Infeccao do Anopheles (Kerteszia) cruzi por Plasmodium vivax e Plasmodium vivax variante VK247 nos Municipios de Sao Vicente e Juquitiba, Sao Paulo / Infection of Anopheles (Kerteszia) cruzi with Plasmodium vivax and Plasmodium vivax variant VK247 in the municipalities of Sao Vicente and Juquitiva, Sao Paulo

O Estado de São Paulo, situado na região Sudeste do Brasil, apresenta esporadicamente casos autóctones de malária que se caracterizam pela presença de quadro clínico benigno com parasitemias baixas e sintomatologia branda, identificados como malária vivax. Pouco se sabe a respeito da sintomatologia e resposta imune desenvolvidas pelo ser humano para as variantes Plasmodium vivax VK247 e Plasmodium vivax-like humano. Estas variantes são transmitidas pelo mosquito Anopheles (Kerteszia) cruzii, uma das espécies mais abundantes no Sudeste brasileiro. O objetivo deste trabalho foi verificar a infecção em anofelinos desta região, através do teste imunoenzimático ELISA com utilização de anticorpos monoclonais específicos dirigidos contra as regiões repetitivas da proteína circunsporozoíta de P. vivax clássico, P. brasilianum/P. malariae e P. vivax VK247. Coletas entomológicas foram realizadas no período de 1991 a 1993 em São Vicente e Juquitiba, municípios localizados em área remanescente da Mata Atlântica do Estado de São Paulo. A Mata Atlântica é rica em plantas da família Bromeliaceae, criadouros de formas imaturas de anofelinos do subgênero Kerteszia. De um total de 1 117 espécimes de An. (Ker.) cruzii capturados no Município de São Vicente, 0,179% foram positivos para P. vivax clássico. Em Juquitiba, dentre 1 161 An. (Ker.) cruzii pesquisados, 0,086% foram positivos para o P. vivax VK247, o que demonstra a presença da variante na região. Embora o índice de infecção encontrado seja baixo, a alta densidade destes mosquitos e sua voracidade (picam durante as 24 h do dia) poderiam compensar a baixa porcentagem de espécimes infectados

Sporadic cases of autochthonous malaria have been recorded in São Paulo State, located in the Southeast region of Brazil. These cases are characterized by their benign course, low parasitemia, and mild symptomatology and have been identified as vivax malaria. Little is known about the symptoms and immune response elicited in humans by the variants Plasmodium vivax VK247 and P. vivax-like human malaria parasites. These variants are transmitted by Anopheles (Kerteszia) cruzii, one of the most common species of mosquitoes in the Southeast of Brazil. The objective of the study described in this paper was to investigate infection in anophelines using ELISA immunoenzymatic assay with specific monoclonal antibodies directed against the repetitive regions of the circumsporozoite protein in classic P. vivax, P. brasilianum/P. malariae, and P. vivax VK247. Between 1991 and 1993, mosquitoes were collected in São Vicente and Juquitiba, municipalites located in a remnant of the Brazilian Atlantic forest in São Paulo State, an ecosystem rich in plants of the Bromeliaceae family. These plants function as nurseries for immature forms of anophelines of the subgenus Kerteszia. Of 1 117 An. (Ker.) cruzii captured in São Vicente, 0.179% were positive for classic P. vivax. In Juquitiba, of 1 161 An. (Ker.) cruzii, 0.086% were positive for P. vivax VK247, confirming the presence of this variant in the region. Although the infection rate is low, the high density of these mosquitoes and their voracity (they exhibit 24-h biting activity) could compensate for the low percentage of infected specimens

Antibodies anti Bloodstream and Circumsporozoite antigens (Plasmodium

During 1992-1994, 33 malaria cases were reported in two regions in Brazil were few sporadic atypical cases occur, most of them in home owners, who are weekenders, while home caretakers live there permanently. Indirect Flurescent antibody Test (IFLAT), with Plasmodium vivax, and Enzime Linked Immunosorbent Assay (ELISA) with repeat peptides of the circumsporozoite (CS) proteins of the 3 known P. vivax variants and P. malarie/P. brasilianum, were performed on 277 sera, obtained within a 5 to 10 km range of malaria cases. Very rarely did any of these donors recall typical malaria episodes. Blood smears of all but 5 were negative. One of the 5 malaria cases included in our serology was of a home owner, 1 of a permanent resident, 3 from Superintendencia de Controle de Endemias employees who went there to capture mosquitoes. In region 1the prevalence of IFLAT positive sera was 73 per cent and 28 per cent among caretakers, 18 per cent and 9.6 per cent among home owners. In region 2 (3 localities) no distinction was possible between caretakers and home owners, IFAT positivity being 38 per cent, 28 per cent and 7 per cent. The relative percentage of positive anti-CS repeats ELISA, differed for each of the peptides among localities. Dwellings are in the vicinity of woods, where monkeys are frequently seen. The origin of these malaria cases, geographical differences and high seropositivity is discussed.

Morphological aspects of the myocarditis and myositis in Calomys callosus experimentally infected with Trypanosoma cruzi: fibrogenesis and spontaneous regression of fibrosis

Calomys callosus a wild rodent, is a natural host of Trypanosoma cruzi. Twelve C. callosus were infected with 10(5) trypomastigotes of the F strain (a myotropic strain) of T. cruzi. Parasitemia decreased on the 21 st day becoming negative around the 40th day of infection. All animals survived but had positive parasitological tests, until the end of the experiment. The infected animals developed severe inflammation in the myocardium and skeletal muscle. This process was pronounced from the 26 th to the 30th day and gradually subsided from the 50 th day becoming absent or residual on the 64 th day after infection. Collagen was identified by the picro Sirius red method. Fibrogenesis developed early, but regression of fibrosis occurred between the 50th and 64th day. Ultrastructural study disclosed a predominance of macrophages and fibroblasts in the inflammatory infiltrates, with small numbers of lymphocytes. Macrophages had active phagocytosis and showed points of contact with altered muscle cells. Different degrees of matrix expansion were present, with granular and fibrilar deposits and collagen bundles. These alterations subsided by the 64th days. Macrophages seem to be the main immune effector cell in the C. callosus model of infection with T. cruzi. The mechanisms involved in the rapid fibrogenesis and its regression deserve further investigation.

Macrophage activation and histopathological findings in Calomys callosus and Swiss mice infected with several strains of Trypanosoma cruzi

Peritoneal macrophage activation as measured by H2O2 release and histopathology was compared between Swiss mice and Calomys callosus, a wild rodent, reservoir of Trypanosoma cruzi, during the course of infection with four strains of this parasite. In mice F and Y strain infections result in high parasitemia and mortality while with silvatic strains Costalimai and M226 parasitemia is sub-patent, with very low mortality. H2O2 release peaked at 33,6 and 59 nM/2 x 10(elevado a sexta potência) cells for strains Y and F, respectively, 48 and 50 nM/2 x 10 (elevado a sexta potência) for strains Costalimai and M226, at different days after infection. Histopathological findings of myositis, myocarditis, necrotizing artheritis and abscence of macrophage parasitism were foud for strains F and Costalimai. Y strain infection presented moderate myocarditis and myositis, with parasites multiplying within macrophages. In C. callosus all four strains resulted in patent parasitemia wich was eventually overcome, with scarce mortality. H2O2 release for strains Y or F was comparable to that of mice-peaks of 27 and 53 nM/2 x 10 (elevado a sexta potência) cells, with lower values for strains Costalimai and M226 - 16.5 and 4.6 nM/2 x 10(elevado a sexta potência)cells, respectively. Histopathological lesions with Y and F strain injected animals were comparable to those of mice at the onset of infections; they subsided completely at the later stages with Y strain and partially with F strain infected C. callosus. In Costalimai infected C. callosus practically no histopathological alterations were observed