At the turn of the 19thcentury the first observations of a female-biased sex ratio in broods and populations of the head louse,Pediculus humanus capitis, had been reported. A study by Buxton in 1940 on the sex ratio of lice on prisoners in Ceylon is still today the subject of reanalyses. This sex ratio distortion had been detected in ten different countries. In the last sixty years no new data have been collected, especially on scalp infestations under economically and socially more developed conditions.
Here we report a female bias of head lice in a survey of 480 school children in Argentina. This bias is independent of the intensity of the pediculosis, which makes local mate competition highly unlikely as the source of the aberrant sex ratio; however, other possible adaptive mechanisms cannot be discounted. These lice as well as lice from pupils in Britain were carrying several strains of the endosymbiotic bacteriumWolbachia pipientis, one of the most wide spread intracellular sex ratio distorters. SimilarWolbachiastrains are also present in the pig louse,Haematopinus suis, suggesting that this endosymbiont might have a marked influence on the biology of the whole order. The presence of a related obligate nutritional bacterium in lice prevents the investigation of a causal link between sex ratio and endosymbionts.
Regardless of its origin, this sex ratio distortion in head lice that has been reported world wide, is stable over time and is a remarkable deviation from the stability of frequency-dependent selection of Fisher's sex ratio. A female bias first reported in 1898 is still present over a hundred years and a thousand generations later.
The early but comprehensive literature on human head lice,Pediculus humanus capitis, reveals a surprisingly homogeneous female bias of the sex ratio world wide [1–3]. The first reported observation of more female than male lice on human heads reaches back to Harding in 1898 in the USA . Records of sex ratios in human head lice in Britain [2,3], Kenya [3,4], Tanzania, Colombia, Australia , Nigeria, Ceylon, Palestine , India [4,5], and North America  show ~65% of the adult lice to be female. Reanalyses of data collected in 1938 are still employed to deduce life history traits of human head lice [4,7,8]. The female bias of natural populations on heads is conserved in the sex ratio of individual broods of experimental infestations [2,6,7]. Many of the people sampled in these studies had been afflicted by poverty, confinement or war. However, in the last sixty years no data have been collected, especially on more normal levels of infestations. Local and temporary deviations from equality of the operational sex ratio should be expected as natural fluctuations. We wanted to find out whether this deviation is also maintained over time. Roughly one hundred years after the original surveys, we determined the sex ratio of adult head lice on pupils from 6 different schools in Argentina. This cohort is different from earlier studies in that it does no longer show any extremely high infestations due to an increase in general living standards. Nevertheless, a female bias is still preserved.
Sex ratio distortions in arthropods frequently originate from cytoplasmic or extrachromosomal factors and parasites of the host and are most often associated with the endosymbiontWolbachia pipientis.Wolbachiahas been shown to induce parthenogenesis in haplodiploid Hymenoptera and diplodiploid Collembola, feminisation in terrestrial isopods, and male killing in many insect species [9–13]. A new bacterium from the Bacteroidetes group (Cytophaga-Flavobacterium-Bacteroides, CFB) has been linked with feminisation and parthenogenesis in mites and insects [14–16]. We screened human lice from Argentina and Britain and pig lice form Poland for the presence ofWolbachiaand CFB bacteria.
Results and discussion
A total of 480 heads were screened for adult lice along 6 schools exhibiting a prevalence of 29.8% (infested heads with at least 1 adult louse/head). 10.5% of the infested heads (15 heads, 94 lice) showed a male bias, 16.8% of the infested heads (24 heads, 32 lice) had only males, 14.7% of the infested heads (21 heads, 72 lice) had an equal sex ratio, 28.0% (40 heads, 344 lice) had a female bias and an additional 30.0% of the children (43 heads, 55 lice) did not carry any male lice, Fig.1. This translates into an overall female bias of 59.6% (1.48) and a relative sex ratio of 0.40 (males/(males + females)) in all the populations based on 356 females and 241 males. The regression line for the distribution of female and male lice differs from an equal sex ratio distribution by a power of p < 0.01 using Fisher's exact test (Fig.1). There is no difference between boys and girls. This is also the first survey of sex ratio in human head lice for South America. Applying the standard deviation of the data in Fig.1, Fig.2shows the frequencies of heads that deviate from a normal distribution of sex ratio. Each of the six schools shows individually a female bias and replicate the bias of all the populations, Fig.3. There is no difference between urban and rural schools. These results in female bias correspond with the data by Buxton and others [5–7]. The probability of a sampling error is p < 0.05; the difference of the actual percentages from 50 is 3.34 times the standard error of this difference [7,18]. Fig.4shows that this bias is independent of the intensity of infestation confirming earlier studies by Lang and others . This suggests that the female bias is both conserved in space and time.
Pediculid lice are diploid amphimictic and exhibit an extra mitotic division following meiosis during spermatogenesis.Pediculusare sexually dimorphic with a small proportion of hermaphrodites. Siblings are not gregarious, males are abundant, both sexes eclose at similar times, mating starts within one day after eclosure or encounter, males are very promiscuous, females do not seem to store sperm, frequent copulation is a requirement for laying fertile eggs and both sexes show active migratory behaviour. At the moment it is difficult to determine the sex of immature stages and the sex-specific mortality of immature stages directly. However, single-pair matings sometimes produce all of one sex. Differential mortality of nymphs does not account for the unusual sex ratio under non-crowding conditions.P. capitisdoes not exhibit parthenogenesis or delayed fertilisation. The sex ratio does not change with increasing age of the mother. No evidence has been found that any environmental factor has any effect upon the sex ratio. Only in a single case under very crowded conditions, a male bias has been observed on some heads by Buxton [7,17]. He attributes this to a severely reduced life span of females . The shortened life expectancy of females is ascribed to copulation prior to full sclerotisation leading to injury and death . A selective reduction in life expectancy of females under crowded condition has also been observed in other insect taxa, e.g., tsetse flies. However, highly infested heads with a maximum of 1,434 lice in a study by Roy and Ghosh still showed a female bias .
Focusing on the data which Buxton obtained in the Colombo prison in Sri Lanka from 1934 to 1936 that also showed a female bias, Rózsa suggests that the prison environment could increase inbreeding in lice. He argues that the transmission rate was likely to be low simply because the prison host population consisted of adult males only and because the prisoners couldn't get rid of their lice; these infrapopulations would subsist through several generations. These arguments were employed by Rózsa as indications for local mate competition leading to an adaptive sex-ratio manipulation by the lice . This is neither supported by our data nor the data of Buxton, Roy and Ghosh, or Lang [5–7]. There is no evidence that female lice can manipulate the sex ratio of their offspring. Rózsa claims that both, individual heads of the men in jail and the prison itself constitute viscous populations in Hamilton's sense – that is to say, one where the individual louse can mate only with a rather permanent set of neighbours who tend also to be his relatives . Whoever has or has had school children to look after can confirm that individual heads of pupils do not constitute a viscous population. Exchange of adult lice between heads is constantly ongoing and is a major reason for the continuous spread of lice in our society. Our data show that the female bias is present on individual heads as well as in all six schools surveyed. All the schools are coeducational.
Hamilton has proposed local mate competition as an explanation of female biased sex ratios in insect and mite populations. All the arthropod populations listed by Hamilton are characterised by inbreeding and haplodiploidy . An ideal for an extreme biofacies may be described by eight properties. One, the primary sex ratio is spanandrous – that is, females greatly preponderate. In human lice, the operational sex ratio is close to equality. The sex ratio determined by dissecting second instar nymphs and the sex ratio at eclosion of imagines of experimental broods is not more spanandrous than the operational sex ratio. Broods of individual female lice exhibit the whole spectrum from male only offspring to female only offspring. Two, reproduction is arrhenotokous. Lice are diplodiploid and reproduction is amphimictic. Three, there is at least one male in every batch of offspring. Egg laying in the human head louse starts with the first blood meal regardless of insemination; it is more continuous given sufficient food than in batches. The complete brood of a female might contain only males, only females or any ratio in between. Four, there is gregarious development, as a group of siblings, from egg to adult. Unlike the body louse where the female tends to return to the same spot for oviposition and which will lead to a clustering of eggs, siblings of head lice are practically not gregarious. Five, adult males eclose first and can mate many times. Both sexes of head lice eclose at similar times but males are very promiscuous. Six, mating takes place immediately after (or even before) eclosure of adult females. Mating continues to take place at any time of the day or night and during the whole adult life span of lice. Mating happens as much before as after dispersal and both sexes show the same active migratory behaviour. Seven, males are disinclined, or unable, to emigrate from the batch. Male lice disperse as eagerly as females. This is very obvious in our data in the number of heads carrying male lice only (Fig.2). Eight, females can store sperm; one insemination serves to fertilise the whole egg production. Female lice are stated to have no receptaculum seminiis (spermatheca) and therefore are considered not to be capable of storing sperm. Nevertheless, Bacot reported in 1916 a record observation for a female being able of laying fertile eggs twelve days after the removal of the male; however, the maximum ever observed by Nuttall in 1917 is only five days, which is in line with the assumption of limited or no sperm storage capability. These eight reproductive properties of lice make local mate competition as the cause of a female-biased sex ratio completely impossible. Further work on Hamilton's hypothesis has shown that within each local group, even if founded by a single female, the sex ratio favoured by individual selection is equality [20–23]. However, groups founded by female-biased genotypes contribute more individuals to the population as a whole than groups founded by unbiased genotypes . This requires the ability of kin recognition and selection. However, in the female-biased parasitoid waspNasonia vitripennis, which is often used in textbooks as an example of local mate competition, mothers cannot discriminate between kin . In many cases in which the female bias could not be attributed to local mate competition, local resource competition among females or female-biased dispersal have been put forward as alternative explanations [eg., [26,27]]. Local resource competition and differential dispersal can be ruled out in head lice for the same reasons discussed earlier for local mate competition. Why, for example, parasitoid wasps likeMelittobia digitatathat seemingly fit all the requirements set out by Hamilton fail to meet the sex ratio prediction of the local mate competition hypothesis remains unsolved . Orzack emphasises that the occurrence of local mate competition is not documented for most species whose sex ratios have been explained by it . He also documents that the original evidence presented by Hamilton in support of local mate competition is not as clear as originally assumed. This suggests that major adaptive and parasitic sex ratio effecting mechanisms still remain to be discovered.
Hamilton himself detected a maternally inherited microorganism, later identified as the endosymbiontWolbachia, in four species of parasitoid wasps belonging to the genusTrichogramma, a genus originally listed as an example of an extreme biofacies leading to local mate competition. Removal of the bacterium changed reproduction from female only thelytoky to biparental arrhenotoky . The possibility that maternally inherited bacteria might bias the sex ratio in favour of females has long been predicted . Parthenogenesis-inducingWolbachiaare quite common in parasitoid wasp species . However, in some species of female-biased parasitoid waspsWolbachiadoes not influence the sex ratio directly. In double infectedNasoniafor example, two strains ofWolbachiainduce cytoplasmic incompatibility, inAsobara tabida, one of the threeWolbachiastrains of the triple infection is essential for oocyte maturation, and inMelittobia australica, the effect ofWolbachiaremains to be determined [33–35].
A sex ratio bias is often more likely related to the physiological state of its host and is consequently not directly controlled by the mother . The physiological state includes the manipulation by symbiotic microorganisms. In the analysis and interpretation of sex ratio deviations, the discrimination between primary sex ratio and functional sex ratio is pivotal . This allows the identification of symbiotic sex ratio distorters.
Using the polymerase chain reaction and specific primers for 16S rDNA and theWolbachiaouter surface protein genewsp, we demonstrated the presence ofWolbachia pipientisin two blood-sucking Anoplura species, the human lousePediculus humanus capitis, Pediculidae, and the pig louse,Haematopinus suis, Haematopinidae. Primers for insect-like CFB bacteria did not amplify any product; primers for mite-like CFB bacteria resulted only in unrelated lice sequences indicative for the absence of a specific target sequence. The highest amounts ofWolbachiawere detected in thorax and head. All lice tested of both species harbouredWolbachia. TheWolbachiainfection is likely close to fixation, which suggests either a relatively young infection showing no signs of host resistance or indicates an essential function forWolbachiain the development and survival of its lice hosts. The fact that two phylogenetically very different lice species with two distinct hosts show similar high levels of penetrance ofWolbachiainfection on two different continents leads us to expectWolbachiainfections to be widespread in many lice species. Thewspgene ofWolbachiais one of the fastest evolving.Wspsequences ofWolbachiafrom human and animal lice overlap. NoWolbachialineage specific to a louse species or to a louse host could be identified. Comparison of thewspsequences revealed no special position of liceWolbachiaamong other insectWolbachiastrains (Fig.5). All lice showed double infections with two differentWolbachiastrains based onwspsequence. Human head lice from two continents have been analysed. Head lice from South America, Argentina, exhibit infections of two different strains ofWolbachiafrom supergroup A,wMel and a new group, which we propose to callwPcap, while from Europe, Wales, only two similar strains of supergroup A (wRi) have been detected. In contrast, pig lice harbourWolbachiafrom supergroup A (wRi) and supergroup B (wCon closest to strainwStr1). While double infections with two A supergroupWolbachiamight reflect recombination events or in-host diversification ofWolbachia, double infections with A and B supergroup bacteria are likely to originate from repeated episodes of horizontal transmission. The diversity of A and B supergroupWolbachiamake it seem possible that lice have received recent horizontal transfer from a wide spectrum ofWolbachiadonors. An infectious form ofWolbachiais not known. It is always vertically transmitted within a species. Lice are one of very few insect taxa that are not attacked by parasitoid wasps and endoparasitic Strepsiptera. Parasitoid wasps are the only so far confirmed vectors for horizontalWolbachiatransmission; the role of Strepsiptera in interspecies transmission is still controversal . Interestingly, we were unable to find any report about lice-specific mites or nematodes, theorised vectors ofWolbachia. The literature is limited to the protozoan gut parasite of body lice, 'Crithidia' orHerpetomonas pediculiand omniphagous steinernematid and heterorhabditid nematodes, which do not carryWolbachia[39–42]. This lack of parasites might be due in part to a deficiency of research; however, it requires at present to postulate a new route for the horizontal transmission ofWolbachiato and within lice species.
Microscopic analysis shows that intracellularWolbachia-like bacteria are not associated with the well described but yet unidentified nutritional lice endosymbionts found in mycetomes (Fig.6). While the bacteria originating from the stomach disc mycetome migrate to the ovaries and enter the developing oocyte at a specialised invagination forming the future mycetome [43–45], intracellularWolbachia-like bacteria are already present in the egg cell and are dispersed in the cytoplasm of the egg. Due to the difficulty of cutting thin sections of the yolk part of eggs,Wolbachiainfections are easily missed in ultrastructural investigations.
The sex ratio bias reported here for the human head louse does not seem to be an isolated phenomenon. Unusual sex ratios have also been reported for the human body louse,Pediculus humanus humanus(P. corporis,P. vestimenti), the human pubic louse,Pthirus pubis, the cattle biting louseBovicola bovis, the shortnosed cattle louse,Haematopinus eurysternus, the longnosed cattle louse,Linognathus vituli, and the little blue cattle louse,Solenopotes capillatus[3,46,47,48,49]. The biting louseB. bovisalso exhibits parthenogenetic reproduction. The search forWolbachiain many biting and sucking lice (Anoplura, Mallophaga) is ongoing .
Human head lice show a female biased sex ratio that has been conserved for over 100 years with a global distribution which represents a remarkable deviation from the stability of frequency-dependent selection of Fisher's sex ratio [1,51]. The association of this sex ratio distortion with a sex-ratio distorting endosymbiont is intriguing. A direct treatment of lice with antibiotics to cure them ofWolbachiais not feasible at the moment because of the lethal effect on mobile stages of lice, as it eliminates the Gram-negative obligate lice endosymbionts as well . Male killing is one of several possible mechanisms leading to distorted sex ratios. In other insects, male-killingWolbachiaact at the earliest stages of development and manifest as eggs that fail to hatch . Indeed, Buxton identified the failure of eggs to hatch as an important cause of mortality inPediculus humanuscorresponding to what would be expected with low-level male killing as it is well known, for example in lady bird beetles [54,55]. Mortality data have not been reported for head lice. In a new study we determined the number of empty eggs, alive eggs, nymphs, and adults of 300 children of two coeducational schools at an age between 6 and 8 years, Fig.7. Per head, alive eggs represent 90% of the accountable metapopulation, nymphs and adults, which can be combined as mobiles, account for the further 10%. This relationship is not affected by the social status of the pupils. The living standard of the children might be used as a proxy of environmental influences on the lice. In Fig.8, we compared the data from a school (A, 161 children) in a deprived neighbourhood with the data from a school in an affluent surrounding (B, 139 children). The pattern is identical. The correlation between living eggs and mobiles is significant (p < 0.01) and suggests a high mortality at the egg stage, Fig.9, the origin of which remains to be determined.
Adaptive sex ratio distortions fluctuate over time and are often specific to local habitats and environmental conditions. Mechanisms such as local mate competition, local resource competition or differential dispersal can lead to female bias populations. The female bias in the human head louse cannot be ascribed to any of these three mechanisms. This bias is found on 4 continents. It is stable over more than one century. This makes it one of the best documented deviations from the stability of frequency-dependent selection of Fisher's equal sex ratio.
The surveys and collections of head lice have been conducted between October 2000 and August 2003. In Argentina, the schools are situated in urban and rural parts of the provinces of La Rioja and Córdoba. The lice were collected by the authors [AVO and SSC]. The hair was wetted and treated with conditioner. With the help of a metal comb, eggs, nits and adults were collected under water and immediately transferred into 95% alcohol. This method of collecting lice preludes any sampling bias favouring larger females over smaller males as suggested by Nuttall and Marshall . Eggs and empty egg cases were distinguished and the sexes of imagines were determined using a light microscope. The lice samples from Britain were collected by their parents in Llandudno, Conwy, and Bangor, Gwynedd, both in northern Wales, United Kingdom. The pig lice were collected from domestic pigs kept on a small farm near Kraków, Poland.
Total genomic DNA was extracted from single lice. Males and females were sectioned in two parts: head-thorax and abdomen and DNA was extracted separately for both sections. QIAGEN DNAeasy™ Tissue Kit was used for DNA extraction following the DNeasy Protocol for Animal Tissues. The DNA obtained was purified with 10% CHELEX®100 at 60°C for 2 h. The samples were centrifuged at 8,000 rpm for 5 min and the supernatant was stored at -20°C. PCR was performed with specific primers forWolbachia16S rDNA, 99F and 994R ,Wolbachiaouter surface protein,wsp81F andwsp691R  and universal primers for 28S rDNA, 28Sa and 28Sb  as control. CFB bacteria were detected with primers for 16S rDNA. Primers for insect-like CFB bacteria were based on sequences derived from the parasitoid wasps of the genus Encarsia, EPS-f and EPS-r , mite-like CFB bacteria were designed with the help of the sequence from the feminised miteBrevipalpus phoenicis, GenBank accession AF350221, CFBmite16S-F 5'-CCT GCG GGG GCT CTT GA-3' and CFBmite16S-R 5'-GGG TTT CGC TCG TTA TAG GAC TTA-3' amplifying a 644 bp fragment inB. phoenicis. Relative amounts were estimated with serial dilutions of the template before amplifications. The products were ligated into QUIAGEN pDrive Cloning Vectors and 8 positive colonies per ligation were sequenced in both directions. The sequences are deposited in GenBank with accession numbers AY596781-AY596786.
Field and laboratory work in Argentina (SSC and AO) have been supported by Fundación Barceló. MAP and HRB are supported by funding from the Natural Environment Research Council (GR3/13199) and HRB acknowledges funding by the European Commission (EUWOL, QLRT-2000-01079).
School of Biological Sciences, University of Wales
Fundación Barceló Crilar,
Department of Systematic Zoology, Institute of Zoology, Jagiellonian University
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