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      Forest Fragmentation as Cause of Bacterial Transmission among Nonhuman Primates, Humans, and Livestock, Uganda

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          Abstract

          Anthropogenic disturbance increases bacterial transmission.

          Abstract

          We conducted a prospective study of bacterial transmission among humans, nonhuman primates (primates hereafter), and livestock in western Uganda. Humans living near forest fragments harbored Escherichia coli bacteria that were ≈75% more similar to bacteria from primates in those fragments than to bacteria from primates in nearby undisturbed forests. Genetic similarity between human/livestock and primate bacteria increased ≈3-fold as anthropogenic disturbance within forest fragments increased from moderate to high. Bacteria harbored by humans and livestock were approximately twice as similar to those of red-tailed guenons, which habitually enter human settlements to raid crops, than to bacteria of other primate species. Tending livestock, experiencing gastrointestinal symptoms, and residing near a disturbed forest fragment increased genetic similarity between a participant’s bacteria and those of nearby primates. Forest fragmentation, anthropogenic disturbance within fragments, primate ecology, and human behavior all influence bidirectional, interspecific bacterial transmission. Targeted interventions on any of these levels should reduce disease transmission and emergence.

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          Most cited references24

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          Distribution of repetitive DNA sequences in eubacteria and application to fingerprinting of bacterial genomes.

          Dispersed repetitive DNA sequences have been described recently in eubacteria. To assess the distribution and evolutionary conservation of two distinct prokaryotic repetitive elements, consensus oligonucleotides were used in polymerase chain reaction [PCR] amplification and slot blot hybridization experiments with genomic DNA from diverse eubacterial species. Oligonucleotides matching Repetitive Extragenic Palindromic [REP] elements and Enterobacterial Repetitive Intergenic Consensus [ERIC] sequences were synthesized and tested as opposing PCR primers in the amplification of eubacterial genomic DNA. REP and ERIC consensus oligonucleotides produced clearly resolvable bands by agarose gel electrophoresis following PCR amplification. These band patterns provided unambiguous DNA fingerprints of different eubacterial species and strains. Both REP and ERIC probes hybridized preferentially to genomic DNA from Gram-negative enteric bacteria and related species. Widespread distribution of these repetitive DNA elements in the genomes of various microorganisms should enable rapid identification of bacterial species and strains, and be useful for the analysis of prokaryotic genomes.
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            Pandemic human viruses cause decline of endangered great apes.

            Commercial hunting and habitat loss are major drivers of the rapid decline of great apes [1]. Ecotourism and research have been widely promoted as a means of providing alternative value for apes and their habitats [2]. However, close contact between humans and habituated apes during ape tourism and research has raised concerns that disease transmission risks might outweigh benefits [3-7]. To date only bacterial and parasitic infections of typically low virulence have been shown to move from humans to wild apes [8, 9]. Here, we present the first direct evidence of virus transmission from humans to wild apes. Tissue samples from habituated chimpanzees that died during three respiratory-disease outbreaks at our research site, Côte d'Ivoire, contained two common human paramyxoviruses. Viral strains sampled from chimpanzees were closely related to strains circulating in contemporaneous, worldwide human epidemics. Twenty-four years of mortality data from observed chimpanzees reveal that such respiratory outbreaks could have a long history. In contrast, survey data show that research presence has had a strong positive effect in suppressing poaching around the research site. These observations illustrate the challenge of maximizing the benefit of research and tourism to great apes while minimizing the negative side effects.
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              Temporal patterns of crop-raiding by primates: linking food availability in croplands and adjacent forest

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                Author and article information

                Journal
                Emerg Infect Dis
                EID
                Emerging Infectious Diseases
                Centers for Disease Control and Prevention
                1080-6040
                1080-6059
                September 2008
                : 14
                : 9
                : 1375-1382
                Affiliations
                [1]University of Illinois, Urbana, Illinois, USA (T.L. Goldberg, T.R. Gillespie, E.L. Estoff)
                [2]Makerere University, Kampala, Uganda (T.L. Goldberg, I.B. Rwego, C.A. Chapman)
                [3]McGill University, Montreal, Quebec, Canada (C.A. Chapman)
                [4]Wildlife Conservation Society, Bronx, New York, USA (C.A. Chapman)
                [1 ]Current affiliation: University of Wisconsin, Madison, Wisconsin, USA.
                Author notes
                Address for correspondence: Tony L. Goldberg, University of Wisconsin–Madison, Department of Pathobiological Sciences, 2015 Linden Dr, Madison, WI 53706, USA; email: tgoldberg@ 123456vetmed.wisc.edu
                Article
                07-1196
                10.3201/eid1409.071196
                2603117
                18760003
                50552f18-1ab2-4b25-9441-dfb16fb5d67c
                History
                Categories
                Research

                Infectious disease & Microbiology
                zoonoses,domestic animals,ecology,epidemiology,escherichia coli,nonhuman primates,africa,uganda,research

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