GS
Soares, CMA
机构
[1] Univ Fed Goias, Inst Ciencias Biol, Mol Biol Lab, ICBII, BR-74001970 Goiania, Go, Brazil
[2] Hosp Evandro Chagas, Fundacao Oswaldo Cruz, Lab Micol Med, Rio De Janeiro, Brazil
[3] Univ Brasilia, Inst Biol, Mol Biol Lab, Brasilia, DF, Brazil
[4] Univ Cincinnati, Coll Med, Div Infect Dis, Cincinnati, OH 45267 USA
关键词
D O I
10.1128/CDLI.9.2.374-377.2002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The complete coding cDNA of HSP60 from Paracoccidioides brasiliensis was overexpressed in an Escherichia coli host to produce high levels of recombinant protein. The protein was purified by affinity chromatography. A total of 169 human serum samples were tested for reactivity by Western blot analysis with the purified HSP60 recombinant protein. Immunoblots indicated that the recombinant A brasiliensis HSP60 was recognized by antibodies in 72 of 75 sera from paracoccidioidomycosis patients. No cross-reactivity was detected with individual sera from patients with aspergillosis, sporotrichosis, cryptococcosis, and tuberculosis. Reactivity to HSP60 was observed in sera from 9.52% of control healthy individuals and 11.5% of patients with histoplasmosis. The high sensitivity and specificity (97.3 and 92.5%, respectively) for HSP60 suggested that the recombinant protein can be used singly or in association with other recombinant antigens to detect antibody responses in A brasiliensis-infected patients.
引用
收藏
页码:374 / 377
页数:4
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