Host-Pathogen Interactions in Anaplasma phagocytophilum and Ehrlichia chaffeensis, Notas de estudo de Engenharia Elétrica

Baixe Host-Pathogen Interactions in Anaplasma phagocytophilum and Ehrlichia chaffeensis e outras Notas de estudo em PDF para Engenharia Elétrica, somente na Docsity! The family Anaplasmataceae (FIG. 1) is composed of patho- genic and non-pathogenic (either commensal or mutualis- tic) obligate intracellular bacteria that infect invertebrates; some species can also target cells of haematopoietic origin in mammals and birds (TABLE 1). The family belongs to the order Rickettsiales, along with the family Rickettsiaceae, which comprises obligate intracellular bacteria that are transmitted by blood-sucking arthropods and that cause potentially fatal diseases such as epidemic typhus. A major biological difference between members of these two families is that the Anaplasmataceae are confined within membrane-bound compartments in the host cytoplasm, whereas the Rickettsiaceae are not. The first Anaplasmataceae species to be identified was the veterinary pathogen Anaplasma marginale, which was found in the red blood cells of cattle with severe anaemia in 1910 by Theiler1. To date, Anaplasma phagocytophilum, Ehrlichia chaffeensis, Ehrlichia ewingii, Ehrlichia canis, Neorickettsia sennetsu and, potentially, Ehrlichia ruminantium are known to infect humans (TABLE 1). Apart from E. chaffeensis and N. sennetsu, Anaplasmataceae species were known as veterinary pathogens before they were shown to infect humans. A. phagocytophilum, E. chaffeensis and E. ewingii cause the important emerging zoonoses human granulocytic anaplasmosis, human monocytic ehrlichiosis and human ewingii ehrlichiosis, respectively2. The clinical signs of these diseases are similar and include fever, headache, myalgia, anorexia and chills, frequently accompanied by leukopenia followed by the appearance of immature cells (rebound leukocytosis), thrombocytopenia, anaemia and an increased level of serum hepatic aminotransferases2–4. The severity of disease varies from asymptomatic sero- conversion to frequently documented severe morbidity and death2–4. These diseases are the most prevalent life- threatening tick-borne zoonoses in the United States4,5 and were collectively designated nationally notifiable diseases in the United States in 1998 (REF. 6). They are less frequently reported in other parts of the world. Clinical diagnosis is made on the basis of retrospective seroconversion or PCR analysis. No vaccines are available for these diseases, and doxycycline, a broad-spectrum antibiotic, remains the drug of choice for treating patients. The first bacterium in the family Anaplasmataceae to be identified as a cause of human ehrlichiosis was N. sennetsu. This bacterium has been isolated from the blood of sev- eral patients with infectious-mononucleosis-like clini- cal signs in Japan and Malaysia, and it has recently been detected in a patient in Laos7. Other Neorickettsia spp. are well-known veterinary pathogens in the United States. Unlike Anaplasma spp. and Ehrlichia spp., Neorickettsia spp. are transmitted to mammals by the ingestion of fish or aquatic insects that harbour infected trematodes. The global canine pathogen E. canis has been isolated from a human, and in Venezuela several patients with clinical signs compatible with human monocytic ehrlichiosis were Department of Veterinary Biosciences, College of Veterinary Medicine, The Ohio State University, 1925 Coffey Road, Columbus, Ohio 43210, USA. e‑mail: rikihisa.1@osu.edu doi:10.1038/nrmicro2318 Published online 7 April 2010 Anaplasma phagocytophilum and Ehrlichia chaffeensis: subversive manipulators of host cells Yasuko Rikihisa Abstract | Anaplasma spp. and Ehrlichia spp. cause several emerging human infectious diseases. Anaplasma phagocytophilum and Ehrlichia chaffeensis are transmitted between mammals by blood-sucking ticks and replicate inside mammalian white blood cells and tick salivary-gland and midgut cells. Adaptation to a life in eukaryotic cells and transmission between hosts has been assisted by the deletion of many genes that are present in the genomes of free-living bacteria (including genes required for the biosynthesis of lipopolysaccharide and peptidoglycan), by the acquisition of a cholesterol uptake pathway and by the expansion of the repertoire of genes encoding the outer-membrane porins and type IV secretion system. Here, I review the specialized properties and other adaptations of these intracellular bacteria. R E V I E W S 328 | MAy 2010 | VOLUMe 8 www.nature.com/reviews/micro © 20 Macmillan Publishers Limited. All rights reserved10 Nature Reviews | Microbiology Anaplasma phagocytophilum Anaplasma platys Anaplasma marginale Ehrlichia canis Ehrlichia chaffeensis Ehrlichia muris Ehrlichia ewingii Ehrlichia ruminantium Neorickettsia risticii Neorickettsia sennetsu Wolbachia pipientis Wolbachia endosymbiont of Dirofilaria immitis Ehrlichia Anaplasma Wolbachia Neorickettsia Neorickettsia helminthoeca Candidatus Xenohaliotis Candidatus Neoehrlichia Aegyptianella found to be infected with E. canis8,9. The brown dog tick transmits E. canis between dogs, and human infestation with this species of tick is common in certain geographical regions, including Venezuela. This suggests that E. canis can cause human monocytic ehrlichiosis under certain circumstances. Three fatal human infections with E. rumi­ nantium, a ruminant pathogen, have been reported in Africa, although they were not confirmed by cytology or bacterial isolation10. These species provide a useful model system to dissect the mechanisms of obligatory intracellular parasitism, inter-kingdom bidirectional signalling, vector trans- mission and leukocyte-targeted disease pathogenesis, thereby also contributing to our understanding of eukaryotes. Key questions that relate to Anaplasma spp. and Ehrlichia spp. include how they subvert the host immune system, how they manipulate host cells to cre- ate an effective replicative niche, how they regulate the dichotomous tasks of intracellular replication and inter- cellular spreading, and how they cause human disease. The focus of this Review will be on recent studies of A. phagocytophilum and E. chaffeensis that are relevant to these questions, observed primarily from the bacterial perspective. New information on the host cell response to infection and the nature of the inclusions that has come to light since this topic was last reviewed11–15 is also included here. Life cycle and intracellular development In nature, the life cycles of A. phagocytophilum, E. chaffeensis and E. ewingii consist of mammalian and tick stages. Wild animals such as white-footed mice and white-tailed deer are primary reservoirs, and domestic animals such as dogs can occasionally serve as secondary reservoirs for human infection16–19. Humans are infected acciden- tally by the bite of infected ticks. A. phagocytophilum is transmitted by the black-legged tick (Ixodes scapularis) and the Western black-legged tick (Ixodes pacificus) in the United States, by the castor bean tick (Ixodes ricinus) in europe and by the taiga tick (Ixodes persulcatus) in Asia2. The lone-star tick (Amblyomma americanum) serves as the biological vector for both E. chaffeensis and E. ewingii transmission16,20,21 (FIG. 2). Human-to-human nosocomial transmission of A. phagocytophilum might have occurred in China, although this case was not confirmed by blood smears or cultures22,23. The fact that E. ewingii has not been isolated in pure culture has hindered molecular analysis of the pathogenesis of this species, and it will therefore not be covered further in this Review. Once transmitted to mammals, A. phagocytophilum and E. chaffeensis replicate primarily in granulocytes and in monocytes or macrophages, respectively, by subverting several host innate immune responses11. Unlike Rickettsia spp. and most other Gram-negative bacteria, the genomes of A. phagocytophilum and E. chaffeensis lack the genes for biosynthesis of the lipopolysaccharide and peptidoglycan that activate host leukocytes. These bacteria must therefore incorporate cholesterol derived from host cells into their membranes to support membrane integrity24. The most studied host cell receptor for A. phagocytophilum infection is P-selectin glycoprotein ligand 1 (PSGL1); little informa- tion is available about the host cell receptors for E. chaffeen­ sis. Binding of A. phagocytophilum to cells of the human leukaemia cell line HL-60 is dependent on the expression of both PSGL1 and an α(1,3)-fucosyltransferase25. However, sialic acid- and PSGL1-independent adhesion activity has been reported in a sub-line of A. phagocytophilum str. NCH-126, and A. phagocytophilum can infect cultured vascular endothelial cells27, which do not usually express PSGL1. Binding of A. phagocytophilum to mouse neutro- phils requires expression of α(1,3)-fucosyltransferases but not PSGL1 (REF. 28). The cognate A. phagocytophilum Figure 1 | A phylogram of the family Anaplasmataceae, based on 16S ribosomal RNA gene sequences. Genera are in bold. The phylogenetic tree was constructed from on sequence alignments by the Clustal W method using the MegAlign program from the Lasergene package. R E V I E W S NATURe ReVIeWS | MicRobiology VOLUMe 8 | MAy 2010 | 329 © 20 Macmillan Publishers Limited. All rights reserved10 Nature Reviews | Microbiology Anaplasma phagocytophilum Ehrlichia chaffeensis Exocytosis ExocytosisHost cell lysis and release Host cell lysis and release Fusion Phagosome VAMP2 and CD-MPR Caveola Beclin 1 and LC3 NCF1 NCF2 NOX2 and CYBA ? ? ?? Lysosome TFR, TF, EEA1, Rab5, VAMP2 and vacuolar (H+) ATPase TFR An A. phagocytophilum population therefore natu- rally encodes a mixture of p44ES alleles, and a cloned A. phagocytophilum expressing a single p44 gene was used to show that antigenic variation of p44 occurs in infected horses and severe combined immunodeficient (SCID) mice62. Donor p44 genes that are frequently expressed were found to be concentrated near the p44ES62. Diverse p44 genes were also expressed in various developmental stages of I. scapularis ticks71. Furthermore, the popula- tions of expressed p44 genes were different in the blood and spleen of A. phagocytophilum-infected mice and also in the salivary glands and midgut of I. scapularis removed from these mice following A. phagocytophilum transmis- sion72. Diverse p44 sequences were also detected in the p44ES loci of A. phagocytophilum strains from various animals and geographical locations73. Taken together, these data indicate that p44 recombination is an inherent property of A. phagocytophilum. The expression of p44 mRNA by A. phagocytophilum is significantly upregulated in the spleens of mice compared with expression in salivary glands of I. scapularis, and mRNA levels are also higher in HL-60 cells than in ISe6 tick cells74. ApxR, a hypothetical protein from A. phagocyto­ philum that was originally isolated by DNA affinity puri- fication and then identified by proteomics75, can bind to the promoter regions of p44ES and apxR and trans activate p44ES 74. In addition, apxR is upregulated approximately 1,000-fold in HL-60 cells compared with levels in ISe6 tick cells74. These results indicate that p44ES and apxR are upregulated in the mammalian host environment and suggest that ApxR not only positively autoregulates itself but also transcriptionally regulates p44ES74. A recent study reported that 43% of A. phagocytophilum genes that are upregulated more than twofold in HL-60 cells com- pared with levels in ISe6 tick cells are predicted to encode membrane-associated proteins and 54% encode hypotheti- cal proteins. Similarly, 46% of the genes that are upregulated more than twofold in ISe6 tick cells compared with levels in HL-60 cells are predicted to encode membrane-associated proteins and 93% encode hypothetical proteins76. This finding reinforces the notion that A. phagocytophilum is a ‘microbial chameleon’ that can change its surface coating to adapt to the host environment. OMP1–P28 proteins. Members of the OMP1–P28 pro- tein family in E. chaffeensis are encoded by a polymorphic multigene family composed of 22 paralogues that are clus- tered in a 29 kb gene locus, and this locus is downstream of the transcriptional regulator gene tr1, as is p44ES in A. phagocytophilum77 (FIG. 4). The gene organization and genomic locus of the E. chaffeensis omp1–p28 gene cluster are conserved among Ehrlichia species, including E. canis, E. ruminantium and E. ewingii77–79. The omp1–p28 locus is among the most strain-variable genomic regions found to date80–83. Although there is no evidence for recombination, multiple OMP1–P28 proteins are expressed by E. chaf­ feensis in infected animals and in cell culture51,77,82,84–86. Given that most of the omp1–p28 paralogues are tran- scribed in DH82 cells77, it is possible that each organism expresses more than one of these proteins. Alternatively, each organism might express a single OMP1–P28 protein, but in a given bacterial population multiple OMP1–P28 family proteins could be expressed. Of note, OMP1B (also known as OMP14–P28) is the only OMP1–P28 paralogue for which a transcript is detected in three developmental stages of A. americanum ticks (which are a proven vector of E. chaffeensis transmission11) before or after E. chaffeen­ sis transmission to naive dogs84. OMP1B was also the only OMP1–P28 paralogue detected by proteomics in E. chaf­ feensis cultured in the ISe6 tick cell line86. OMP1B is an orthologue of E. canis P30-10, the expression of which is upregulated in cell culture at 25 °C compared with expres- sion at 37 °C87. Therefore, the E. chaffeensis OMP1–P28 multigene family may be differentially expressed in mammalian and tick hosts84,86. Functions of P44 and OMP1–P28 proteins. Antibodies specific to P44 inhibit A. phagocytophilum infection in mice and HL-60 cell culture64,88–90, indicating that Figure 3 | The intracellular niches of Anaplasma phagocytophilum and Ehrlichia chaffeensis in human cells. Caveolae-mediated endocytosis directs Anaplasma phagocytophilum and Ehrlichia chaffeensis into intracellular compartments (morulae) that do not fuse with lysosomes or assemble NADPH oxidase (the components of which are NADPH oxidase 2 (NOX2; also known as gp91phox homologue 2), cytochrome b245 light chain (CYBA, also known as p22phox), neutrophil cytosol factor 1 (NCF1; also known as p47phox) and NCF2 (also known as p67phox)), thus providing protection from non-oxidative and oxidative damage. E. chaffeensis inclusions are early endosomes, being positive for early-endosome antigen 1 (EEA1), Rab5, transferrin (TF), transferrin receptor (TFR), vacuolar (H+)ATPase and vesicle-associated membrane protein 2 (VAMP2). Some A. phagocytophilum morulae are positive for VAMP2 and cation-dependent mannose-6-phosphate receptor (CD-MPR; also known as M6PR) and acquire early- autophagosome-like features (they are positive for beclin 1 and LC3). It is thought that these bacteria exit through host cell lysis or exocytosis, but this has yet to be proved experimentally (as indicated by the question marks). R E V I E W S 332 | MAy 2010 | VOLUMe 8 www.nature.com/reviews/micro © 20 Macmillan Publishers Limited. All rights reserved10 Nature Reviews | Microbiology tr1 omp1X omp1N oriC 4.4 kb p44 distribution 700,000 600,000 500,000 400,000 300,000 200,000 100,0001,400,000 1,300,000 1,200,000 1,100,000 1,000,000 900,000 2,200 4,400 6,600 8,800 1,100 13,200 15,400 217,600 19,800 22,000 24,200 800,000 1 Ap 1.47 Mb Ec 1.18 Mb 28.9 kb oriC p44ES a b tr1 M N Q P T U V W X Y S H Z A B C D E F p28 secA p28-1 p28-2 antigenic variation of P44 proteins may help A. phago­ cytophilum to escape host immune surveillance. Likewise, immunization with recombinant P28 protects mice from E. chaffeensis challenge91. Polyclonal antibodies specific to E. chaffeensis or monoclonal antibodies specific to P28 (also known as OMP1G) mediate protection of SCID mice from fatal infection with E. chaffeensis92,93. So what is the physiological function, if any, of P44 and OMP1–P28 proteins in bacteria? Isolated native P44, P28 and OMP1F have transmembrane β-strands and exhibit porin activ- ity94,95. Porin activity allows passive diffusion across the outer membrane of l-glutamine, the mono saccharides arabinose and glucose, the disaccharide sucrose and even the tetrasaccharide stachyose. Notably, P28 and OMP1F of E. chaffeensis have different solute diffusion rates94, suggesting that differential expression of this gene fam- ily could affect the effectiveness of nutrient acquisition by the bacteria. Other surface proteins. In addition to P44, proteomics analysis in A. phagocytophilum has shown bacterial sur- face expression of two hypothetical proteins (named in this study as Asp55 and Asp62) and OMP85, OMP1A and components of the T4SS apparatus50 (see Supplementary information S1 (table)). Asp55 and Asp62 are predicted to contain 22 transmembrane β-strands forming a β-barrel and, thus, might be involved in membrane transport. Sera specific to Asp55 and Asp62 partially inhibit A. phago­ cytophilum infection of HL-60 cells in vitro50. The genes encoding Asp55 and Asp62 are co-transcribed and are con- served among members of the family Anaplasmataceae51. OMP85 is a conserved outer-membrane protein in Gram- negative bacteria96 and a central component of the apparatus for outer-membrane protein assembly97. In addition to the OMP1–P28 family proteins, there are other surface-exposed proteins in E. chaffeensis; including the hypothetical protein esp73 (which is an Asp55 orthologue), OMP85, tandem-repeat protein 47 (TRP47; also known as gp47), proteases and components of the T4SS apparatus51. TRP47, TRP32 and TRP120 (also known as gp120) were previously reported to be exposed on the surface of E. chaffeensis98–100. None of these three proteins has a predicted signal peptide or transmembrane segment, and they probably adhere to the bacterial sur- face. TRP120 was suggested to play a part in adhesion or invasion of mammalian cells on the basis of experiments using TRP120-transformed E. coli, although its expres- sion on the surface of E. coli was not shown98. In addition, Figure 4 | The p44 and omp1–p28 loci. a | The Anaplasma phagocytophilum (Ap) p44 expression locus (p44ES) is downstream of transcriptional regulator 1 (tr1), outer-membrane protein 1X (omp1X) and omp1N, near the predicted replication origin (oriC). More than 100 p44 genes are concentrated around p44ES, as shown in the genome representation, and serve as donors for recombination at p44ES. From outside to inside in the distribution diagram, the two circles represent p44 genes on the plus and minus strands. The full-length p44 genes (that each have an ORF longer than 1,000 bp and contain conserved start and stop codons and a central hypervariable region of approximately 280 bp) are indicated in red. The silent p44 genes (that each have an ORF less than 1,000 bp long, contain either conserved or alternative start or stop codons and cannot be expressed as full-length p44 genes at the current genomic location) are shown in black. b | The Ehrlichia chaffeensis (Ec) omp1–p28 locus contains a cluster of 22 omp1–p28 genes (shown in magenta; letters represent the relevant omp1 gene, such that M is omp1M and so on) flanked by tr1 and secA near the predicted oriC. R E V I E W S NATURe ReVIeWS | MicRobiology VOLUMe 8 | MAy 2010 | 333 © 20 Macmillan Publishers Limited. All rights reserved10 these proteins are highly immunogenic in infected ani- mals and patients99,101,102. Although genes encoding the proteins involved in glycosylation have not been found in A. phagocytophilum and E. chaffeensis37, the tandem- repeat proteins were reported to be glycosylated99,103. Recently, however, the same laboratory reported that some of these proteins are not glycosylated104. In E. chaffeensis, 15 predicted lipoproteins are expressed in cell culture, and orthologues of these lipoproteins are encoded in the A. phagocytophilum genome105. Some are predicted to be exposed on the bacterial surface and are thought to be responsible for the delayed hypersensitiv- ity reaction in infected mammals105. Dynamic expression of diverse surface proteins, both as a bacterial population and during the life cycle of an individual cell, is key for bacterial survival and persistence and, in addition to the variation of surface proteins according to bacterial strain, poses a challenge to effective vaccine design. Intracellular replication and maturation Anaplasma spp. and Ehrlichia spp. form dense intracellular microcolonies, which are called morulae, as they look like mulberries when blood smears, tissue samples or cultured cells are Romanowsky stained and observed under the light microscope (the term ‘morulae’ is derived from the Latin word for mulberry: ‘morus’) (reviewed in REF 106). Under an electron microscope, A. phagocytophilum and E. chaf­ feensis can be seen to be enveloped with inner and outer membranes. They are polymorphic bacteria (ranging from 0.2 to 2.0 μm in diameter) that can sometimes be catego- rized into dense-cored cells and reticulate cells in cultured human cells as well as in infected blood and tick mid- gut cells27,106–112. In cell culture, a biphasic developmental cycle has been reported (FIG. 5): initially, small dense-cored cells bind to host cells, are internalized and develop into large reticulate cells; these reticulate cells then mature into dense-cored cells or compact into clumps110–112. The infectivity of populations that are rich in dense-cored cells is notably greater than that of populations that are rich in reticulate cells111,112. Dense-cored cells and reticulate cells might not always be distinct, because various intermediate or aberrant forms exist110,112. In addition, caution should be taken, as the ultrastructure of this group of bacteria is influenced not only by the physiological conditions in the host cell, but also by fixation and other sample preparation methods used in electron microscopy113. When an A. phagocytophilum or E. chaffeensis popula- tion enriched in dense-cored cells was used to inoculate a human leukaemia cell line, quantitative PCR showed that after a lag phase of growth lasting for approximately 24 h, an exponential growth phase occurred from 24 h to 72 h followed by a short stationary phase from 72 h to 96 h114,115. Under different culture conditions, trans- mission electron microscopy showed a considerable amount of replication by 24 h, and shortly thereafter the reticulate cells recondensed to dense-cored cells to re- initiate the infection cycle111,112. During the first hour, only one to a few bacteria per host cell can be seen under the light microscope (at this stage, the bacteria are gener- ally not distinct and immunofluorescence labelling using bacteria-specific antibodies is required to confirm their presence)25,114–116. During exponential growth, both the number and the size of the morulae increase in every infected cell. During stationary phase, morulae become loose and swollen and the bacteria disperse and begin to be liberated from the host cells, eventually resulting in bursting of the infected cell114–116. Proteins belonging to the A. phagocytophilum and E. chaffeensis T4SS apparatus and two-component sys- tems as well as several E. chaffeensis surface proteins (P28, OMP1F, TRP47 and TRP120) are differentially expressed during intracellular development94,98,99,112. These pro- teins can therefore be used as surface markers to distin- guish dense-cored cell and reticulate cell populations by immunofluorescence microscopy. Within less than 1 h of incubation, only small-form A. phagocytophilum (consist- ing of mostly dense-cored cells) in which the VirB9 com- ponent of the T4SS cannot be detected are associated with human peripheral blood neutrophils, whereas in HL-60 cells a VirB9-expressing form (consisting of mostly reticu- late cells) is also found116. Most dense-cored cells remain attached to the HL-60 cell surface, but reticulate cells are internalized and co-localize with lysosome-associated membrane glycoprotein 1 (LAMP1), a lysosomal marker116, suggesting that some reticulate cells are rapidly internalized and degraded, depending on the cell type. Taken together, the different stages of the A. phagocyto­ philum and E. chaffeensis developmental cycle influence the nature of binding to host cells and the early avoidance of the late-endosome–lysosome pathway. Although the A. phagocytophilum and E. chaffeensis developmental cycles resemble those of Chlamydia spp. and Coxiella spp., eukaryotic histone H1 homologues, which are required for chromosomal condensation dur- ing the elementary body stages of the Chlamydia spp. and Coxiella spp. cycles117,118, are not found in members of the family Anaplasmataceae. Many questions remain regard- ing the intracellular replication and maturation of Erlichia spp. and Anaplasma spp., including how these processes are regulated and coordinated. Although conversion to dense-cored cells resembles stress or quorum responses, genes encoding the nutritional stress response proteins RelA and SpoT or proteins required for the biosynthesis of a quorum-sensing pheromone have not been found in the genomes of Anaplasma spp. or Ehrlichia spp. Furthermore, Anaplasma spp. and Ehrlichia spp. encode only two RNA polymerase σ-factor homologues: a constitutive σ70 (also known as RpoD) and a single alternative σ-factor, σ32 (also known as RpoH). The paucity of alternative σ-factors suggests that the intracellular development of these bacteria requires regulation of constitutive σ70-type promoters by transcription factors. In fact, DNA-binding proteins that can transactivate downstream genes have been identified: ApxR in A. phagocytophilum75 and ecxR in E. chaffeensis114. In addition, genome sequence analy- sis predicts several DNA-interacting proteins: a putative transcriptional regulator encoded by tr1 that has a winged helix–turn–helix motif, a basic histone-like HU protein, a putative transcription factor of the barrier to autointe- gration factor (BAF) family, a transcriptional regulator of the MerR (mercuric resistance operon regulator) family, integration host factor α-subunit (IHFα) and IHFβ, and Alternative σ-factor A σ-factor that is produced under specific conditions, allowing the RNA polymerase to transcribe a different set of genes than the housekeeping σ factor, σ70, allows. R E V I E W S 334 | MAy 2010 | VOLUMe 8 www.nature.com/reviews/micro © 20 Macmillan Publishers Limited. All rights reserved10 therefore hijacks cholesterol by manipulating the cellu- lar LDL cholesterol uptake system to facilitate bacterial replication. Future prospects Since the first complete genome sequence data for A. phagocytophilum and E. chaffeensis became availa- ble 4 years ago, we have made good progress in under- standing the surface proteins of these bacteria and their signalling and regulatory potential. Many ‘hypo- thetical’ proteins have been shown to be expressed, and several have been shown to have, or are predicted to have, important functions. Our eventual under- standing of how A. phagocytophilum and E. chaffeensis cause disease will entail integration of this knowledge with an understanding of the host cell response to infection. It is likely that further surprising functions will be discovered for ‘hypothetical’ proteins in these bacteria. On the one hand, the unique surface proteins that have evolved in this group of pathogens continue to provide insights into the niche adaptation of these bacteria and their interplay with the host immune system. On the other hand, A. phagocytophilum and E. chaffeensis proteins that are found in other bac- teria, including certain two-component systems and the T4SS, offer the opportunity to study the roles of these proteins in the pathogenesis of eukaryotic host cells. Although space limitations precluded their dis- cussion in this Review, ongoing studies of immunity and host defence against these pathogens, of tick gene knockdowns and of the ecology and evolution of this group of bacteria should also fill important gaps in our knowledge. As the choice of antibiotics available to treat infection with this group of pathogens is limited and the effec- tiveness of treatment is reduced when the initiation of therapy is delayed, non-antimicrobial compounds that inhibit the replication of these bacteria may have thera- peutic and prophylactic applications. Recombinant bac- terial antigens and synthetic peptides offer a novel set of compounds that could be used to aid rapid diagnosis and to develop a vaccine for high-risk populations. 1. Theiler, A. Anaplasma marginale (gen. and spec. nov.) The marginal points in the blood of cattle suffering from specific disease. Transvaal S. Afr. Rep.Vet. Bacteriol. Dept. Agr. 1908–1909, 7–64 (1910). 2. Thomas, R. J., Dumler, J. S. & Carlyon, J. A. Current management of human granulocytic anaplasmosis, human monocytic ehrlichiosis and Ehrlichia ewingii ehrlichiosis. Expert Rev. Anti Infect. Ther. 7, 709–722 (2009). 3. Paddock, C. D. & Childs, J. E. 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Identification of Ehrlichia chaffeensis morulae in cerebrospinal fluid mononuclear cells. J. Clin. Microbiol. 30, 2207–2210 (1992). 149. Ratnasamy, N., Everett, E. D., Roland, W. E., McDonald, G. & Caldwell, C. W. Central nervous system manifestations of human ehrlichiosis. Clin. Infect. Dis. 23, 314–319 (1996). Acknowledgements I thank all former and current members of my laboratory for their scientific contributions, T. Vojt for preparing the figures, V. L. Popov for the electron micrographs and K. Hayes-Ozello for editorial assistance. I also acknowledge grants from the US National Institutes of Health. Competing interests statement The author declares no competing financial interests. DATABASES Entrez Genome Project: http://www.ncbi.nlm.nih.gov/ genomeprj Amblyomma americanum | Anaplasma marginale | Anaplasma phagocytophilum | Chlamydia trachomatis str. D/UW-3/CX | Coxiella burnetii str. RSA 493 | Ehrlichia canis | Ehrlichia chaffeensis | Ehrlichia ruminantium | Escherichia coli | Ixodes scapularis | Neorickettsia sennetsu | Rickettsia prowazekii str. Madrid E Pfam: http://pfam.sanger.ac.uk PF01617 UniProtKB: http://www.uniprot.org σ32 | σ70 | ABI1 | ABL1 | AnkA | ApxR | Asp62 | Asp55 | Ats1 | DnaA | Esp73 | HU | IHFα | IHFβ | OMP1A | OMP1B | OMP1F | OMP85 | P30-10 | PSGL1 | RecF | TRP47 FURTHER INFORMATION Yasuko Rikihisa’s homepage: http://riki-lb1.vet.ohio-state.edu/ ehrlichia JCVI Comprehensive Microbial Resource: http://cmr.jcvi.org/ tigr-scripts/CMR/CmrHomePage.cgi SUPPLEMENTARY INFORMATION See online article: S1 (table) All liNkS ARe AcTiVe iN THe oNliNe PDf R E V I E W S NATURe ReVIeWS | MicRobiology VOLUMe 8 | MAy 2010 | 339 © 20 Macmillan Publishers Limited. All rights reserved10