Chitnis, A., Rawls, D. & Moore, J. (2000). Origin of HIV-1 in colonial French Equatorial Africa? AIDS Res. Hum. Retroviruses. 16: 5-8.
2014: I've written up some comments on Faria et al. (2014) "The early spread and epidemic ignition of HIV-1 in human populations" Science 346: 56 - 61, located here. The paper makes some important contributions to our understanding of the spread of HIV, but appears in passing to deliberately mislead readers about colonial history and the origin of HIV-1.
Because this topic is important and controversial, and because the background of this paper is unusual, I (Jim Moore) thought it worth writing a brief account of how it came to be written. Brevity has never been my strong suit; to ignore this history, skip to the paper.
Edward Hooper's response to Chitnis et al. and this preamble |
New material from Edward Hooper, summer 2001 |
Press release from Edward Hooper, 9/28/01: New evidence |
25 September 2000: I've added some material;
if you've already seen this preamble (or don't care),
skip ahead to the new bits.
10 May 2001
Another "new bit" -- there have been several developments re the debate over HIV's origins.
Marx et al. point out that the probability of spontaneous mutation from SIV to HIV is a function of viral population size, and that since "[n]ormally, human host defences would suppress poorly adapted SIV strains", some mechanism must be found to permit the SIV to remain at high levels in the new host for long enough that such a spontaneous mutation might occur (where "long enough" is on the order of months, and normal immune suppression of unfit virus is on the order of 1-2 weeks). Visually, in (a) SIV titres have to be high for a long time (red curve) to have a realistic chance of mutating to HIV, but normally they are suppressed (black curve) too soon.
The suggested mechanism is serial passaging of virus via unsterile needles, which they tie to the postwar introduction of disposable syringes. High viral population levels are maintained (through a series of bottlenecks) in a series of different individual hosts (figure b). Chitnis et al. postulate a slightly different mechanism, that of immune suppression due to chronic stress associated with colonial labor camps etc. plus a much lower rate of serial passage via unsterile needles or arm-to-arm vaccination (figure c). |
The two papers (Marx et al. and Chitnis et al.) postulate similar mechanisms for the origin of HIV but place the critical events and immediate causes in two very different time periods. In this connection there is a glaring discrepancy between our papers concerning the history of injections in Africa during the colonial period. I do not fully understand the basis for the discrepancy, so only note it here.
Marx et al. provide a table of "History of injectable medications and needle reuse in Africa, 1900-1998", in which the only entry prior to 1920 is for treatment of syphilis, 1900-1920, and it is stated that this "antedates awareness of transmission of infectious diseases by unsterile injections". They also state that prior to WWII injectable drugs were administered "on site and under medical supervision, while closely controlling access to the relatively costly drugs and injecting equipment (UNICEF 1987), using sterile injecting procedures and with access to sterilization equipment on hand. There is little evidence of injection-related transmission of disease in the pre-WWII colonial period (Alland 1970)." [p. 6]. The only indications they list prior to 1952 are syphilis, diabetes and VD.
In total and complete contrast, Headrick (1994) presents tables of numerous specific vaccination campaigns against smallpox and other diseases prior to 1920. For example, Table 3.8 (p. 65) lists 19 separate documented smallpox vaccination campaigns in French Equatorial Africa between 1893 - 1912; the total vaccinated in the 15 for which numbers are available is 82,091. She then states, "In addition, continual vaccination of recruits and porters went on and doctors, missionaries, and sometimes administrators carried out informal, small-scale vaccination tours in their immediate surroundings. Compared to French West Africa, where 1,003,000 vaccinations were performed in 1911 alone, the figures for French Equatorial Africa are not impressive (Delrieu 1914, 375)." [p. 66]. In addition there were (according to Headrick) massive campaigns against sleeping sickness and bacillary dysentery during the 1920s. As to the qualifications and supervision of people administering injections, see Headrick pp. 241-253. One illustrative quote: "Most white missionaries, administrators, company agents, army nurses, agents sanitaires, and hygienistes adjoints went well beyond what their occupations permitted. All dispensed drugs, gave injections, made diagnoses, or performed minor surgery without the direct supervision of a doctor." [p. 244]. As to awareness that unsterile injections could carry disease, Headrick notes e.g. that in 1920, nurses (local technicians) in the sleeping sickness campaigns were trained in "concrete operations: sterilizing water, instruments, and the skin, cleaning slides and ... giving injections. These courses lasted from 4 to 8 weeks." [p. 246; she notes this was the only formal training course for local nurses given at the time.] See also Copeman (1899) for a contemporary discussion of the importance of sterile instruments.
I have no idea how to reconcile these two images of colonial medical practice. For the interested reader, here are the references cited above:
In late 1998/early 1999, several seemingly unrelated elements came together for me:
The obvious way to link these was for Amit to do a paper reviewing what was known about the origins of HIV-1, and how the new chimpanzee data fitted into it. Then...
King Leopold's Ghost" made a huge impact on me. According to Hochschild, at one stage those in charge of enforcing colonial rule were required to account for every spent cartridge with proof of a dead African; a severed hand was acceptable. Because cartridges often went astray, it became standard practice to cut the hand from a living person and turn that in; photographs of amputees that were (eventually) distributed in Europe played a role in the "Red Rubber" movement against the abuses of Belgian colonial rule -- the first international human rights campaign. Reading the Discover passage quite frankly infuriated me; the colonial governments did not prevent travel, they regulated it -- those impressed into forced labor camps, or as porters, certainly traveled widely. And post-colonial pogroms need to be viewed in context of the up to 10 million people who died during this period as a result of colonial policies. Not to mention that the urbanization of e.g. Brazzaville and Leopoldville/Kinshasa began well prior to WWII.
Thus it seemed to me (and Amit and Diana) that while the end of colonial rule certainly brought with it the risk factors Wain-Hobson mentions, there was an apparent ignorance of comparable risk factors present during the half-century preceding WWII as well. The purpose of our paper is to bring these factors to the attention of the HIV/AIDS research community. We make no claim to having "demonstrated" an origin scenario for HIV, but we hope to have pointed to a plausible, but seemingly ignored, place to look.
Which brings me to Edward Hooper's book, "The River". This came out after we had written our paper, and what with one thing and another I wasn't able to finish it until December 1999.
First off, I realize now that we are not the first to suggest an HIV origin in colonial, rather than postcolonial, times. The scenario was new to us and reviewers found it acceptable without pointing us to a canonical reference, so there we are. I hope we have added something of real value, at least (e.g., calling attention to the lack of epidemiological information for Guinea may lead to something).
Only after reading Hooper's book do I realize (only partially, I'm sure) the nature of the controversy into which we have wandered. Broadly speaking, there are currently two main scientific schools regarding the origin of HIV (see Hooper, chapter 10):
To the extent that our paper is seen as supporting one school or the other it is participating in a controversy, so I want to be clear where I personally stand on this (Amit and Diana have moved, and I will update this note as appropriate when I reach them). My stance is developing as I learn about the issues involved; feedback is welcome.
Hooper's book represents a magnificent effort and is a persuasive analysis. I would feel ridiculous comparing it with our brief sketch, but need to at least address points of conflict. Let me be explicit: at this point in time, I suspect that the OPV hypothesis is less likely to be correct than is something along the much vaguer lines we propose -- but this is a weak suspicion only. Hooper does not offer proof, but his argument cannot be dismissed.
It is of course critical to determine whether any eastern chimpanzees (P. t. schweinfurthii) carry an SIVcpz that could be ancestral to any of the three known HIV-1 lineages. This should be doable with noninvasive methods; I am sure the work is ongoing.
I believe that our scenario and Hooper's OPV account differ with respect to the first two reasons, but do not differ at all with respect to the latter two. Neither scenario seems likely to be provable beyond a shadow of legal doubt, but both are plausible enough that to ignore the implications or lessons of either would be foolish. Hooper convinces me that the OPV scenario could have happened, and in my opinion that possibility is the important thing.
And maybe it did, with a different virus. See The Virus and the Vaccine (Atlantic Monthly, Feb. '00), an account of SV40.
ADDITIONAL references on forced labor practices in the region, recommended by Adam Hochschild in response to this website:
Of interest:
Vaccination was introduced by Jenner in 1796, and consists of substituting cowpox (vaccinia) for smallpox. The benefits of not using smallpox itself are obvious.
All that is old hat. What may be significant regarding the HIV origins debate is that for a long time, the mechanism of transfer of the culture (variola or vaccinia) was the same. When Copeman writes of vaccination rather than inoculation, at least at times he appears to be distinguishing between the content of the pustules, no more. Vaccinia strains were carried serially from child to child (p. 52), starting with a strain Jenner originated in 1798. See pages 67 through 72. Reference is made to a strain of "humanized lymph [which] was obtained from Birmingham [in 1892], where, to the best of my belief, the same strain has been continuously carried on by means of arm-to-arm vaccination for the past thirty-eight years" (p. 131). This does not necessarily imply a continuous 8-day cycle; it was known from 1853 that lymph could be stored for up to 6 months between host passages (p. 156). Arm-to-arm methods were known to carry risks of transmitting e.g. syphilis (p. 151). The method was abandoned slowly (as best as I can tell, over a period of > 30-50 years), first on the continent and then in England in the late 19th century (p. 149). France was the last country to give it up on the continent.
Copeman and his colleague Richard Thorne Thorne did a survey of methods used on the continent that started in December 1896; Thorne Thorne wrote the report which is appended in the book. Of note:
The report then goes on to explain that in Paris, "certain classes" were so suspicious of lymph delivered to a vaccination site in tubes -- thinking it derived from humans, and so potentially carrying syphilis, tuberculosis, etc -- that vaccination could only be done by bringing a tethered calf to the site and "vaccinating" people with lymph material scraped directly from the calf.
---Clearly, while arm-to-arm methods had fallen from favor in Europe by 1900, the pace of medical change was slow and doctors practicing in the late 19th century would have been educated (and often practiced) when it was an acceptable if second-choice method. One can also read the suspicion among "certain classes" of Parisians as evidence that vaccine stocks could not always be trusted. Note that it appears to have been somewhat difficult to grow lymph in calves, and (I am speculating here) it may have been that human-passaged lymph was simply easier to obtain--wherever one wants fresh vaccine, there are by definition plenty of humans but not always young calves.
This is relevant to the discussion of HIV-1 origins in two ways. First, arm-to-arm serial passaging would have seemed an acceptable second choice in a region where cattle were scarce and people available. Second, it suggests that one needs to be very careful of the word "vaccination" in the context of the period; it appears initially to have meant only "use of vaccinia" and only later gained generic secondary implications of batch-tested stocks, sterile methods, etc.
ABSTRACT
Sociocultural factors during the postcolonial period have been
implicated as paramount in generating conditions that promoted both the
origin and subsequent epidemic spread of HIV-1 in Africa. We suggest,
however, that the origin of the disease may lie in the interaction between
colonial practices (e.g., labor camps, non-sterile vaccination campaigns) and
traditional bushmeat hunting in French Equatorial Africa. Both the
epidemiology of HIV-2 and the colonial history of West Africa appear more
complex, but similar conditions existed there and may have contributed to
the origin of HIV-2. Focusing the search for the origins of HIV-1 and HIV-2
on this earlier time period may contribute to understanding the evolution of
the HIV viruses and the dynamics of emerging diseases.
Human Immunodeficiency Virus Type 1 (HIV-1) seems to have
originated in at least three zoonotic transmissions of SIVcpz from
chimpanzees (Pan troglodytes troglodytes) to humans, 1 placing the origin of the disease in Central
Africa (Cameroon, Gabon, R. P. Congo, lower Central African Republic, and
Rio Muni [Equatorial Guinea]). This most probably occurred in the course
of hunting and butchering apes for food. Because such hunting is
traditional, an obvious question is, "Why now?"
The earliest direct evidence of HIV-1 comes from a blood sample
collected in Kinshasa in 1959, 2 and
this has led some to concentrate attention on post-World War II (WWII)
social changes connected with the end of European colonial power in the
region (basically, urbanization combined with "breakdown of colonial
control" leading to increased opportunities for transmission of sexually
transmitted diseases [STDs]). However, while the post-WWII period did
bring many changes to Central Africa that have probably played a role in
the origin of the current epidemic, the origin of the
disease must lie some years earlier. We suggest that the origin of
the disease may have occurred prior to WWII, during the period of French
colonial administration of French Equatorial Africa (see Table 1 for chronology). What factors might have
contributed to the initial zoonosis and to its subsequent spread during
this period, in the absence of evidence of endemic HIV-1?
It seems likely that transmission of SIVcpz to humans has taken
place regularly at some low frequency for thousands of years; previously
either strains were nonpathogenic in humans (and lost owing to random
factors), nontransmissible between humans, or infected individuals died
without spreading the virus (owing either to low population density or to
[hypothetical] traditional practices limiting sexual promiscuity). We are
thus looking for factors associated with the colonial period that would do
the following:
1) EXPOSURE RISK: Colonial authorities conscripted people
for work as porters and as forced labor on railroads and other
infrastructure projects; during WWI, they also required villagers to harvest
large quantities of rubber. 3-5 All these
led to (a) some people fleeing villages to live in the forest, and (b) those
conscripted having little time, energy, or opportunity to devote to
agriculture. It may be conjectured that both would have led to significant
increases in reliance on bushmeat. In addition, increasing access to guns
would have played a role in obtaining large animals like chimpanzees.
2) VIRAL TRANSMISSION: There was a massive influx of
people into the major cities following WW II, constituting "... movement of
previously isolated people into the newly expanding cities" 6 (e.g., the population of Kinshasa increased
almost 10-fold from 49,000 in 1940 to 420,000 in 1961; Fig. 1 7). Whatever role this influx may have had in
the development of the epidemic, it should be kept in mind that the cities
were not "newly" expanding; the population of Kinshasa (and Brazzaville)
also increased about 10-fold between 1905 and 1940 (Fig. 1). This earlier
period of urbanization would have created conditions favorable to the
initial establishment of the disease.
In addition, the social turmoil associated with forced resettlements
and labor undoubtedly disrupted traditional sexual practices and
networks. More directly, some of the labor camps (of thousands of men)
encouraged the presence of women for "recreational" purposes. 5 Finally, massive vaccination campaigns were
carried out with limited resources (e.g., six syringes used to screen and
treat nearly 90,000 people for sleeping sickness in 1917-19) 8. An unknown proportion of nearly 100,000
smallpox vaccinations prior to 1914 employed arm-arm direct inoculation
with material from pox vesicles5, 9
(containing a high concentration of lymphocytes, the primary target of
HIV-1).
3) VIRAL ADAPTATION: Arm-arm inoculation may have
resulted in passaging of virus through a series of hosts over a relatively
short period of time, a process that can select for more virulent pathogen
strains. 10 Without knowing more
about the details of the arm-arm campaigns (how many successive
"donors" were used in the course of a campaign? how many people
vaccinated?) the importance of this possible serial passaging cannot be
evaluated.
It is not clear whether understanding the origins of HIV-1 will make
a difference in treating AIDS, and the above scenario presents only
plausible risk factors--it is not clear how or if any of them can be
confirmed as playing a role in the origin of AIDS. However, to the extent
that it is useful/interesting to understand the origin of HIV-1, if this
scenario is correct it suggests that investigation should be concentrated in
French archives pertaining to French Equatorial Africa between 1890 and
1930, with special reference to
We have not dealt in detail with conditions in West Africa that might
have been associated with the origin of HIV-2 from SIVsm carried by sooty
mangabeys (reviewed in Ref. 13). Unlike
the comparatively sudden impact of colonialism on small-scale societies in
French Equatorial Africa, in the west European contact began in the 15th
century and interacted in a complex way with existing kingdoms through
some 400 years of trade and exploitation--prominently including the slave
trade 14. In addition, in West Africa
(but apparently not in French Equatorial Africa) smallpox inoculation
(variolation) was either indigenous or introduced early 15. These differences make it more difficult to
point to a specific time and place as the likely site of the origin of the
disease.
It is, however, worth noting that while the highest reported
seroprevalence of HIV-2 is in Guinea-Bissau, the greatest diversity of
subtypes is in Sierra Leone 13, 16-18.
These countries straddle Guinea, a country for which there seems to be
relatively little information published about HIV seroprevalence.
Northwestern Guinea includes the heart of the 19th century state of Fouta
Djalon, which played a major role in the slave trade and did not fall to the
French until 1895, not long after the rubber boom began in the area
14 Entire districts were depopulated,
and then repopulated, as Fouta fell and antislavery laws were slowly
enforced over the next decade. Because it took time to re-clear fields and
rebuild abandoned villages, many of these returning people were forced
to live by hunting bushmeat. Over 50,000 porters were used per year to
headload rubber from the interior to the coast by 1906; a railroad was
under construction from 1899 through 1913, mostly with slave labor.
The "[d]iversion of labor was so great that food was in short supply and
had to be imported" and if laborers sickened they received no rations,
having to scavenge in the forests 14.
Finally, the French army of the Sudan operating in the late 19th century
(mostly in what is now northeastern Guinea and western Mali) made
extensive use of slaves for both labor and sex; officers regularly got their
choice of slave women and promiscuity was high 14.
In short, similar risk factors were present. They peaked slightly
earlier (the turmoil was greatest roughly in 1880-1910) and less sharply
(e.g., indigenous variolation was practiced for hundreds of years), but
they were present. While spread throughout the region, the combination
of clashing states and intensive forced labor was slightly greater in the
region of Fouta Djalon and neighboring Wasulu, both located primarily
within the modern nation of Guinea.
The widespread occurrence of these epidemiologically-relevant
factors prior to WWII suggests that HIV-1, and possibly HIV-2, emerged as
infectious human pathogens earlier than generally believed, a conclusion
consistent with recent and ongoing genetic analyses. 19
We thank Kathy Creely, David Ho, Bette Korber and Richard Nisbett for
their help and encouragement.
Suppose: a single person is infected, and on average transmits the virus to 2 people over the next 5 years. Given obvious uncertainties about sexual practices, infectability etc. this is very rough; I am assuming here that if the virus originally transferred during a hunting/butchery episode, the early years are in rural, small-village settings; prostitution was not a factor early on. Basically, I'm postulating a doubling every 5 years. What does that look like?
In about 1930, the population of French Equatorial Africa was very roughly about 1.2 million adults (Headrick, 1994). The figure shows the number of "cases" as a percent of 1.2 million, starting with N = 1 in 1900 and doubling every 5 years. Note the vertical axis goes only up to 5.5%.
IMPORTANT Please note that these numbers are not intended to accurately model HIV seroprevalence in Africa. Really the ONLY point here is the trivial--but often forgotten--power of nonlinear processes to (a) appear nonexistent at first, and then (b) suddenly "burst" into being. In the case above, all I intend to show is that even with no change in human behavior, given a disease having relatively low infectivity one would expect a period of years/decades with prevalence too low to be detected (without extraordinary, well-focussed effort or astounding good luck)to precede a "sudden" appearance. For an interesting discussion of this issue applied to a very different problem--the apparently discontinuous acquisition of vocabulary by human infants--see chapter 4 of
Arguments against 'natural transfer' (and rebuttals)
Whose side are we on? [sic]
Why might we care about the origin of HIV?
ADDITIONAL references to early vaccination campaigns that may have employed arm-to-arm methods for carrying vaccine to the interior regions of French Equatorial Africa (taken from Headrick 1994; I have not consulted the originals -- I hope that some Francophone interested in this issue will do so!
I recently came across the following items.
---This is certainly consistent with the idea that prior to the rubber boom, hunting gorillas was unusual and that colonial pressure for taxes and rubber created an expanded market for hunting bushmeat.
---This is evidence that guns, and hunting game difficult to get without them, were uncommon under colonial rule. WWI must have put some into circulation, and certainly the supply has been increasing. Point is, while shotguns may have been known in the region for centuries, they were not available. [Interestingly, he tells of being threatened by Maka "cannibals" (just north of Avebe) and astonishing them by shooting a flying parrot with his shotgun; they knew only about rifles and so thought him a supernatural marksman (p. 39).]
---This seems relevant to the idea that if HIV-1 had existed in the interior prior to 1960, it would have been reported by Colonial doctors.
"It will be noted that in each of the countries concerned, vaccination with calf lymph has become the habitual, if not the universal practice. In some, indeed, we were informed that, although vaccination with humanized lymph is not definitely prohibited under any statute or regulation, yet resort to such lymph by any medical practitioner having official responsibility to the Government is altogether discouraged.
In only one of the places visited -- namely, Paris -- did we find that vaccination was carried out under official sanction with crude calf lymph, and even there the process was limited to vaccination direct from calf to arm, all lymph stored for distribution being glycerinated calf lymph" (p. 190). (Glycerin was found to kill most of the bacterial contaminants of crude lymph.)
Origin of HIV Type 1 in Colonial
French Equatorial Africa?
Amit Chitnis, Diana Rawls, Jim Moore*
University of California, San Diego
AIDS Research and Human Retroviruses 16(1): 5-8
University of California, San Diego
9500 Gilman Drive
La Jolla CA 92093-0532
jjmoore@ucsd.edu
[eprint note: formatting is not that of the journal]
back to text
back to text
back to text
back to text
back to text
back to text
back to text
back to text
back to text
back to text
back to text
back to text
back to text
back to text
back to text
back to text
back to text
back to text
back to text
TABLE 1: CHRONOLOGY
----------------------------------
a See Ref. 5.
b See Ref. 6.
back to
text
The initial draft of our paper included a simple numerical 'model' to illustrate how long it might take for HIV/AIDS to be detected in Africa. Reviewers all thought it went beyond "simple" to simplistic, and it got pulled. Since webspace isn't as expensive, and since it might help some people, here is a very slightly improved version.
since 5 Jan 00
Last update: 24 Jan 2000