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M A Marques

Publications and source records attributed to M A Marques.

21 records · Page 2Linked to original sources

Serological response of patients with leprosy to a 28- to 30-kilodalton protein doublet from early cultures of Mycobacterium bovis BCG.

Analysis by Western immunoblotting of Mycobacterium bovis BCG short-term culture filtrates with a pool of serum samples from lepromatous leprosy patients revealed an immunodominant protein doublet with apparent molecular masses of 28 and 30 kilodaltons (kDa). The humoral response to these antigens was also investigated by using individual serum samples from patients representative of the whole spectrum of leprosy and from tuberculosis patients, as well as from contacts of leprosy patients and control groups. The protein doublet was recognized by 92% of the sera from patients with lepromatous leprosy (51 of 56), whereas essentially negative results were obtained with sera from the other groups. Similar immunodominant bands were also detected by Western blotting analysis of sonic extracts of seven other slow- and fast-growing mycobacterial species, suggesting a broad distribution of these antigens within the genus. Analysis of the purified doublet by Western blotting after two-dimensional gel electrophoresis fractionation showed that the 28- and 30-kDa doublet consisted of at least five different components with pls from 5.2 to 5.7 and molecular masses from 28 to 31 kDa. These results indicate that the protein doublet could be used as a potential marker in the diagnosis of lepromatous leprosy.

Antibodies, Bacterial↗

Gradual changes of influenza virions during passage of undiluted material.

Defective influenza virions undergo gradual changes during passage of undiluted material: the amount of RNA in virions diminishes, the equimolarity of the RNA segments is lost and the interfering activity of defective virions decreases. Defective virions of early passages have a small deficiency in genetic material and at a high m.o.i. induce the synthesis of the complete set of virus-specific proteins. Defective virions from later passages are characterized by a considerable deficiency in genetic material and a decrease in the amount of high mol. wt. RNA segments. They do not demonstrate complementation and at a high m.o.i. do not induce the synthesis of virus-specific proteins, thus revealing analogous defects in the genome of the majority of defective virions. The characteristics of protein synthesis in cells infected with these virions are similar to those in uninfected cells. During undiluted passage of influenza virus the cyclic production of defective and infectious virions takes place.

Animals↗