Volume 2, Number 4—October 1996
Emerging Infectious Diseases and the Depopulation of French Polynesia in the 19th Century
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|EID||Martin PM, Combes C. Emerging Infectious Diseases and the Depopulation of French Polynesia in the 19th Century. Emerg Infect Dis. 1996;2(4):359-361. https://dx.doi.org/10.3201/eid0204.960416|
|AMA||Martin PM, Combes C. Emerging Infectious Diseases and the Depopulation of French Polynesia in the 19th Century. Emerging Infectious Diseases. 1996;2(4):359-361. doi:10.3201/eid0204.960416.|
|APA||Martin, P. M., & Combes, C. (1996). Emerging Infectious Diseases and the Depopulation of French Polynesia in the 19th Century. Emerging Infectious Diseases, 2(4), 359-361. https://dx.doi.org/10.3201/eid0204.960416.|
To the Editor: The same dynamics now considered factors in the emergence of infectious diseases may have been involved in the dramatic depopulation of French Polynesia in the 19th century. Temporal and geographic variation in the frequency and severity of infectious diseases are the result of the encounter and interaction of a population of parasites and a population of hosts. J. Musser reviewed the "bacterial side of the equation" (1). On the host side, there are two historical models that describe the influence of parasitism on human populations (2-4): 1) the South American model, in which new pathogens were introduced into native populations by the European conquistadores, causing the death of 50 million people; and 2) the African model, in which infectious diseases present in native populations protected them from the effects of colonization until modern times when the discovery of quinine and other efficient antipathogenic drugs provided added protection. The second model is well illustrated by the attempted colonization of Madagascar, where the French lost five men to war and 5,000 to malaria (2). This letter intends to illustrate the first model. We suggest that during their first contacts with European navigators in the very late 18th century and the 19th century, Polynesian islanders, much like populations in the South American model, were decimated by newly introduced infectious diseases.
It is difficult to know precisely which infectious diseases were present in Tahiti and the other French Polynesian islands before the arrival of the first Europeans. However, a study of Polynesian languages indicates that Bancroftian filariasis and leprosy were already present, while syphilis and other venereal diseases, influenza, and tuberculosis (TB) were probably unknown. Epidemic diarrhea and dysenteriae could have existed, although first reports mentioned that the oldest Polynesians "never heard of dysenteriae before" (5). In the Marquesian language, names exist for leprosy, bronchitis, abscesses, and impetigo.
The number of inhabitants in Tahiti, as well as in the Marquesas and the Austral Archipelago, was at first only estimated by European explorers. However, a precise census was performed as soon as missionaries and French authorities noted the high death rates in most of the islands (5,7,15,16). Tahiti was annexed by France in 1843; the first census was performed in 1848, and the population size was assessed approximately every 5 years until 1911.
Four major epidemic diseases (TB, typhoid, influenza, and smallpox) devastated the Marquesas from 1791 to 1863/64; approximately 80% of the population died. During that period, exchange of populations between the Marquesas Islands also increased, as a consequence of colonization. Thus, leprosy increased dramatically during the second half of the 19th century, to a prevalence of 4.11% in 1884 (6).
In Rapa, the remote, southern island of the Austral Archipelago, at least three epidemics were reported, resulting in the loss of more than 90% of the population. Although the cause of the first epidemic remained unknown, dysenteriae and smallpox were identified as causes of the second and third epidemics, respectively.
From Rapa, a missionary went to Mangareva in 1831 or 1832, and his visit there was followed by an epidemic that the natives attributed "to his god." He had to flee back to Rapa. The second recorded epidemic disease was "Chinese scabies" in 1865, which decimated the child population. Then, the warship "La Zélée" brought an epidemic of influenza in 1908. In 1910, TB and leprosy were reported "to spread rapidly" (7), and in 1911, the ship "La Gauloise" brought whooping cough to Mangareva.
In Tahiti and the Society Islands, the number and diversity of international and interisland exchanges, involving numerous commercial ships and whalers, make the origin of epidemics more difficult to trace. However, at least five were reported successively in the Leeward Islands in 1843, 1848, 1854, and 1864 (7), and at least 11 in Tahiti: influenza (1772 to 1774), pulmonary TB (1775), dysentery following the passage of the ship of Vancouver (1790), dysentery after the passage of the whaler "Britania" (1807), disastrous influenza in 1820, whooping cough in 1840, smallpox in 1841, dysentery again in 1843, scarlet fever in 1847, measles in 1852-1854 (800 deaths were recorded) and typhoid fever after the passage of "La Magicienne" in 1877 (8).
Almost without exception, authors attributed the dramatic depopulation of French Polynesia during the 19th century to infectious diseases. Other causes, such as alcohol, opium, local wars, infanticides, and even orgiastic behavior were also mentioned as possible causes. Depopulation occurred to a similar extent in other South Pacific countries (9), e.g., the Cook Islands, Hawaii, Tonga, Samoa, and particularly Fiji, where 50% of the population died. Thus, after limited initial contact with persons exposed to infectious diseases, most of the Polynesian populations died. Why did it happen? Why were epidemics so intense and so severe? It is unlikely that clones of bacteria, viruses, fungi, or parasites with particularly high virulence were introduced into native populations since the long crossing by sailing boats would have selected clones with lower virulence. Moreover, epidemics are also intense and severe in animal populations when new infectious agents are introduced. In Hawaii, the introduction of Plasmodium from birds had catastrophic consequences for the local fauna (10).
Host population factors that may influence the spread of an infectious agent (i.e., the intensity of an epidemic) are diverse: 1) social disruption was certainly a major cause for the increase of leprosy and TB in the Marquesas during the 19th century: pacification of the archipelago by Dupetit-Thouars changed traditional behavior and destroyed tribal barriers against leprosy by permitting the development of interisland exchanges, thus contributing to the spread of both leprosy (within the Marquesas) and TB (from Tahiti to one Marquesas island, then between the Marquesas) (11); 2) the absence of most infectious diseases in Polynesia before the 18th century probably slowed the selection of behavioral methods of prevention and the development of traditional medicine; 3) a small population without exposure to infectious diseases would not have selected resistance genes against nonexistent infectious agents; and 4) the lack of population immunity probably had a major role in the spread of new infectious agents.
Host population factors that can influence the virulence of parasites (i.e., the severity of an epidemic) are less frequent. Successive epidemics of closely related viruses or bacteria can enhance the severity of the disease, as in dengue fever (12), or can inversely provide cross-protection, as was suggested between yaws and syphilis (13), whose causative organisms are almost indistinguishable. Reduced genetic polymorphism of 19th century Polynesians who had no immunity to infectious diseases could have contributed to the severity of epidemics in the South Pacific, as it was speculated for South America (4 14,).
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The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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