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Suitability of current typing procedures to identify epidemiologically linked human Giardia duodenalis isolates

BACKGROUND: Giardia duodenalis is a leading cause of gastroenteritis worldwide. Humans are mainly infected by two different subtypes, i.e., assemblage A and B. Genotyping is hampered by allelic sequence heterozygosity (ASH) mainly in assemblage B, and by occurrence of mixed infections. Here we asses...

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Autores principales: Woschke, Andreas, Faber, Mirko, Stark, Klaus, Holtfreter, Martha, Mockenhaupt, Frank, Richter, Joachim, Regnath, Thomas, Sobottka, Ingo, Reiter-Owona, Ingrid, Diefenbach, Andreas, Gosten-Heinrich, Petra, Friesen, Johannes, Ignatius, Ralf, Aebischer, Toni, Klotz, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8023459/
https://www.ncbi.nlm.nih.gov/pubmed/33764999
http://dx.doi.org/10.1371/journal.pntd.0009277
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author Woschke, Andreas
Faber, Mirko
Stark, Klaus
Holtfreter, Martha
Mockenhaupt, Frank
Richter, Joachim
Regnath, Thomas
Sobottka, Ingo
Reiter-Owona, Ingrid
Diefenbach, Andreas
Gosten-Heinrich, Petra
Friesen, Johannes
Ignatius, Ralf
Aebischer, Toni
Klotz, Christian
author_facet Woschke, Andreas
Faber, Mirko
Stark, Klaus
Holtfreter, Martha
Mockenhaupt, Frank
Richter, Joachim
Regnath, Thomas
Sobottka, Ingo
Reiter-Owona, Ingrid
Diefenbach, Andreas
Gosten-Heinrich, Petra
Friesen, Johannes
Ignatius, Ralf
Aebischer, Toni
Klotz, Christian
author_sort Woschke, Andreas
collection PubMed
description BACKGROUND: Giardia duodenalis is a leading cause of gastroenteritis worldwide. Humans are mainly infected by two different subtypes, i.e., assemblage A and B. Genotyping is hampered by allelic sequence heterozygosity (ASH) mainly in assemblage B, and by occurrence of mixed infections. Here we assessed the suitability of current genotyping protocols of G. duodenalis for epidemiological applications such as molecular tracing of transmission chains. METHODOLOGY/PRINCIPAL FINDINGS: Two G. duodenalis isolate collections, from an outpatient tropical medicine clinic and from several primary care laboratories, were characterized by assemblage-specific qPCR (TIF, CATH gene loci) and a common multi locus sequence typing (MLST; TPI, BG, GDH gene loci). Assemblage A isolates were further typed at additional loci (HCMP22547, CID1, RHP26, HCMP6372, DIS3, NEK15411). Of 175/202 (86.6%) patients the G. duodenalis assemblage could be identified: Assemblages A 25/175 (14.3%), B 115/175 (65.7%) and A+B mixed 35/175 (20.0%). By incorporating allelic sequence heterozygosity in the analysis, the three marker MLST correctly identified 6/9 (66,7%) and 4/5 (80.0%) consecutive samples from chronic assemblage B infections in the two collections, respectively, and identified a cluster of five independent patients carrying assemblage B parasites of identical MLST type. Extended MLST for assemblage A altogether identified 5/6 (83,3%) consecutive samples from chronic assemblage A infections and 15 novel genotypes. Based on the observed A+B mixed infections it is estimated that only 75% and 50% of assemblage A or B only cases represent single strain infections, respectively. We demonstrate that typing results are consistent with this prediction. CONCLUSIONS/SIGNIFICANCE: Typing of assemblage A and B isolates with resolution for epidemiological applications is possible but requires separate genotyping protocols. The high frequency of multiple infections and their impact on typing results are findings with immediate consequences for result interpretation in this field.
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spelling pubmed-80234592021-04-15 Suitability of current typing procedures to identify epidemiologically linked human Giardia duodenalis isolates Woschke, Andreas Faber, Mirko Stark, Klaus Holtfreter, Martha Mockenhaupt, Frank Richter, Joachim Regnath, Thomas Sobottka, Ingo Reiter-Owona, Ingrid Diefenbach, Andreas Gosten-Heinrich, Petra Friesen, Johannes Ignatius, Ralf Aebischer, Toni Klotz, Christian PLoS Negl Trop Dis Research Article BACKGROUND: Giardia duodenalis is a leading cause of gastroenteritis worldwide. Humans are mainly infected by two different subtypes, i.e., assemblage A and B. Genotyping is hampered by allelic sequence heterozygosity (ASH) mainly in assemblage B, and by occurrence of mixed infections. Here we assessed the suitability of current genotyping protocols of G. duodenalis for epidemiological applications such as molecular tracing of transmission chains. METHODOLOGY/PRINCIPAL FINDINGS: Two G. duodenalis isolate collections, from an outpatient tropical medicine clinic and from several primary care laboratories, were characterized by assemblage-specific qPCR (TIF, CATH gene loci) and a common multi locus sequence typing (MLST; TPI, BG, GDH gene loci). Assemblage A isolates were further typed at additional loci (HCMP22547, CID1, RHP26, HCMP6372, DIS3, NEK15411). Of 175/202 (86.6%) patients the G. duodenalis assemblage could be identified: Assemblages A 25/175 (14.3%), B 115/175 (65.7%) and A+B mixed 35/175 (20.0%). By incorporating allelic sequence heterozygosity in the analysis, the three marker MLST correctly identified 6/9 (66,7%) and 4/5 (80.0%) consecutive samples from chronic assemblage B infections in the two collections, respectively, and identified a cluster of five independent patients carrying assemblage B parasites of identical MLST type. Extended MLST for assemblage A altogether identified 5/6 (83,3%) consecutive samples from chronic assemblage A infections and 15 novel genotypes. Based on the observed A+B mixed infections it is estimated that only 75% and 50% of assemblage A or B only cases represent single strain infections, respectively. We demonstrate that typing results are consistent with this prediction. CONCLUSIONS/SIGNIFICANCE: Typing of assemblage A and B isolates with resolution for epidemiological applications is possible but requires separate genotyping protocols. The high frequency of multiple infections and their impact on typing results are findings with immediate consequences for result interpretation in this field. Public Library of Science 2021-03-25 /pmc/articles/PMC8023459/ /pubmed/33764999 http://dx.doi.org/10.1371/journal.pntd.0009277 Text en © 2021 Woschke et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Woschke, Andreas
Faber, Mirko
Stark, Klaus
Holtfreter, Martha
Mockenhaupt, Frank
Richter, Joachim
Regnath, Thomas
Sobottka, Ingo
Reiter-Owona, Ingrid
Diefenbach, Andreas
Gosten-Heinrich, Petra
Friesen, Johannes
Ignatius, Ralf
Aebischer, Toni
Klotz, Christian
Suitability of current typing procedures to identify epidemiologically linked human Giardia duodenalis isolates
title Suitability of current typing procedures to identify epidemiologically linked human Giardia duodenalis isolates
title_full Suitability of current typing procedures to identify epidemiologically linked human Giardia duodenalis isolates
title_fullStr Suitability of current typing procedures to identify epidemiologically linked human Giardia duodenalis isolates
title_full_unstemmed Suitability of current typing procedures to identify epidemiologically linked human Giardia duodenalis isolates
title_short Suitability of current typing procedures to identify epidemiologically linked human Giardia duodenalis isolates
title_sort suitability of current typing procedures to identify epidemiologically linked human giardia duodenalis isolates
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8023459/
https://www.ncbi.nlm.nih.gov/pubmed/33764999
http://dx.doi.org/10.1371/journal.pntd.0009277
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