Corrigendum: Comparison of 21-Plex PCR and API 20C AUX, MALDI-TOF MS, and rDNA Sequencing for a Wide Range of Clinically Isolated Yeast Species: Improved Identification by Combining 21-Plex PCR and API 20C AUX as an Alternative Strategy for Developing Countries

Arastehfar, Amir; Daneshnia, Farnaz; Kord, Mohammad; Roudbary, Maryam; Zarrinfar, Hossein; Fang, Wenjie; Hashemi, Sayed Jamal; Najafzadeh, Mohammad Javad; Khodavaisy, Sadegh; Pan, Weihua; Liao, Wanqing; Badali, Hamid; Rezaie, Sassan; Zomorodian, Kamiar; Hagen, Ferry; Boekhout, Teun

doi:10.3389/fcimb.2019.00176

CORRECTION article

Front. Cell. Infect. Microbiol. , 28 May 2019

Sec. Clinical Microbiology

Volume 9 - 2019 | https://doi.org/10.3389/fcimb.2019.00176

Corrigendum: Comparison of 21-Plex PCR and API 20C AUX, MALDI-TOF MS, and rDNA Sequencing for a Wide Range of Clinically Isolated Yeast Species: Improved Identification by Combining 21-Plex PCR and API 20C AUX as an Alternative Strategy for Developing Countries

This article is a correction to:

Comparison of 21-Plex PCR and API 20C AUX, MALDI-TOF MS, and rDNA Sequencing for a Wide Range of Clinically Isolated Yeast Species: Improved Identification by Combining 21-Plex PCR and API 20C AUX as an Alternative Strategy for Developing Countries
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$\nAmir Arastehfar&#x;$ Amir Arastehfar¹^†

Farnaz Daneshnia¹^†

Mohammad Kord²

Maryam Roudbary³

Hossein Zarrinfar⁴

Wenjie Fang⁵

Sayed Jamal Hashemi^2,6

Mohammad Javad Najafzadeh⁷

Sadegh Khodavaisy^2,8^*

Weihua Pan⁵^*

Wanqing Liao⁵

Hamid Badali⁹

Sassan Rezaie²

Kamiar Zomorodian¹⁰

Ferry Hagen¹

Teun Boekhout^1,5,11

¹Yeast Biodiversity Department, Westerdijk Fungal Biodiversity Institute, Utrecht, Netherlands
²Department of Medical Parasitology and Mycology, Tehran University of Medical Sciences, Tehran, Iran
³Department of Medical Mycology and Parasitology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran
⁴Allergy Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
⁵Shanghai Key Laboratory of Molecular Medical Mycology, Department of Dermatology, Shanghai Institute of Medical Mycology, Shanghai Changzheng Hospital, Second Military Medical University, Shanghai, China
⁶Food Microbiology Research Center, Tehran University of Medical Sciences, Tehran, Iran
⁷Department of Parasitology and Mycology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
⁸Zoonoses Research Center, Kurdistan University of Medical Sciences, Sanandaj, Iran
⁹Department of Medical Mycology, Invasive Fungi Research Center, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran
¹⁰Department of Medical Mycology and Parasitology, Basic Sciences in Infectious Diseases Research Center, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran
¹¹Yeast Biodiversity Department, Institute of Biodiversity and Ecosystem Dynamics, University of Amsterdam, Amsterdam, Netherlands

A Corrigendum on
Comparison of 21-Plex PCR and API 20C AUX, MALDI-TOF MS, and rDNA Sequencing for a Wide Range of Clinically Isolated Yeast Species: Improved Identification by Combining 21-Plex PCR and API 20C AUX as an Alternative Strategy for Developing Countries

by Arastehfar, A., Daneshnia, F., Kord, M., Roudbary, M., Zarrinfar, H., Fang, W., et al. (2019). Front. Cell. Infect. Microbiol. 9:21. doi: 10.3389/fcimb.2019.00021

An author's name was incorrectly spelled as “Amir Aarstehfar.” The correct spelling is “Amir Arastehfar”.

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Keywords: API 20C AUX, 21-plex PCR, MALDI-TOF MS, LSU rDNA sequencing, developing countries

Citation: Arastehfar A, Daneshnia F, Kord M, Roudbary M, Zarrinfar H, Fang W, Hashemi SJ, Najafzadeh MJ, Khodavaisy S, Pan W, Liao W, Badali H, Rezaie S, Zomorodian K, Hagen F and Boekhout T (2019) Corrigendum: Comparison of 21-Plex PCR and API 20C AUX, MALDI-TOF MS, and rDNA Sequencing for a Wide Range of Clinically Isolated Yeast Species: Improved Identification by Combining 21-Plex PCR and API 20C AUX as an Alternative Strategy for Developing Countries. Front. Cell. Infect. Microbiol. 9:176. doi: 10.3389/fcimb.2019.00176

Received: 21 April 2019; Accepted: 08 May 2019;
Published: 28 May 2019.

Approved by:

Frontiers Editorial Office, Frontiers Media SA, Switzerland

Copyright © 2019 Arastehfar, Daneshnia, Kord, Roudbary, Zarrinfar, Fang, Hashemi, Najafzadeh, Khodavaisy, Pan, Liao, Badali, Rezaie, Zomorodian, Hagen and Boekhout. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Sadegh Khodavaisy, c2FkZWdoXzczOTIwMDhAeWFob28uY29t; Weihua Pan, cGFud2VpaHVhQHNtbXUuZWR1LmNu

^†These authors have contributed equally to this work

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

Corrigendum: Comparison of 21-Plex PCR and API 20C AUX, MALDI-TOF MS, and rDNA Sequencing for a Wide Range of Clinically Isolated Yeast Species: Improved Identification by Combining 21-Plex PCR and API 20C AUX as an Alternative Strategy for Developing Countries

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