Paradoxopsyllus scorodumovi (Aphaniptera) flea, an effective vector of plague in a Gorno-Altai natural focus

A study was conducted on the fleas of P. scorodumovi and five local strains of the plague microbe, one of which is typical of the strains of the Altai subspecies and four are non-typical of this nidus. The fleas of this species are capable to transmit not only the plague agent of the strains typical of this nidus but also non-typical ones which differ in some biological properties and are avirulent for most carriers but Pallas's pika. Biological peculiarities of fleas of P. scorodumovi in addition to their high efficiency as vectors of the plague microbe enable us to associate the more active autumn epizooty with fleas of this species.     

Peculiarities of thoracic and abdominal combs of fleas (Siphonaptera)

The structure of pseudosetae, spinelets, and spines of combs (ctenidia) was studied by means of light and SE microscopy in 80% of genera and subgenera of the World fauna. It is found out that peculiarities of ctenidiae in the prothorax and in tergites of the abdomen are characteristics of families and infraorders of fleas. Some characters of ctenidiae found in certain flea genera are reductions and apparently caused by habitation in some extremal conditions. An absence of ctenidiae in the unfraorder Pulicomorpha is compensated by more developed posterior margin of prothorax and general abbreviation of all thoracal segments. Reasons of ctenidiae absence, which is observed in certain genera of the infraorders Ceratophyllomorpha, Pygiopsyllomorpha and Hystricopsillomorpha associated with the same hosts, is not clear. It is confirmed, that distance between ctenidiae in different flea species associated with the same species host species, however it is recovered, that this distance correlates with the diameter of most thin hair of host. In some flea species the distance between ctenidia spices in females is larger, than in males. It is found, that sexual dimorphism by this character may not be expressed in certain species of closely related species group of fleas. It is suggested that ctenidiae were present even in the common ancestor of fleas. The hypothesis on origin of spines and pseudosetae from setae of the posterior walls of toracal and abdominal segments in the common ancestor of fleas is proposed.     

Epizootological role of fleas in the Gorno-Altai natural plague focus (a review)

Epizootological role of fleas in the Gorno-Altai natural plague focus (Sailugemsk focus) and numerous data on the flea viability are analyzed and generalized. Information concerning the flea natural infectivity with Yersinia pestis altaica is represented. Ecological peculiarities of some flea species parasitizing the main host, Mongolian pika Ochotona pallasi, and nature of their interrelations with Y. pestis are investigated. It is shown that the flea taxocenosis provides the permanent all year-round circulation of Y. pestis in the Gorno-Altai natural focus. Certain combinations of structural elements of the flea taxocenosis have a dominant significance in determination the circulation process at different phases of the annual epizootic cycle.     

Adaptations of fleas (Siphonaptera) to parasitism

The paper deals with peculiarities of flea structure determined by their parasitism on mammals and birds. On the basis of the data on diversity of morphological characters, the leading role of structures of the frontal and nototrochanteral complexes in the adaptive evolution of Siphonaptera is substantiated. Peculiarities of the pulicoid, ischnopsylloid, palaeopsylloid, and generalized morphological types are analyzed together with examples of narrow morphological specializations. Distribution of fleas of these morphological types over five groups of hosts differing in the degree of mobility and association with nests and burrows is also analyzed.     

Characteristics of distribution of fleas from small mammals and birds in the southern taiga of Priirtysh'ie]

The analysis of the landscape distribution of fleas from small mammals and birds in the southern taiga of Priirtishje is given. According to their abundance and faunistic composition the population of fleas from small mammals can be arranged into four groups: fleas of forest floodland landscape, those of forest-meadow floodland landscape, fleas of settlements and bogs.     

Fleas of the Lake Evoron vole (Siphonaptera)

In Lower Priamurje in summer of 1977-1979 Microtus evoronensis was parasitized mainly by fleas of Ceratophyllus calcarifer. Other seven species of fleas recorded from this animal are very rare. They are connected, in general, with other small mammals and birds.     

Reproductive success of cat fleas,Ctenocephalides felis,on calves as unusual hosts

Abstract. Cat fleas, Ctenocephalides felis, were released onto calves as unusual hosts, and sampled at intervals for histological examination. Egg output from fleas on age-matched male and female calves was monitored. Using indicators of reproductive maturation and regression together with egg output data, the reproductive success and fertility of cat fleas on male and female calves were estimated. Comparisons were made with fleas taken from cats. The mean egg output of fleas on the bull calf was highly significantly different from that on the age-matched female calf: 28.14 ± 2.96 (SE) eggs/h compared with 16.21 ± 1.96 (SE) eggs/h. A higher proportion of sampled fleas (83.0%) was reproductively mature on the feline hosts compared with the calves (45.4-62.5%). Blue bodies resulting from oocyte resorption were present in the ovarioles of 10.4-19.0% of fleas sampled from the calves. No blue bodies were present in fleas removed from cats. Eggs laid by fleas on calves were viable and larvae were reared to adulthood. The mean percentage hatching success on the age-matched male and female calves was 46.7% and 51.7%. This represents a reduction in viability of 28-33% compared with eggs laid by fleas on cats. Factors which may account for reduced reproductive maturation of fleas on calves, including protein content of the host's blood, are discussed.     

Geographic variation in rodent-flea relationships in the presence of black-tailed prairie dog colonies

We characterized the relationship between fleas and their rodent hosts in the presence of prairie dog colonies and compared them to adjacent assemblages away from colonies. We evaluated the rodent-flea relationship by quantifying prevalence, probability of infestation, flea load, and intensity of fleas on rodents. As prairie dog burrows provide refugia for fleas, we hypothesized that prevalence, flea load, and intensity would be higher for rodents that are associated with black-tailed prairie dog colonies. Rodents were trapped at off- and on-colony grids, resulting in the collection of 4,509 fleas from 1,430 rodents in six study areas. The rodent community composition varied between these study areas. Flea species richness was not different between prairie dog colonies and the surrounding grasslands (p = 0.883) but was positively correlated with rodent species richness (p = 0.055). Prairie dog colonies did not increase the prevalence of fleas (p > 0.10). Flea loads on rodents did not vary between off- and on-colony grids at three of the study areas (p > 0.10). Based on the prevalence, infestation rates, and flea loads, we identified Peromyscus maniculatus, Onychomys leucogaster, and two Neotoma species as important rodent hosts for fleas and Aetheca wagneri, Orchopeus leucopus, Peromyscopsylla hesperomys, Pleochaetis exilis, and Thrassisfotus as the most important fleas associated with these rodents. Prairie dog colonies did not seem to facilitate transmission of fleas between rodent hosts, and the few rodent-flea associations exhibited significant differences between off- and on-colony grids.     

Spatial distribution of fleas (Siphonaptera) in the burrows of the greater gerbil in the south central Kara-Kum

It has been established that only a negligible part of fleas occurs on animals while the main habitats where the greater part of micropopulation is concentrated from April to September are mouth, passages and food chambers situated at a depth up to 60 cm. In March, October, November and December fleas are restricted to the passages of burrows at a depth over 100 cm.     

Sampling fleas: the reliability of host infestation data

The use of measures of host infestation as a reliable indicator of a flea population size to be used in interspecific comparisons was considered. The abundance of fleas collected from host bodies and collected from host burrows was compared among 55 flea species, controlling for the effect of flea phylogeny. The mean number of fleas on host bodies correlated positively with the mean number of fleas in host burrows/nests both when the entire data pool was analysed and for separate subsets of data on 'fur' fleas and 'nest' fleas. This was also true for a within-host (Microtus californicus) between-flea comparison. The results of this study demonstrate that, in general, the index of host body infestation by fleas can be used reliably as an indicator of the entire population size.     

Factors influencing the breeding of the rabbit flea (Spilopsyllus cuniculi): A spring-time accelerator and a kairomone in nestling rabbit urine with notes on Cediopsylla simplex, another "hormone bound" species

Accelerated impregnation and maturation of the rabbit flea coincides with the spring peak litter-size of the rabbit, but its breeding performance falls off before that of the domestic host. A kairomone nestling factor, which boosts copulation, impregnation and development of fleas feeding on the newborn young, is also present in relatively feeble amounts in baby rabbit urine. This urine boosts pairing of matured (="primed") fleas united in tubes away from a host, but impregnation is increased only if fleas are feeding on newborn young while exposed to the urine.
Undeveloped fleas matured on the pregnant doe require a transfer to another host before they will pair, whereas fleas matured on the nestlings copulate without a transfer. A variable time-lag between transfer and copulation of fleas, dependent on the "priming" qualities of the preparatory host, suggests that a chemical intermediary is involved.
If the antennae of the females are coated with vaseline, the maturation of these fleas is delayed feeding on nestlings, but not on the prepartum doe. This delay is less marked during the spring acceleration than at other times of the year.
The breeding of a North American species of hare flea ( Cediopsyllu simplex (Baker)) parasitizing Sylvilagus floridanus (Allen) is also controlled by the sex hormones of the host.     

The ability of flea species on the common vole from mountainous Dagestan to transmit and preserve the causative agent of plague

The infection ability and terms of preservation of plague microbe in fleas of common vole from Dagestan high-mountain plague focus (Frontopsylla causasica, Megabothris turbidus, Ctenophthalmus intermedius and Amphipsylla rossica) was studied experimentally. Block formation and transmission of the infection by F. caucasica and M. turbidus was observed. The transmission of plague microbe by Ct. intermedius fleas was first carried out. These species of fleas preserve the infection for a long time. Experiments with fleas of A. rossica yielded negative results.     

Experimental study of the infecting ability of the flea Coptopsylla lamellifer rostrata in the Kyzylkum natural focus of plague

Experimental infecting of the fleas Coptopsylla lamellifer rostrata by plague was carried out. The fleas were infected by feeding through biomembrane (skin of a white mouse) with a mixture of defibrinated blood of guinea-pig and plague microbes. Under concentration 2-3 milliard of the microbes in 1 millilitre, from 60 to 100% of the fleas were infected. Forming of the block of proventriculus was observed in 9-13 day. Mean percent of blocking for all experiments was less than 1%. Maximal rate of blocking (2.8%) was observed in the experiment under everyday 3-hour feeding. After planting of the fleas with blocks on great gerbil (2 fleas on one gerbil) 20% of the gerbils were infected. The conclusion had been made that C. lamellifer rostrata has only insignificant effectiveness as a vector of plague agent in Kyzylkum. Probably it is caused by some specific features of this subspecies.     

Fleas of small mammals and birds in the forest-park area of the city of Novosibirsk

The distribution of fleas of small mammals and birds in the nidi of tick-borne encephalitis was analysed. 23 species were recorded from the forest-park zone. Palaeopsylla soricis starki, Amalaraeus penicilliger penicilliger, Megabothris rectangulatus, Ctenophthalmus assimilis, Hystrichopsylla talpae were dominant. They amounted to 90% of the total number of fleas. The greatest species variety of fleas was noted in afforested low-lying parts with rich species composition of hosts.     

云南省玉龙鼠疫疫源地野外鼠形动物寄生蚤丰盛度影响因素分析

【目的】分析云南省玉龙鼠疫疫源地野外鼠形动物寄生蚤丰盛度的影响因素。【方法】选取云南省玉龙鼠疫疫源地3个海拔区域,按4个季节进行野外捕鼠,捕获的鼠形动物用梳检法收集体表寄生蚤并在显微镜下分类鉴定。通过实际测量和实地观察相结合的方式收集潜在影响鼠形动物寄生蚤丰盛度的因素包括鼠形动物特征变量指标(如种类、年龄、性别、体长、体重)、环境和气象因子(如海拔、季节)等数据。采用EpiData 3.02软件建立数据库,在R软件下使用跨栏负二项分布回归分析鼠形动物寄生蚤丰盛度的影响因素。【结果】从捕获的884只鼠形动物中检获寄生蚤9种484头,以特新蚤指名亚种、方叶栉眼蚤、无值大锥蚤、云南栉眼蚤为主(86.16%)。回归分析显示： 2 700-3 000 m和3 000 m以上海拔鼠形动物染蚤概率较2 400-2 700 m分别增加1.27和3.72倍;湿度高于70%时,鼠形动物染蚤概率较湿度≤70%时减少41%;与齐氏姬鼠的染蚤概率相比,中华姬鼠的染蚤概率降低50%,大绒鼠的染蚤概率增加79%;体长超过104 mm的鼠形动物染蚤概率较体长≤104 mm的鼠形动物染蚤概率增加76%;气温高于15℃时,鼠形动物染蚤数量较温度≤15℃时降低67%;成年鼠形动物的染蚤数量较未成年鼠形动物的染蚤数量增加2.25倍;与春季相比,夏季的染蚤数量增加2.00倍,秋季的染蚤概率减少48%,冬季的染蚤概率和染蚤数量分别增加1.44和1.06倍。【结论】玉龙鼠疫疫源地野外鼠形动物寄生蚤以特新蚤指名亚种、方叶栉眼蚤、无值大锥蚤、云南栉眼蚤为优势蚤种。鼠形动物寄生蚤丰盛度与海拔、季节、气温、湿度等环境气象因子及鼠形动物种类、体长、年龄等鼠形动物特征变量密切相关。     

The Ectoparasites of the European Badger, Meles meles, and the Behavior of the Host-Specific Flea, Paraceras melis

The badger-specific flea, Paraceras melis, jumps repeatedly when separated from its host Meles meles; thereafter fleas settled into sheltered positions. After separation from badgers, some 42% of fleas (n = 63) voided their gut contents; this was associated with a significant increase in mean jumping distance. The maximum longevity of fleas away from the host was 89 days, with 50% mortality at around 35 days. Badger lice, Trichodectes melis, survived for up to 3 days postcapture. We conclude that the badger's habit of frequently swapping dens with a mean period of return of 6 days is unlikely to bring about significant mortality of adult fleas but may effectively eradicate lice. Fleas abandoned in bedding in a simulated badger sett were mobile, being drawn toward light and moving upward. This response would draw the fleas to the den entrance, which may be a suitable site to intercept returning badgers. The fleas responded to stimuli which might signal the proximity of the host: they jumped toward sources of carbon dioxide and of carbon dioxide in air current directed at the flea. The strongest response was seen when a mixture of stimuli consisting of carbon dioxide, a dark circle of card, and movement were tested; the majority of fleas jumped toward the mixed stimulus. Finally, fleas separated from the host responded to exhaled air by running and jumping; this is in marked contrast to their response to those stimuli when on the host, when fleas run downward and very rarely jump. These contrasting observations find adaptive explanation in the two contexts.     

The flea epifauna of a suburban fox (Vulpes vulpes) population

Five hundred and thirteen fleas, of eight different species, were collected from a sample of 252 foxes killed in suburban London. 25–8% of foxes carried fleas, with a mean of 204 fleas per fox. Levels of infestation of male and female hosts did not differ significantly. Possible sources of the fleas infesting foxes are discussed with respect to their seasonal occurrence and fox prey composition. No evidence was found to support the suggestion that foxes obtain the majority of their fleas from prey items, although occasional heavy infestations of some flea species were probably derived from recent meals. Although Pulex irritans, Paraceras m. melis and Ctenocephalides canis , which contributed 35 % of the flea epifauna, could be considered parasitic on the fox, it seems probable that foxes pick up the majority of their fleas from the habitat through which they move. Thus, two particularly heavily infested categories of foxes were found: (1) juveniles during July-September, their fleas probably being accumulated during exploratory and play activities, and (2) all animals during the period October-December.     

An attempt to protect cats against infestation with Ctenocephalides felis felis using gut membrane antigens as a vaccine

Cats (n = 5) were vaccinated with membrane antigens extracted from the gut of unfed fleas (Ctenocephalides felis felis) together with Quil A and RIBI as adjuvants. Five unvaccinated cats were retained as controls. All the cats were infested on 6 separate occasions with fleas (46–250 per challenge). Protection was assessed from the number of fleas retrieved and the fecundity of the female fleas, measured as the number of developed oocytes contained in the reproductive tract. Cats injected with gut membrane antigens had significantly elevated levels of anti-flea antibodies in their sera, but they were neither protected significantly against infestation with fleas nor was the apparent fecundity of fleas which had fed on vaccinated cats decreased. The possible reason why gut membrane antigens failed to protect cats against fleas are discussed.     

Notes on the life-history of the rabbit flea Caenopsylla laptevi ibera Beaucournu & Marquez, 1987 (Siphonaptera: Ceratophyllidae) in eastern Spain

The rabbit flea Caenopsylla laptevi ibera occurs in arid environments of central and eastern Spain. Although the fleas breed during the coolest, most humid part of the year, the larvae survive and grow in sand at only 50-60% relative humidity. At 22 degrees C and 80% relative humidity eggs hatch in six days and the cocoon stage is reached 10-11 days after hatching. Female fleas emerge from pupation at about 17 days after cocoon spinning; males emerge a little later at a mean of 20 days. Adult fleas are mainly found on the host Oryctolagus cuniculus. Measurements of burrow microclimate confirmed that in south-eastern Spain burrow humidity was adequate for the development of C. I. ibera larvae over most of the year. However, breeding may be restricted for at least part of the year, as the larvae of C. I. ibera apparently cannot complete development at 25 degrees C or above. In the laboratory, fleas can enter a prolonged quiescent period while in the cocoon. This is possibly a facultative, pre-pupal diapause and the likely mechanism that accounts for the disappearance of adult fleas from the field by spring and their reappearance each autumn.     

Driven to distraction: detecting the hidden costs of flea parasitism through foraging behaviour in gerbils

Gerbilline rodents such as Allenby's gerbils (Gerbillus andersoni allenbyi), when parasitized by fleas such as Synosternus cleopatrae pyramidis, devote long hours of grooming to remove the ectoparasites. Yet no detrimental energetic or immunological effects of the ectoparasites have been found in adult Allenby's gerbil. Why should gerbils go to such trouble? We tested for the various ways that fleas can negatively affect gerbils by manipulating flea infestation on gerbils and the presence of a fox. We demonstrate that gerbils responded to fleas by leaving resource patches at higher giving-up densities. Furthermore, they stayed in those resource patches less time and left them at higher quitting harvest rates so long as a fox was also present. When flea-ridden, gerbils also abandoned using vigilance to manage risk and relied mainly on time allocation. Thus, having fleas imposed a foraging cost similar in nature to that arising from the risk of predation from foxes and may be even larger in magnitude. More than that, the presence of fleas acted as a magnifier of foraging costs, especially those arising from the risk of predation. The fleas reduced the gerbils' foraging aptitude and altered how they went about managing risk of predation. We hypothesize that fleas reduce the attention that gerbils otherwise have for foraging and predator detection. We suggest that this is the major cost of ectoparasitism.