2023
DOI: 10.1016/j.exppara.2023.108478
|View full text |Cite
|
Sign up to set email alerts
|

Outbreak of Chagas disease in Brazil: Validation of a molecular diagnostic method

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
5
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
5

Relationship

3
2

Authors

Journals

citations
Cited by 5 publications
(6 citation statements)
references
References 36 publications
0
5
0
Order By: Relevance
“…No Brasil, a PCR quantitativa também foi exitosa na avaliação da DC aguda em amostras de 77 pacientes pernambucanos, chegando-se a conclusão de que a qPCR deveria ser incorporada ao diagnóstico de casos suspeitos de DC aguda (68). Além disso, o qPCR foi considerado uma ferramenta auxiliar para estudos que requeiram o isolamento do T. cruzi da corrente sanguínea de pacientes com DC crônica, após o estabelecimento de um ponto de corte de carga parasitária que garanta uma taxa relativa de sucesso (44,54,62).…”
Section: Resultsunclassified
“…No Brasil, a PCR quantitativa também foi exitosa na avaliação da DC aguda em amostras de 77 pacientes pernambucanos, chegando-se a conclusão de que a qPCR deveria ser incorporada ao diagnóstico de casos suspeitos de DC aguda (68). Além disso, o qPCR foi considerado uma ferramenta auxiliar para estudos que requeiram o isolamento do T. cruzi da corrente sanguínea de pacientes com DC crônica, após o estabelecimento de um ponto de corte de carga parasitária que garanta uma taxa relativa de sucesso (44,54,62).…”
Section: Resultsunclassified
“…Then, the final pellet was transferred to 1.5 mL microtubes, and extraction was performed with the QIAamp DNA Mini Kit – QIAGEN according to the manufacturer‘s recommendations. The primers TcSAT1 – F (5′AAATTCCTCCAAGCAGCGGA3′) and TcSAT2 – R (5′ ATGAATGGCGGGAGTCAGAG3′) were used to amplify the T. cruzi satellite DNA (SAT-DNA), as described previously ( 21 ). T. cruzi genomic DNA (strain Y) was used to generate a standard curve to quantify the parasite load in samples by quantitative PCR (qPCR).…”
Section: Methodsmentioning
confidence: 99%
“…T. cruzi genomic DNA (strain Y) was used to generate a standard curve to quantify the parasite load in samples by quantitative PCR (qPCR). Quantification of parasite load was performed with the QuantStudio 5 Real-Time PCR System (Thermo Fisher Scientific) using the TcSAT-IAM system ( 21 ). Samples were tested in duplicate at all stages.…”
Section: Methodsmentioning
confidence: 99%
“…7,17 Conflicting results may be explained by an insufficient antibody production, and, in these cases, molecular methods for detection of T. cruzi DNA have been used as an excellent alternative for these cases. [18][19][20] Immunochromatography (rapid test) has been used for point-of-care testing of T-cruzi infection among family members of patients in field works or at outpatient clinics. 21 Serological tests are subsequently performed to confirm.…”
Section: Laboratorymentioning
confidence: 99%
“…Recently, one of the largest outbreaks in Brazil has occurred in Pernambuco, and the diagnosis of suspected cases was only possible by real-time polymerase chain reaction (PCR) using the TcSAT-IAM. 18 Besides, this method has been suggested to monitor the etiological treatment in the chronic phase, 22 since today the criteria for cure of CD is antibody decay analyzed by serological techniques, which may take many years.…”
Section: Laboratorymentioning
confidence: 99%