scholarly journals SYBR green-based detection of Leishmania infantum DNA using peripheral blood samples

2014 ◽  
Vol 40 (1) ◽  
pp. 81-87 ◽  
Author(s):  
Mehrdad Ghasemian ◽  
Mohammad Javad Gharavi ◽  
Lame Akhlaghi ◽  
Mehdi Mohebali ◽  
Ahmad Reza Meamar ◽  
...  
2008 ◽  
Vol 7 (2) ◽  
pp. 175-181
Author(s):  
Mohammad Ali Hossein . ◽  
Leila Mehdizadeh Fan . ◽  
Abbass Ali Hosseinpo . ◽  
Mohammad Ali Mahmood . ◽  
Safar Farajnia . ◽  
...  

2017 ◽  
Vol 2017 ◽  
pp. 1-10 ◽  
Author(s):  
Fernanda Alvarenga Cardoso Medeiros ◽  
Luciana Inácia Gomes ◽  
Edward Oliveira ◽  
Carolina Senra Alves de Souza ◽  
Maria Vitória Mourão ◽  
...  

AkDNAPCR enzyme-linked immunosorbent assay (kDNAPCR-ELISA) for the diagnosis of human visceral leishmaniasis (HVL) was developed. The detection limit of the reaction, precision measurements, and cut-off of thekDNAPCR-ELISA were defined in a proof-of-concept phase. A reference strain ofLeishmania (Leishmania) infantumand a bank of 14 peripheral blood samples from immunocompetent patients with VL were characterized using techniques considered gold standards, and 11 blood samples obtained from healthy individuals of an endemic area were also assessed. Phase II evaluation determined the performance of the assay in peripheral blood samples from 105 patients with VL (adults and children), 25 patients withLeishmania/HIV coinfection, 40 healthy individuals, and 33 asymptomatic individuals living in endemic areas. ThekDNAPCR-ELISA exhibited satisfactory precision, with a detection limit of 0.07 fg of DNA fromL.(L.) infantumand 1 parasite/mL blood. The overall sensitivity of the assay for all groups studied was 100% (95% confidence interval [CI]: 97.1–100%), and the specificity was 95% (95% CI: 83.5–98.6%). ThekDNAPCR-ELISA was shown to be a useful tool for VL symptomatic and asymptomatic individuals diagnosis and its use in endemic countries may help monitor control interventions.


2021 ◽  
Vol 134 ◽  
pp. 58-63
Author(s):  
Matheus Fujimura Soares ◽  
Larissa Martins Melo ◽  
Jaqueline Poleto Bragato ◽  
Amanda de Oliveira Furlan ◽  
Natália Francisco Scaramele ◽  
...  

HPB ◽  
2018 ◽  
Vol 20 ◽  
pp. S262
Author(s):  
R. Martins ◽  
C. Martín-Sierra ◽  
P. Laranjeira ◽  
A.M. Abrantes ◽  
J.G. Tralhão ◽  
...  

2003 ◽  
Vol 71 (11) ◽  
pp. 6668-6671 ◽  
Author(s):  
W. Evan Secor ◽  
Amil Shah ◽  
Pauline M. N. Mwinzi ◽  
Bryson A. Ndenga ◽  
Caroline O. Watta ◽  
...  

ABSTRACT Distribution of chemokine receptors CCR5 and CXCR4, which are also coreceptors for human immunodeficiency virus type 1 invasion of cells, was measured on the surfaces of CD4+ T cells and monocytes in peripheral blood samples from a group of Kenyan car washers. Patients with active schistosomiasis displayed higher cell surface densities of these receptors than did cured schistosomiasis patients.


Author(s):  
Erik Artur Cortinhas Alves ◽  
Raissa Coelho Andrade ◽  
Carlos Eduardo de Melo Amaral ◽  
Milena Coelho Fernandes Caldato ◽  
Adriana Maria Rocha Bastos ◽  
...  

AbstractPrimary congenital hypothyroidism (PCH) has an incidence of approximately 1 in each 3000–4000 live births. In the last two decades, nearly 50 types of the distinct inactivating mutations have already been described in the coding region of the tshr gene. The aim of present study was to investigate tshr gene mutations in patients with primary congenital hypothyroidism, analyzing a sample of 106 patients that were diagnosed with PCH. Genomic DNA was isolated from peripheral blood samples, and 10 exons from the TSH receptor were automatically sequenced. Five nucleotide alterations (P52T, N187N, A459A, L645L, and D727E. N187N and D727E polymorphisms) were associated with positive medical history. In view of the clinical, biochemical and molecular heterogeneity of the etiology of the PCH, the study of polymorphisms is critical for investigating the possible associations with prevailing symptoms of this disorder.


2017 ◽  
Vol 2017 ◽  
pp. 1-6 ◽  
Author(s):  
Fengjie Wu ◽  
Jun Zhu ◽  
Yongjiang Mao ◽  
Xiaomei Li ◽  
Baoguang Hu ◽  
...  

In this study, we identified CTCs using the previously reported CanPatrol CTC enrichment technique from peripheral blood samples of 126 patients with colorectal cancer (CRC) and found that CTCs could be classified into three subpopulations based on expression of epithelial cell adhesion molecule (EpCAM) (E-CTCs), the mesenchymal cell marker vimentin (M-CTCs), or both EpCAM and vimentin (biphenotypic E/M-CTCs). Circulating tumor microemboli (CTMs) were also identified in peripheral blood samples. Meanwhile, E-CTCs, M-CTCs, E/M-CTCs, and CTMs were detected in 76.98%, 42.06%, 56.35%, and 36.51% of the 126 patients, respectively. Interestingly, the presence of CTMs and each CTC subpopulation was significantly associated with blood lymphocyte counts and tumor-node-metastasis stage (P<0.001). Lymphocyte counts and the neutrophil-to-lymphocyte ratio (NLR) in patients lacking CTCs were significantly different from those in patients testing positive for CTMs and each CTC subpopulation (P<0.001). Our results indicate that tumor metastasis is more significantly associated with the presence of CTMs and M-CTCs than with other CTC subpopulations and suggest that EMT may be involved in CTC evasion of lymphocyte-mediated clearance.


Author(s):  
T. Aper ◽  
O. Teebken ◽  
A. Krüger ◽  
A. Heisterkamp ◽  
A. Hilfiker ◽  
...  

1998 ◽  
Vol 36 (1) ◽  
pp. 105-109 ◽  
Author(s):  
François Blot ◽  
Eric Schmidt ◽  
Gérard Nitenberg ◽  
Cyrille Tancrède ◽  
Bernard Leclercq ◽  
...  

To diagnose catheter-related sepsis without removing the catheter, we evaluated the differential positivity times of cultures of blood drawn simultaneously from central venous catheter and peripheral sites. In a 450-bed cancer reference center, simultaneous central- and peripheral-blood cultures were prospectively performed for patients with suspicion of catheter-related sepsis over an 18-month period. Data for 64 patients for whom the same microorganisms were found when central- and peripheral-blood samples were cultured were retrospectively reviewed by two independent physicians blinded to the differential positivity time values in order to establish or refute the diagnosis of catheter-related sepsis. The diagnosis was established in 28 cases, refuted in 14, and indeterminate in the remaining 22. The differential positivity time was significantly greater for patients with catheter-related sepsis (P < 10−4). A cutoff limit of +120 min had 100% specificity and 96.4% sensitivity for the diagnosis of catheter-related sepsis. These results strongly suggest that measurement of the differential positivity time might be a reliable tool facilitating the diagnosis of catheter-related sepsis in patients with an indwelling catheter.


2003 ◽  
Vol 2 (1) ◽  
pp. 179
Author(s):  
A. Meye ◽  
U. Bilkenroth ◽  
U. Schmidt ◽  
Ms. Blümke ◽  
S. Füssel ◽  
...  

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