- Research article
- Open Access
Pair of lice lost or parasites regained: the evolutionary history of anthropoid primate lice
© Reed et al; licensee BioMed Central Ltd. 2007
- Received: 15 September 2006
- Accepted: 07 March 2007
- Published: 07 March 2007
The parasitic sucking lice of primates are known to have undergone at least 25 million years of coevolution with their hosts. For example, chimpanzee lice and human head/body lice last shared a common ancestor roughly six million years ago, a divergence that is contemporaneous with their hosts. In an assemblage where lice are often highly host specific, humans host two different genera of lice, one that is shared with chimpanzees and another that is shared with gorillas. In this study, we reconstruct the evolutionary history of primate lice and infer the historical events that explain the current distribution of these lice on their primate hosts.
Phylogenetic and cophylogenetic analyses suggest that the louse genera Pediculus and Pthirus are each monophyletic, and are sister taxa to one another. The age of the most recent common ancestor of the two Pediculus species studied matches the age predicted by host divergence (ca. 6 million years), whereas the age of the ancestor of Pthirus does not. The two species of Pthirus (Pthirus gorillae and Pthirus pubis) last shared a common ancestor ca. 3–4 million years ago, which is considerably younger than the divergence between their hosts (gorillas and humans, respectively), of approximately 7 million years ago.
Reconciliation analysis determines that there are two alternative explanations that account for the current distribution of anthropoid primate lice. The more parsimonious of the two solutions suggests that a Pthirus species switched from gorillas to humans. This analysis assumes that the divergence between Pediculus and Pthirus was contemporaneous with the split (i.e., a node of cospeciation) between gorillas and the lineage leading to chimpanzees and humans. Divergence date estimates, however, show that the nodes in the host and parasite trees are not contemporaneous. Rather, the shared coevolutionary history of the anthropoid primates and their lice contains a mixture of evolutionary events including cospeciation, parasite duplication, parasite extinction, and host switching. Based on these data, the coevolutionary history of primates and their lice has been anything but parsimonious.
- Much Recent Common Ancestor
- Host Switch
- Partition Homogeneity Test
- Parasite Tree
- Coevolutionary History
Sucking lice (Phthiraptera: Anoplura) are permanent and obligate ectoparasites of eutherian mammals. These highly specialized blood-sucking insects live in close association with their hosts and complete their entire life cycle on the host . Anoplurans have modified mouthparts for feeding on host blood and because mammalian blood differs widely among species in terms of its suitability for louse nutrition , sucking lice can be highly host specific [1, 3]. Host specificity could also be reinforced by interactions with the host's immune system. High host specificity can arise from a long history of cospeciation between hosts and their parasites. Cospeciation is speciation (or cladogenesis) in a parasite lineage as a result of, or at the same time as, host cladogenesis . The current distribution of parasites on host taxa (the host-parasite associations) can be the result of cospeciation or various historical events  such as host switching, sorting events (extinction and lineage sorting), duplication events (parasites speciating on a single host lineage), and failure of the parasite to speciate when the host speciates ('missing the boat'; ). These historical processes can be detected by comparing the phylogenies of hosts and their parasites using methodologies such as reconciliation analysis . Previous cophylogenetic studies of lice (both sucking lice and chewing lice) have documented each of these historical events in various combinations (for a review, see ).
The alternative hypothesis involves an ancient louse duplication event that occurred on the ancestor of gorillas, chimpanzees, and humans, which would have created the lineages leading to the two extant genera, Pediculus and Pthirus (Figure 2B). In this case, the timing of the divergence between Pthirus pubis and Pthirus gorillae would correspond to that of their hosts (ca. 7 MYA; ). In this scenario, humans would have retained both genera, but chimpanzees would have lost a Pthirus species and gorillas would have lost a Pediculus species to extinction (Figure 2B). Such parasite duplications and extinctions are common in the lice of birds and mammals (e.g., ). This parasite extinction or 'pair of lice lost' model is less parsimonious than the 'recent host switch' hypothesis listed above because it requires at least three evolutionary steps (a duplication of the parasite on a primate common ancestor as well as the extinction of one Pediculus and one Pthirus lineage, Figure 2B). Although the 'recent host switch' hypothesis is more parsimonious, it is not necessarily more likely than the 'pair of lice lost' hypothesis. Each of the historical events (host switch, duplication, and extinction) has some probability of occurrence, the quantification of which is beyond the scope of this paper. There are additional hypotheses that can be postulated that have more evolutionary steps than the two presented above, however there are no other hypotheses that have an equal number of steps or fewer steps. For instance, one might assume that the current distribution of lice resulted from a host switch of Pthirus from humans to gorillas (the opposite direction of the switch in the 'recent host switch' model). However, this evolutionary scenario would require at least five evolutionary steps.
The two hypotheses of parasite distributions ('pair of lice lost' and 'recent host switch') are based on the premise of maximizing the number of cospeciation events and minimizing the number of events that deviate from cospeciation, which are typical of analyses that attempt to reconcile host and parasite associations that are based on the concept of evolutionary parsimony (reconciliation analysis as implemented in TreeMap; ). However, parsimony-based reconciliation analyses do not take into account branch lengths and divergence times – information that is essential to distinguish between the 'recent host switch' and 'pair of lice lost' hypotheses. In the presence of significant cospeciation we can use the timing of speciation events to differentiate among alternative hypotheses of host-parasite associations .
We have performed phylogenetic and cophylogenetic analyses of two genes, the mitochondrial cytochrome c oxidase subunit I (Cox1) gene and nuclear gene elongation factor 1 alpha (EF-1α) gene, to determine the shared evolutionary history of primate lice and their hosts. We also investigate the use of standard phylogenetic methods for reconstructing coevolutionary histories when standard cophylogenetic methods (e.g., reconciliation analysis) cannot always find the solution that best fits the observed data.
Phylogenetic and cophylogenetic analyses
Cophylogenetic analyses using TreeMap  produced two reconciliations of host and parasite phylogenies in agreement with the 'recent host switch' and 'pair of lice lost' hypotheses presented in Figure 2. The reconciliation concordant with the 'recent host switch' hypothesis (Figure 2A) included five cospeciation events and one host switch for a total cost of 1.0. The reconstruction concordant with the 'pair of lice lost' hypothesis (Figure 2B) was less parsimonious. While this reconstruction included five cospeciation events, there was also a single duplication event and two losses resulting in a total cost of 3.0. Both reconciliations show significantly greater similarity between the host and parasite trees than would be expected based on chance alone (i.e., both reconciliations show significant cospeciation, p < 0.05).
Divergence date estimation
Divergence date estimates.
MRCA (clade number)
Cox1 and EF1α
Cox1 and EF1α (r8s, 20 MYA)
Cox1 and EF1α (r8s, 25 MYA)
Cox1 (r8s, 20 MYA)
Cox1 (r8s, 25 MYA)
P. schaeffi and P. humanus (2)
Pediculus and Pthirus (4)
Reconciliation analysis using TreeMap corroborates earlier reports of significant cospeciation between primate lice and their hosts . These cophylogenetic analyses also result in two reconciliations of the host and parasite phylogenies where the most parsimonious reconstruction favors the 'recent host switch' hypothesis (Figure 2A). However, divergence date estimates conflict with the results of the reconciliation analysis because the 'recent host switch' hypothesis predicts that the divergence of Pediculus and Pthirus would be roughly contemporaneous with the split between gorillas and the lineage leading to humans and chimpanzees. Our estimates of the MRCA of Pediculus and Pthirus dates to roughly 13 MYA, not remotely consistent with the MRCA of humans, chimpanzees, and gorillas (ca. 7 MYA; ). Given the much older age of our MRCA of Pediculus and Pthirus, it is more appropriate, although less parsimonious, to assume that the origin of the two genera was the result of a parasite duplication event rather than a cospeciation event ('pair of lice lost' hypothesis; Figure 2B). It is curious that the estimate of the MRCA of Pthirus and Pediculus (13 MYA) is contemporaneous with the divergence of Orangutans from other apes , however this is possibly coincidental. Lice do not parasitize orangutans; therefore, reconstructing their role in the evolutionary history of primate sucking lice will be difficult.
The 'pair of lice lost' hypothesis is also unsatisfactory when compared to divergence date estimates. For the 'pair of lice lost' hypothesis to be correct we must assume that divergence between Pthirus pubis and Pthirus gorillae is roughly contemporaneous with the split of gorilla from the lineage leading to chimpanzees and humans (i.e., ca. 7 MYA). Our divergence date estimates of roughly 3–4 MYA (Table 1) is much younger than the host divergence of 7 MYA  and is even younger than the divergence between chimpanzees and humans (ca. 6 MYA).
The estimates of divergence dates argue for a more complex evolutionary history than estimated by reconciliation analysis. While reconciliation analysis serves to find the most parsimonious reconstruction of host and parasite evolutionary history by maximizing cospeciation events and minimizing the cost of the reconstruction, it can only identify possible scenarios describing the evolutionary history between associated taxa. Incorporating branch length data in other analyses is necessary to determine which scenario best fits the observed data. For example, post-hoc Mantel tests are commonly used to look for overall correlation in host and parasite data sets . However, we have too few taxa to perform such an analysis, and we have instead relied upon ad-hoc phylogenetic tests to determine whether certain nodes of cospeciation were contemporaneous.
To further examine the validity of the 'pair of lice lost' hypothesis, we assessed whether the divergence of the two Pthirus species was contemporaneous with the host divergence of roughly 7 MYA. The branch length between the two Pthirus species in the best-fit ML louse tree was artificially lengthened to approximate a branch that is the same age as the branch between Pediculus schaeffi and Pediculus humanus, thereby representing the split between chimp and human lice. It is widely known that the gorilla, chimpanzees, and human divergence times are very close in age, so if our estimate is contemporaneous with the divergence of chimpanzees and humans (the most conservative expected age), then we cannot rule out true contemporaneous times of divergence between the two Pthirus species and their hosts. The likelihood score of this constrained tree (with a branch length approximating a 6 million year divergence between Pthirus gorillae and Pthirus pubis) was significantly worse than the true louse tree (where the estimated divergence was closer to 3–4 MYA; d.f. = 6, χ2 = 12.91, p = 0.044). We can therefore reject contemporaneous divergence events and we can conclude that the split between the human and gorilla species of Pthirus diverged much more recently than the split between humans and gorillas or even humans and chimpanzees. The divergence within Pthirus is therefore the result of a host switch from gorillas to humans (loosely defined) roughly 3–4 MYA, as predicted in the 'recent host switch' hypothesis.
We can similarly examine the divergence date estimation for the branch between Pthirus and Pediculus, which the 'recent host switch' model would predict to be 7 MYA. Our estimates were much older (Table 1), and shortening the branch length artificially between Pthirus and Pediculus to resemble a divergence near 7 MYA can be easily rejected (p < 0.01). These analyses support an ancient duplication at that node, consistent with the 'pair of lice lost' model. Therefore, contrary to the results of the reconciliation analysis, the divergence date estimates predict a much less parsimonious explanation of current primate louse distributions: a combination of the 'recent host switch' and 'pair of lice lost' hypotheses.
Evidence suggests that Pthirus pubis has been associated with humans for several million years, and likely arrived on humans via a host switch from gorillas. Despite the fact that human pubic lice are primarily transmitted via sexual contact, such contact is not required to explain the host switch. Parasites often switch from a given species to a predator of that species , and are sometimes found to switch to unrelated hosts in communally used areas, such as roosting or nesting sites . The host switch in question could have resulted from any form of contact between archaic humans and gorillas including, but not limited to, feeding on or living among gorillas. Regardless of how the transfer occurred, suitable habitat had to be available on the new human host for the host switch to be successful. For example, it is possible that the switch of Pthirus from gorillas to humans coincides with a change in available niche space in humans, such as the loss of body hair. Further study, however, is required to test such a hypothesis.
Because Pthirus has been associated with humans for several million years, this taxon can be examined in the same way that Pediculus humanus has to study the evolutionary history of its human host [9, 19, 20]. Pthirus pubis represents an independent, ecological replicate that went through the same evolutionary history on humans as their head/body lice, and can be used to test predictions made from Pediculus humanus. Pediculus humanus shows genetic evidence of population expansion out of Africa roughly 100,000 years ago, which is concordant with host evolutionary history . However, in contrast to the shallow mitochondrial DNA (mtDNA) gene history of humans (human mtDNA coalesce to a common ancestor within 200,000 years, [21–23]), Pediculus humanus has three deeply divergent mtDNA lineages that share a MRCA ca. 2 million years ago, which is far older than the age of their modern human hosts . Perhaps a worldwide sample of Pthirus pubis will mirror that of Pediculus humanus, and show both the population expansion 100,000 years ago and the three deeply divergent mtDNA lineages. Understanding human evolutionary history from the perspective of its parasites may provide useful insight into a brief period of history that is not fully recorded in the host fossil record or in host DNA . However, if parasites are to provide much clarity, it will likely be only after many human parasites have been examined.
The advent of parsimony-based reconciliation analysis has permitted many researchers to assess phylogenetic congruence in a wide array of host-parasite assemblages. However, this method is more limited than Bayesian approaches  to studying cophylogenetics, which evaluate not only topological congruence but also the comparative timing of host and parasite divergences. It is imperative that we continue to put into practice the theoretical work that has propelled systematists forward in recent years. Only then can we hope to uncover the more complex interactions between hosts and parasites.
Specimen collection and preparation
Specimens examined. Louse taxa included in phylogenetic and cophylogenetic analyses.
Genbank Accession Numbers
Host Species Voucher ID
USA, Florida, West Palm Beach
Homo sapiens (WP007)
UK, Scotland, Glasgow
Homo sapiens (GLA 140)
Gorilla gorilla (051122CAWBB001)
Captive (SW Found for Biomed. Res.)
USA, Nevada, Tonopah
Perognathus longimembris (MLZ 2039)
PCR and sequencing
PCR amplification and sequencing of a portion of the mitochondrial cytochrome c oxidase subunit I gene (Cox1; 858 bp) was performed using the primers LCO1718  and H7005 . PCR amplification and sequencing of 345 bp of the nuclear elongation factor 1 alpha (EF-1α) gene were performed using the primers For3 and Cho10 . Double-stranded PCR amplifications for both Cox1 and EF-1α were performed in 25 μl reaction volumes using 10 μl of Eppendorf HotMaster PCR Mix (Fisher Scientific), 1 μl of each primer (at 10 mM), and 2 μl of DNA template. The amplification protocol required an initial denaturation step of 94°C for 10 min, followed by 5 cycles of 94°C (1 min), 48°C (1 min), and 65°C (2 min), then 30 cycles of 94°C (1 min), 52°C (1 min), and 65°C (2 min) and a final extension of 65°C for 10 minutes. Amplified fragments were purified using ExoSAP-IT (USB Corporation) and sequenced in both directions. Sequences were edited using Sequencher v. 4.2.2 (Gene Codes Corporation, Ann Arbor, Michigan) and aligned by eye using Se-Al v2.0a11 http://evolve.zps.ox.ac.uk/Se-Al/Se-Al.html. Primer sequences were removed and sequences were trimmed in reference to the translated protein sequence using Se-AL v2.01a11 and MacClade 4.0 . All sequences were submitted to [Genbank: EF152552-EF152564] and alignments to [TreeBase: #SN3269]. Sequences of the Cox1 gene from the primate host taxa were downloaded [Genbank: NC001807, NC001643, NC001645, NC001992, NC008219]. EF-1α sequences were not available for several primate taxa, and were therefore not examined.
Phylogenetic and cophylogenetic analyses
The partition homogeneity test  in PAUP*4.0b10  was used to evaluate phylogenetic congruence of the louse Cox1 and EF-1α data sets. One thousand partition replicates were analyzed by maximum parsimony (heuristic search option with random addition replicates and tree bisection-reconnection branch swapping). Modeltest  was used to determine the best-fit ML model for the molecular data. Phylogenetic analyses were conducted on host and parasite data sets using maximum likelihood (ML) with branch and bound searches using the best-fit model in PAUP* 4.0b10 . Nonparametric bootstraps (100 replicates) were performed to assess nodal support for the louse phylogeny. ML searches were performed with and without the 'enforce clock' constraint in order to test the hypothesis of a molecular clock in the Cox1 and EF-1α louse datasets. The resulting ML host and parasite trees with branch lengths estimated from the best-fit ML model were then used in cophylogenetic analyses.
TreeMap (v. 2.0.2; ) was used to determine whether host and parasite trees were more similar to one another than would be expected by chance. Default costs for evolutionary events (codivergence = 0, host switching = 1, duplication = 1, and loss = 1) were used. Significance values were calculated from a sample of 1,000 randomly generated trees.
Divergence date estimation
Because the lice and their primate hosts showed significant codivergence and because molecular data did not differ significantly from clocklike behavior, divergence dates were estimated using methods that both adhere to and relax the molecular clock. Divergence dates were estimated in the program r8s , using the Langley and Fitch (LF) model which assumes a molecular clock. Dates were also estimated using a parametric Bayesian approach  in the program multidivtime. This method relaxes the molecular clock and allows rate variation among genes and lineages, and it is therefore appropriate for datasets that utilize more than one molecular marker. The topology resulting from ML analysis of the combined 2-gene data set was used in multidivtime. The Cox1 best-fit ML tree and the combined 2-gene topologies were used in r8s. Divergence dates were estimated using each individual gene (with branch lengths optimized on the best ML tree) as well as a combined 2-gene dataset.
For the parametric Bayesian analysis, model parameters for the F84+Γ model were estimated for each gene separately using the baseml program in PAML v3.14 . These parameters were then used in the program estbranches [34, 36] to estimate the ML and the variance-covariance matrix of the branch length estimates for each gene. Lastly, the program multidivtime [34, 36], utilizing the output files from estbranches and implementing Markov chain Monte Carlo (MCMC) sampling, was used to estimate prior and posterior distribution of rates and divergence time estimates among lineages. The prior assumption for the mean and standard deviation of the time of the ingroup root node (rttm) was set to 3.0 time units, where 1 time unit represents 10 million years. This value corresponds to the upper limit of the split between hominoid and cercopithecoid primates. The mean and standard deviation for the prior distribution of the rate of evolution at the ingroup node (rtrate and rtratesd) was determined following the protocol of Jansa et al. (rttm; ). To avoid violation of the definition of the prior, rtratesd was set to its maximum value (equal to rtrate). The Markov chain was initialized by randomly selecting the initial parameter value and each Markov chain was sampled every 100 cycles for 1,000,000 generations with a burn in of 100,000 cycles.
A calibration point of 22.5 ± 2.5 MYA was used for the split between Pedicinus and Pediculus+Pthirus. This divergence of 20–25 MYA corresponds to the split between OWM and apes [38–41]. Since lice and their primate hosts show significant cospeciation, we can use this well-established host calibration based on fossil data to calibrate the louse phylogenetic trees. It is preferable to use more than one calibration point when estimating divergence dates [42, 43], however the small number of nodes in our trees make that impossible. Furthermore, Reed et al.  showed that the calibration point of 20–25 MYA yielded estimated clade ages that were very similar to those estimated from a calibration of 5–7 million years between the human and chimpanzee lice (P. humanus and P. schaeffi, respectively).
We wish to thank K. Shepherd at Lice Solutions and D. Clayton at the University of Utah for samples of head lice, Debbie Cox (Chimpanzee Sanctuary, Wildlife Conservation Trust and the Jane Goodall Institute) for samples of chimpanzee lice, D. Dean (Salt Lake City Public Health Center) for pubic lice, C. Whittier and M. Cranfield (Maryland Zoo Gorilla Veterinary Project) for gorilla lice, and K. Rice (Southwest Foundation for Biomedical Research) for baboon lice. We thank F. K. Barker for assistance with multidivtime and two anonymous reviewers for the helpful comments and suggestions. This work was funded in part by The National Science Foundation (DBI 0102112, DBI 0445712, and DEB 0555024) and the University of Florida Research Opportunity Fund to DLR.
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