Cuterebra buccata

Ge­o­graphic Range

Rab­bit bot flies (Cutere­bra buc­cata) are pri­mar­ily Nearc­tic and na­tive to the east­ern United States and Canada. Their range in­cludes much of the east coast from New Hamp­shire and Long Is­land, New York, south­ward through Vir­ginia, Mary­land, Ten­nessee, Geor­gia, and Florida. They are ab­sent from Maine, Rhode Is­land, and Ver­mont. Rab­bit bot flies have been doc­u­mented as far west as North Dakota, Kansas, New Mex­ico, and Ari­zona. They have also been reared from rab­bits in Texas. There have been ad­di­tional ob­ser­va­tions of this species in Wis­con­sin, north­ern Illi­nois, and Iowa.

Rab­bit bot flies have been doc­u­mented in Canada in south­ern On­tario and Nova Sco­tia.

Mu­seum records also doc­u­ment one spec­i­men from the state of Querétaro, Mex­ico, and there are re­ports of rab­bit bot flies as far south as Neotrop­i­cal re­gions in Guatemala and Hon­duras. (GBIF Sec­re­tariat, 2022; Sabrosky, 1986)

Habi­tat

As lar­vae, rab­bit bot flies bury them­selves within a mam­malian host, the typ­i­cal host being cot­ton­tail rab­bits (Sylvi­la­gus flori­danus). How­ever, they also use atyp­i­cal hosts such as snow­shoe hares (Lepus amer­i­canus) and do­mes­tic rab­bits (Oryc­to­la­gus cu­nicu­lus). They have also been re­ported to use non-na­tive rat species like black rats (Rat­tus rat­tus) and Nor­way rats (Rat­tus norvegi­cus).

Rab­bit bot fly lar­vae typ­i­cally bur­row into the hip or groin re­gion of their hosts, but may also set­tle in the neck and shoul­der re­gions. They de­velop a breath­ing hole at the sur­face of the skin of the host. After feed­ing on their hosts, lar­vae emerge from these breath­ing holes and bur­row them­selves into the ground. Lar­vae then meta­mor­phose into pupae and re­main un­der­ground for sev­eral months be­fore emerg­ing as adult flies. Rab­bit bot flies can be found on the edges of forests and around the dens of their ro­dent hosts, where they lay their eggs. Like most bot fly species in the east­ern United States, rab­bit bot flies are ac­tive at am­bi­ent tem­per­a­tures above 20°C and re­quire sub­stan­tial sun­light.

El­e­va­tion ranges for rab­bit bot flies have not been re­ported. (Cog­ley, 1991; Kauf­man and Wood, 2015; Sabrosky, 1986)

Phys­i­cal De­scrip­tion

Adult rab­bit bot flies have a long red stripe and a red dot in their eyes, typ­i­cal of bot fly species that use hosts in the order Lago­mor­pha. They have white hair with a pat­tern of black spots on their face and three spots on their cheeks. These three spots are unique to rab­bit bot flies. The most ven­tral spot is also the largest of the three. The tho­raxes of rab­bit bot flies are white or light gray with fine hairs. There is also a clus­ter of black spots along their ab­domens.

Fe­male rab­bit bot flies have shorter hairs on their tho­raxes com­pared to males. Males mea­sure a total length be­tween 16.5 and 17.5 mm, while fe­males are typ­i­cally 18 to 20 mm. Re­ported wingspans are 14.5 to 16.5 mm in males and 16.5 to 18.0 mm in fe­males.

Whereas other bot fly species, such as mouse bot flies (Cutere­bra fontinella), pos­sess mul­ti­ply-pointed spines along their bod­ies, rab­bit bot flies have singly-pointed spines. Rab­bit bot fly lar­vae vary in size by in­star. For ex­am­ple, at the be­gin­ning of the sec­ond in­star, they mea­sure about 5.8 mm long by 1.6 mm wide. By the end of the sec­ond in­star, they mea­sure 10.5 mm by 4.5 mm. At the end of their third in­star, they are 26 to 32 mm long, and 13 to 16 mm wide. Rab­bit bot fly lar­vae re­main in their hosts for ap­prox­i­mately two weeks to com­plete their three in­star stages be­fore leav­ing hosts to pu­pate. A study in Geor­gia re­ported that pu­pa­tion time lasted 103 to 129 days. How­ever, the pupal stage can last longer in north­ern parts of their range. (Col­well, 2001; Kni­pling and Brody, 1940; Sabrosky, 1986)

  • Sexual Dimorphism
  • female larger
  • sexes shaped differently
  • Range length
    16.5 to 20 mm
    0.65 to 0.79 in
  • Range wingspan
    14.5 to 18 mm
    0.57 to 0.71 in

De­vel­op­ment

Rab­bit bot flies lay their eggs out­side of the dens of their hosts. Upon hatch­ing, lar­vae bur­row into the skin of host an­i­mals. Hatch­ing is stag­gered as an evo­lu­tion­ary de­fense to pre­vent an en­tire clus­ter of eggs at­tach­ing to an atyp­i­cal host. Heat and fric­tion are a cat­a­lyst for eggs hatch­ing and will cause them to hatch quicker. Cold tem­per­a­tures in­hibit the hatch­ing and growth of the eggs.

Lar­vae bur­row into their hosts through any ori­fice or open wound. They then mi­grate through the body and set­tle within the neck, shoul­ders, pos­te­rior, or hips of their rab­bit hosts. The rear or gen­i­tals of male rab­bits are ideal for lar­val de­vel­op­ment.

Lar­vae em­bed­ded in a host form a "war­ble" un­der­neath the skin. War­bles have three parts to them, all of which aid in de­vel­op­ment. Pores are holes which allow the bots to breathe under the skin of their hosts. Cap­sules are a thick­ened layer of host skin that pro­tects the lar­vae. The cap­sule layer gets thicker as lar­vae de­velop due to the at­tempts of hosts to heal the open wound. Fi­nally, cav­i­ties are the areas in which lar­vae re­side dur­ing de­vel­op­ment.

Rab­bit bot fly lar­vae com­plete three in­stars in their hosts. At the be­gin­ning of the sec­ond in­star, they mea­sure about 5.8 mm long by 1.6 mm wide. By the end of the sec­ond in­star, they are 10.5 mm long by 4.5 mm wide. At the end of their third in­star, they are 26 to 32 mm long, and 13 to 16 mm wide. A study in Geor­gia re­ported that rab­bit bot fly lar­vae re­mained in their hosts for roughly two weeks to com­plete the three in­stars be­fore leav­ing hosts to pu­pate. How­ever, in colder re­gions this de­vel­op­ment can take up to 30 days.

After 14 to 30 days, rab­bit bot flies exit their hosts through the breath­ing hole in the war­ble and set­tle into soil sub­strate. Upon en­ter­ing the soil, lar­vae will enter di­a­pause in the soil through­out cold pe­ri­ods and ex­hibit de­layed de­vel­op­ment. Di­a­pause ends when warmer months come, at which point lar­vae pu­pate. De­pend­ing on re­gional cli­mate and di­a­pause use, the pu­pa­tion process can take 1 to 12 months. How­ever, stud­ies in Geor­gia mea­sured pu­pa­tion times of 103 to 129 days.

Adult rab­bit bot flies live for ap­prox­i­mately two weeks and do not feed; in­stead they focus solely on re­pro­duc­tion. They mate and lay eggs, be­gin­ning the cycle for the next gen­er­a­tion. (Kni­pling and Brody, 1940; Sabrosky, 1986)

Re­pro­duc­tion

Mat­ing sys­tems of rab­bit bot flies are not well known. Due to their short adult lifes­pan, they are thought to be monog­a­mous.

Once a year, males con­gre­gate in an area to wait for fe­males. It is un­clear what trig­gers the con­gre­ga­tion. Whether it is a pre­de­ter­mined time or if there is some de­cid­ing stim­u­lus is un­known. Fe­males lay eggs out­side of rab­bit dens to im­prove the chances of hatched lar­vae find­ing a host.

The re­pro­duc­tive sys­tems of rab­bit bot flies are thought to mir­ror those of other mam­malian-host bot fly species in the genus Cutere­bra. Typ­i­cally, they are not able to fly in colder tem­per­a­tures, so they will ag­gre­gate to mate when it is sunny and above 20 °C. Males fly to pa­trol and pro­tect a ter­ri­tory from com­peti­tors. Fe­males fly less often, and only fly to find a land­ing site where males can find them. In­ter­course typ­i­cally lasts around 3 min­utes. (Col­well, 2001; Had­wen, 1915; Hunter and Web­ster, 2012; Sabrosky, 1986; Shif­fer, 1983)

Rab­bit bot flies reach sex­ual ma­tu­rity once they reach their adult stage, which can take 2 to 12 months. They breed in sum­mer months at am­bi­ent tem­per­a­tures above 20°C. How­ever, one study found that rab­bit bots in south­ern Geor­gia ex­pe­ri­enced two bouts of re­pro­duc­tion per year. In this case, a larva from June pu­pated for 75 days and then reached adult­hood by Au­gust of the same year. Then, lar­vae from No­vem­ber pu­pated for 103 to 129 days and reached adult­hood the fol­low­ing spring, be­tween March and April. It is likely that tem­per­a­ture lim­its re­pro­duc­tive ca­pa­bil­ity at sites far­ther north in their range.

Fer­til­iza­tion in rab­bit bot flies is in­ter­nal, as fe­males use their ovipos­i­tor to gather sperm from males. Fe­male flies die soon after lay­ing eggs. Al­though fe­males bots of other species lay about 2,000 eggs in the breed­ing sea­son, exact brood num­bers have not been re­ported for rab­bit bot flies.

Rab­bit bot fly eggs do not hatch all at once. In­stead, they are stag­gered to pro­tect all lar­vae from bur­row­ing into the same un­suit­able host, the eggs stag­ger in their hatch­ing and will not hatch at the same time. Lar­vae are im­me­di­ately in­de­pen­dent upon hatch­ing.

In­cu­ba­tion pe­riod and birth mass for rab­bit bot fly lar­vae are not re­ported in the lit­er­a­ture. (Col­well, 2001; Kni­pling and Brody, 1940; Sabrosky, 1986)

  • Breeding interval
    Once a year but sometimes two generations/year in souther locales
  • Breeding season
    Temperatures above 20C, typically just a few weeks long
  • Average time to independence
    0 minutes
  • Range age at sexual or reproductive maturity (female)
    2 to 12 months
  • Range age at sexual or reproductive maturity (male)
    2 to 12 months

After fe­male rab­bit bot flies lay eggs, there is no fur­ther parental in­volve­ment with off­spring as they de­velop. Adults die ap­prox­i­mately two weeks after emerg­ing from the pupal stage. (Sabrosky, 1986)

  • Parental Investment
  • no parental involvement

Lifes­pan/Longevity

Adult rab­bit bot flies have an av­er­age lifes­pan of ap­prox­i­mately two weeks in the wild. Lar­vae typ­i­cally stay within a host for 14 to 30 days, after which they exit their host and bur­row in the ground to pu­pate. Pupae re­main in the soil for 2 to 10 months de­pend­ing on sea­son and local cli­mate. For ex­am­ple, in Geor­gia, pu­pa­tion was mea­sured from 75 to 129 days; some over­win­tered as pupae while oth­ers emerged in the fall the same year as they hatched.

Rab­bit bot flies are not known to be kept in cap­tiv­ity due to the dif­fi­culty of repli­cat­ing the con­di­tions for pu­pa­tion. The longest known lifes­pan in the wild is 12 months. (Kni­pling and Brody, 1940; Sabrosky, 1986)

  • Range lifespan
    Status: wild
    12 (high) months

Be­hav­ior

Rab­bit bot flies have a par­a­sitic lar­val stage and, upon emer­gence from their host, they bur­row in the ground to pu­pate. This makes them fos­so­r­ial dur­ing part of their life cycle. As pupae, rab­bit bot flies enter a state of di­a­pause - sim­i­lar to hi­ber­na­tion - when tem­per­a­tures are cool dur­ing late fall, win­ter months, and early spring months.

Rab­bit bot flies typ­i­cally use cot­ton­tail rab­bits (Sylvi­la­gus flori­danus) as hosts, bur­row­ing into the rear or hip area. Atyp­i­cal hosts in­clude snow­shoe hares (Lepus amer­i­canus), do­mes­tic rab­bits (Oryc­to­la­gus cu­nicu­lus), black rats (Rat­tus rat­tus), and Nor­way rats (Rat­tus norvegi­cus).

Rab­bit bot flies do not so­cial­ize with each other out­side of mat­ing. They are soli­tary as lar­vae and pupae as a re­sult of their par­a­sitism and stag­gered stages of de­vel­op­ment.

Adult rab­bit bot flies are ac­tive dur­ing the day at tem­per­a­tures above 20 °C. Adult males pa­trol ter­ri­to­ries dur­ing the day, but only fly when there is sun­light, or for short pe­ri­ods (ap­prox­i­mately 15 min­utes) when the sun is cov­ered. Fe­males do not fly un­less they are ac­tively seek­ing a mate.

If an air­borne in­sect en­ters the ter­ri­tory of a male rab­bit bot fly, the male will at­tack and at­tempt to bring the in­truder to the ground. If they can not di­rectly at­tack an in­truder, they chase it out of their ter­ri­tory. (Col­well, 2001; Sabrosky, 1986; Shif­fer, 1983; Slan­sky, et al., 2008; Wolf and Batzil, 2001)

Home Range

There is lit­tle in­for­ma­tion on the home range of adult rab­bit bot flies. Adult males de­fend a ter­ri­tory dur­ing the few weeks that they are alive and seek­ing mates. (Col­well, 2001)

Com­mu­ni­ca­tion and Per­cep­tion

Lit­tle is known about the com­mu­ni­ca­tion of rab­bit bot flies with con­specifics or re­lated bot fly species.

Bot flies con­gre­gate for two weeks in warmer months to mate. The spe­cific weeks vary de­pend­ing on whether the pu­pa­tion pe­riod ends in sum­mer or fall. It is un­known what draws males to con­gre­gate in a spe­cific area, al­though most lit­er­a­ture sug­gests it in­volves chem­i­cal sig­nal­ing. Males re­lease pheromones that help them at­tract fe­males and fly around so that fe­males see them. Males also guard ter­ri­to­ries and will at­tack or chase in­sect in­trud­ers.

Rab­bit bot flies have com­pound eyes, which al­lows them to dis­tin­guish shades of col­ors and re­spond quickly to ex­ter­nal vi­sual stim­uli. They use tac­tile com­mu­ni­ca­tion to find mates and pro­cre­ate, as well as move through hosts. (Kni­pling and Brody, 1940; Sabrosky, 1986)

Food Habits

As lar­vae, rab­bit bot flies bury them­selves in a host and feed off of the flesh and bod­ily flu­ids of that an­i­mal. The main host that rab­bit bot flies use are east­ern cot­ton­tails (Sylvi­la­gus flori­danus).

Rab­bit bot flies do not feed as pupae. As adults they lack a mouth, and thus can­not eat. In­stead, they use stored en­ergy from their lar­val stage to sur­vive for roughly two weeks, dur­ing which time they search for mates. (Cramer, 2006; Cramer and Cameron, 2006; Dur­den, 1995; Sabrosky, 1986)

Pre­da­tion

Lit­tle is known re­gard­ing preda­tors of rab­bit bot flies. Lar­vae and pupae avoid preda­tors by bur­row­ing into hosts or the ground, re­spec­tively. Pre­da­tion is likely rare for adult rab­bit bot flies, as they are only alive and ac­tive for ap­prox­i­mately two weeks. (Col­well, 2001; Sabrosky, 1986)

Ecosys­tem Roles

Rab­bit bot flies are par­a­sitic, which can have a neg­a­tive ef­fect on the ecosys­tems they in­habit. They typ­i­cally feed off of hosts in the order (Lago­mor­pha). Their typ­i­cal hosts, east­ern cot­ton­tails (Sylvi­la­gus flori­danus), have evolved to sur­vive being par­a­sitized. Atyp­i­cal lago­morph hosts in­clude snow­shoe hares (Lepus amer­i­canus) and do­mes­tic rab­bits (Oryc­to­la­gus cu­nicu­lus), with the lat­ter being re­ported to host up to 9 lar­vae in one in­di­vid­ual. One re­port found that rab­bit bot flies can be reared from non-na­tive rats such as black rats (Rat­tus rat­tus) and Nor­way rats (Rat­tus norvegi­cus). (Kni­pling and Brody, 1940; Sabrosky, 1986; Slan­sky, et al., 2008; Wolf and Batzil, 2001)

Species Used as Host

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Rab­bit bot flies pro­vide no known eco­nomic ben­e­fit for hu­mans.

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Rab­bit bot flies pose a minor health risk to hu­mans. There is one re­port of lar­vae found in an el­derly man in Con­necti­cut. Mul­ti­ple bots on this in­di­vid­ual reached the sec­ond in­star stage, caus­ing pain, lethargy, and minor skin dam­age. Re­moval of bot fly lar­vae re­quires surgery.

Rab­bit bot flies are also known to par­a­sitize do­mes­tic rab­bits (Oryc­to­la­gus cu­nicu­lus), with as many as 9 lar­vae pre­sent in a sin­gle in­di­vid­ual. (Kni­pling and Brody, 1940; Sabrosky, 1986; Stafford, et al., 2021)

Con­ser­va­tion Sta­tus

Rab­bit bot flies have no spe­cial sta­tus on the U.S fed­eral list, CITES, or the State of Michi­gan list. These flies have not been eval­u­ated by the IUCN Red List.

No con­ser­va­tion ef­forts are cur­rently in place for rab­bit bot flies.

A threat to this species is for­est and pas­ture fires. Rab­bit bot flies are very sen­si­tive to tem­per­a­ture and the change in tem­per­a­ture of the soil causes mor­tal­ity of eggs, lar­vae, and pupae. (Col­well, 2001)

Con­trib­u­tors

Dave Brown (au­thor), Rad­ford Uni­ver­sity, Karen Pow­ers (ed­i­tor), Rad­ford Uni­ver­sity, Galen Bur­rell (ed­i­tor), Spe­cial Pro­jects.

Glossary

Nearctic

living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.

World Map

Neotropical

living in the southern part of the New World. In other words, Central and South America.

World Map

bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.

carnivore

an animal that mainly eats meat

causes or carries domestic animal disease

either directly causes, or indirectly transmits, a disease to a domestic animal

chemical

uses smells or other chemicals to communicate

diapause

a period of time when growth or development is suspended in insects and other invertebrates, it can usually only be ended the appropriate environmental stimulus.

diurnal
  1. active during the day, 2. lasting for one day.
ectothermic

animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature

fertilization

union of egg and spermatozoan

forest

forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.

fossorial

Referring to a burrowing life-style or behavior, specialized for digging or burrowing.

hibernation

the state that some animals enter during winter in which normal physiological processes are significantly reduced, thus lowering the animal's energy requirements. The act or condition of passing winter in a torpid or resting state, typically involving the abandonment of homoiothermy in mammals.

internal fertilization

fertilization takes place within the female's body

metamorphosis

A large change in the shape or structure of an animal that happens as the animal grows. In insects, "incomplete metamorphosis" is when young animals are similar to adults and change gradually into the adult form, and "complete metamorphosis" is when there is a profound change between larval and adult forms. Butterflies have complete metamorphosis, grasshoppers have incomplete metamorphosis.

monogamous

Having one mate at a time.

motile

having the capacity to move from one place to another.

native range

the area in which the animal is naturally found, the region in which it is endemic.

oviparous

reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.

parasite

an organism that obtains nutrients from other organisms in a harmful way that doesn't cause immediate death

pheromones

chemicals released into air or water that are detected by and responded to by other animals of the same species

sanguivore

an animal that mainly eats blood

seasonal breeding

breeding is confined to a particular season

semelparous

offspring are all produced in a single group (litter, clutch, etc.), after which the parent usually dies. Semelparous organisms often only live through a single season/year (or other periodic change in conditions) but may live for many seasons. In both cases reproduction occurs as a single investment of energy in offspring, with no future chance for investment in reproduction.

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

solitary

lives alone

tactile

uses touch to communicate

temperate

that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).

terrestrial

Living on the ground.

territorial

defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement

visual

uses sight to communicate

year-round breeding

breeding takes place throughout the year

Ref­er­ences

Cameron, A. 1926. The oc­cur­rence of Cutere­bra (Diptera, Oestri­dae) in west­ern Canada. Par­a­sitol­ogy, 18/4: 430-435.

Cog­ley, T. 1991. War­ble de­vel­op­ment by the ro­dent bot Cutere­bra fontinella (Diptera: Cutere­bri­dae) in the deer mouse. Vet­eri­nary Par­a­sitol­ogy, 38/4: 275-288.

Col­well, D. 2001. Par­a­sitic Dis­eases of Wild Mam­mals, Sec­ond Edi­tion. Iowa: Iowa State Uni­ver­sity Press.

Cramer, M. 2006. The Ef­fects of Bot Fly (Cutere­bra fontinella) Par­a­sitism on the Ecol­ogy and Be­hav­ior of the White-footed Mouse (Per­omyscus leu­co­pus). (Mas­ter's The­sis). Cincin­nati, Ohio: Uni­ver­sity of Cincin­nati.

Cramer, M., G. Cameron. 2006. Ef­fects of bot fly (Cutere­bra fontinella) par­a­sitism on a pop­u­la­tion of white-footed mice (Per­omyscus leu­co­pus). Jour­nal of Mam­mal­ogy, 87/6: 1103-1111.

Dur­den, L. 1995. Bot fly (Cutere­bra fontinella fontinella) par­a­sitism of cot­ton mice (Per­omyscus gossyp­i­nus) on St. Cather­ines Is­land, Geor­gia. The Jour­nal of Par­a­sitol­ogy, 81/5: 787-790.

GBIF Sec­re­tariat, 2022. "Cu­ture­bra buc­cata" (On-line). GBIF. Ac­cessed June 19, 2022 at https://​www.​gbif.​org/​occurrence/​search?​taxon_​key=1587508.

Gin­grich, R. 1981. Mi­gra­tory ki­net­ics of Cutere­bra fontinella (Diptera: Cutere­bri­dae) in the white-footed mouse, Per­omyscus leu­co­pus. The Jour­nal of Par­a­sitol­ogy, 67/3: 398-402.

Had­wen, S. 1915. A de­scrip­tion the egg and ovipos­i­tor of Cutere­bra fontinella, Clark (Cot­ton­tail Bot.). Jour­nal of the En­to­mo­log­i­cal So­ci­ety of British Co­lum­bia, N/A: 88-91.

Hunter, D., J. Web­ster. 2012. AG­GRE­GA­TION BE­HAV­IOR OF ADULT CUTERE­BRA GRISEA AND C. TENE­BROSA (DIPTERA: CUTERE­BRI­DAE). The Cana­dian En­to­mol­o­gist, 105/10: 1301-1307.

Jen­ni­son, C., L. Rodas, G. Bar­ret. 2006. Cutere­bra fontinella par­a­sitism on Per­omyscus leu­co­pus and Ochro­to­mys nut­talli. South­east­ern Nat­u­ral­ist, 5/1: 157-167.

John­son, A., T. Barzee, K. Hol­bert, S. Poarch, J. Storm. 2018. Ef­fect of Cutere­bra fontinella (mouse bot fly) on the move­ment of Per­omyscus leu­co­pus (white-footed mouse). South­east­ern Nat­u­ral­ist, 17/4: 597-604.

Kauf­man, P., L. Wood. 2015. Dis­cov­ery and suc­cess­ful de­vel­op­ment of Cutere­bra amer­i­cana (Diptera: Oestri­dae) from an atyp­i­cal host, Rat­tus rat­tus (Ro­den­tia: Muri­dae), in Florida, U.S.A.. Florida En­to­mol­o­gist, 98/1: 349-351.

Kni­pling, E., A. Brody. 1940. Some tax­o­nomic char­ac­ters of Cutere­brine (Diptera) lar­vae, with lar­val de­scrip­tions of two species from Geor­gia. The Jour­nal of Par­a­sitol­ogy, 26/1: 33-43.

Noel, S., N. Tessier, B. Angers, D. Wood, F. La­pointe. 2004. Mol­e­c­u­lar iden­ti­fi­ca­tion of two species of myi­a­sis-caus­ing Cutere­bra by mul­ti­plex PCR and RFLP. Med­ical and Vet­eri­nary En­to­mol­ogy, 18/2: 161-166.

Pezzi, M., T. Bonacci, M. Leis. 2019. Myi­a­sis in do­mes­tic cats: a global re­view.. Par­a­sites Vec­tors, 12: 372.

Sabrosky, C. 1986. North Amer­i­can Species of Cutere­bra and Rab­bit and Ro­dent Bot flies.. Col­lege Park, Mary­land: En­to­mo­log­i­cal So­ci­ety of Amer­ica.

Scholl, P. 1991. Gonotrophic de­vel­op­ment in the ro­dent bot fly Cutere­bra fontinella (Diptera: Oestri­dae). Jour­nal of Med­ical En­to­mol­ogy, 28/3: 474-476.

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Slan­sky, F. 2006. Cutere­bra Bot Flies (Diptera: Oestri­dae) and Their In­dige­nous Hosts and Po­ten­tial Hosts in Florida. Florida En­to­mol­o­gist, 89/2: 152-160.

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