Multiplex <scp>qPCR</scp> assay to determine <i>Leishmania infantum</i> load in <i>Lutzomyia longipalpis</i> sandfly samples-Reference-Cited by-同舟云学术

Multiplex qPCR assay to determine Leishmania infantum load in Lutzomyia longipalpis sandfly samples

Published:2022-01-28 Issue:2 Volume:36 Page:176-184
ISSN:0269-283X
Container-title:Medical and Veterinary Entomology
language:en
Short-container-title:Medical Vet Entomology

Author:

Mota Tiago Feitosa¹^ORCID,Brodskyn Claudia Ida¹^ORCID,Morello Luis Gustavo²³^ORCID,Marchini Fabricio Klerynton²³^ORCID,Krieger Marco Aurelio²^ORCID,Cássia Pontello Rampazzo Rita³^ORCID,Fraga Deborah Bittencourt Mothé¹⁴^ORCID

Affiliation:

1. Laboratório de Interação Parasito‐Hospedeiro e Epidemiologia (LaIPHE), Instituto Gonçalo Moniz (IGM) FIOCRUZ‐BA, Rua Waldemar Falcão Salvador Brazil

2. Instituto Carlos Chagas (ICC), FIOCRUZ‐PR Rua Prof. Algacyr Munhoz Mader Curitiba Brazil

3. Instituto de Biologia Molecular do Paraná (IBMP) Rua Professor Algacyr Munhoz Mader Curitiba Brazil

4. Departamento de Medicina Veterinária Preventiva e Produção Animal, Escola de Medicina Veterinária e Zootecnia Universidade Federal da Bahia (UFBA) Salvador Brazil

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

Wiley

Subject

Insect Science,General Veterinary,Ecology, Evolution, Behavior and Systematics,Parasitology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/mve.12564

Reference40 articles.

1. An overview of the sandfly fauna (Diptera: Psychodidae) followed by the detection of Leishmania DNA and blood meal identification in the state of Acre, Amazonian Brazil

2. Multiple internal controls enhance reliability for PCR and real time PCR detection of Rathayibacter toxicus

3. Estimation of population at risk of infection and number of cases of Leishmaniasis

4. The period gene and genetic differentiation between three Brazilian populations of Lutzomyia longipalpis

5. Real-time PCR to assess the Leishmania load in Lutzomyia longipalpis sand flies: Screening of target genes and assessment of quantitative methods

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