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1.
Braz. j. med. biol. res ; 41(7): 596-599, July 2008. ilus
Article in English | LILACS | ID: lil-489522

ABSTRACT

Hantavirus cardiopulmonary syndrome (HCPS) has been recognized as an important public heath problem. Five hantaviruses associated with HCPS are currently known in Brazil: Juquitiba, Araraquara, Laguna Negra-like, Castelo dos Sonhos, and Anajatuba viruses. The laboratory diagnosis of HCPS is routinely carried out by the detection of anti-hantavirus IgM and/or IgG antibodies. The present study describes the expression of the N protein of a hantavirus detected in the blood sample of an HCPS patient. The entire S segment of the virus was amplified and found to be 1858 nucleotides long, with an open reading frame of 1287 nucleotides that encodes a protein of 429 amino acids. The nucleotide sequence described here showed a high identity with the N protein gene of Araraquara virus. The entire N protein was expressed using the vector pET200D and the Escherichia coli BL21 strain. The expression of the recombinant protein was confirmed by the detection of a 52-kDa protein by Western blot using a pool of human sera obtained from HCPS patients, and by specific IgG detection in five serum samples of HCPS patients tested by ELISA. These results suggest that the recombinant N protein could be used as an antigen for the serological screening of hantavirus infection.


Subject(s)
Humans , Antigens, Viral , Hantavirus Pulmonary Syndrome/diagnosis , Orthohantavirus/immunology , Nucleocapsid Proteins , Antigens, Viral/genetics , Antigens, Viral/immunology , Capsid Proteins/immunology , Enzyme-Linked Immunosorbent Assay , Escherichia coli , Genetic Vectors , Immunoglobulin G/immunology , Nucleocapsid Proteins/genetics , Nucleocapsid Proteins/immunology , Viral Core Proteins/immunology
2.
Braz. j. med. biol. res ; 34(1): 93-101, Jan. 2001. tab, graf
Article in English | LILACS | ID: lil-277061

ABSTRACT

A prospective study of cytomegalovirus (CMV) infection was carried out on 34 renal transplant recipients managed at a General Hospital in Ribeirão Preto, SP, Brazil. Serologic tests showed that all patients were infected with CMV before renal transplantation. Two nested-PCR techniques with primers that recognize sequences of the glycoprotein B (gB) and H (gH) genes were used for CMV detection in blood and urine samples during the post-transplantation period. CMV was detected more frequently in blood samples than in urine samples (P<0.001). Thirty-three patients had CMV detected at least once in blood and/or urine samples. Seven of these patients (21.2 percent) were diagnosed as having symptomatic CMV infection and showed a worse clinical outcome, with a higher death rate (P = 0.03). No association between CMV viremia and graft rejection was observed. Nested-PCR was not useful to identify patients at risk for symptomatic CMV infection since only 21.2 percent of the patients with CMV infection were symptomatic


Subject(s)
Humans , Cytomegalovirus Infections/diagnosis , Kidney Transplantation , Polymerase Chain Reaction/methods , Base Sequence , Cytomegalovirus Infections/blood , Cytomegalovirus Infections/urine , DNA Primers , Immunoglobulin G/isolation & purification , Immunoglobulin M/isolation & purification , Prospective Studies , Viral Envelope Proteins/genetics
3.
Braz. j. med. biol. res ; 32(8): 953-9, Aug. 1999. tab
Article in English | LILACS | ID: lil-238963

ABSTRACT

Cytomegalovirus (CMV) is the single most important infectious agent affecting recipients of organ transplants. To evaluate the incidence and the clinical importance of CMV infection in renal transplants in Brazil, 37 patients submitted to renal allograft transplants were tested periodically for the presence of cytomegalovirus DNA in urine using the polymerase chain reaction (PCR), and for the presence of IgM and IgG antibodies against CMV by enzyme-linked immunosorbent assay (ELISA) and indirect immunofluorescence (IIF). The PCR-amplified products were detected by gel electrophoresis and confirmed by dot-blot hybridization with oligonucleotide probes. Thirty-two of the 37 patients (86.4 percent) were positive by at least one of the three methods. In six patients, PCR was the only test which detected the probable CMV infection. Ten patients had a positive result by PCR before transplantation. In general, the diagnosis was achieved earlier by PCR than by serologic tests. Active infection occurred more frequently during the first four months after transplantation. Sixteen of the 32 patients (50 percent) with active CMV infection presented clinical symptoms consistent with CMV infection. Five patients without evidence of active CMV infection by the three tests had only minor clinical manifestations during follow-up. Our results indicate that PCR is a highly sensitive procedure for the early detection of CMV infection and that CMV infection in renal transplant patients is a frequent problem in Brazil


Subject(s)
Humans , Cytomegalovirus Infections/diagnosis , Cytomegalovirus Infections/epidemiology , Cytomegalovirus/isolation & purification , Kidney Transplantation , Polymerase Chain Reaction , Postoperative Complications , Cytomegalovirus Infections/complications , Cytomegalovirus Infections/virology , Enzyme-Linked Immunosorbent Assay , Incidence , Prevalence , Prospective Studies , Serologic Tests
4.
Braz. j. med. biol. res ; 27(11): 2573-8, Nov. 1994. ilus, tab, graf
Article in English | LILACS | ID: lil-153978

ABSTRACT

Two patients receiving the same cadaver kidney graft were investigated prospectively for cytomegalovirus (CMV) infection using the polymerase chain reaction (PCR) and serologic tests (ELISA and IFI). The data indicate that a strain of CMV was probably transmitted from the same donor to both kidney recipients including one who was seropositive for CMV


Subject(s)
Humans , Male , Adolescent , Cytomegalovirus Infections/transmission , Postoperative Complications/diagnosis , Kidney Transplantation , Tissue Donors , Antibodies, Viral/blood , Base Sequence , Cytomegalovirus Infections/diagnosis , Cytomegalovirus Infections/immunology , Cytomegalovirus/immunology , Postoperative Complications/immunology , DNA, Viral/urine , Enzyme-Linked Immunosorbent Assay , Fluorescent Antibody Technique , Immunoglobulin G/blood , Immunoglobulin M/blood , Polymerase Chain Reaction
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