Sabrina Krief
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Sabrina Krief has a total of 58 co-authors. Here are the top co-authors by number of shared publications:
- Jacques Guillot
Department of Dermatology, Parasitology, Mycology, Oniris, Nantes, France
6 shared publications - Georges Snounou
Écologie et Émergence des Pathogènes Transmis par les Arthropodes (CNRS UMR2000). Centre François Jacob, Institut Pasteur, 28 Rue du Dr. Roux, 75724 Paris, France; Department of Parasitology and Entomology, Faculty of Public Health, Mahidol University, Bangkok 10400, Thailand
4 shared publications Jean-Michel Krief
Projet pour la conservation des grands singes, Kibale National Park, Fort Portal, Uganda
4 shared publicationsThierry Sévenet
4 shared publicationsAndrew Seguya
Uganda Wildlife Authority, Kampala, Uganda
3 shared publicationsClaude Marcel Hladik
3 shared publications
Latest Publications
- Open Access
- 22 October 2014
- Published by Public Library of Science (PLoS) in PLOS ONE
- Vol. 9 (10) , e109925
Wild Chimpanzees on the Edge: Nocturnal Activities in Croplands
In a rapidly changing landscape highly impacted by anthropogenic activities, the great apes are facing new challenges to coexist with humans. For chimpanzee communities inhabiting encroached territories, not bordered by rival conspecifics but by human agricultural fields, such boundaries are risky areas. To investigate the hypothesis that they use specific strategies for incursions out of the forest into maize fields to prevent the risk of detection by humans guarding their field, we carried out video recordings of chimpanzees at the edge of the forest bordered by a maize plantation in Kibale National Park, Uganda. Contrary to our expectations, large parties are engaged in crop-raids, including vulnerable individuals such as females with clinging infants. More surprisingly chimpanzees were crop-raiding during the night. They also stayed longer in the maize field and presented few signs of vigilance and anxiety during these nocturnal crop-raids. While nocturnal activities of chimpanzees have been reported during full moon periods, this is the first record of frequent and repeated nocturnal activities after twilight, in darkness. Habitat destruction may have promoted behavioural adjustments such as nocturnal exploitation of open croplands.
- 22 October 2014
- Published by Public Library of Science (PLoS) in PLOS ONE
- Vol. 9 (10) , e109925
Open AccessWild Chimpanzees on the Edge: Nocturnal Activities in Croplands
In a rapidly changing landscape highly impacted by anthropogenic activities, the great apes are facing new challenges to coexist with humans. For chimpanzee communities inhabiting encroached territories, not bordered by rival conspecifics but by human agricultural fields, such boundaries are risky areas. To investigate the hypothesis that they use specific strategies for incursions out of the forest into maize fields to prevent the risk of detection by humans guarding their field, we carried out video recordings of chimpanzees at the edge of the forest bordered by a maize plantation in Kibale National Park, Uganda. Contrary to our expectations, large parties are engaged in crop-raids, including vulnerable individuals such as females with clinging infants. More surprisingly chimpanzees were crop-raiding during the night. They also stayed longer in the maize field and presented few signs of vigilance and anxiety during these nocturnal crop-raids. While nocturnal activities of chimpanzees have been reported during full moon periods, this is the first record of frequent and repeated nocturnal activities after twilight, in darkness. Habitat destruction may have promoted behavioural adjustments such as nocturnal exploitation of open croplands.
- 22 May 2014
- Published by Wiley in Journal of Medical Primatology
- Vol. 43 (4) , 280-283
Facial dysplasia in wild chimpanzees
At least 10% of the Sebitoli chimpanzee community of the Kibale National Park (Uganda) present a characteristic facial phenotype with flattened nose, reduced nostrils, and concave mid‐face. Affected individuals do not present skin lesions, and also young infants are affected. We suggest, therefore, a congenital origin of this defect.
- 22 May 2014
- Published by Wiley in Journal of Medical Primatology
- Vol. 43 (4) , 280-283
Facial dysplasia in wild chimpanzees
At least 10% of the Sebitoli chimpanzee community of the Kibale National Park (Uganda) present a characteristic facial phenotype with flattened nose, reduced nostrils, and concave mid‐face. Affected individuals do not present skin lesions, and also young infants are affected. We suggest, therefore, a congenital origin of this defect.
- Open Access
- 1 January 2013
- Published by PERSEE Program in Bulletin de l'Académie Vétérinaire de France
- Vol. 166 (3) , 276-285
Proximités géographiques et phylogénétiques entre les chimpanzés et les humains et conséquences sanitaires. Exemple du parc national de Kibale en Ouganda
COMMUNICATION Le Chimpanzé, espèce vivante la plus proche phylogénétiquement de l'homme, est aujourd'hui menacée de disparition en particulier par la fragmentation des forêts tropicales. Afin d'évaluer les risques pour les deux espèces de cette proximité spatiale en potentielle augmentation, notre objectif est d'étudier si les chimpanzés évitent les interfaces et si leur santé témoignent de ces éventuels contacts. Quinze années de recherche sur deux communautés de chimpanzés sauvages du parc national de Kibale (Ouganda) montrent que les chimpanzés n'évitent pas les lisières, traversent une route à fort trafic et que les activités humaines en forêt sont fréquentes. Nos observations révèlent des conséquences sévères sur leur santé: mutilations dues au braconnage et détection d'agents pathogènes similaires, impliquant probablement des transmissions interspécifiques. Dans un contexte où les maladies émergentes peuvent entraîner des conséquences fatales sur la santé des hommes et des chimpanzés, il est primordial d'approfondir ces travaux pour la santé publique et la conservation.
- 1 January 2013
- Published by PERSEE Program in Bulletin de l'Académie Vétérinaire de France
- Vol. 166 (3) , 276-285
Open AccessProximités géographiques et phylogénétiques entre les chimpanzés et les humains et conséquences sanitaires. Exemple du parc national de Kibale en Ouganda
COMMUNICATION Le Chimpanzé, espèce vivante la plus proche phylogénétiquement de l'homme, est aujourd'hui menacée de disparition en particulier par la fragmentation des forêts tropicales. Afin d'évaluer les risques pour les deux espèces de cette proximité spatiale en potentielle augmentation, notre objectif est d'étudier si les chimpanzés évitent les interfaces et si leur santé témoignent de ces éventuels contacts. Quinze années de recherche sur deux communautés de chimpanzés sauvages du parc national de Kibale (Ouganda) montrent que les chimpanzés n'évitent pas les lisières, traversent une route à fort trafic et que les activités humaines en forêt sont fréquentes. Nos observations révèlent des conséquences sévères sur leur santé: mutilations dues au braconnage et détection d'agents pathogènes similaires, impliquant probablement des transmissions interspécifiques. Dans un contexte où les maladies émergentes peuvent entraîner des conséquences fatales sur la santé des hommes et des chimpanzés, il est primordial d'approfondir ces travaux pour la santé publique et la conservation.
- Open Access
- 17 April 2012
- Published by Springer Nature in Malaria Journal
- Vol. 11 (1) , 1-11
Investigations on anopheline mosquitoes close to the nest sites of chimpanzees subject to malaria infection in Ugandan Highlands
Malaria parasites (Plasmodium sp.), including new species, have recently been discovered as low grade mixed infections in three wild chimpanzees (Pan troglodytes schweinfurthii) sampled randomly in Kibale National Park, Uganda. This suggested a high prevalence of malaria infection in this community. The clinical course of malaria in chimpanzees and the species of the vectors that transmit their parasites are not known. The fact that these apes display a specific behaviour in which they consume plant parts of low nutritional value but that contain compounds with anti-malarial properties suggests that the apes health might be affected by the parasite. The avoidance of the night-biting anopheline mosquitoes is another potential behavioural adaptation that would lead to a decrease in the number of infectious bites and consequently malaria. Mosquitoes were collected over two years using suction-light traps and yeast-generated CO2 traps at the nesting and the feeding sites of two chimpanzee communities in Kibale National Park. The species of the female Anopheles caught were then determined and the presence of Plasmodium was sought in these insects by PCR amplification. The mosquito catches yielded a total of 309 female Anopheles specimens, the only known vectors of malaria parasites of mammalians. These specimens belonged to 10 species, of which Anopheles implexus, Anopheles vinckei and Anopheles demeilloni dominated. Sensitive DNA amplification techniques failed to detect any Plasmodium-positive Anopheles specimens. Humidity and trap height influenced the Anopheles capture success, and there was a negative correlation between nest numbers and mosquito abundance. The anopheline mosquitoes were also less diverse and numerous in sites where chimpanzees were nesting as compared to those where they were feeding. These observations suggest that the sites where chimpanzees build their nests every night might be selected, at least in part, in order to minimize contact with anopheline mosquitoes, which might lead to a reduced risk in acquiring malaria infections.
- 17 April 2012
- Published by Springer Nature in Malaria Journal
- Vol. 11 (1) , 1-11
Open AccessInvestigations on anopheline mosquitoes close to the nest sites of chimpanzees subject to malaria infection in Ugandan Highlands
Malaria parasites (Plasmodium sp.), including new species, have recently been discovered as low grade mixed infections in three wild chimpanzees (Pan troglodytes schweinfurthii) sampled randomly in Kibale National Park, Uganda. This suggested a high prevalence of malaria infection in this community. The clinical course of malaria in chimpanzees and the species of the vectors that transmit their parasites are not known. The fact that these apes display a specific behaviour in which they consume plant parts of low nutritional value but that contain compounds with anti-malarial properties suggests that the apes health might be affected by the parasite. The avoidance of the night-biting anopheline mosquitoes is another potential behavioural adaptation that would lead to a decrease in the number of infectious bites and consequently malaria. Mosquitoes were collected over two years using suction-light traps and yeast-generated CO2 traps at the nesting and the feeding sites of two chimpanzee communities in Kibale National Park. The species of the female Anopheles caught were then determined and the presence of Plasmodium was sought in these insects by PCR amplification. The mosquito catches yielded a total of 309 female Anopheles specimens, the only known vectors of malaria parasites of mammalians. These specimens belonged to 10 species, of which Anopheles implexus, Anopheles vinckei and Anopheles demeilloni dominated. Sensitive DNA amplification techniques failed to detect any Plasmodium-positive Anopheles specimens. Humidity and trap height influenced the Anopheles capture success, and there was a negative correlation between nest numbers and mosquito abundance. The anopheline mosquitoes were also less diverse and numerous in sites where chimpanzees were nesting as compared to those where they were feeding. These observations suggest that the sites where chimpanzees build their nests every night might be selected, at least in part, in order to minimize contact with anopheline mosquitoes, which might lead to a reduced risk in acquiring malaria infections.
- 15 November 2011
- Published by Walter de Gruyter GmbH
- p. 159-170
Do animals use natural properties of plants to self-medicate?
"Do animals use natural properties of plants to self-medicate?" published on 15 Nov 2011 by Wageningen Academic.
- 15 November 2011
- Published by Walter de Gruyter GmbH
- p. 159-170
Do animals use natural properties of plants to self-medicate?
"Do animals use natural properties of plants to self-medicate?" published on 15 Nov 2011 by Wageningen Academic.
- 1 November 2011
- Vol. 195 (8) , 1927
[Great apes: who are they? Are they able to self-medicate?].
Six great ape species (chimpanzees, bonobos, Western gorillas, Eastern gorillas, Sumatran orangutans and Bornean orangutans) live in tropical forests of Africa and South-East Asia. Their habitat, severely threatened by deforestation, contains a vast chemical and biological diversity. During the last decade, we have isolated and identified novel pharmacologically active compounds from plants used by wild chimpanzees in Kibale National Park, Uganda. Our continuous observations over the last 12 years confirm that chimpanzees, when sick, may ingest plant material that are not generally eaten, supporting the existence of self-medication among great apes. Knowledge of great-ape diseases, and the medicinal resources of tropical forests, may be improved by preserving and studying our closest relatives in their natural habitat.
- 1 November 2011
- Vol. 195 (8) , 1927
[Great apes: who are they? Are they able to self-medicate?].
Six great ape species (chimpanzees, bonobos, Western gorillas, Eastern gorillas, Sumatran orangutans and Bornean orangutans) live in tropical forests of Africa and South-East Asia. Their habitat, severely threatened by deforestation, contains a vast chemical and biological diversity. During the last decade, we have isolated and identified novel pharmacologically active compounds from plants used by wild chimpanzees in Kibale National Park, Uganda. Our continuous observations over the last 12 years confirm that chimpanzees, when sick, may ingest plant material that are not generally eaten, supporting the existence of self-medication among great apes. Knowledge of great-ape diseases, and the medicinal resources of tropical forests, may be improved by preserving and studying our closest relatives in their natural habitat.
- 1 November 2011
- Vol. 195 (8) , 1945-54
[Malaria in hominids].
Malaria parasites (Plasmodium spp) that infect great apes are very poorly documented Malaria was first described in gorillas, chimpanzees and orangutans in the early 20th century, but most studies were confined to a handful of chimpanzees in the 1930-1950s and a few orangutans in the 1970s. The three Plasmodium species described in African great apes were very similar to those infecting humans. The most extensively studied was P reichenowi, because of its close phylogenetic relation to P. falciparum, the predominant parasite in Africa and the most dangerous for humans. In the last three years, independent molecular studies of various chimpanzee and gorilla populations have revealed an unexpected diversity in the Plasmodium species they harbor, which are also phylogenetically close to P falciparum. In addition, cases of non human primate infection by human malaria parasites have been observed. These observations shed fresh light on the origin and evolutionary history of P. falciparum and provide a unique opportunity to probe the biological specificities of this major human parasite.
- 1 November 2011
- Vol. 195 (8) , 1945-54
[Malaria in hominids].
Malaria parasites (Plasmodium spp) that infect great apes are very poorly documented Malaria was first described in gorillas, chimpanzees and orangutans in the early 20th century, but most studies were confined to a handful of chimpanzees in the 1930-1950s and a few orangutans in the 1970s. The three Plasmodium species described in African great apes were very similar to those infecting humans. The most extensively studied was P reichenowi, because of its close phylogenetic relation to P. falciparum, the predominant parasite in Africa and the most dangerous for humans. In the last three years, independent molecular studies of various chimpanzee and gorilla populations have revealed an unexpected diversity in the Plasmodium species they harbor, which are also phylogenetically close to P falciparum. In addition, cases of non human primate infection by human malaria parasites have been observed. These observations shed fresh light on the origin and evolutionary history of P. falciparum and provide a unique opportunity to probe the biological specificities of this major human parasite.
- 1 November 2011
- Vol. 195 (8) , 1955
[Nematodes of the genus Oesophagostomum: an emerging risk for humans and apes in Africa?].
Nematodes of the genus Oesophagostomum are common intestinal parasites found in cattle, pigs and primates. They can cause severe illness, resulting from the formation of granulomas, caseous lesions and abscesses in the intestinal wall. Human oesophagostomosis is endemic in northern Ghana and Togo. In these regions, epidemiological investigations have been conducted to determine the biological characteristics, transmission dynamics and optimal management of clinical cases. Nodular oesophagostomosis has also been described in free-ranging chimpanzees and gorillas. Clinical signs associated with nodules have been observed in great apes raised in sanctuaries, while the health status of their wild counterparts does not seem to be significantly affected It has been suggested that some nonhuman primates may act as reservoirs for human oesophagostomosis. In Ghana, identification of genetic differences among Oesophagostomum nematodes infecting different primate hosts suggests that oesophagostomosis is a rare zoonosis. In Uganda, where the situation is diferent, cross-infection is probably more frequent.
- 1 November 2011
- Vol. 195 (8) , 1955
[Nematodes of the genus Oesophagostomum: an emerging risk for humans and apes in Africa?].
Nematodes of the genus Oesophagostomum are common intestinal parasites found in cattle, pigs and primates. They can cause severe illness, resulting from the formation of granulomas, caseous lesions and abscesses in the intestinal wall. Human oesophagostomosis is endemic in northern Ghana and Togo. In these regions, epidemiological investigations have been conducted to determine the biological characteristics, transmission dynamics and optimal management of clinical cases. Nodular oesophagostomosis has also been described in free-ranging chimpanzees and gorillas. Clinical signs associated with nodules have been observed in great apes raised in sanctuaries, while the health status of their wild counterparts does not seem to be significantly affected It has been suggested that some nonhuman primates may act as reservoirs for human oesophagostomosis. In Ghana, identification of genetic differences among Oesophagostomum nematodes infecting different primate hosts suggests that oesophagostomosis is a rare zoonosis. In Uganda, where the situation is diferent, cross-infection is probably more frequent.
- 1 November 2011
- Published by Elsevier in Bulletin de l'Académie Nationale de Médecine
- Vol. 195 (8) , 1927-1944
Les grands singes : qui sont-ils ? Sont-ils capables d’automédication ?
- 1 November 2011
- Published by Elsevier in Bulletin de l'Académie Nationale de Médecine
- Vol. 195 (8) , 1927-1944
Les grands singes : qui sont-ils ? Sont-ils capables d’automédication ?
- 1 January 2011
- Published by Brill
- p. 159-170
Do animals use natural properties of plants to self-medicate?
For more than 30 years, field studies have shown that chimpanzees ingest items of low nutritional value such as rough leaves, bitter stems of Vernonia amygdalinaand clay, apparently thereby...
- 1 January 2011
- Published by Brill
- p. 159-170
Do animals use natural properties of plants to self-medicate?
For more than 30 years, field studies have shown that chimpanzees ingest items of low nutritional value such as rough leaves, bitter stems of Vernonia amygdalinaand clay, apparently thereby...