Natural infection in anopheline species and its implications for autochthonous malaria in the Atlantic Forest in Brazil
A descriptive study was carried out in an area of the Atlantic Forest with autochthonous malaria in the Parelheiros subdistrict on the periphery of the municipality of São Paulo to identify anopheline fauna and anophelines naturally infected with Plasmodium as well as to discuss their role in this p...
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Published in | Parasites & vectors Vol. 6; no. 1; p. 58 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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BioMed Central
07.03.2013
BioMed Central Ltd |
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Abstract | A descriptive study was carried out in an area of the Atlantic Forest with autochthonous malaria in the Parelheiros subdistrict on the periphery of the municipality of São Paulo to identify anopheline fauna and anophelines naturally infected with Plasmodium as well as to discuss their role in this peculiar epidemiological context.
Entomological captures were made from May 2009 to April 2011 using Shannon traps and automatic CDC traps in four areas chosen for their different patterns of human presence and incidences of malaria (anthropic zone 1, anthropic zone 2, transition zone and sylvatic zone). Natural Plasmodium infection was detected by nested PCR based on amplification of the 18S rRNA gene.
In total, 6,073 anophelines were collected from May 2009 to April 2011, and six species were identified in the four zones. Anopheles cruzii was the predominant species in the three environments but was more abundant in the sylvatic zone. Anopheles (Kerteszia) cruzii specimens from the anthropic and sylvatic zones were positive for P. vivax and P. malariae. An. (Ker.) bellator, An. (Nys.) triannulatus, An. (Nys.) strodei, An. (Nys.) lutzi and An. (Ano) maculipes were found in small numbers. Of these, An. (Nys.) triannulatus and An. (Nys.) lutzi, which were collected in the anthropic zone, were naturally infected with P. vivax while An. (Nys.) triannulatus from the anthropic zones and An. (Nys.) strodei from the transition zone were positive for P. malariae.
These results confirm that Anopheles (Kerteszia) cruzii plays an important role as a major Plasmodium vector. However, the finding of other naturally infected species may indicate that secondary vectors are also involved in the transmission of malaria in the study areas. These findings can be expected to help in the implementation of new measures to control autochthonous malaria in areas of the Atlantic Forest. |
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AbstractList | BACKGROUND: A descriptive study was carried out in an area of the Atlantic Forest with autochthonous malaria in the Parelheiros subdistrict on the periphery of the municipality of São Paulo to identify anopheline fauna and anophelines naturally infected with Plasmodium as well as to discuss their role in this peculiar epidemiological context. METHODS: Entomological captures were made from May 2009 to April 2011 using Shannon traps and automatic CDC traps in four areas chosen for their different patterns of human presence and incidences of malaria (anthropic zone 1, anthropic zone 2, transition zone and sylvatic zone). Natural Plasmodium infection was detected by nested PCR based on amplification of the 18S rRNA gene. RESULTS: In total, 6,073 anophelines were collected from May 2009 to April 2011, and six species were identified in the four zones. Anopheles cruzii was the predominant species in the three environments but was more abundant in the sylvatic zone.Anopheles (Kerteszia) cruzii specimens from the anthropic and sylvatic zones were positive for P. vivax and P. malariae. An. (Ker.) bellator, An. (Nys.) triannulatus, An. (Nys.) strodei, An. (Nys.) lutzi and An. (Ano) maculipes were found in small numbers. Of these, An. (Nys.) triannulatus and An. (Nys.) lutzi, which were collected in the anthropic zone, were naturally infected with P. vivax while An. (Nys.) triannulatus from the anthropic zones and An. (Nys.) strodei from the transition zone were positive for P. malariae. CONCLUSION: These results confirm that Anopheles (Kerteszia) cruzii plays an important role as a major Plasmodium vector. However, the finding of other naturally infected species may indicate that secondary vectors are also involved in the transmission of malaria in the study areas. These findings can be expected to help in the implementation of new measures to control autochthonous malaria in areas of the Atlantic Forest. Doc number: 58 Abstract Background: A descriptive study was carried out in an area of the Atlantic Forest with autochthonous malaria in the Parelheiros subdistrict on the periphery of the municipality of São Paulo to identify anopheline fauna and anophelines naturally infected with Plasmodium as well as to discuss their role in this peculiar epidemiological context. Methods: Entomological captures were made from May 2009 to April 2011 using Shannon traps and automatic CDC traps in four areas chosen for their different patterns of human presence and incidences of malaria (anthropic zone 1, anthropic zone 2, transition zone and sylvatic zone). Natural Plasmodium infection was detected by nested PCR based on amplification of the 18S rRNA gene. Results: In total, 6,073 anophelines were collected from May 2009 to April 2011, and six species were identified in the four zones. Anopheles cruzii was the predominant species in the three environments but was more abundant in the sylvatic zone. Anopheles (Kerteszia) cruzii specimens from the anthropic and sylvatic zones were positive for P. vivax and P. malariae . An. (Ker.) bellator , An. (Nys.) triannulatus , An. (Nys.) strodei , An. (Nys.) lu tzi and An. (Ano) maculipes were found in small numbers. Of these, An. (Nys.) triannulatus and An. (Nys.) lutzi, which were collected in the anthropic zone, were naturally infected with P. vivax while An. (Nys.) triannulatus from the anthropic zones and An. (Nys.) strodei from the transition zone were positive for P. malariae . Conclusion: These results confirm that Anopheles (Kerteszia) cruzii plays an important role as a major Plasmodium vector. However, the finding of other naturally infected species may indicate that secondary vectors are also involved in the transmission of malaria in the study areas. These findings can be expected to help in the implementation of new measures to control autochthonous malaria in areas of the Atlantic Forest. A descriptive study was carried out in an area of the Atlantic Forest with autochthonous malaria in the Parelheiros subdistrict on the periphery of the municipality of São Paulo to identify anopheline fauna and anophelines naturally infected with Plasmodium as well as to discuss their role in this peculiar epidemiological context. Entomological captures were made from May 2009 to April 2011 using Shannon traps and automatic CDC traps in four areas chosen for their different patterns of human presence and incidences of malaria (anthropic zone 1, anthropic zone 2, transition zone and sylvatic zone). Natural Plasmodium infection was detected by nested PCR based on amplification of the 18S rRNA gene. In total, 6,073 anophelines were collected from May 2009 to April 2011, and six species were identified in the four zones. Anopheles cruzii was the predominant species in the three environments but was more abundant in the sylvatic zone. Anopheles (Kerteszia) cruzii specimens from the anthropic and sylvatic zones were positive for P. vivax and P. malariae. An. (Ker.) bellator, An. (Nys.) triannulatus, An. (Nys.) strodei, An. (Nys.) lutzi and An. (Ano) maculipes were found in small numbers. Of these, An. (Nys.) triannulatus and An. (Nys.) lutzi, which were collected in the anthropic zone, were naturally infected with P. vivax while An. (Nys.) triannulatus from the anthropic zones and An. (Nys.) strodei from the transition zone were positive for P. malariae. These results confirm that Anopheles (Kerteszia) cruzii plays an important role as a major Plasmodium vector. However, the finding of other naturally infected species may indicate that secondary vectors are also involved in the transmission of malaria in the study areas. These findings can be expected to help in the implementation of new measures to control autochthonous malaria in areas of the Atlantic Forest. BACKGROUNDA descriptive study was carried out in an area of the Atlantic Forest with autochthonous malaria in the Parelheiros subdistrict on the periphery of the municipality of São Paulo to identify anopheline fauna and anophelines naturally infected with Plasmodium as well as to discuss their role in this peculiar epidemiological context. METHODSEntomological captures were made from May 2009 to April 2011 using Shannon traps and automatic CDC traps in four areas chosen for their different patterns of human presence and incidences of malaria (anthropic zone 1, anthropic zone 2, transition zone and sylvatic zone). Natural Plasmodium infection was detected by nested PCR based on amplification of the 18S rRNA gene. RESULTSIn total, 6,073 anophelines were collected from May 2009 to April 2011, and six species were identified in the four zones. Anopheles cruzii was the predominant species in the three environments but was more abundant in the sylvatic zone. Anopheles (Kerteszia) cruzii specimens from the anthropic and sylvatic zones were positive for P. vivax and P. malariae. An. (Ker.) bellator, An. (Nys.) triannulatus, An. (Nys.) strodei, An. (Nys.) lutzi and An. (Ano) maculipes were found in small numbers. Of these, An. (Nys.) triannulatus and An. (Nys.) lutzi, which were collected in the anthropic zone, were naturally infected with P. vivax while An. (Nys.) triannulatus from the anthropic zones and An. (Nys.) strodei from the transition zone were positive for P. malariae. CONCLUSIONThese results confirm that Anopheles (Kerteszia) cruzii plays an important role as a major Plasmodium vector. However, the finding of other naturally infected species may indicate that secondary vectors are also involved in the transmission of malaria in the study areas. These findings can be expected to help in the implementation of new measures to control autochthonous malaria in areas of the Atlantic Forest. Background: A descriptive study was carried out in an area of the Atlantic Forest with autochthonous malaria in the Parelheiros subdistrict on the periphery of the municipality of Sao Paulo to identify anopheline fauna and anophelines naturally infected with Plasmodium as well as to discuss their role in this peculiar epidemiological context. Methods: Entomological captures were made from May 2009 to April 2011 using Shannon traps and automatic CDC traps in four areas chosen for their different patterns of human presence and incidences of malaria (anthropic zone 1, anthropic zone 2, transition zone and sylvatic zone). Natural Plasmodium infection was detected by nested PCR based on amplification of the 18S rRNA gene. Results: In total, 6,073 anophelines were collected from May 2009 to April 2011, and six species were identified in the four zones. Anopheles cruzii was the predominant species in the three environments but was more abundant in the sylvatic zone. Anopheles (Kerteszia) cruzii specimens from the anthropic and sylvatic zones were positive for P. vivax and P. malariae. An. (Ker.) bellator, An. (Nys.) triannulatus, An. (Nys.) strodei, An. (Nys.) lutzi and An. (Ano) maculipes were found in small numbers. Of these, An. (Nys.) triannulatus and An. (Nys.) lutzi, which were collected in the anthropic zone, were naturally infected with P. vivax while An. (Nys.) triannulatus from the anthropic zones and An. (Nys.) strodei from the transition zone were positive for P. malariae. Conclusion: These results confirm that Anopheles (Kerteszia) cruzii plays an important role as a major Plasmodium vector. However, the finding of other naturally infected species may indicate that secondary vectors are also involved in the transmission of malaria in the study areas. These findings can be expected to help in the implementation of new measures to control autochthonous malaria in areas of the Atlantic Forest. |
ArticleNumber | 58 |
Author | Pereira, Diego M Fernandes, Lícia N Malafronte, Rosely S Urbinatti, Paulo R Mello, Maria Helena S H Mucci, Luís F Ribeiro, Andressa F Natal, Delsio Fernandes, Aristides Duarte, Ana Maria R C Matos, Jr, Marco O de Paula, Marcia B |
AuthorAffiliation | 4 Culicid Laboratory/SR-03, SUCEN, Pça. Coronel Vitoriano 23, Taubaté 12020-020, Brazil 6 Department of Infectious and Parasitic Diseases, Faculty of Medicine, University of São Paulo, Av Dr Arnaldo 455, São Paulo, 01246-903, Brazil 1 Biochemistry and Molecular Biology Laboratory, Superintendency for the Control of Endemic Diseases (SUCEN), Rua Paula Souza 166, São Paulo 01027-000, Brazil 2 Epidemiology Department, Faculty of Public Health, University of São Paulo, Av. Dr. Arnaldo715, São Paulo 01246-904, Brazil 3 Zoonosis Control Center, Laboratory for the Identification of and Research into Synanthropic Fauna/Lab-Fauna, Rua Santa Eulália 86, São Paulo 02031-020, Brazil 5 Protozoology Laboratory, Institute of Tropical Medicine, University of São Paulo, Av. Dr. Enéas de Carvalho Aguiar 470, São Paulo 05403-000, Brazil |
AuthorAffiliation_xml | – name: 3 Zoonosis Control Center, Laboratory for the Identification of and Research into Synanthropic Fauna/Lab-Fauna, Rua Santa Eulália 86, São Paulo 02031-020, Brazil – name: 2 Epidemiology Department, Faculty of Public Health, University of São Paulo, Av. Dr. Arnaldo715, São Paulo 01246-904, Brazil – name: 4 Culicid Laboratory/SR-03, SUCEN, Pça. Coronel Vitoriano 23, Taubaté 12020-020, Brazil – name: 5 Protozoology Laboratory, Institute of Tropical Medicine, University of São Paulo, Av. Dr. Enéas de Carvalho Aguiar 470, São Paulo 05403-000, Brazil – name: 1 Biochemistry and Molecular Biology Laboratory, Superintendency for the Control of Endemic Diseases (SUCEN), Rua Paula Souza 166, São Paulo 01027-000, Brazil – name: 6 Department of Infectious and Parasitic Diseases, Faculty of Medicine, University of São Paulo, Av Dr Arnaldo 455, São Paulo, 01246-903, Brazil |
Author_xml | – sequence: 1 givenname: Ana Maria R C surname: Duarte fullname: Duarte, Ana Maria R C email: amrcd2@gmail.com organization: Biochemistry and Molecular Biology Laboratory, Superintendency for the Control of Endemic Diseases, Rua Paula Souza 166, São Paulo 01027-000, Brazil. amrcd2@gmail.com – sequence: 2 givenname: Diego M surname: Pereira fullname: Pereira, Diego M – sequence: 3 givenname: Marcia B surname: de Paula fullname: de Paula, Marcia B – sequence: 4 givenname: Aristides surname: Fernandes fullname: Fernandes, Aristides – sequence: 5 givenname: Paulo R surname: Urbinatti fullname: Urbinatti, Paulo R – sequence: 6 givenname: Andressa F surname: Ribeiro fullname: Ribeiro, Andressa F – sequence: 7 givenname: Maria Helena S H surname: Mello fullname: Mello, Maria Helena S H – sequence: 8 givenname: Marco O surname: Matos, Jr fullname: Matos, Jr, Marco O – sequence: 9 givenname: Luís F surname: Mucci fullname: Mucci, Luís F – sequence: 10 givenname: Lícia N surname: Fernandes fullname: Fernandes, Lícia N – sequence: 11 givenname: Delsio surname: Natal fullname: Natal, Delsio – sequence: 12 givenname: Rosely S surname: Malafronte fullname: Malafronte, Rosely S |
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SubjectTerms | Animals Anopheles Anopheles - parasitology Anopheles cruzii Bellator Brazil - epidemiology Ecosystem Female Humans Insect Vectors - parasitology Kerteszia Malaria - epidemiology Malaria - parasitology Plasmodium Plasmodium - classification Plasmodium - genetics Plasmodium - isolation & purification Trees |
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Title | Natural infection in anopheline species and its implications for autochthonous malaria in the Atlantic Forest in Brazil |
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