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Biology subjects

Ferguson, A. W.

Publications and source records attributed to Ferguson, A. W..

4 recordsLinked to original sources

Biodiversity databases as underutilized resources for pathogen discovery: a quantitative synthesis of bat and rodent tissue collections in natural history museums

Zoonotic spillovers are becoming increasingly frequent, and the devastating effects of the SARS-CoV-2 pandemic demonstrate our continued inability to combat their consequences effectively. Natural history museums can enhance the study of zoonoses by serving as valuable resources for understanding the ecology and evolutionary history of pathogens and their wildlife hosts. Despite the growing interest in the role museums can play in pathobiology research and zoonotic risk assessment, there remains a lack of centralized resources for locating tissue samples that may be leveraged for pathogen discovery. Using the worlds most significant global aggregator of museum specimens, The Global Biodiversity Information Facility (GBIF), we examined how such tools could be adopted to identify specimens that might be sources of viral genetic material. Focusing on tissue samples from the mammalian orders Rodentia and Chiroptera, speciose taxa that host a high diversity of known zoonotic viruses, we examined temporal, spatial, and taxonomic gaps and patterns in the available tissue samples. Our analyses reveal a heavy bias toward tissue samples collected from the Americas (and consequently, taxonomic groups found in the Americas), with most collected samples housed in North American institutions. This limits the scope of future pathogen discovery efforts and presents a barrier to pandemic preparedness in the Global South. We also examine gaps in metadata quality (e.g., descriptions of preservation method and storage medium) and outline recommendations for GBIF to facilitate future biosurveillance projects and effectively incorporate natural history museums into One Health disease research. Author SummaryThe SARS-CoV-2 pandemic has driven a greater research focus on understanding wildlife reservoirs of zoonotic pathogens. As a complement to field-based sampling of wildlife, natural history museum collections house millions of specimens that could be used by researchers to study pathogens quickly, safely, and cost-effectively. Digital databases of museum specimens and their associated tissue samples were originally created for biodiversity research, but these could be adapted to guide pathogen discovery research. Using the largest of these databases, The Global Biodiversity Information Facility, we explored tissue samples from rodents and bats, which have been shown to carry a disproportionate number of zoonotic pathogens. We searched for keywords that would indicate the presence of relevant tissue samples and then mapped the results visually. This revealed disproportionate distributions of tissue samples across time, space, and taxonomy. Our study is the first attempt to assess how a biodiversity database can be used for this novel purpose. We suggest changes that would improve these databases for zoonotic disease research.

ecology↗

Museum collections and machine learning guide discovery of novel coronaviruses and paramyxoviruses

Natural history museum collections are valuable but underutilized resources for viral discovery, offering opportunities to test hypotheses about viral occurrence across space, time, and taxonomic groups. We developed machine learning models of bat host suitability to guide coronavirus and paramyxovirus screening of 1330 and 491 tissues, respectively, in a museum collection. For the first time, we recovered coronavirus (n = 16) and paramyxovirus (n = 3) sequences from archived museum tissues, confirming three novel coronavirus host species and three novel paramyxovirus host species (3% and 33% prediction success rate, respectively). These sequences included a SARS-like coronavirus and an orthoparamyxovirus from Angolan Rhinolophus fumigatus specimens collected in June 2019, suggesting that viruses with epidemic potential may be more widespread in sub-Saharan Africa than previously believed. Our study demonstrates the value of combining predictive modeling and collections-based viral discovery, particularly for filling outstanding sampling gaps and investigating changes in host-virus associations over time.

ecology↗

Prospecting for zoonotic pathogens using targeted DNA enrichment

There are over 60 zoonoses linked to small mammals, including some of the most devastating pathogens in human history. Meanwhile, millions of museum-archived tissues are available to understand natural history of these pathogens. Our goal is to maximize the value of museum collections for pathogen-based research using targeted sequence capture. To this end, we have generated a probe panel that includes 39,916, 80bp RNA probes targeting 32 pathogen groups, including bacteria, helminths, fungi, and protozoans. Lab generated, mock control samples show that we are capable of enriching targeted loci from pathogen DNA 2,882 to 6,746-fold. Further, we were able to identify bacterial species in museum-archived samples, including Bartonella, a known human zoonosis. These results show that probe-based enrichment of pathogens is a highly customizable and efficient method for identifying pathogens from museum-archived tissues.

genomics↗

Phylogenomic systematics of the spotted skunks (Carnivora, Mephitidae, Spilogale): Additional species diversity and Pleistocene climate change as a major driver of diversification

Four species of spotted skunks (Carnivora, Mephitidae, Spilogale) are currently recognized: Spilogale angustifrons, S. gracilis, S. putorius, and S. pygmaea. Understanding species boundaries within this group is critical for effective conservation given that regional populations or subspecies (e.g., S. p. interrupta) have experienced significant population declines. Further, there may be currently unrecognized diversity within this genus as some taxa (e.g., S. angustifrons) and geographic regions (e.g., Central America) never have been assessed using DNA sequence data. We analyzed species limits and diversification patterns in spotted skunks using multilocus nuclear (ultraconserved elements) and mitochondrial (whole mitogenomes and single gene analysis) data sets from broad geographic sampling representing all currently recognized species and subspecies. We found a high degree of genetic divergence among Spilogale that reflects seven distinct species and eight unique mitochondrial lineages. Initial divergence between S. pygmaea and all other Spilogale occurred 29 in the Early Pliocene (~ 5.0 million years ago) which was followed by subsequent diversification of the remaining Spilogale into an "eastern" and "western" lineage during the Early Pleistocene (~1.5 million years ago). These two lineages experienced temporally coincident patterns of diversification at ~0.66 and ~0.35 million years ago into two and ultimately three distinct evolutionary units, respectively. Diversification was confined almost entirely within the Pleistocene during a timeframe characterized by alternating glacial-interglacial cycles, with the origin of this diversity occurring in northeastern Mexico and the southwestern United States of America. Mitochondrial-nuclear discordance was recovered across three lineages in geographic regions consistent with secondary contact, including a distinct mitochondrial lineage confined to the Sonoran Desert. Our results have direct consequences for conservation of threatened populations, or species, as well as for our understanding of the evolution of delayed implantation in this enigmatic group of small carnivores.

evolutionary biology↗