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1.
J Water Health, v. 21, n. 3, 443, mar. 2023
Artículo en Inglés | Sec. Est. Saúde SP, SESSP-IBPROD, Sec. Est. Saúde SP | ID: bud-4886

RESUMEN

Despite the Naegleria genus being isolated from different natural environments such as water, soil, and air, not all Naegleria species are capable of causing infections in humans, and they are capable of completing their life cycle in environmental niches. However, the presence of this genus may suggest the existence of one of the highly pathogenic free-living amoeba (FLA) species: Naegleria fowleri or the brain-eating amoeba. This facultative parasitic protozoon represents a risk to public health, mainly related to domestic and agricultural waters. In this research, our main objective was to determine the existence of pathogenic protozoa in the Santa Cruz wastewater treatment plant, Santiago Island. Using 5 L of water we confirmed the presence of potentially pathogenic Naegleria australiensis, being the first report on Naegleria species in Cape Verde. This fact demonstrates the low efficiency in the treatment of wastewater and, consequently, a potential threat to public health. Nevertheless, more studies will be needed for the prevention and control of possible infections in this Macaronesian country.

2.
Acta Trop ; 98(1): 1-5, 2006 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-16529708

RESUMEN

The natural infection of Lutzomyia neivai with Leishmania in the endemic area of American cutaneous leishmaniasis (ACL) in northwestern Argentina was analyzed by the polymerase chain reaction (PCR)-hybridization technique. Phlebotominae sand flies were captured in the provinces of Tucumán and Salta between 1999 and 2003. From a sample of 440 Lu. neivai females analysed for the detection of the Leishmania (Viannia) and Leishmania (Leishmania) subgenera, 9.1% of the samples resulted infected with a parasite of the subgenus Viannia and none with the Leishmania. This is the first report of naturally infected sand flies in Argentina besides the first report of infected Lu. neivai sensu strictu. Our results contributed to further incrimination of this specie as vector of leishmaniasis in the area and the identification of the main circulating parasite as belonging to the Leishmania (Viannia) subgenera.


Asunto(s)
Leishmania/fisiología , Leishmaniasis Cutánea/transmisión , Psychodidae/parasitología , Animales , Argentina/epidemiología , Interacciones Huésped-Parásitos , Insectos Vectores/parasitología , Leishmaniasis Cutánea/epidemiología
3.
Mem Inst Oswaldo Cruz ; 100(2): 187-92, 2005 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-16021307

RESUMEN

American cutaneous leishmaniasis (ACL) is an endemic disease in Northern Argentina. We applied the polymerase chain reaction (PCR) followed by a hybridization labelled probe to 21 paraffin embedded human skin biopsies, already analyzed histologically, from leishmaniasis endemic areas in the province of Tucumán, Argentina. We used primers previously designed to detect a Leishmania-specific 120-base-pair fragment of kinetoplast DNA minicircle, other two primer pairs that amplify kDNA minicircles belonging to the L. braziliensis and L. mexicana complexes respectively, and specific oligonucleotide primers to detect L. (V.) braziliensis which amplify the sequence of the ribosomal protein L-14 of this species. The PCR-hybridization showed a sensitivity of 90.5% when compared to the histopathology test which was 61.9%. Five of the total samples analyzed were positive for the L. braziliensis complex whilst none was positive for the L. mexicana complex. The specific primers for L. (V.) braziliensis detected the parasite in four samples. These results are consistent with those reported for close endemic areas and demonstrate that the causative agent of human leishmaniasis in the analyzed cases was L. (V.) braziliensis. PCR should be used as a diagnostic tool for tegumentary leishmaniasis, especially in the mucosal form, and as a valuable technique for the identification of the Leishmania species that causes the disease in certain areas.


Asunto(s)
Leishmania braziliensis/aislamiento & purificación , Leishmaniasis Cutánea/diagnóstico , Piel/parasitología , Animales , Argentina , Biopsia , Southern Blotting , ADN de Cinetoplasto/análisis , ADN Protozoario/análisis , Enfermedades Endémicas , Humanos , Leishmania braziliensis/genética , Leishmaniasis Cutánea/parasitología , Leishmaniasis Cutánea/patología , Adhesión en Parafina , Reacción en Cadena de la Polimerasa , Sensibilidad y Especificidad , Piel/patología
4.
Mem. Inst. Oswaldo Cruz ; 100(2): 187-192, Apr. 2005. ilus, tab
Artículo en Inglés | LILACS | ID: lil-410858

RESUMEN

American cutaneous leishmaniasis (ACL) is an endemic disease in Northern Argentina. We applied the polymerase chain reaction (PCR) followed by a hybridization labelled probe to 21 paraffin embedded human skin biopsies, already analyzed histologically, from leishmaniasis endemic areas in the province of Tucumán, Argentina. We used primers previously designed to detect a Leishmania-specific 120-base-pair fragment of kinetoplast DNA minicircle, other two primer pairs that amplify kDNA minicircles belonging to the L. braziliensis and L. mexicana complexes respectively, and specific oligonucleotide primers to detect L. (V.) braziliensis which amplify the sequence of the ribosomal protein L-14 of this species. The PCR-hybridization showed a sensitivity of 90.5 percent when compared to the histopathology test which was 61.9 percent. Five of the total samples analyzed were positive for the L. braziliensis complex whilst none was positive for the L. mexicana complex. The specific primers for L. (V.) braziliensis detected the parasite in four samples. These results are consistent with those reported for close endemic areas and demonstrate that the causative agent of human leishmaniasis in the analyzed cases was L. (V.) braziliensis. PCR should be used as a diagnostic tool for tegumentary leishmaniasis, especially in the mucosal form, and as a valuable technique for the identification of the Leishmania species that causes the disease in certain areas.


Asunto(s)
Animales , Humanos , Leishmania braziliensis/aislamiento & purificación , Leishmaniasis Cutánea/diagnóstico , Piel/parasitología , Argentina , Biopsia , Southern Blotting , ADN de Cinetoplasto/análisis , ADN Protozoario/análisis , Enfermedades Endémicas , Leishmania braziliensis/genética , Leishmaniasis Cutánea/parasitología , Leishmaniasis Cutánea/patología , Adhesión en Parafina , Reacción en Cadena de la Polimerasa , Sensibilidad y Especificidad , Piel/patología
5.
Clin Diagn Lab Immunol ; 9(4): 808-11, 2002 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-12093677

RESUMEN

The humoral immune response against Leishmania braziliensis histone H1 by patients with cutaneous leishmaniasis is described. For this purpose, the protein was purified as a recombinant protein in a prokaryotic expression system and was assayed by enzyme-linked immunosorbent assay (ELISA) with a collection of sera from patients with cutaneous leishmaniasis and Chagas' disease. The assays showed that L. braziliensis histone H1 was recognized by 66% of the serum samples from patients with leishmaniasis and by 40% of the serum samples from patients with Chagas' disease, indicating that it acts as an immunogen during cutaneous leishmaniasis. In order to locate the linear antigenic determinants of this protein, a collection of synthetic peptides covering the L. braziliensis histone H1sequence was tested by ELISA. The experiments showed that the main antigenic determinant is located in the central region of this protein. Our results show that the recombinant L. braziliensis histone H1 is recognized by a significant percentage of serum samples from patients with cutaneous leishmaniasis, but use of this protein as a tool for the diagnosis of cutaneous leishmaniasis is hampered by the cross-reaction with sera from patients with Chagas' disease.


Asunto(s)
Histonas/inmunología , Leishmania braziliensis/inmunología , Leishmaniasis Cutánea/inmunología , Animales , Anticuerpos Antiprotozoarios/sangre , Anticuerpos Antiprotozoarios/inmunología , Formación de Anticuerpos , Especificidad de Anticuerpos , Antígenos de Protozoos/inmunología , Clonación Molecular , Mapeo Epitopo , Epítopos , Humanos
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