Transient infection of the zebrafish notochord with E. coli induces chronic inflammation

Zebrafish embryos and larvae are now well-established models in which to study infectious diseases. Infections with non-pathogenic Gram-negative Escherichia coli induce a strong and reproducible inflammatory response. Here, we study the cellular response of zebrafish larvae when E. coli bacteria are...

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Main Authors: Mai Nguyen-Chi, Quang Tien Phan, Catherine Gonzalez, Jean-François Dubremetz, Jean-Pierre Levraud, Georges Lutfalla
Format: Article
Language:English
Published: The Company of Biologists 2014-07-01
Series:Disease Models & Mechanisms
Subjects:
Online Access:http://dmm.biologists.org/content/7/7/871
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spelling doaj-9db47b3c6f6549b989de7300348bdd9c2020-11-25T01:51:46ZengThe Company of BiologistsDisease Models & Mechanisms1754-84031754-84112014-07-017787188210.1242/dmm.014498014498Transient infection of the zebrafish notochord with E. coli induces chronic inflammationMai Nguyen-ChiQuang Tien PhanCatherine GonzalezJean-François DubremetzJean-Pierre LevraudGeorges LutfallaZebrafish embryos and larvae are now well-established models in which to study infectious diseases. Infections with non-pathogenic Gram-negative Escherichia coli induce a strong and reproducible inflammatory response. Here, we study the cellular response of zebrafish larvae when E. coli bacteria are injected into the notochord and describe the effects. First, we provide direct evidence that the notochord is a unique organ that is inaccessible to leukocytes (macrophages and neutrophils) during the early stages of inflammation. Second, we show that notochord infection induces a host response that is characterised by rapid clearance of the bacteria, strong leukocyte recruitment around the notochord and prolonged inflammation that lasts several days after bacteria clearance. During this inflammatory response, il1b is first expressed in macrophages and subsequently at high levels in neutrophils. Moreover, knock down of il1b alters the recruitment of neutrophils to the notochord, demonstrating the important role of this cytokine in the maintenance of inflammation in the notochord. Eventually, infection of the notochord induces severe defects of the notochord that correlate with neutrophil degranulation occurring around this tissue. This is the first in vivo evidence that neutrophils can degranulate in the absence of a direct encounter with a pathogen. Persistent inflammation, neutrophil infiltration and restructuring of the extracellular matrix are defects that resemble those seen in bone infection and in some chondropathies. As the notochord is a transient embryonic structure that is closely related to cartilage and bone and that contributes to vertebral column formation, we propose infection of the notochord in zebrafish larvae as a new model to study the cellular and molecular mechanisms underlying cartilage and bone inflammation.http://dmm.biologists.org/content/7/7/871ZebrafishNeutrophilsInflammationInterleukin-1β
collection DOAJ
language English
format Article
sources DOAJ
author Mai Nguyen-Chi
Quang Tien Phan
Catherine Gonzalez
Jean-François Dubremetz
Jean-Pierre Levraud
Georges Lutfalla
spellingShingle Mai Nguyen-Chi
Quang Tien Phan
Catherine Gonzalez
Jean-François Dubremetz
Jean-Pierre Levraud
Georges Lutfalla
Transient infection of the zebrafish notochord with E. coli induces chronic inflammation
Disease Models & Mechanisms
Zebrafish
Neutrophils
Inflammation
Interleukin-1β
author_facet Mai Nguyen-Chi
Quang Tien Phan
Catherine Gonzalez
Jean-François Dubremetz
Jean-Pierre Levraud
Georges Lutfalla
author_sort Mai Nguyen-Chi
title Transient infection of the zebrafish notochord with E. coli induces chronic inflammation
title_short Transient infection of the zebrafish notochord with E. coli induces chronic inflammation
title_full Transient infection of the zebrafish notochord with E. coli induces chronic inflammation
title_fullStr Transient infection of the zebrafish notochord with E. coli induces chronic inflammation
title_full_unstemmed Transient infection of the zebrafish notochord with E. coli induces chronic inflammation
title_sort transient infection of the zebrafish notochord with e. coli induces chronic inflammation
publisher The Company of Biologists
series Disease Models & Mechanisms
issn 1754-8403
1754-8411
publishDate 2014-07-01
description Zebrafish embryos and larvae are now well-established models in which to study infectious diseases. Infections with non-pathogenic Gram-negative Escherichia coli induce a strong and reproducible inflammatory response. Here, we study the cellular response of zebrafish larvae when E. coli bacteria are injected into the notochord and describe the effects. First, we provide direct evidence that the notochord is a unique organ that is inaccessible to leukocytes (macrophages and neutrophils) during the early stages of inflammation. Second, we show that notochord infection induces a host response that is characterised by rapid clearance of the bacteria, strong leukocyte recruitment around the notochord and prolonged inflammation that lasts several days after bacteria clearance. During this inflammatory response, il1b is first expressed in macrophages and subsequently at high levels in neutrophils. Moreover, knock down of il1b alters the recruitment of neutrophils to the notochord, demonstrating the important role of this cytokine in the maintenance of inflammation in the notochord. Eventually, infection of the notochord induces severe defects of the notochord that correlate with neutrophil degranulation occurring around this tissue. This is the first in vivo evidence that neutrophils can degranulate in the absence of a direct encounter with a pathogen. Persistent inflammation, neutrophil infiltration and restructuring of the extracellular matrix are defects that resemble those seen in bone infection and in some chondropathies. As the notochord is a transient embryonic structure that is closely related to cartilage and bone and that contributes to vertebral column formation, we propose infection of the notochord in zebrafish larvae as a new model to study the cellular and molecular mechanisms underlying cartilage and bone inflammation.
topic Zebrafish
Neutrophils
Inflammation
Interleukin-1β
url http://dmm.biologists.org/content/7/7/871
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