scholarly journals Intracellular Behaviour of Three Legionella pneumophila Strains within Three Amoeba Strains, Including Willaertia magna C2c Maky

Pathogens ◽  
2020 ◽  
Vol 9 (2) ◽  
pp. 105 ◽  
Author(s):  
Issam Hasni ◽  
Antoine Jarry ◽  
Benjamin Quelard ◽  
Antoine Carlino ◽  
Jean-Baptiste Eberst ◽  
...  
Keyword(s):  
Legionella Pneumophila ◽  
Acanthamoeba Castellanii ◽  
Aquatic Environments ◽  
Intracellular Pathogen ◽  
Planktonic Cells ◽  
Intracellular Growth ◽  
Free Living ◽  
Intracellular Parasites ◽  
Elimination Mechanism

Legionella pneumophila is a facultative intracellular pathogen found in aquatic environments as planktonic cells within biofilms and as intracellular parasites of free-living amoebae such as Acanthamoeba castellanii. This pathogen bypasses the elimination mechanism to replicate within amoebae; however, not all amoeba species support the growth of L. pneumophila. Willaertia magna C2c Maky, a non-pathogenic amoeba, was previously demonstrated to possess the ability to eliminate the L. pneumophila strain Paris. Here, we study the intracellular behaviour of three L. pneumophila strains (Paris, Philadelphia, and Lens) within W. magna C2c Maky and compare this strain to A. castellanii and W. magna Z503, which are used as controls. We observe the intracellular growth of strain Lens within W. magna Z503 and A. castellanii at 22 °C and 37 °C. Strain Paris grows within A. castellanii at any temperature, while it only grows at 22 °C within W. magna Z503. Strain Philadelphia proliferates only within A. castellanii at 37 °C. Within W. magna C2c Maky, none of the three legionella strains exhibit intracellular growth. Additionally, the ability of W. magna C2c Maky to decrease the number of internalized L. pneumophila is confirmed. These results support the idea that W. magna C2c Maky possesses unique behaviour in regard to L. pneumophila strains.

scholarly journals Mitigation of Expression of Virulence Genes in Legionella pneumophila Internalized in the Free-Living Amoeba Willaertia magna C2c Maky

Pathogens ◽  
2020 ◽  
Vol 9 (6) ◽  
pp. 447 ◽  
Author(s):  
Rayane Mouh Mameri ◽  
Jacques Bodennec ◽  
Laurent Bezin ◽  
Sandrine Demanèche
Keyword(s):  
Gene Expression ◽  
Legionella Pneumophila ◽  
Virulence Genes ◽  
Natural Habitat ◽  
Acanthamoeba Castellanii ◽  
Severe Form ◽  
Aquatic Environments ◽  
Free Living ◽  
Intracellular Parasites ◽  
Free Living Amoeba

Legionella pneumophila is a human pathogen responsible for a severe form of pneumonia named Legionnaire disease. Its natural habitat is aquatic environments, being in a free state or intracellular parasites of free-living amoebae, such as Acanthamoeba castellanii. This pathogen is able to replicate within some amoebae. Willaertia magna C2c Maky, a non-pathogenic amoeba, was previously demonstrated to resist to L. pneumophila and even to be able to eliminate the L. pneumophila strains Philadelphia, Lens, and Paris. Here, we studied the induction of seven virulence genes of three L. pneumophila strains (Paris, Philadelphia, and Lens) within W. magna C2c Maky in comparison within A. castellanii and with the gene expression level of L. pneumophila strains alone used as controls. We defined a gene expression-based virulence index to compare easily and without bias the transcript levels in different conditions and demonstrated that W. magna C2c Maky did not increase the virulence of L. pneumophila strains in contrast to A. castellanii. These results confirmed the non-permissiveness of W. magna C2c Maky toward L. pneumophila strains.

scholarly journals Intracellular Growth in Acanthamoeba castellanii Affects Monocyte Entry Mechanisms and Enhances Virulence of Legionella pneumophila

1999 ◽  
Vol 67 (9) ◽  
pp. 4427-4434 ◽  
Author(s):  
Jeffrey D. Cirillo ◽  
Suat L. G. Cirillo ◽  
Ling Yan ◽  
Luiz E. Bermudez ◽  
Stanley Falkow ◽  
...  
Keyword(s):  
Legionella Pneumophila ◽  
Acanthamoeba Castellanii ◽  
Host Cells ◽  
Intracellular Pathogen ◽  
Activated Macrophages ◽  
Standard Laboratory ◽  
Intracellular Growth ◽  
Growth Environment ◽  
Pathogen Entry ◽  
First Time

ABSTRACT Since Legionella pneumophila is an intracellular pathogen, entry into and replication within host cells are thought to be critical to its ability to cause disease. L. pneumophilagrown in one of its environmental hosts, Acanthamoeba castellanii, is phenotypically different from L. pneumophila grown on standard laboratory medium (BCYE agar). Although amoeba-grown L. pneumophila displays enhanced entry into monocytes compared to BCYE-grown bacteria, the mechanisms of entry used and the effects on virulence have not been examined. To explore whether amoeba-grown L. pneumophila differs from BCYE-grown L. pneumophila in these characteristics, we examined entry into monocytes, replication in activated macrophages, and virulence in mice. Entry of amoeba-grown L. pneumophilainto monocytes occurred more frequently by coiling phagocytosis, was less affected by complement opsonization, and was less sensitive to microtubule and microfilament inhibitors than was entry of BCYE-grown bacteria. In addition, amoeba-grown L. pneumophila displays increased replication in monocytes and is more virulent in A/J, C57BL/6 Beige, and C57BL/6 mice. These data demonstrate for the first time that the intra-amoebal growth environment affects the entry mechanisms and virulence of L. pneumophila.

scholarly journals Functional Similarities between the icm/dot Pathogenesis Systems of Coxiella burnetii and Legionella pneumophila

2003 ◽  
Vol 71 (7) ◽  
pp. 3714-3723 ◽  
Author(s):  
Tal Zusman ◽  
Gal Yerushalmi ◽  
Gil Segal
Keyword(s):  
Coxiella Burnetii ◽  
Legionella Pneumophila ◽  
Q Fever ◽  
Acanthamoeba Castellanii ◽  
Insertion Mutant ◽  
Homologous Gene ◽  
Intracellular Pathogen ◽  
Intracellular Growth ◽  
Human Macrophages ◽  
Homologous Genes

ABSTRACT Coxiella burnetii, the etiological agent of Q fever, is an obligate intracellular pathogen, whereas Legionella pneumophila, the causative agent of Legionnaires' disease, is a facultative intracellular pathogen. During infection of humans both of these pathogens multiply in alveolar macrophages inside a closed phagosome. L. pneumophila intracellular multiplication was shown to be dependent on the icm/dot system, which probably encodes a type IV-related translocation apparatus. Recently, genes homologous to all of the L. pneumophila icm/dot genes (besides icmR) were found in C. burnetii. To explore the similarities and differences between the icm/dot pathogenesis systems of these two pathogens, interspecies complementation analysis was performed. Nine C. burnetii icm homologous genes (icmT, icmS, icmQ, icmP, icmO, icmJ, icmB, icmW, and icmX) were cloned under regulation of the corresponding L. pneumophila icm genes and examined for the ability to complement L. pneumophila mutants with mutations in these genes. The C. burnetii icmS and icmW homologous genes were found to complement the corresponding L. pneumophila icm mutants to wild-type levels of intracellular growth in both HL-60-derived human macrophages and Acanthamoeba castellanii. In addition, the C. burnetii icmT homologous gene was found to completely complement an L. pneumophila insertion mutant for intracellular growth in HL-60-derived human macrophages, but it only partially complemented the same mutant for intracellular growth in A. castellanii. Moreover, as previously shown for L. pneumophila, the proteins encoded by the C. burnetii icmS and icmW homologous genes were found to interact with one another, and interspecies protein interaction was observed as well. Our results strongly indicate that the Icm/Dot pathogenesis systems of C. burnetii and L. pneumophila have common features.

The amoebae plate test implicates a paralogue of lpxB in the interaction of Legionella pneumophila with Acanthamoeba castellanii

Microbiology ◽  
2005 ◽  
Vol 151 (1) ◽  
pp. 167-182 ◽  
Author(s):  
Urs Albers ◽  
Katrin Reus ◽  
Howard A. Shuman ◽  
Hubert Hilbi
Keyword(s):  
Legionella Pneumophila ◽  
Lipid A ◽  
Sequence Similarity ◽  
Acanthamoeba Castellanii ◽  
Growth Defect ◽  
Wild Type ◽  
Intracellular Growth ◽  
Plate Test ◽  
Raw264.7 Macrophages ◽  
Mutant Strains

Legionella pneumophila is a bacterial parasite of freshwater amoebae which also grows in alveolar macrophages and thus causes the potentially fatal pneumonia Legionnaires' disease. Intracellular growth within amoebae and macrophages is mechanistically similar and requires the Icm/Dot type IV secretion system. This paper reports the development of an assay, the amoebae plate test (APT), to analyse growth of L. pneumophila wild-type and icm/dot mutant strains spotted on agar plates in the presence of Acanthamoeba castellanii. In the APT, wild-type L. pneumophila formed robust colonies even at high dilutions, icmT, -R, -P or dotB mutants failed to grow, and icmS or -G mutants were partially growth defective. The icmS or icmG mutant strains were used to screen an L. pneumophila chromosomal library for genes that suppress the growth defect in the presence of the amoebae. An icmS suppressor plasmid was isolated that harboured the icmS and flanking icm genes, indicating that this plasmid complements the intracellular growth defect of the mutant. In contrast, different icmG suppressor plasmids rendered the icmG mutant more cytotoxic for A. castellanii without enhancing intracellular multiplication in amoebae or RAW264.7 macrophages. Deletion of individual genes in the suppressor plasmids inserts identified lcs (Legionella cytotoxic suppressor) -A, -B, -C and -D as being required for enhanced cytotoxicity of an icmG mutant strain. The corresponding proteins show sequence similarity to hydrolases, NlpD-related metalloproteases, lipid A disaccharide synthases and ABC transporters, respectively. Overexpression of LcsC, a putative paralogue of the lipid A disaccharide synthase LpxB, increased cytotoxicity of an icmG mutant but not that of other icm/dot or rpoS mutant strains against A. castellanii. Based on sequence comparison and chromosomal location, lcsB and lcsC probably encode enzymes involved in cell wall maintenance and peptidoglycan metabolism. The APT established here may prove useful to identify other bacterial factors relevant for interactions with amoeba hosts.

scholarly journals Legionella pneumophila Contains a Type II General Secretion Pathway Required for Growth in Amoebae as Well as for Secretion of the Msp Protease

1999 ◽  
Vol 67 (7) ◽  
pp. 3662-3666 ◽  
Author(s):  
Laura M. Hales ◽  
Howard A. Shuman
Keyword(s):  
Legionella Pneumophila ◽  
Acanthamoeba Castellanii ◽  
Gram Negative Bacteria ◽  
Type Ii ◽  
Free Living ◽  
Gram Negative ◽  
Secretion Pathway ◽  
Free Living Amoeba ◽  
Substitution Mutation

ABSTRACT We report the identification of a set of Legionella pneumophila genes that encode products with homology to proteins of the type II general secretion pathway of gram-negative bacteria. A strain containing a deletion-substitution mutation of two of these genes was unable to secrete the Msp protease. This strain was unable to multiply within the free-living amoeba Acanthamoeba castellanii yet was able to kill HL-60-derived macrophages. Because Msp is not required for growth in amoebae, other proteins which are important for growth in amoebae are likely secreted by this pathway.

scholarly journals Balamuthia mandrillaris, Free-Living Ameba and Opportunistic Agent of Encephalitis, Is a Potential Host for Legionella pneumophila Bacteria

2005 ◽  
Vol 71 (5) ◽  
pp. 2244-2249 ◽  
Author(s):  
Winlet Sheba Shadrach ◽  
Kerstin Rydzewski ◽  
Ulrike Laube ◽  
Gudrun Holland ◽  
Muhsin Özel ◽  
...  
Keyword(s):  
Legionella Pneumophila ◽  
Mammalian Cells ◽  
Mammalian Species ◽  
Acanthamoeba Castellanii ◽  
Electron Microscopic ◽  
Free Living ◽  
Balamuthia Mandrillaris ◽  
Microscopic Studies ◽  
Legionnaires Disease ◽  
Free Living Ameba

ABSTRACT Balamuthia mandrillaris is a free-living ameba and an opportunistic agent of granulomatous encephalitis in humans and other mammalian species. Other free-living amebas, such as Acanthamoeba and Hartmannella, can provide a niche for intracellular survival of bacteria, including the causative agent of Legionnaires' disease, Legionella pneumophila. Infection of amebas by L. pneumophila enhances the bacterial infectivity for mammalian cells and lung tissues. Likewise, the pathogenicity of amebas may be enhanced when they host bacteria. So far, the colonization of B. mandrillaris by bacteria has not been convincingly shown. In this study, we investigated whether this ameba could host L. pneumophila bacteria. Our experiments showed that L. pneumophila could initiate uptake by B. mandrillaris and could replicate within the ameba about 4 to 5 log cycles from 24 to 72 h after infection. On the other hand, a dotA mutant, known to be unable to propagate in Acanthamoeba castellanii, also did not replicate within B. mandrillaris. Approaching completion of the intracellular cycle, L. pneumophila wild-type bacteria were able to destroy their ameboid hosts. Observations by light microscopy paralleled our quantitative data and revealed the rounding, collapse, clumping, and complete destruction of the infected amebas. Electron microscopic studies unveiled the replication of the bacteria in a compartment surrounded by a structure resembling rough endoplasmic reticulum. The course of intracellular infection, the degree of bacterial multiplication, and the ultrastructural features of a L. pneumophila-infected B. mandrillaris ameba resembled those described for other amebas hosting Legionella bacteria. We hence speculate that B. mandrillaris might serve as a host for bacteria in its natural environment.

scholarly journals Temperature-Dependent Parasitic Relationship between Legionella pneumophila and a Free-Living Amoeba (Acanthamoeba castellanii)

2008 ◽  
Vol 74 (14) ◽  
pp. 4585-4588 ◽  
Author(s):  
Akira Ohno ◽  
Naoyuki Kato ◽  
Ryota Sakamoto ◽  
Soichiro Kimura ◽  
Keizo Yamaguchi
Keyword(s):  
Legionella Pneumophila ◽  
Low Temperatures ◽  
Acanthamoeba Castellanii ◽  
Temperature Dependent ◽  
Free Living ◽  
Free Living Amoeba ◽  
Effects Of Temperature ◽  
Number Of Bacteria

ABSTRACT We analyzed the effects of temperature on the interaction of Legionella pneumophila with Acanthamoeba castellanii. At <20°C, overexpression of type 1 metacaspase, a stimulator of A. castellanii encystation, was associated with a reduced number of bacteria within amoeba. At low temperatures, A. castellanii seems to eliminate L. pneumophila by encystation and digestion.

scholarly journals Intracellular growth of Legionella pneumophila within Acanthamoeba castellanii Neff.

1984 ◽  
Vol 45 (1) ◽  
pp. 18-24 ◽  
Author(s):  
E P Holden ◽  
H H Winkler ◽  
D O Wood ◽  
E D Leinbach
Keyword(s):  
Legionella Pneumophila ◽  
Acanthamoeba Castellanii ◽  
Intracellular Growth

scholarly journals ArgR-Regulated Genes Are Derepressed in the Legionella-Containing Vacuole

2010 ◽  
Vol 192 (17) ◽  
pp. 4504-4516 ◽  
Author(s):  
Galadriel Hovel-Miner ◽  
Sebastien P. Faucher ◽  
Xavier Charpentier ◽  
Howard A. Shuman
Keyword(s):  
Legionella Pneumophila ◽  
Acanthamoeba Castellanii ◽  
Transcriptional Response ◽  
Global Gene Expression ◽  
Host Cells ◽  
Intracellular Growth ◽  
Arginine Repressor ◽  
Legionnaires Disease ◽  
Global Gene Expression Analysis ◽  
Eukaryotic Organisms

ABSTRACT Legionella pneumophila is an intracellular pathogen that infects protozoa in aquatic environments and when inhaled by susceptible human hosts replicates in alveolar macrophages and can result in the often fatal pneumonia called Legionnaires' disease. The ability of L. pneumophila to replicate within host cells requires the establishment of a specialized compartment that evades normal phagolysosome fusion called the Legionella-containing vacuole (LCV). Elucidation of the biochemical composition of the LCV and the identification of the regulatory signals sensed during intracellular replication are inherently challenging. l-Arginine is a critical nutrient in the metabolism of both prokaryotic and eukaryotic organisms. We showed that the L. pneumophila arginine repressor homolog, ArgR, is required for maximal intracellular growth in the unicellular host Acanthamoeba castellanii. In this study, we present evidence that the concentration of l-arginine in the LCV is sensed by ArgR to produce an intracellular transcriptional response. We characterized the L. pneumophila ArgR regulon by global gene expression analysis, identified genes highly affected by ArgR, showed that ArgR repression is dependent upon the presence of l-arginine, and demonstrated that ArgR-regulated genes are derepressed during intracellular growth. Additional targets of ArgR that may account for the argR mutant's intracellular multiplication defect are discussed. These results suggest that l-arginine availability functions as a regulatory signal during Legionella intracellular growth.

scholarly journals Acanthamoeba castellanii Promotes the Survival of Vibrio parahaemolyticus

2008 ◽  
Vol 74 (23) ◽  
pp. 7183-7188 ◽  
Author(s):  
Michelle A. Laskowski-Arce ◽  
Kim Orth
Keyword(s):  
Vibrio Parahaemolyticus ◽  
Acanthamoeba Castellanii ◽  
Survival Advantage ◽  
Aquatic Environments ◽  
Pathogenic Species ◽  
Free Living ◽  
Food Borne ◽  
And Function ◽  
Living Bacteria

ABSTRACT Vibrio parahaemolyticus is a food-borne pathogen that naturally inhabits both marine and estuarine environments. Free-living protozoa exist in similar aquatic environments and function to control bacterial numbers by grazing on free-living bacteria. Protozoa also play an important role in the survival and spread of some pathogenic species of bacteria. We investigated the interaction between the protozoan Acanthamoeba castellanii and the bacterium Vibrio parahaemolyticus. We found that Acanthamoeba castellanii does not prey on Vibrio parahaemolyticus but instead secretes a factor that promotes the survival of Vibrio parahaemolyticus in coculture. These studies suggest that protozoa may provide a survival advantage to an extracellular pathogen in the environment.

Sign in / Sign up

Export Citation Format

Share Document