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Author Correction: A multicentric evaluation of dipstick test for serodiagnosis of visceral leishmaniasis in India, Nepal, Sri Lanka, Brazil, Ethiopia and Spain

Authors :
Helina Fikre
V. N. R. Das
Nadira D. Karunaweera
Sarfaraz Ahmad Ejazi
Anirban Bhattacharyya
Yamuna Siriwardana
Yara M. Gomes
Arega Yeshanew
Carlos Henrique Nery Costa
Mitali Chatterjee
Samiran Saha
Sneha Ghosh
Bhagya Deepachandi
Basudha Khanal
Rama Prosad Goswami
Nahid Ali
Ermias Diro
Javier Moreno
Krishna Pandey
Mineo Nakazawa
Narayan Raj Bhattarai
Emebet Adem
Mehebubar Rahaman
Zewdu Hurissa
Keshav Rai
Pradeep Das
Maria Edileuza Felinto deBrito
Roma Melkamu
Eugenia Carrillo
Somsubhra Thakur Choudhury
Source :
Scientific Reports, Scientific Reports, Vol 11, Iss 1, Pp 1-2 (2021)
Publication Year :
2021
Publisher :
Nature Publishing Group UK, 2021.

Abstract

Correction to: Scientific Reports https://doi.org/10.1038/s41598-019-46283-9, published online 09 July 2019 The original version of this Article contained an error. The information in the “Dipstick development and assay” section was incomplete. Therefore, the original text, “The assay comprises of incubation of the dipstick with diluted serum samples (1:2000) for 30 min which is followed by washing with TBST (twice). Subsequently, it is incubated with HRP conjugated anti-human IgG (1: 2000) for 30 min. Finally, after two washes in TBST and one in TBS, the strips are dipped in a freshly prepared substrate composed of 0.05% 3, 3′-diaminobenzidine tetrahydrochloride (DAB, Sigma, USA) containing 0.05% of H2O2 in 100 mM TBS. The reaction is stopped by dipping in distilled water. The appearance of dark brown coloured bands at both the test and control line indicates VL positivity and a single band at the control line is indicative of VL negativity.” now reads: “The general assay consists of incubation of the dipsticks with diluted serum (1:2000) samples for 30 min, followed by washing with TBST (twice). Subsequently, it is incubated with HRP conjugated anti-human IgG (1:2000) for 30 min. Finally, after two washes in TBST and one in TBS, the strips are dipped in a freshly prepared substrate composed of 0.05% 3, 3′-diaminobenzidine tetrahydrochloride (DAB, Sigma, USA), containing 0.05% of H2O2 in 100 mM TBS. The reaction is stopped by dipping in distilled water, and the strips dried at RT. In Spain, there were several modifications to the assay; the dipsticks are incubated in diluted serum (1:100), and HRP conjugated anti-human IgG, for 60 min, followed by a 10 min incubation in substrate composed of 0.07% of DAB and 0.2% of H2O2 in 60 mM TBS, before being dried at RT. The appearance of dark brown coloured bands at both the test and control line indicates VL positivity and a single band at the control line is indicative of VL negativity. Whenever this signal was hard to assess, we classified it as not clear, and therefore grouped it together with those displaying no bands. Dipsticks that did not present with a reactive band, or a control band, were excluded from further consideration.” These changes do not affect the overall conclusions of the Article. This has now been corrected in the PDF and HTML versions of the Article.

Details

Language :
English
ISSN :
20452322
Volume :
11
Database :
OpenAIRE
Journal :
Scientific Reports
Accession number :
edsair.doi.dedup.....4ca10ca7f4449c3e8c63abca1e5e1c1b