AUTONOMOUS SENTINELS FOR THE DETECTION OF INVASIVE PATHOGENS

Keyword(s):  
2007 ◽  
Vol 28 (5) ◽  
pp. 397-418 ◽  
Author(s):  
Diana F. Tomback ◽  
Lynn M. Resler

2010 ◽  
Vol 7 (2) ◽  
pp. 241-244 ◽  
Author(s):  
Robert Poulin

Cryptic species cause problems for estimates of biodiversity. In the case of parasites, cryptic species also plague efforts to detect potential zoonotic diseases or invasive pathogens. It is crucial to determine whether the likelihood of finding cryptic species differs among higher parasite taxa, to better calibrate estimates of diversity and monitor diseases. Using published reports of cryptic species of helminth parasites identified using molecular tools, I show that the number of species found is strongly related to the number of parasite individuals sequenced, weakly influenced by the number of host species from which parasites were obtained, and unaffected by the genetic markers used. After correction for these factors, more cryptic species of trematodes are found than in other helminth taxa. Although several features distinguish trematodes from other helminths, it is probable that our inability to discriminate among sibling species of trematodes results from their lack of structures serving as species-specific morphological markers. The available data suggest that current estimates of helminth diversity may need to be doubled (tripled for trematodes) to better reflect extant diversity.


2020 ◽  
Author(s):  
◽  
Lea Stauber

Invasive pathogens are a threat to forest and agroecosystems, as well as animal and human health. Identifying genomic determinants of pathogen evolution, as well as investigations into the genetic structure of invasive pathogen populations provide fundamental insights to why species can emerge as invasive pathogens. In this PhD project I investigated the emergence and population genomics of the invasive chestnut blight fungus Cryphonectria parasitica, using comparative and population genomic approaches. C. parasitica recently emerged as an invasive bark pathogen on non-Asian Castanea species in North America and Europe. In the first chapter, I investigated genomic determinants of lifestyle transitions in the genus Cryphonectria, by genome comparisons of C. parasitica and its sister species. The study uncovered a striking loss of genes associated with carbohydrate metabolism in the invasive pathogen C. parasitica, which may have promoted its pathogenicity on Castanea species. The second chapter explores the emergence and diversification of a highly invasive chestnut blight lineage across south-eastern Europe. By analyzing the genome-wide diversity of a large set of C. parasitica isolates of predominantly European origin, the study showed that a highly successful clonal pathogen lineage can emerge from a recombinant bridgehead population within Europe. Interestingly, the emergence of this clonal lineage was accompanied by an evolutionary transition from mixed mating type populations to single mating type outbreak populations. Lastly, in the third chapter I investigated temporal changes in genetic diversity of established C. parasitica populations in southern Switzerland, as well as potential links between the presence of the deleterious hyperparasitic mycovirus Cryphonectria hypovirus 1 (CHV1) and fungal genome-wide diversity. The results indicate increased mating among related fungal individuals, resulting in high genetic similarity of genotypes and facilitated CHV1 transmission. There were no substantial changes in fungal population structure and after ˜30 years and no detectable impact of CHV1 presence on fungal genome-wide diversity. Although our results show stable CHV1 incidence in fungal populations over three decades, the short-term interaction dynamics are likely highly volatile. The overall findings of this PhD thesis highlight the relevance of genomic determinants facilitating pathogen emergence and invasions. C. parasitica is a useful model to study fundamental questions of pathogen evolution and invasive processes, as well as antagonistic pathogen-hyperparasite interactions.


Cell Reports ◽  
2020 ◽  
Vol 33 (11) ◽  
pp. 108515
Author(s):  
Thomas Macleod ◽  
Joseph S. Ainscough ◽  
Christina Hesse ◽  
Sebastian Konzok ◽  
Armin Braun ◽  
...  

2010 ◽  
Vol 48 (1) ◽  
pp. 177-180 ◽  
Author(s):  
Kris A. Murray ◽  
Richard W. R. Retallick ◽  
Robert Puschendorf ◽  
Lee F. Skerratt ◽  
Dan Rosauer ◽  
...  
Keyword(s):  

2018 ◽  
Author(s):  
Patricia E. Collins ◽  
Domenico Somma ◽  
David Kerrigan ◽  
Felicity Herrington ◽  
Karen R. Keeshan ◽  
...  

AbstractThe ability of the innate immune system to distinguish between low level microbial presence and invasive pathogens is fundamental for immune homeostasis and immunity. However, the molecular mechanisms underlying threat discrimination by innate immune cells are not clearly defined. Here we describe the integration of the NF-ĸB and MAPK pathways in the nucleus by the IĸB protein BCL-3 and the MAP3K TPL-2. Our data reveals that TPL-2 is a nucleocytoplasmic shuttling protein and demonstrates that the nucleus is the primary site for TPL-2 ubiquitination and proteasomal degradation. BCL-3 promotes TPL-2 degradation through interaction in the nucleus. As a consequence, Bcl3-/- macrophages have increased TPL-2 stability and MAPK activity following TLR stimulation. The enhanced stability of TPL-2 in Bcl3-/- macrophages lowers the MAPK activation threshold and the level of TLR ligand required to initiate an inflammatory response. This study establishes the nucleus as a key regulatory site for TLR-induced MAPK activity and identifies BCL-3 as a regulator of the cellular decision to initiate inflammation


2021 ◽  
Author(s):  
Jean A Berube ◽  
Jeremy D. Allison ◽  
Kate Van Rooyen ◽  
Cory Hughes ◽  
Patrick N. Gagné ◽  
...  

Abstract Surveillance for early detection of non-native, invasive pathogens requires simple, sturdy, and easy to use collecting devices. In this study, we compared the fungal species detected in wet collection cups of Lindgren traps versus those detected on slides with oiled cheesecloth as aerial spore collectors. DNA was extracted and amplified from both using the primers ITS1F -ITS7G, and Illumina sequencing was used for metabarcoding of fungi present in samples. In 90 samples there were 1277 fungal OTUs. For fungal OTUs only detected by one collection method, insect traps had three times the number of fungal OTUs compared to slides, and this pattern persisted when analyses were restricted to pathogens and forest pathogens. Annually, thousands of insect traps are deployed in North America and the associated trap fluids have added value in forest disease research and monitoring.


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