No abstract
Most hosts, including humans, are simultaneously or sequentially infected with several parasites. A key question is whether patterns of coinfection arise because infection by one parasite species affects susceptibility to others or because of inherent differences between hosts. We used timeseries data from individual hosts in natural populations to analyze patterns of infection risk for a microparasite community, detecting large positive and negative effects of other infections. Patterns remain once variations in host susceptibility and exposure are accounted for. Indeed, effects are typically of greater magnitude, and explain more variation in infection risk, than the effects associated with host and environmental factors more commonly considered in disease studies. We highlight the danger of mistaken inference when considering parasite species in isolation rather than parasite communities.Macroparasites (helminths and arthropods) and microparasites (viruses, bacteria, and protozoa) are integral components of the ecological communities that include their hosts (1), and it is likely that most hosts, most of the time, are infected with more than one parasite species (2). Interactions between parasites in natural populations, however, have been studied only rarely. A community ecology perspective is particularly relevant for studies of coinfection, as parasites may interact directly by competing for resources or indirectly via the host immune system (3). Interactions may be antagonistic to at least one of the parasites, either as a result of resource shortage or where there are cross-effective immune responses, or they may be beneficial to one or both parasites, as a result of parasite-induced immunosuppression or down-regulation of all or part of the immune system (1). Table 1 for details of their biology). Infection risk will depend on both the probability of encountering an infectious dose and the probability of infection given exposure (host susceptibility). We aimed to determine whether susceptibility to infection by a microparasite was influenced by other microparasites. Therefore, for each microparasite, we investigated whether the other microparasites influenced the probability that a susceptible animal became infected at a given time point (t 0 ), adding infection status for these other microparasites as explanatory variables to baseline statistical models that accounted for environmental and individual variables (e.g., sex and season) (12) (table S1). Thus, we guard against detecting spurious associations, which, in reality, reflect correlated exposure risk (e.g., a positive association simply because both parasites are most prevalent in late summer). For parasites causing self-limiting infections, infection status at both t 0 and/ or the previous month (t −1 ) were considered as explanatory variables, whereas for B. microti infections, which are chronic, a three-level covariate was used: uninfected, newly infected (infected at t 0 but not before), and chronically infected (first infected prior ...
Ticks are obligate haematophagous acarines that parasitise every class of vertebrate (including man) and have a worldwide distribution. An increasing awareness of tick-borne diseases among clinicians and scientific researchers has led to the recent description of a number of emerging tick-borne bacterial diseases. Since the identification of Borrelia burgdorferi as the agent of Lyme disease in 1982, 11 tick-borne human bacterial pathogens have been described in Europe. Aetiological diagnosis of tick-transmitted diseases is often difficult and relies on specialised laboratories using very specific tools. Interpretation of laboratory data is very important in order to establish the diagnosis. These guidelines aim to help clinicians and microbiologists in diagnosing infection transmitted by tick bites and to provide the scientific and medical community with a better understanding of these infectious diseases.
The bacterial genus Bartonella comprises 21 pathogens causing characteristic intraerythrocytic infections. Bartonella bacilliformis is a severe pathogen representing an ancestral lineage, whereas the other species are benign pathogens that evolved by radial speciation. Here, we have used comparative and functional genomics to infer pathogenicity genes specific to the radiating lineage, and we suggest that these genes may have facilitated adaptation to the host environment. We determined the complete genome sequence of Bartonella tribocorum by shotgun sequencing and functionally identified 97 pathogenicity genes by signature-tagged mutagenesis. Eighty-one pathogenicity genes belong to the core genome (1,097 genes) of the radiating lineage inferred from genome comparison of B. tribocorum, Bartonella henselae and Bartonella quintana. Sixty-six pathogenicity genes are present in B. bacilliformis, and one has been lost by deletion. The 14 pathogenicity genes specific for the radiating lineage encode two laterally acquired type IV secretion systems, suggesting that these systems have a role in host adaptability.
Bartonella spp. are facultative intracellular bacteria that cause characteristic host-restricted hemotropic infections in mammals and are typically transmitted by blood-sucking arthropods. In the mammalian reservoir, these bacteria initially infect a yet unrecognized primary niche, which seeds organisms into the blood stream leading to the establishment of a long-lasting intra-erythrocytic bacteremia as the hall-mark of infection. Bacterial type IV secretion systems, which are supra-molecular transporters ancestrally related to bacterial conjugation systems, represent crucial pathogenicity factors that have contributed to a radial expansion of the Bartonella lineage in nature by facilitating adaptation to unique mammalian hosts. On the molecular level, the type IV secretion system VirB/VirD4 is known to translocate a cocktail of different effector proteins into host cells, which subvert multiple cellular functions to the benefit of the infecting pathogen. Furthermore, bacterial adhesins mediate a critical, early step in the pathogenesis of the bartonellae by binding to extracellular matrix components of host cells, which leads to firm bacterial adhesion to the cell surface as a prerequisite for the efficient translocation of type IV secretion effector proteins. The best-studied adhesins in bartonellae are the orthologous trimeric autotransporter adhesins, BadA in Bartonella henselae and the Vomp family in Bartonella quintana. Genetic diversity and strain variability also appear to enhance the ability of bartonellae to invade not only specific reservoir hosts, but also accidental hosts, as shown for B. henselae. Bartonellae have been identified in many different blood-sucking arthropods, in which they are typically found to cause extracellular infections of the mid-gut epithelium. Adaptation to specific vectors and reservoirs seems to be a common strategy of bartonellae for transmission and host diversity. However, knowledge regarding arthropod specificity/restriction, the mode of transmission, and the bacterial factors involved in arthropod infection and transmission is still limited.
Nucleotide base sequence data were obtained for a 940-bp fragment of the citrate synthase-encoding gene @.A) of representatives of the eight validly described Burtonella species and seven uncharacterized Burtonella strains obtained from small mammals. Complete 16s rRNA gene sequences were also determined for the uncharacterized strains, and these sequences revealed that each strain had a unique sequence which was very similar to the sequences of the previously recognized Bartonellu species. A comparison of the gltA sequences of the different Burtonella species revealed that the levels of similarity between sequences were 83.8 to 93.5%, whereas comparisons of sequences obtained from different strains of the same species revealed that the levels of similarity were more than 99.8%. One of the uncharacterized strains had a gZtA sequence that matched the sequence of Burtonelk elizabethue, three uncharacterized strains had sequences which were more than 99.6% similar to each other (but less than 93.5% similar to any other sequence), and the remaining three uncharacterized strains each exhibited less than 93.5% sequence similarity to other Burtonella species or isolates. Phylogenetic trees were inferred from multiple alignments of both g U and 16s ribosomal DNA (rDNA) sequences. Whereas the proposed intra-Burtonella architecture of trees inferred from 16s rDNA sequence data by using both distance matrix and parsimony methods had virtually no statistical support, the trees inferred from the gk-4 sequence data contained four well-supported lineages in the genus. The gU-derived phylogeny appears to be more useful than the phylogeny derived from 16s rDNA sequence data for investigating the evolutionary relationships of Burtonella species, and the validity of the lineages identified by the gltA analysis is discussed in this paper.The family Bartonellaceae has recently been subjected to considerable taxonomic reassessment, which has resulted in (i) the transfer of members of the genus Rochalirnaea (formerly placed in the Rickettsiaceae) to the genus Bartonella (7), (ii) the unification of the two established genera in the family, the genera Bartonella and Grahamella, with the name of the former taking precedence (5), (iii) the proposal of several new species and subspecies (5,6), and (iv) the removal of the family from the order Rickettsiales (7). The restructured family now includes the single genus Bartonella, which contains eight species. A polyphasic approach was used to develop all of these proposals, and phylogenetic data derived from a comparison of 16s rRNA gene sequences provided important supporting evidence. These studies also revealed that the Bartonella species are very closely related and that they exhibit very high levels of 16s rRNA gene sequence similarity (>97.8%) and significant levels of DNA-DNA homology (16 to 67%) (5, 7, 8). The paucity of 16s rRNA gene sequence differences between species limits the usefulness of this tool for inferring intragenus phylogeny and, as in other closely related taxa, does n...
This study used a PCR-based approach targeting 16S rRNA gene fragments to determine the occurrence and association of the three bovine digital dermatitis (BDD) treponeme phylogroups within lesions found in cattle from the United Kingdom. Examination of 51 BDD lesions collected from infected cattle across the United Kingdom revealed that BDD treponeme group 1 (Treponema medium/Treponema vincentii-like), group 2 (Treponema phagedenis-like), and group 3 (Treponema putidum/Treponema denticola-like) were present in 96.1%, 98%, and 76.5% of BDD lesions, respectively. The three phylogroups were present together in 74.5% of lesions. The PCR assays enabled the isolation of further treponeme strains from previously mixed primary BDD lesion cultures. Here a representative from each of the three distinct treponeme phylogroups was isolated from a single BDD lesion for the first time. These data highlight the extent to which this disease is polytreponemal. Immunohistochemistry and electron microscopy were used to investigate lesional hoof tissues, resulting in treponemes being identified copiously in hair follicles and sebaceous glands, suggesting a potential route of exit and/or entry for these pathogens. This study gives further evidence for the importance of the three treponeme groups in BDD pathogenesis and reiterates the value of molecular genetic approaches for isolating and identifying fastidious anaerobes.
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