Polycystic Kidney Disease: An Unrecognized Emerging Infectious Disease?

Polycystic kidney disease (PKD) is one of the most common genetic diseases in humans. We contend that it may be an emerging infectious disease and/or microbial toxicosis in a vulnerable human subpopulation. Use of a differential activation protocol for the Limulus amebocyte lysate (LAL) assay showed...

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Main Authors: Marcia A. Miller-Hjelle, J. Thomas Hjelle, Monica Jones, William R. Mayberry, Mary Ann Dombrink-Kurtzman, Stephen W. Peterson, Deborah M. Nowak, Frank S. Darras
Format: Article
Language:English
Published: Centers for Disease Control and Prevention 1997-06-01
Series:Emerging Infectious Diseases
Subjects:
Online Access:https://wwwnc.cdc.gov/eid/article/3/2/97-0204_article
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spelling doaj-10796ecc120c48609a4841ef59bc84802020-11-25T00:36:31ZengCenters for Disease Control and PreventionEmerging Infectious Diseases1080-60401080-60591997-06-013211312710.3201/eid0302.970204Polycystic Kidney Disease: An Unrecognized Emerging Infectious Disease?Marcia A. Miller-HjelleJ. Thomas HjelleMonica JonesWilliam R. MayberryMary Ann Dombrink-KurtzmanStephen W. PetersonDeborah M. NowakFrank S. DarrasPolycystic kidney disease (PKD) is one of the most common genetic diseases in humans. We contend that it may be an emerging infectious disease and/or microbial toxicosis in a vulnerable human subpopulation. Use of a differential activation protocol for the Limulus amebocyte lysate (LAL) assay showed bacterial endotoxin and fungal (13)-ß-D-glucans in cyst fluids from human kidneys with PKD. Fatty acid analysis of cyst fluid confirmed the presence of 3-hydroxy fatty acids characteristic of endotoxin. Tissue and cyst fluid from three PKD patients were examined for fungal components. Serologic tests showed Fusarium, Aspergillus, and Candida antigens. IgE, but not IgG, reactive with Fusarium and Candida were also detected in cyst fluid. Fungal DNA was detected in kidney tissue and cyst fluid from these three PKD patients, but not in healthy human kidney tissue. We examine the intertwined nature of the actions of endotoxin and fungal components, sphingolipid biology in PKD, the structure of PKD gene products, infections, and integrity of gut function to establish a mechanistic hypothesis for microbial provocation of human cystic disease. Proof of this hypothesis will require identification of the microbes and microbial components involved and multifaceted studies of PKD cell biology.https://wwwnc.cdc.gov/eid/article/3/2/97-0204_articleUnited States
collection DOAJ
language English
format Article
sources DOAJ
author Marcia A. Miller-Hjelle
J. Thomas Hjelle
Monica Jones
William R. Mayberry
Mary Ann Dombrink-Kurtzman
Stephen W. Peterson
Deborah M. Nowak
Frank S. Darras
spellingShingle Marcia A. Miller-Hjelle
J. Thomas Hjelle
Monica Jones
William R. Mayberry
Mary Ann Dombrink-Kurtzman
Stephen W. Peterson
Deborah M. Nowak
Frank S. Darras
Polycystic Kidney Disease: An Unrecognized Emerging Infectious Disease?
Emerging Infectious Diseases
United States
author_facet Marcia A. Miller-Hjelle
J. Thomas Hjelle
Monica Jones
William R. Mayberry
Mary Ann Dombrink-Kurtzman
Stephen W. Peterson
Deborah M. Nowak
Frank S. Darras
author_sort Marcia A. Miller-Hjelle
title Polycystic Kidney Disease: An Unrecognized Emerging Infectious Disease?
title_short Polycystic Kidney Disease: An Unrecognized Emerging Infectious Disease?
title_full Polycystic Kidney Disease: An Unrecognized Emerging Infectious Disease?
title_fullStr Polycystic Kidney Disease: An Unrecognized Emerging Infectious Disease?
title_full_unstemmed Polycystic Kidney Disease: An Unrecognized Emerging Infectious Disease?
title_sort polycystic kidney disease: an unrecognized emerging infectious disease?
publisher Centers for Disease Control and Prevention
series Emerging Infectious Diseases
issn 1080-6040
1080-6059
publishDate 1997-06-01
description Polycystic kidney disease (PKD) is one of the most common genetic diseases in humans. We contend that it may be an emerging infectious disease and/or microbial toxicosis in a vulnerable human subpopulation. Use of a differential activation protocol for the Limulus amebocyte lysate (LAL) assay showed bacterial endotoxin and fungal (13)-ß-D-glucans in cyst fluids from human kidneys with PKD. Fatty acid analysis of cyst fluid confirmed the presence of 3-hydroxy fatty acids characteristic of endotoxin. Tissue and cyst fluid from three PKD patients were examined for fungal components. Serologic tests showed Fusarium, Aspergillus, and Candida antigens. IgE, but not IgG, reactive with Fusarium and Candida were also detected in cyst fluid. Fungal DNA was detected in kidney tissue and cyst fluid from these three PKD patients, but not in healthy human kidney tissue. We examine the intertwined nature of the actions of endotoxin and fungal components, sphingolipid biology in PKD, the structure of PKD gene products, infections, and integrity of gut function to establish a mechanistic hypothesis for microbial provocation of human cystic disease. Proof of this hypothesis will require identification of the microbes and microbial components involved and multifaceted studies of PKD cell biology.
topic United States
url https://wwwnc.cdc.gov/eid/article/3/2/97-0204_article
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