Why the Donkey Did Not Go South: Disease as a Constraint on the Spread of Equus asinus into Southern Africa
Donkeys are the only ungulate definitely known to have been domesticated in Africa and were widely employed in the north of the continent and through the Sahara and the Sahel as pack animals, as well as spreading through much of the Old World. Used in Egypt by 4000 bc, they are attested in Nubia in the third millennium bc, in eastern Sudan in the second millennium bc and, in a Pastoral Neolithic context, at Narosura, Kenya, in the first millennium bc. However, they went completely unremarked by early European observers in southern Africa and appear never to have reached that region, unlike cattle and sheep, both of which reached it before the beginning of the Christian era in a process that linguistic and genetic data now firmly link to the migration of herders from East Africa. Taking its lead from previous studies of the impact of epizootic disease on the expansion through Sub-Saharan Africa of cattle and dogs, this paper asks if disease also constrained the southward movement of donkeys and, if so, what the consequences of this may have been.
KeywordsDonkeys Africa Pastoralism Infectious disease Trypanosomiasis Equine piroplasmosis African horse sickness
Les ânes sont les seules ongulés certainement connus pour avoir été domestiqués en Afrique et ont été largement utilisés dans le nord du continent et à travers le Sahara et le Sahel comme animaux de bât, ainsi qu’ils se sont diffuses à travers une grande partie de l’Ancien Monde. Utilisés en Egypte par 4000 av. J.-C., ils sont attestés en Nubie dans le troisième millénaire avant J.-C. dans l’est du Soudan dans le deuxième millénaire avant J.-C. et dans un contexte Néolithique pastoral au Narosura, au Kenya, au cours du premier millénaire avant notre ère. Cependant, les premiers observateurs européens en Afrique méridionale ne nous en donnent aucune mentione et il semble donc que les ânes n’y sont jamais arrivés, une situation très differente de celle du bétail et des moutons, qui ont atteint l’Afrique méridionale avant le début de l’ère chrétienne dans un processus pour lequel les données linguistiques et génétiques maintenant soutiennent un fort lien à la migration des éleveurs originant en Afrique orientale. Prenant son avance des études précédentes de l’impact de les maladies épizootiques sur l’expansion à travers l’Afrique sub-saharienne du bétail et des chiens, cet article demande si les maladies ont également contraint le déplacement vers le sud des ânes et, si oui, quelles sont les conséquences de ceci.
Relative to Eurasia, Africa is the original home of very few of the world’s domesticated mammals. Claims for a separate early Holocene domestication of cattle (Bos taurus) are disputed on both osteological and genetic grounds (di Lernia 2013; Stock and Gifford-Gonzalez, 2013), although some input from African individuals is likely once cattle arrived in Northeast Africa from the Near East (Pérez-Pardal et al. 2010), followed by further admixture with ultimately South Asian-derived zebu (Bos indicus) in and after the Bronze Age (Hanotte et al. 2000). Cats (Felis catus) have also been considered an African domesticate based on their strong archaeological presence in Pharaonic Egypt, but while tamed as early as the late Predynastic period (Van Neer et al. 2014), genetic and archaeological data now also point to another (and earlier) domestication event in the Near East (O’Brien et al. 2008). This leaves donkeys (Equus asinus) as the only domestic mammal for which a uniquely African centre of origin can still plausibly be argued (Kimura et al. 2013), although even then southwestern Arabia may have been an additional domestication locus (Rosenbom et al. 2014).
Recent research has emphasised that early pastoralists in Northeast Africa likely found African wild asses (Equus africanus) increasingly useful as a substitute for cattle in moving water, firewood and their own possessions as climate became drier in the middle Holocene. Asses are not only adapted to hot, dry conditions, but also need less food, can digest coarser grasses and have several important water-sparing adaptations (Kimura et al. 2013). Significant morphological change may have taken some considerable time to appear, with osteological damage caused by carrying heavy loads a more certain indicator of domestication than reduction in size (Rossel et al. 2008). The archaeozoological record nevertheless indicates that donkeys were in use in Egypt and had spread into the Near East by the onset of the third millennium bc, occurred widely in Sudan by the following millennium and had reached southern Kenya/northern Tanzania and the central Sahara by or soon after 3000 years ago. In all of these contexts, they are associated with human populations who also kept cattle and caprines.
However, while other species of domestic livestock underwent a significant further expansion as far as southern Africa in the last couple of centuries bc (Orton 2015) and were subsequently kept there in large numbers by both Khoe-speaking herders and (from the middle centuries of the first millennium ad) Bantu-speaking agropastoralists (Huffman 2007; Sadr 2013), donkeys remained behind in East Africa. Unless this is the result of widespread taphonomic bias, given their many advantages for East African pastoralists today, their widespread utility for more settled, agricultural populations in the Sahel, North Africa and beyond and their presence in East Africa before herders spread south from there, this requires explanation.
Earlier research that explored the possible roles of infectious diseases in constraining the spread within Sub-Saharan Africa of both cattle (Gifford-Gonzalez 2000, 2016) and dogs (Mitchell 2015) suggests that this may be a productive line of enquiry for explaining why donkeys did not expand into southern Africa in precolonial times. Indeed, Blench (2000, p. 350) noted some time ago that in recent times “the clearing of savanna forest of the Sahel and the consequent decline in tsetse challenge has permitted donkeys to spread southwards” in West Africa [emphasis added]. To investigate the possible role of disease, I first review the archaeological and historical evidence for the donkey’s presence in Northeast and East Africa and the subsequent southward spread of other livestock taxa. I then show that there is no historical or archaeological evidence for donkeys having been present in southern Africa before European settlement. To understand this, I look at three disease challenges—trypanosomiasis, equine babesiosis/piroplasmosis and African horse sickness—discussing their epidemiology, pathology and current distribution. While these infections may not on their own account for the donkey’s absence from southern Africa, I argue that the dangers they pose to E. asinus require us to include them in any explanation of the latter’s otherwise curious omission from the domestic animals kept there by precolonial African populations.
Origins and Spread of the Donkey in Sub-Saharan Africa
Genetic studies have thrown considerable new light on the origins of donkeys and consistently divide them into two evolutionary groups. Conventionally named clades I and II, they are found across the world in roughly equal proportions without any clear geographic pattern (Kimura et al. 2013). Clade I is closely related to the Nubian wild ass (E. africanus africanus), one of two surviving but genetically well-separated subspecies of the African wild ass (Beja-Pereira et al. 2004; Kimura et al. 2011). However, thus far, it has not been possible to establish the ancestry of clade II, except to exclude from consideration the other extant subspecies, the Somali wild ass (Equus africanus somaliensis) (Kimura et al. 2011). This is consistent with a lack of evidence for this subspecies hybridising with domestic donkeys (Kebede 2013). A now extinct wild relative of both subspecies is a not-unlikely alternative ancestor for clade II (Kimura et al. 2013, p. 89).
Early archaeological occurrences of domesticated donkeys (Equus asinus) in Northeast, Saharan and East Africa (after Marshall 2007; directly dated specimens have their dates given in italics)
4600–4400 cal. bc
Boessneck and von den Driesch (1998)
4000–3500 cal. bc
Boessneck von den Driesch and Ziegler (1989)
3600 cal. bc
Van Neer et al. (2004)
Gautier and Van Neer (2009)
von den Driesch (1997)
Rossel et al. (2008)
ca. 3000–2850 bc
Burleigh et al. (1991)
4390 ± 130bp (OxA-566)
3497–2670 cal. bc
ca. 2950 bc
Boessneck et al. (1992)
Third millennium cal. bc
3560 ± 150bp (KN-5318)
2340–1527 cal. bc
Jesse et al. (2004)
Gautier and Van Neer (2006)
2200–1700 cal. bc
ca. 1460 bc
Kimura et al. (2011)
1300–200 cal. bc
Gifford-Gonzalez and Kimengich (1984)
ca. 1000 bc–ad 500
Prendergast and Mutundu (2009)
1100 bc–ca. ad 500
Prendergast and Mutundu (2009)
Prendergast et al. (2014)
First millennium cal. bc
D’Andrea et al. (2011)
Gala Abu Ahmed
Linseele and Pöllath (2015)
ca. ad 1–400
MacDonald and MacDonald (2000)
The oldest archaeological examples of domestic donkeys come from Predynastic and Archaic Egypt, with the earliest at El Omari in contexts dated to 4600–4400 cal. bc (Boessneck and von den Driesch 1998), followed by others at a number of sites in both Upper Egypt and the Nile Delta (e.g., Van Neer et al. 2004; Dębowska-Ludwin 2012). Iconographic representations—notably on the Libyan Palette (Dochniak 1991)—are also known. Deliberate interments with elite associations dated to the First Dynasty or shortly thereafter come from Abydos in Upper Egypt (Rossel et al. 2008) and three sites near Memphis, just south of Cairo: Abusir (Boessneck et al. 1992), Helwan (Flores 2003) and Tarkhan (Burleigh et al. 1991). There is then considerable epigraphic and iconographic evidence for the employment of donkeys in agricultural activities and as pack animals in the Old Kingdom and all subsequent periods of Pharaonic history (e.g., Closse 1998; El-Menshawy 2009). Donkeys were also used to facilitate Egyptian expeditions into the Western Desert, reaching up to at least 600 km west of the Nile as early as 2600 bc (Kuper 2006; Förster 2013) and were introduced into the Near East from around 3000 bc (Grigson 2006).
The archaeozoological record for donkeys along the Middle Nile and elsewhere in northeastern Africa is patchier. Several finds document their presence at Kerma from the third millennium bc (Chaix 1993), and a complete skeleton has been directly dated to 3560 ± 150 bp (KN-5318, 2340–1527 cal. bc at 95 % probability using IntCal13) from a pastoralist (Handessi Horizon) context at Wadi Hariq, 400 km west of the Nile (Jesse et al. 2004). Still further into the Sahara, donkeys were present in southwestern Libya by 1000 bc (Kimura et al. 2011) and had expanded beyond the southern limits of the desert into the Sahel by the early centuries ad (MacDonald and MacDonald 2000). East of the Nile the Gash Delta has produced remains dated to the second millennium bc (Gautier and Van Neer 2006), broadly contemporary with representations of donkeys in the land of Pwnt (probably equivalent to the coast of northern Eritrea) in the reliefs of Queen Hatshepsut’s funerary temple at Deir el-Bahri ca. 1460 bc (Houlihan 2002, p. 124). The oldest archaeological specimens from Eritrea/Ethiopia are younger than this, however, and come from Pre-Aksumite contexts of the first millennium bc at Mezber (D’Andrea et al. 2011), followed by later examples at and near Aksum itself in the first millennium ad (Cain 1999; Chaix 2013). Also of first millennium bc date are finds from Napatan contexts at the fortress of Gala Abu Ahmed in Wadi Howar, 110 km west of the Nile (Linseele and Pöllath 2015, p. 566), although donkeys are rare in other Kushite sites (Chaix 2008).
Within East Africa, donkey teeth are known from Narosura, southwestern Kenya (Gifford-Gonzalez and Kimengich 1984, p. 470; Marshall 2007, p. 385), in Pastoral Neolithic contexts dated to the first millennium bc (Odner 1972). Their identification seems secure as it reflects the independent assessment of two of the region’s leading archaeozoologists. Marshall (2000, Table 10.3) also notes the presence of donkeys at the first millennium bc Elmenteitan site of Ngamuriak, also in southwestern Kenya, but they are not reported in her detailed analysis of its fauna (Marshall 1990, p. 211). They do, however, occur at Jangwani 2 and Gileodabeshta 2 in the Lake Eyasi Basin of northern Tanzania. While both sites have undergone a degree of bioturbation and some of the radiocarbon dates from them are suspect, only Pastoral Neolithic (mostly Narosuran) ceramics were recovered and a first millennium bc/earlier first millennium ad date is plausible (Prendergast and Mutundu 2009, p. 219). Recent direct dating of a Narosuran sherd from Gileodabeshta 2 to 2910 ± 20 bp (1126–929 cal. bc, ISGS-A2368) strengthens this interpretation (Prendergast et al. 2014).
Documentary references from the nineteenth and twentieth centuries nevertheless make it plain that donkeys had a limited presence in East Africa as a whole during and immediately before the colonial era, a situation that has only recently begun to change. In Kenya and Tanzania, they were effectively confined to those arid and semiarid areas where pastoralism was a major activity and were virtually absent toward the Great Lakes and from the southern lowlands of Tanzania (Wilson 2013). They may, however, have been kept in Swahili settlements along the Tanzanian and Kenyan coast, having been introduced from southern Arabia or elsewhere in the Middle East (Blench 2000). Further south, donkey numbers in Central and south-central Africa are extremely low today, although showing some increase, for example in Malawi and Zambia, as part of ongoing development initiatives (Starkey and Starkey 2004). Nowhere in these regions, however, is there any suggestion that they were present before the advent of Europeans. Indeed, in July 1866, David Livingstone noted in his diary when approaching Lake Malawi from the east that local residents greeted his one remaining donkey (brought south from Zanzibar) with as much curiosity and laughter as they did himself (Wilson 2013, p. 39).
Donkeys in Southern Africa?
Much of south-central Africa (southern Tanzania, Malawi, Zambia) is not propitious for cattle due to the presence of a range of serious infectious diseases, particularly trypanosomiasis (Gifford-Gonzalez 2000), and many local populations, such as the Bemba (Richards 1939) and Yao (Mitchell 1963), consequently did not keep them. Cattle and caprines did, however, pass through these areas to form a cornerstone of herder and agropastoralist economies in much of Africa south of the Zambezi. Might the same have been true of donkeys?
From a historical standpoint, the answer seems to be a definitive no. Dent (1972, p. 123), for example, is unequivocal in stating that “there were no asses in southern Africa until the arrival of the Dutch” in the seventeenth century, while Jacobs (2001, p. 485) is equally categorical: “Donkeys are not indigenous to South Africa…they arrived through European expansion.” Lying behind these statements are the observations of numerous European explorers, scientists and other observers from 1488, when the Portuguese first skirted southern Africa’s Atlantic coast, into the nineteenth century. None found any difficulty in noting that the Khoe-speaking herders living in the more arid western third of the subcontinent kept large numbers of sheep and cattle, along with some goats, or that Bantu-speaking agropastoralists further east did the same wherever the absence of disease made this possible. However, not one historical observation exists of even a single donkey in indigenous hands (e.g., Kolbe 1731; Schapera and Farrington 1933; Mossop 1935; Thom 1952, 1954, 1958; Burchell 1953; Thompson 1967, 1968; Raven-Hart 1971; Valentyn 1971, 1973; Smith 1975; Sparrman 1975, 1977; Thunberg 1986). Moreover, the only references to “wild horses and mules” explicitly note that they were covered with stripes (e.g., Schapera and Farrington 1933, p. 33), an unambiguous indicator that the animals in question were, in fact, zebras. Given that European observers, including scientists of international repute such as Anders Sparrman, Carl Peter Thunberg and William Burchell, were so unanimous in not mentioning the presence of donkeys among southern African herders and farmers, while having no difficulty in commenting on the presence of equally familiar cattle, sheep, goats and dogs, it seems reasonable to conclude that donkeys were not kept by native southern African populations at the time of European contact.
Size of faunal assemblages at selected early herder sites and agropastoralist sites in southern Africa
NISP/MNI (large mammal)
Robbins et al. (2008)
Smith and Jacobson (1995)
Pleurdeau et al. (2012)
South Africa (Western Cape)
Boomplaas (DGL Member)
South Africa (Western Cape)
Klein and Cruz-Uribe (1989)
South Africa (Western Cape)
Klein and Cruz-Uribe (1989)
Denbow et al. (2008)
South Africa (Limpopo)
South Africa (Limpopo)
Donkeys in archaeozoological assemblages from southern Africa
Date (ad) of context
Sehonghong (Layer GAP)
ca. 250–1000 (fresh; later intrusion, likely post-1878)
Plug and Mitchell (2008)
South Africa (Eastern Cape)
Voigt et al. (1995)
South Africa (KwaZulu-Natal)
1873–1879 (later intrusion?)
Watson and Watson (1990)
South Africa (Limpopo)
Badenhorst et al. (2002)
If donkeys were not present in southern Africa, archaeological, historical and ethnographic evidence do all confirm that Khoe-speaking herders in South Africa and Namibia kept sheep cattle and goats (Sadr 2013), just like Bantu-speaking agropastoralists did in the better-watered parts of the subcontinent’s summer rainfall region (Voigt 1986; Huffman 2007). In both cases, livestock and the milk that they produced were not only a core element of the diet but also essential to human social reproduction because of the powerful symbolic associations that they held (e.g., Huffman 1998; Lombard and Parsons 2015).
Early archaeological occurrences of domesticated livestock in southern Africa (directly dated specimens are given in bold)
Calibrated date (95 %)
2270 ± 40
Pleurdeau et al. (2012)
2190 ± 40
Pleurdeau et al. (2012)
2105 ± 65
Sealy and Yates (1994)
2070 ± 40
Robbins et al. 2008)
2020 ± 40
Robbins et al. (2008)
1980 ± 120
349 cal. bc–cal. ad 364
1960 ± 50
1880 ± 55
1790 ± 80
Smith and Jacobson (1995)
1700 ± 55
cal. ad 245–525
Deacon et al. (1978)
1630 ± 60
Sealy and Yates (1994)
1625 ± 25
Orton et al. (2013)
1550 ± 50
Sandelowsky et al. (1979)
1510 ± 75
cal. ad 415–681
Deacon et al. (1978)
Disease Challenges for Donkeys
Much of the eastern, south-central and southern regions of sub-Saharan Africa, on the other hand, was, and remains, home to one or more other equid species. Three such taxa survive today: Grévy’s zebra (E. grevyi) in the semi-arid grasslands of Ethiopia and northern Kenya; the plains zebra (E. quagga) from Kenya south into South Africa; and the mountain zebra (E. zebra) in the Western and Eastern Cape Provinces of South Africa and in Namibia. As in the analogous cases of cattle (Gifford-Gonzalez 2000) and dogs (Mitchell 2015), when domesticated equids entered areas south of the Sahara and the Horn to which they were strangers they may have encountered pathogens to which they had no prior experience. The susceptibility of domestic horses to diseases originally restricted to Africa south of the Sahara is well established, and trypanosomiasis and African horse sickness, in particular, severely constrained their expansion south of the Sahel and in South Africa (Clutton-Brock 2000, pp. 30–31; Swart 2010). What has not been considered until now is whether these diseases, or others, similarly hindered the expansion of the donkey.
Direct evidence of many infectious diseases is difficult to recover from the archaeozoological record, although the identification of tick vectors, such as the brown dog tick (Rhipicephalus sanguineus), in mummified dogs in Egypt (Hutchet et al. 2013), or of a range of parasites in dog coprolites from Peru (Richardson et al. 2012), indicates what is possible when preservation conditions are favourable. Recovery of parasite genetic material is also possible in some circumstances, as in the case of the DNA of Trypanosoma cruzi, which causes Chagas disease, retrieved from the rib of a well-preserved pre-Columbian person in Brazil (Lima et al. 2008). Pending similar exceptional finds in the African context, the existing veterinary literature can help us to establish which diseases affect donkeys in Africa today, the conditions under which they occur and the effects that they produce. If one species or population (i.e., donkeys) exhibits more virulent forms of a given disease than another (e.g., zebras), then the former likely received it more recently, while if African populations show some degree of tolerance to a particular pathogen, then not only is this likely to have taken some time evolve, but also the disease itself probably once posed a more serious threat within Africa itself (cf. Gifford-Gonzalez 2000).
However, while donkeys are of considerable—and in many areas growing—importance to people, the diseases from which they suffer remain woefully understudied (Pearson et al. 1999, p. 194). This reflects two things. First, since donkeys are primarily used to transport people and goods rather than reared for food, export (alive or dead) or being kept as companions, they are perceived to be of lower economic value and thus attract less veterinary attention than other domestic animals (Stringer et al. 2015, p. 6). Second, the individuals (often women) and communities for whom donkeys are particularly important are themselves typically among the poorer, more marginal sections of the population (Jacobs 2001; Geiger and Hovorka 2015). Once again, this has reduced the amount of veterinary research directed at them, even if they are increasingly understood to offer important tools of empowerment for those same groups (Starkey 1995).
Compounding these difficulties, all too often statements about the effects of major infectious diseases on donkeys are extrapolated from what is known about horses (Segwagwe et al. 2000, p. 179), despite the fact that the two species show many differences (Burden and Thiemann 2015) and exhibit different symptoms that may vary considerably in their severity. As a result, donkeys remain “especially neglected when it comes to disease investigation, control and prevention” (Getachew et al. 2014, p. 236) and overviews of disease in them are few (but see Segwagwe et al. 2000; Getachew et al. 2014; Getachew et al. 2016). What follows may therefore easily underestimate the impacts of the infections that I discuss and the number of significant disease threats to which donkeys are exposed in Africa.
Sleeping sickness is one of the best-known insect-borne diseases in Africa, affecting more than 30 mammal taxa, including wild animals, domestic livestock and people. The causal agents are parasitic protozoa of the genus Trypanosoma that are principally spread by various species of tsetse fly (Glossina spp.), although blood-eating (haematophagous) flies and Trictonid bugs can also act as vectors of some species (Uilenberg 1998). Having been ingested when the vector insect bites and feeds on the blood of a mammalian host, the trypanosome goes through a further part of its life cycle and then moves into the fly’s salivary glands ready to begin another cycle of infection.
Equines (i.e., horses and mules, as well as donkeys) are often less of a preferred target for tsetse flies than cattle (Radostits et al. 2007), but it is widely acknowledged that horses are severely affected by the disease (Namangala and Odongo 2014). What is less commonly appreciated is that donkeys are far from resistant to it (Gifford-Gonzalez 1998, p. 192) and may suffer high rates of infection accompanied by extensive morbidity and mortality. Indeed, in some parts of Africa (for example, southwestern Burkina Faso) they exhibit higher frequencies of infection than cattle (Sow et al. 2014). The omission of donkeys from Namangala and Odongo’s (2014, Table 10.1) list of animals affected by nagana (animal—as opposed to human—trypanosomiasis) is therefore bizarre or, rather, yet another manifestation of the neglect to which African donkeys and their diseases are exposed.
At least three species of Trypanosoma have been identified as causing infection in African donkeys: T. congolense, T. vivax and T. brucei. In addition, donkeys are also susceptible to two other trypanosomal conditions not discussed here, surra (caused by T. evansi) and dourine (caused by T. equiperdum), neither of which involves tsetse flies. Glossina spp., the principal vectors for the other three trypanosomes and the only one reported for Trypanosoma brucei (Namangala and Odongo 2014, p. 233), currently range between 14° N and 29° S of the Equator. They need shady bush environments in which to rest and reproduce and find their most common animal hosts among nonmigratory mammals living in such conditions. Broadly speaking, this limits them to areas where mean annual rainfall is greater than 500–700 mm (Nash 1969), with infection rates peaking in the wet season when circumstances are most favourable for their reproduction and survival.
Several studies exist regarding the impact on donkeys of the various primarily tsetse-borne infections. In southern Ethiopia, for instance, Kanchula and Abebe (1997) documented a trypanosomiasis infection rate of 21 %, equal to that found in the same area among horses, and with Trypanosoma vivax the most common agent. Later work by Assefa and Abebe (2001) indicated, however, that T. congolense was the most prevalent source of infection, consistent with studies in Kenya (Nudungu et al. 1998) and The Gambia (Mattioli et al. 1994). The savanna-dwelling tsetse species G. morsitans, G. pallidipes and G. submorsitans were the predominant vectors involved. Conversely, a second Gambian study documented an infection rate of 78 % for T. vivax, one of 36 % for T. congolense and one of 28 % for T. brucei, with half of all the donkeys examined being infected with two, and sometimes as many as five, different parasite taxa (Pinchbeck et al. 2008). The significance of this study lies also in its employment of species-specific PCR after Whole Genome Amplification, which demonstrated a more than fourfold increase in levels of infection compared to conventional microscope-based detection methods (83 % compared to 18 %). While infection rates may vary considerably between regions (e.g., Bedada and Dagnachew 2012), the moral of this research is clearly that previous investigations indicating a lower prevalence of trypanosomiasis in donkeys relative to horses, or other livestock, need to be reassessed (cf. Dhollander et al. 2006). Such reassessments ought also to control for seasonal variation in tsetse activity, tethering practices and level of chemoprophylactic use (Mesele and Leta 2010).
Existing data nevertheless affirm that donkeys seem highly susceptible to Trypanosoma spp. and that infection can cause “severe clinical disease” (Getachew et al. 2016, p. S107), with greatly shortened life expectancies in areas of high tsetse/trypanosomiasis infestation (Sow et al. 2014). Among other studies, Burden et al. (2010) note that trypanosomiasis is “amongst the greatest constraints of donkey keeping” in Kenya’s Lamu Archipelago, while in The Gambia, Faye et al. (2001, p. 102) observe, with respect to horses and donkeys, that “equine mortality rates exceed the foaling rates,” a situation that is clearly unsustainable in the absence of continued importation of new stock from areas that have much less, or even no, disease presence. But although all three of the trypanosomes discussed thus far are significant causes of anaemia, unthriftiness and reduced capacity for work (Burden et al. 2010), they are not equally dangerous. Thus, Assefa and Abebe (2001) suggest that T. vivax produces a milder infection than T. congolense, as is generally true for East African livestock as a whole (Namangala and Odongo 2014).
T. brucei, on the other hand, appears to strike equally at both horses and donkeys, producing a severe infection that is often fatal (Connor 1994). Indeed, in The Gambia, T. brucei infection is more common in donkeys than in horses (Pinchbeck et al. 2008) and both this study and others (e.g., Dhollander et al. 2006; Mesele and Leta 2010) raise the possibility that the relatively low rates of infection attributed to T. brucei may well underestimate its impact on sub-Saharan donkey populations because of the increased pathogenicity, and thus the higher mortality rates, associated with this particular trypanosome. Confirming this, experimental infection of donkeys with T. brucei has been observed to produce symptoms of dullness, weakness, fever and tachycardia, with death resulting in all cases within 8 to 10 weeks of initial infection (Ikede et al. 1977). More recently, Kingston et al. (2016) have documented infection of the central nervous system of donkeys by T. brucei in The Gambia, a condition that results in slowly deteriorating cerebral dysfunction and is usually fatal.
Equine piroplasmosis (or babesiosis) has previously been described as “the most serious infectious disease of horses in southern Africa” (Littlejohn and Walker 1979, p. 309), exceeding even the effects of African horse sickness, which I discuss below. Though best known from South Africa, it is far from restricted to that part of the continent and occurs in most tropical and subtropical regions of the world where suitable tick vectors are present (hence the lack of a distribution map in this paper). Two infectious agents are responsible for the condition, Theileria equi and Babesia caballi. While usually occurring separately, they may also simultaneously coinfect the same animal, although infection with T. equi is more common than infection with B. caballi (Wise et al. 2013). Both are piroplasmic protozoa of the same phylum (Apicomplexa) as Plasmodium, which causes malaria. However, T. equi exhibits several characteristics that distinguish it from other Babesia species, and RNA analysis suggests that it belongs to a phyletic group different from both Babesia and Theileria; its precise taxonomic classification thus remains unclear (Rothschild 2013).
The lifecycle of T. equi is still not completely understood, although, as is also the case for B. caballi, it involves three distinct stages. Like most other Babesia species, in mammals it only targets the red blood cells, with infection starting when the tick vector feeds on an animal. Proliferation of the parasite within the animal’s erythrocytes then paves the way for the infection of any new, uninfected tick (Wise et al. 2013, p. 1336). A wide range of ticks may act as vectors for these parasites, including species of Dermacentor, Rhipicephalus and Hyalomma (Wise et al. 2013; Oduori et al. 2015), and the red-legged tick Rhipicephalus evertsi evertsi, in particular, is often observed on donkeys (De Waal and van Heerden 1994). T. equi can, however, also be transmitted transplacentally and may result in abortion, stillbirth or infection of a live foal (Wise et al. 2013, p. 1337). Horses at least can remain carriers of B. caballi for up to 4 years after initial infection (Holbrook et al. 1973). All three species of zebra have also been identified as carriers (Lampen et al. 2009; Hawkins et al. 2015), and T. equi is likely to have first evolved as an infection of zebras before affecting other equids (Bhoora et al. 2009).
Piroplasmosis has been reported in donkeys in Sudan, Ethiopia and Kenya but is likely to be much more widespread than this, as is the case with its occurrence in horses (Oduori et al. 2015). Clinically visible signs of infection, which are more evident when infection is caused by T. equi than by B. caballi, include loss of appetite, anaemia, oedema, reduced work efficiency, weight loss and abortion, with overwork putting donkeys at increased risk (Oduori et al. 2015, p. 684). Depression, marked thirst, constipation and spleen enlargement may also occur (Kumar et al. 2009). There are fewer donkey-focused studies of the disease than those investigating horses, however, with some suggesting that it is more often chronic than acute in nature (Laus et al. 2015). Indeed, Oduori et al. (2015, p. 685) note that in east-central Kenya, clinical signs could not be identified, “consistent with the nature of the disease in an endemic setting, where equids over time have developed protective immunity.”
Nevertheless, equine piroplasmosis has elsewhere been described as one of the most important tick borne diseases to afflict donkeys (Kumar et al. 2009) and in northeastern South Africa, where donkeys were introduced from the mid-1800s, it caused “a great mortality” at the start of the twentieth century, comparable to its effects in horses (Bowhill 1905, p. 7). Experimental infection of donkeys with T. (formerly B.) equi confirms its pathogenicity (Singh et al. 1980; Kumar et al. 2003), while Segwagwe et al. (2000, p. 181) observe that in Botswana “donkeys are known to be equally as susceptible as horses to B. equi and B. caballi.” It thus seems likely that when donkeys with no previous history of exposure (and resistance) to equine piroplasmosis entered areas where they could be infected by ticks adapted to existing zebra reservoir populations they might well have suffered considerable losses. This possibility would be enhanced should it be possible to associate different clinical signs with the genetically distinct groups of T. equi now beginning to be identified (cf. Lampen et al. 2009, p. 259).
African Horse Sickness
African horse sickness finds its primary natural host in zebras, though it is not impossible that other mammals also act as reservoirs (Wilson et al. 2009, p. 5). There is neither archaeological nor palaeontological evidence for the presence of any of the extant species of zebra within the Sahara or to its north during the Holocene (MacDonald and MacDonald 2000, p. 139; Churcher 2014; Faith 2014). Nor is there likely to have been significant distributional overlap between any zebra species and the African wild ass (Fig. 2). Epidemiologically naïve populations of donkeys encountering African horse sickness for the first time as they moved south might thus have reacted like modern animals in the Middle East on first exposure to the virus, even if they subsequently evolved the degree of immunity that some studies suggest and that their presence in parts of East Africa for some 3000 years would support. Unlike the other two diseases that I have discussed, African horse sickness is thus unlikely to have been a constraint on keeping donkeys in areas where the disease itself is endemic.
Discussion and Conclusion
All three of the diseases I have discussed pose health threats to donkeys, most especially in the cases of equine piroplasmosis and of trypanosomiasis caused by infection with T. brucei. Nevertheless, at least some donkey populations—for example those examined in Kenya by Oduori et al. (2015)—show a degree of resistance to the latter condition, and African donkeys in general appear to suffer much less from African horse sickness than those living elsewhere. The corollary of these propositions is, however, that such immunity must have taken time to evolve and that on first exposure donkey mortality and morbidity rates will have been much higher. This is to be expected given the restriction of the donkey’s ancestor, the African wild ass, to arid and semiarid regions of North and Northeast Africa in the Pleistocene and early Holocene. These regions experienced rainfall that was too low to support populations of Glossina spp., and animals living there cannot therefore have been exposed to trypanosomiasis. That E. africanus only has thin stripes on its lower legs is fully consistent with this since the distribution of zebras shows an almost perfect correlation with that of biting flies, especially Glossina spp., and the width of zebra stripes appears to deter tsetse and tabanid flies from biting them (Caro et al. 2014; Fig. 2).
The absence of zebras from the Sahara, Sudan and most of the Horn of Africa also makes it likely that donkeys living in these areas underwent little, if any, exposure to two other major diseases, both of which find their primary hosts in zebra populations—equine piroplasmosis and African horse sickness. Even the historical distribution of Grévy’s zebra, the more dryland adapted of the two taxa present in East Africa, shows virtually no overlap with that of the wild ass (Fig. 3). Such overlap as may have existed (in western Djibouti, the lower Awash Valley and parts of the Somali Region of Ethiopia) would, in any case, only have been with the Somali subspecies of the wild ass (E. africanus somaliensis), which genetic analyses demonstrate is not ancestral to the domestic donkey and which last shared a common ancestor with donkeys and Nubian wild asses over 100,000 years ago (Kimura et al. 2011).
The archaeozoological record for donkeys in the Pastoral Neolithic of East Africa remains sparse, with relevant observations coming from a mere handful of sites. Nevertheless, it shows that donkeys were present in the region in the first millennium bc, in both the Loita Plains of southwestern Kenya and on the southern side of Lake Eyasi in northern Tanzania. The latter area marks the most southerly known extension of Pastoral Neolithic settlement and it is thus to it, or areas nearby, that we need to look for the origin of those groups that introduced cattle, sheep, ancestral forms of the Khoe language family and, perhaps, pottery, to Africa south of the Zambezi in the last few centuries bc (based on dates from Leopard Cave, Namibia, Spoegrivier, South Africa and Toteng, Botswana; Sealy and Yates 1994; Robbins et al. 2008; Pleurdeau et al. 2012). Gifford-Gonzalez (2000, 2016) has demonstrated that a number of serious infectious diseases, including trypanosomiasis, probably handicapped the southward spread of domestic livestock, especially cattle, into East Africa and between East Africa and southern Africa. The recent elegant analysis of Chritz et al. (2015) reconstructing more open grassland conditions around Gogo Falls on the eastern side of Lake Victoria in the first few centuries ad does not gainsay this since neither its location (too far north) nor date (too recent) are directly relevant to the expansion of livestock to southern Africa. It does, however, highlight the direction that palaeoenvironmental research must take in order to establish where a disease-free corridor lay, however ephemeral it may have been.
But while caprines and cattle took advantage of that corridor to reach southern Africa, donkeys—according to the evidence of early historical accounts and archaeology—did not. The precise reasons for this are likely to have been complex—perhaps in the first instance even specific to the (small?) groups from which those introducing herding to the south in the last couple of centuries bc derived—but the donkey’s failure to spread into southern or, indeed, south-central Africa at any time before European contact suggests the operation of an ongoing and long-standing cause. Disease is, I submit, an obvious possibility, and I have shown that not only are donkeys are susceptible to trypanosomiasis but that they are particularly at risk to the form of the disease caused by T. brucei, which is frequently fatal and at least as dangerous to them as it is to horses. Interestingly, T. brucei is less serious for domestic ruminants than T. vivax and T. congolense (Namangala and Odongo 2014, p. 244), which raises the possibility that sheep, goats and cattle might have been able to pass through areas infected with it, while donkeys were kept at bay. Equine piroplasmosis is also likely to have posed significant dangers, though here the veterinary evidence is arguably more mixed, with the risk varying depending on the specific strain of the protozoa and virus involved. African horse sickness, on the other hand, seems to have been a challenge that was easier to meet and, at least in East Africa, donkeys today display primarily subclinical signs when infected by it.
As with the constraints imposed by disease on the southward spread of other livestock (Gifford-Gonzalez 2016), my hypothesis is easily refutable by future archaeozoological research, but even if donkeys should be identified in archaeological faunas significantly south of the Lake Eyasi area the question must remain why they did not continue south. Had they done so, they would presumably have found most of Namibia and Botswana and large parts of South Africa and Lesotho highly inviting, just like their twentieth- and twenty-first-century successors. Moreover, given their significance for today’s East African pastoralists in enhancing flexible mobility in dryland areas, particularly in transporting water, firewood and other resources (Marshall and Weissbrod 2009), they would presumably have made life considerably easier for Stone Age herders in the semiarid regions of the western half of southern Africa. In their absence, at least some of those herders used cattle to move their mat houses and personal possessions (Smith 1992, pp. 200–201), animals that are slower and energetically less efficient, must rest to ruminate and have significantly higher water and nutritional needs (Marshall 2007). Perhaps learned from Khoekhoe cattle-keepers, southern Nguni groups in South Africa also employed cattle as pack animals, but the practice did not reach beyond them (Wilson 1982, pp. 108–109). Elsewhere in southern and south-central Africa, therefore all goods had to be moved on people’s heads or by canoe. Given that donkeys can carry loads of 80–100 kg for 24–30 km a day (Raepsaet 2008, Table 23, p. 4) compared to the 25–35 kg recorded for precolonial African porters (Alpers 1977, p. 222), agropastoralist societies must have been significantly hampered by the absence of pack animals, for example in moving staples such as basic foodstuffs over long distance given that people would have had to consume some of what they were moving to achieve this (cf. Drennan 1984; for a direct, text-aided comparison, donkeys in the Near Eastern Bronze Age carried 250 % as much as human porters; Dercksen 1996).
To sum up, the donkey’s absence from southern Africa in precolonial times is established by its total omission from early (fifteenth- to nineteenth-century) European accounts of the region and its concomitant lack of identification in pre-nineteenth century archaeological faunas. This absence surely implies the presence of a deterrent or barrier between it and East Africa. That barrier was, I argue, not merely an asinine aversion to more wooded or wetter savanna environments per se, but rather to the diseases that those environments harboured. To take this proposition further, several additional lines of evidence can be investigated.
First, the many specimens currently attributable only to Equus sp. from sites in East Africa might—where collagen is preserved—be investigated using new palaeoproteomic (ZooMS) techniques (e.g., Welker et al. 2015) to determine whether additional donkeys lurk unidentified in Pastoral Neolithic or other faunal assemblages; they and existing specimens would also benefit from direct dating using the AMS radiocarbon technique to confirm their precise age. Along with renewed archaeozoological examinations, the same techniques could also be deployed as part of efforts to exclude conclusively the possibility that donkeys lie “hidden” and unidentified in southern African faunas; Geduld (Smith and Jacobson 1995) and Bosutswe (Denbow et al. 2008) might, for example, be promising in this respect (Table 2). Second, the genomes of donkeys, particularly those thought to represent populations long native to East Africa, could be investigated to ascertain whether they show evidence of having evolved resistance to the diseases I have discussed. Third, improved veterinary understanding of disease in the donkey—rather than mere extrapolation from single sources or studies focused on horses alone—would better establish the precise impact on E. asinus of trypanosomiasis, equine piroplasmosis and African horse sickness, as well as the effects (and origins, in Africa or beyond) of other diseases not considered here, such as equine infectious anaemia that are also spread by insect vectors (Caro et al. 2014, Supplementary Table 1). Finally, as with cattle (Gifford-Gonzalez 2000), it would be worth establishing to what degree African donkey keepers practise forms of livestock management or environmental modification that may protect their animals from infection. By pursuing all these paths, we shall find ourselves looking at—rather than overlooking—the role of infectious disease in the spread within Africa of its one domesticated native ungulate.
I am grateful to Patrick Roberts, Fiona Marshall and an anonymous reviewer for their comments and to Sam Lunn-Rockliffe for producing the maps that accompany this paper. While I have cited the results of studies involving the deliberate infection of donkeys, I do not approve of the use of animals in such work.
Compliance with Ethical Standards
Conflicts of Interest
The author declares that he has no conflicts of interest.
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