White-footed mouse | |
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Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Mammalia |
Order: | Rodentia |
Family: | Cricetidae |
Subfamily: | Neotominae |
Genus: | Peromyscus |
Species: | P. leucopus |
Binomial name | |
Peromyscus leucopus (Rafinesque, 1818) | |
The white-footed mouse (Peromyscus leucopus) is a rodent native to North America from Ontario, Quebec, Labrador, and the Maritime Provinces (excluding the island of Newfoundland) to the southwestern United States and Mexico. [1] In the Maritimes, its only location is a disjunct population in southern Nova Scotia. [2] It is also known as the woodmouse, particularly in Texas.
Adults are 90–100 mm (3.5–3.9 in) in length, not counting the tail, which can add another 63–97 mm (2.5–3.8 in). A young adult weighs 20–30 g (0.7–1.1 oz). While their maximum lifespan is 96 months, the mean life expectancy for the species is 45.5 months for females and 47.5 for males. In northern climates, the average life expectancy is 12–24 months. [3] The species is similar to Peromyscus maniculatus . [4]
White-footed mice are omnivorous, and eat seeds and insects. They are particularly voracious predators of the pupal stage of the invasive spongy moth (formerly termed the gypsy moth). [5] They are timid and generally avoid humans, but they occasionally take up residence in ground-floor walls of homes and apartments, where they build nests and store food. [6] White-footed mice spend substantial time in trees and bushes, sometimes taking unoccupied old bird nests and building roofs on them. [7]
Like the North American deer mouse, this species may carry hantaviruses, which can cause severe illness in humans. It has also been found to be a competent reservoir for the Lyme disease–causing spirochete, Borrelia burgdorferi . [8] The white-footed mouse is the favored host for the parasitic botfly Cuterebra fontinella . [9]
The white-footed mouse is one of the most common mouse species used as laboratory mice after the house mouse, and their domesticated version is called Peromyscus leucopus linville . [10] Such domesticated mice are also kept as pets [11] [12] and have been bred to have many different colors. [13]
Native populations of P. leucopus in New York city are isolated by dense human infrastructure and are largely confined to small urban forest islands such as Prospect Park and Central Park. [14] The limited gene flow caused by human activities and coupled with a bottleneck event in urban populations has been powerful enough to lead to evolutionary divergence of urban white-footed mice. [14] [15]
New York City mice exhibit local adaptations to diet-mediated selective pressures of urban habitats. Being opportunistic feeders, urban P. leucopus populations subsist on food discarded by humans as a readily available source of nutriment, thereby consuming a lot more fat and carbohydrates than rural populations. [16] Results of a landscape genomics study showed evidence of positive selection in mitochondrial genes of urban mice that are responsible for lipid and carbohydrate breakdown and digestion. [16] Isolated P. leucopus populations inhabiting NYC parks show signs of molecular-level adaptation to urban food resources. [16] The differential evolution of metabolic processes in urban P. leucopus populations is thought to contribute to their success and survival in NYC urban forests. [16] Furthermore, the morphology of urban white-footed mice may be changing to adapt to alternative food sources. For instance, the teeth of white-footed mice in New York City are shorter than the teeth of rural mice. [16] This change in physical traits could be explained by the availability of higher-quality food sources in urban forests, which negates the need for long, powerful teeth. [16]
Urban populations of P. leucopus may be under unique selective pressures due to increased routine exposure to pollutants and toxins. A comparative transcriptome study found evidence of positive selection acting on the genes of urban mice that play major roles in detoxification and xenobiotic metabolism. [17] The genes under positive selection pressure include CYP1A1 and Hsp90, which are known to be involved in the metabolism of foreign substances and drugs. [18] High concentrations of heavy metals such as lead and mercury in NYC park soils pose a unique selective pressure that likely led urban populations of P. leucopus to develop metabolic adaptations to the toxicity of urban forest environments. [17] Furthermore, exposure of pollutants is known to induce hypermethylation of DNA. [18] A study showed that in urban white-footed mice, a gene coding for a demethylase enzyme is under positive selection. [18] This means that urban populations of white-footed mice that live in highly polluted environments uniquely benefit from an active demethylase enzyme that removes methyl groups from DNA. [18]
City-dwelling white-footed mouse populations are densely concentrated in isolated urban parks, which makes sperm competition a particularly powerful source of selection in urban environments. [19] Genetic studies have identified signs of molecular-level evolution of reproductive processes in urban white-footed mouse populations. Genes associated with spermatogenesis, sperm locomotion, and sperm-egg interactions in urban mice show a divergent pattern of regulation compared to their rural counterparts. [19] Therefore, the intensified sperm competition of dense mouse populations in urban forests has driven them to develop faster, more efficient sperm than that of rural mice.
Urban environments are saturated with large numbers of novel and familiar pathogens that are introduced by transportation, traffic, and trade. [20] The elevated occurrence of pathogens is a driver of directional selection in which genetic variants that more efficiently resist infection are favored. The outcome of this selection can be seen in genetic divergence between urban and rural P. leucopus populations at loci that regulate the innate immune response and inflammation. [21] Furthermore, a study has found evidence of positive selection acting on genes that modulate pathogen recognition in urban mice. [21] Immunoregulatory proteins that are found on T lymphocytes are overexpressed in urban mice when compared to rural populations. [21] These findings suggest that the immune systems of NYC white-footed mice may be evolving to recognize and respond to pathogens more efficiently. The divergence between rural and urban white-footed mice is especially prominent due to impeded gene flow between these populations, which is caused by landscape barriers including roads, highways, and pedestrian sidewalks. [22] Monitoring the strength of immune defenses in P. leucopus is of special importance because they are commonly infected with dangerous pathogens such as hantaviruses and Borrelia burgdorferi . [22]
A spirochaete or spirochete is a member of the phylum Spirochaetota, which contains distinctive diderm (double-membrane) Gram-negative bacteria, most of which have long, helically coiled cells. Spirochaetes are chemoheterotrophic in nature, with lengths between 3 and 500 μm and diameters around 0.09 to at least 3 μm.
Lyme disease, also known as Lyme borreliosis, is a tick-borne disease caused by species of Borrelia bacteria, transmitted by blood-feeding ticks in the genus Ixodes. The most common sign of infection is an expanding red rash, known as erythema migrans (EM), which appears at the site of the tick bite about a week afterwards. The rash is typically neither itchy nor painful. Approximately 70–80% of infected people develop a rash. Early diagnosis can be difficult. Other early symptoms may include fever, headaches and tiredness. If untreated, symptoms may include loss of the ability to move one or both sides of the face, joint pains, severe headaches with neck stiffness or heart palpitations. Months to years later, repeated episodes of joint pain and swelling may occur. Occasionally, shooting pains or tingling in the arms and legs may develop. Despite appropriate treatment, about 10 to 20% of those affected develop joint pains, memory problems, and tiredness for six months or more; this constellation of symptoms is termed post-treatment Lyme disease syndrome (PTLDS).
Peromyscus is a genus of rodents. They are commonly referred to as deer mice or deermice, not to be confused with the chevrotain or "mouse deer". They are New World mice only distantly related to the common house and laboratory mouse, Mus musculus. From this relative, Peromyscus species are distinguished by relatively larger eyes, and also often two-tone coloring, with darker colors over the dorsum (back), and white abdominal and limb hair-coloring. In reference to the coloring, the word Peromyscus comes from Greek words meaning "booted mouse". They are also accomplished jumpers and runners by comparison to house mice, and their common name of "deer mouse" is in reference to this agility.
Borrelia burgdorferi is a bacterial species of the spirochete class in the genus Borrelia, and is one of the causative agents of Lyme disease in humans. Along with a few similar genospecies, some of which also cause Lyme disease, it makes up the species complex of Borrelia burgdorferi sensu lato. The complex currently comprises 20 accepted and 3 proposed genospecies. B. burgdorferi sensu stricto exists in North America and Eurasia and until 2016 was the only known cause of Lyme disease in North America. Borrelia species are Gram-negative.
Borrelia is a genus of bacteria of the spirochete phylum. Several species cause Lyme disease, also called Lyme borreliosis, a zoonotic, vector-borne disease transmitted by ticks. Other species of Borrelia cause relapsing fever, and are transmitted by ticks or lice, depending on the species of bacteria. A few Borrelia species as Candidatus Borrelia mahuryensis harbor intermediate genetic features between Lyme disease and relapsing fever Borrelia. The genus is named after French biologist Amédée Borrel (1867–1936), who first documented the distinction between a species of Borrelia, B. anserina, and the other known type of spirochete at the time, Treponema pallidum. This bacterium must be viewed using dark-field microscopy, which make the cells appear white against a dark background. Borrelia species are grown in Barbour-Stoenner-Kelly medium. Of 52 known species of Borrelia, 20 are members of the Lyme disease group, 29 belong to the relapsing fever group, and two are members of a genetically distinct third group typically found in reptiles. A proposal has been made to split the Lyme disease group based on genetic diversity and move them to their own genus, Borelliella, but this change is not widely accepted. This bacterium uses hard and soft ticks and lice as vectors. Testing for the presence of the bacteria in a human includes two-tiered serological testing, including immunoassays and immunoblotting.
Lyme disease, or borreliosis, is caused by spirochetal bacteria from the genus Borrelia, which has 52 known species. Three main species are the main causative agents of the disease in humans, while a number of others have been implicated as possibly pathogenic. Borrelia species in the species complex known to cause Lyme disease are collectively called Borrelia burgdorferisensu lato (s.l.) not to be confused with the single species in that complex Borrelia burgdorferi sensu stricto which is responsible for nearly all cases of Lyme disease in North America.
Ixodes scapularis is commonly known as the deer tick or black-legged tick, and in some parts of the US as the bear tick. It was also named Ixodes dammini until it was shown to be the same species in 1993. It is a hard-bodied tick found in the eastern and northern Midwest of the United States as well as in southeastern Canada. It is a vector for several diseases of animals, including humans and is known as the deer tick owing to its habit of parasitizing the white-tailed deer. It is also known to parasitize mice, lizards, migratory birds, etc. especially while the tick is in the larval or nymphal stage.
Jorge Benach is a medical researcher at the Stony Brook University in New York state. Benach is the chair of the Department of Molecular Genetics and Microbiology. Benach's main area of research is the tick-borne spirochete Borrelia burgdorferi, which is the causative agent of Lyme disease.
Virulence-related outer membrane proteins, or outer surface proteins (Osp) in some contexts, are expressed in the outer membrane of gram-negative bacteria and are essential to bacterial survival within macrophages and for eukaryotic cell invasion.
Southern tick-associated rash illness (STARI) is an emerging infectious disease related to Lyme disease that occurs in southeastern and south-central United States. It is spread by tick bites and it was hypothesized that the illness was caused by the bacteria Borrelia lonestari. However, there is insufficient evidence to declare this Borrelia strain as a causative agent.
Deer tick virus (DTV) is a virus in the genus Flavivirus spread via ticks that causes encephalitis.
Borrelia miyamotoi is a bacterium of the spirochete phylum in the genus Borrelia. A zoonotic organism, B. miyamotoi can infect humans through the bite of several species of hard-shell Ixodes ticks, the same kind of ticks that spread B. burgdorferi, the causative bacterium of Lyme disease. Ixodes ticks are also the primary vector in the spread of babesiosis and anaplasmosis.
Borrelia spielmanii is a spirochete bacterium; it routinely infects Ixodes ricinus, and subsequently humans, causing Lyme disease.
Borrelia lusitaniae is a bacterium of the spirochete class of the genus Borrelia, which has a diderm (double-membrane) envelope. It is a part of the Borrelia burgdorferisensu lato genospecies and is a Gram-negative bacterium. B. lusitaniae is tick-borne; he type strain is PotiB2. It can be pathogenic, being involved in cases of Lyme borreliosis. A species of tick, Ixodes ricinus, is the host of B. lusitaniae. It is thought to have originated from Portugal and has since spread to parts of Europe and North Africa. Lizards of the family Lacertidae are now believed to be important reservoir hosts of this bacterium.
Borrelia bissettiae is a spirochete bacterium. The type strain is strain DN127. It is pathogenic and causes Lyme borreliosis in the Americas and Eurasia.
Borrelia kurtenbachii is a spirochete bacterium; it can be pathogenic, being involved in cases of Lyme borreliosis.
Borrelia andersonii is a spirochete bacterium. It can be pathogenic, being involved in cases of Lyme borreliosis.
Borrelia sinica is a spirochete bacterium. Its cells contain only four periplasmic flagella inserted at each end of the spirochaetes, differing from other Borrelia species. It is associated with Lyme disease. CMN3T is the type strain of this species.
Brevinema andersonii, named for John F. Anderson, who first described the organism. This organism is a Gram-negative, microaerophilic, helical shaped, chemoorganotrophic organism from the genus Brevinema. Brevinema andersonii is host associated, strains have been isolated from blood and other tissues of short-tailed shrews and white-footed mice and are infectious for laboratory mice and Syrian hamsters.B. andersonii is readily identified by restriction enzyme analysis, and SDS-PAGE, or fatty acid composition data. Another identifier for B. andersonii is the sheathed periplasmic flagella in the 1-2-1 configuration. While cells are visible by dark-field or phase-contrast microscopy, they cannot be seen when bright-field microscopy is used.
Borrelia mayonii is a Gram-negative, host-associated spirochete that is capable of causing Lyme disease. This organism can infect various vertebrate hosts such as humans via the bite of a black legged tick.