Publications by authors named "Jean-Jacques Letesson"

Brucellosis is a worldwide extended zoonosis caused by pathogens of the genus . While most , , and biovars grow slowly in complex media, they multiply intensely in livestock genitals and placenta indicating high metabolic capacities. Mutant analyses and in infection models emphasize that erythritol (abundant in placenta and genitals) is a preferred substrate of brucellae, and suggest hexoses, pentoses, and gluconeogenic substrates use in host cells.

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  • One Health promotes collaboration across various disciplines to improve health outcomes for humans, animals, and the environment, with a focus on the challenges posed by brucellosis.
  • Key stakeholders include public health officials, veterinarians, microbiologists, and breeders, who must work together to enhance awareness and implementation of effective diagnostic and treatment methods.
  • The initiative faces obstacles like climate change, infrastructure weaknesses, and the need for tailored vaccination strategies, emphasizing the importance of building trust and awareness among affected communities.
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  • Bacteria from the genus Brucella cause brucellosis, a serious disease affecting both animals and humans, and have been controversially merged with other unrelated bacterial species based on genomic findings.
  • Researchers argue this merger is inappropriate due to lack of thorough phylogenetic analysis and exclusion of expert opinions in brucellosis.
  • They warn that combining these groups could lead to confusion and risks in public health, particularly impacting those dealing with brucellosis in under-resourced regions, and call for keeping the Brucella genus distinct.
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The facultative intracellular pathogen Brucella abortus interacts with several organelles of the host cell to reach its replicative niche inside the endoplasmic reticulum. However, little is known about the interplay between the intracellular bacteria and the host cell mitochondria. Here, we showed that B.

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The intracellular pathogens of the genus are phylogenetically close to , a diverse group of free-living bacteria with a few species occasionally infecting medically compromised patients. A group of taxonomists recently included all organisms in the genus based on global genome analyses and alleged equivalences with genera such as . Here, we demonstrate that such equivalencies are incorrect because they overlook the complexities of pathogenicity.

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This study aimed to consolidate current knowledge of wildlife brucellosis in Africa and to analyse available predictors of infection. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines were followed. Information on species, test used, test results, area, rainfall, livestock and wildlife contact and year of study were extracted.

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species cause brucellosis, a worldwide extended zoonosis. The brucellae are related to free-living and plant-associated α2- and, since they multiply within host cells, their metabolism probably reflects this adaptation. To investigate this, we used the rodent-associated biovar 5, which in contrast to the ruminant-associated and and other biovars, is fast-growing and conserves the ancestral Entner-Doudoroff pathway (EDP) present in the plant-associated relatives.

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Mechanistic understanding of the factors that govern host tropism remains incompletely understood for most pathogens. species, which are capable of infecting a wide range of hosts, offer a useful avenue to address this question. We hypothesized that metabolic fine-tuning to intrahost niches is likely an underappreciated axis underlying pathogens' ability to infect new hosts and tropism.

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Live attenuated vaccines play a key role in the control of many human and animal pathogens. Their rational development is usually helped by identification of the reservoir of infection, the lymphoid subpopulations associated with protective immunity as well as the virulence genes involved in pathogen persistence. Here, we compared the course of infection in C57BL/6 mice infected via intraperitoneal (i.

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Allergic asthma is a chronic Th2 inflammatory disease of the lower airways affecting a growing number of people worldwide. The impact of infections and microbiota composition on allergic asthma has been investigated frequently. Until now, however, there have been few attempts to investigate the impact of asthma on the control of infectious microorganisms and the underlying mechanisms.

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  • - The study focuses on a class III zoonotic bacterial pathogen that can survive and replicate within host cells, particularly macrophages, by using a detailed transposon sequencing analysis to identify essential genes.
  • - Researchers created a comprehensive transposon mutant library and mapped nearly a million insertion sites, revealing 491 essential coding sequences, with chromosome I containing a higher percentage of essential genes than chromosome II.
  • - They discovered 48 crucial genes for the bacteria's growth inside macrophages, highlighting the importance of the pyrimidine nucleotide biosynthesis pathway for its proliferation in these immune cells.
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  • * Brucella interrupts ER function and establishes connections with mitochondria, but its replication doesn't rely on mitochondrial energy processes or reactive oxygen species.
  • * Infection with Brucella leads to significant mitochondrial fragmentation in various cell types, which seems to result from impaired mitochondrial fusion rather than its usual control mechanisms, yet it does not affect the bacterium's replication or the infected cells' sensitivity to apoptosis.
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Entry of the facultative intracellular pathogen into host cells results in the formation of endosomal -containing vacuoles (eBCVs) that initially traffic along the endocytic pathway. eBCV acidification triggers the expression of a type IV secretion system that translocates bacterial effector proteins into host cells. This interferes with lysosomal fusion of eBCVs and supports their maturation to replicative -containing vacuoles (rBCVs).

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This study shows the absence of the world's most common bacterial zoonoses caused by Brucella abortus and Brucella melitensis in cattle, goats and dogs in an agro-pastoral community in South Africa, where heifer vaccination against brucellosis with the live Strain 19 vaccine is compulsory. The study site is bordering wildlife reserves with multiple wildlife species infected with brucellosis. The results showed a low seroprevalence (1.

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This study develops an original co-infection model in mice using , the most frequent cause of human brucellosis, and , the agent of African trypanosomiasis. Although the immunosuppressive effects of in natural hosts and mice models are well established, we observed that the injection of in mice chronically infected with induces a drastic reduction in the number of in the spleen, the main reservoir of the infection. Similar results are obtained with - and -infected mice and -infected mice co-infected with , demonstrating that this phenomenon is not due to antigenic cross-reactivity.

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  • * A study on chronic brucellosis infection revealed a significant loss of marginal zone macrophages (MZMs and MMMs) in the spleen, adversely affecting the organ's ability to process antigens and respond to infections.
  • * The reduction in MZ macrophages is linked to persistent low-level inflammation from interferon gamma (IFN-γ), but is not reliant on T cell or TNF receptor pathways, indicating their vulnerability during systemic infections.
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Paratuberculosis, caused by Mycobacterium avium subsp. paratuberculosis (Map), is a chronic granulomatous enteritis which primarily affects domestic and wild ruminants, resulting in serious economic losses for dairy and beef industry around the world. There is no satisfactory cure or vaccine, and actual diagnostic tests need improvement, particularly for the initial stages of the disease.

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Erythritol is the preferential carbon source for most brucellae, a group of facultative intracellular bacteria that cause a worldwide zoonosis. Since this polyol is abundant in genital organs of ruminants and swine, it is widely accepted that erythritol accounts at least in part for the characteristic genital tropism of brucellae. Nevertheless, proof of erythritol availability and essentiality during intracellular multiplication has remained elusive.

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Mycobacterium avium subsp. hominissuis (Mah) represents a health concern for humans and to a lesser extent for pigs, but its zoonotic potential remains elusive. Using multispacer sequence typing (MST) we previously identified 49 different genotypes of Mah among Belgian clinical and porcine isolates, with 5 MSTs shared by both hosts.

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Brucella abortus is a pathogen infecting cattle, able to survive, traffic, and proliferate inside host cells. It belongs to the Alphaproteobacteria, a phylogenetic group comprising bacteria with free living, symbiotic, and pathogenic lifestyles. An essential regulator of cell cycle progression named CtrA was described in the model bacterium Caulobacter crescentus.

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  • The study explores the mucosal immune system's role in defending against Brucella infection, focusing on different immune responses during primary and secondary infections in genetically modified mice.
  • Early control of Brucella in the lungs relies on specific immune factors like TCR-δ, IL-17RA, and TAP1, while later stages are affected by MHC class II and IFN-γR deficiencies across various organs.
  • For secondary infections, a robust memory immune response is primarily driven by CD4(+) and CD8(+) T cells, with IL-12p35 and IL-17A pathways playing crucial roles, emphasizing that protective responses vary based on the infection route.
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Brucellae are facultative intracellular pathogens. The recent development of methods and genetically engineered strains allowed the description of cell-cycle progression of Brucella abortus, including unipolar growth and the ordered initiation of chromosomal replication. B.

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Brucella are facultative intracellular Gram-negative coccobacilli that chronically infect humans as well as domestic and wild-type mammals, and cause brucellosis. Alternatively activated macrophages (M2a) induced by IL-4/IL-13 via STAT6 signaling pathways have been frequently described as a favorable niche for long-term persistence of intracellular pathogens. Based on the observation that M2a-like macrophages are induced in the spleen during the chronic phase of B.

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Eukaryotic cells developed strategies to detect and eradicate infections. The innate immune system, which is the first line of defence against invading pathogens, relies on the recognition of molecular patterns conserved among pathogens. Pathogen associated molecular pattern binding to pattern recognition receptor triggers the activation of several signalling pathways leading to the establishment of a pro-inflammatory state required to control the infection.

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