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Sp110 transcription is induced and required by Anaplasma phagocytophilumfor infection of human promyelocytic cells
© de la Fuente et al; licensee BioMed Central Ltd. 2007
Received: 27 April 2007
Accepted: 20 September 2007
Published: 20 September 2007
The tick-borne intracellular pathogen, Anaplasma phagocytophilum (Rickettsiales: Anaplasmataceae) causes human granulocytic anaplasmosis after infection of polymorphonuclear leucocytes. The human Sp110 gene is a member of the nuclear body (NB) components that functions as a nuclear hormone receptor transcriptional coactivator and plays an important role in immunoprotective mechanisms against pathogens in humans. In this research, we hypothesized that Sp110 may be involved in the infection of human promyelocytic HL-60 cells with A. phagocytophilum.
The human Sp110 and A. phagocytophilum msp4 mRNA levels were evaluated by real-time RT-PCR in infected human HL-60 cells sampled at 0, 12, 24, 48, 72 and 96 hours post-infection. The effect of Sp110 expression on A. phagocytophilum infection was determined by RNA interference (RNAi). The expression of Sp110 was silenced in HL-60 cells by RNAi using pre-designed siRNAs using the Nucleofector 96-well shuttle system (Amaxa Biosystems, Gaithersburg, MD, USA). The A. phagocytophilum infection levels were evaluated in HL-60 cells after RNAi by real-time PCR of msp4 and normalizing against human Alu sequences.
While Sp110 mRNA levels increased concurrently with A. phagocytophilum infections in HL-60 cells, the silencing of Sp110 expression by RNA interference resulted in decreased infection levels.
These results demonstrated that Sp110 expression is required for A. phagocytophilum infection and multiplication in HL-60 cells, and suggest a previously undescribed mechanism by which A. phagocytophilum modulates Sp110 mRNA levels to facilitate establishment of infection of human HL-60 cells.
Anaplasma phagocytophilum (Rickettsiales: Anaplasmataceae) is an obligate intracellular tick-borne pathogen that causes human granulocytic anaplasmosis (HGA), tick-borne fever of ruminants, and equine and canine granulocytic anaplasmosis . HGA, first described in 1994 in the United States, has become a predominant form of anaplasmosis and among the most common tick-borne pathogens in the United States and Europe . HGA is characterized by fever, headache, myalgia, and malaise, as well as leukopenia, thrombocytopenia, and elevated levels of C-reactive protein and liver transaminases, which are indicators of inflammatory response and hepatic injury, respectively . Although the disease is usually self-limiting, severe complications can result, including prolonged fever, shock, seizures, pneumonitis, acute renal failure, hemorrhage, rhabdomyolysis, opportunistic infections and death .
A. phagocytophilum initiates infection of polymorphonuclear leucocytes by adhesion to host cells, a process which involves adhesins, such as the human P-selectin glycoprotein ligand-1 (PSGL-1) that bind cooperatively to neutrophil ligand molecules . After infection, A. phagocytophilum undergoes a developmental cycle in parasitophorous vacuoles that includes reticulated and dense forms, and this infection modulates host cell growth and differentiation .
While the main vector for A. phagocytophilum are tick species belonging to the Ixodes ricinus complex, the pathogen multiplies in a broad range of terrestrial vertebrates [2, 4]. In the laboratory, A. phagocytophilum can be propagated in undifferentiated human promyelocytic HL-60 cells. Infection of HL-60 cells with A. phagocytophilum results in modulation of host cell gene expression (see for example [5, 6].
Sp110 is a member of the nuclear body (NB) components that functions as a nuclear hormone receptor transcriptional coactivator . Sp110 and other NB-associated proteins, induced by type I (α/β) and type II (γ) interferons (IFNs), play a role in IFN response and virus replication . Sp110 expression is induced in human peripheral blood leukocytes and spleen but not in other tissues . Sp110 inhibits vesicular stomatitis virus and influenza virus replication, confers resistance to human Foamy virus, and gene polymorphisms or mutations have been associated with susceptibility to the Hepatitis C virus and immunodeficiency and hepatic veno-occlusive disease [8–10].
Recently, the mouse Sp110 homologue, the intracellular pathogen resistance 1 (Ipr1) gene, was shown to control susceptibility to Mycobacterium tuberculosis in mice . As in mice, Ipr1-like expression was higher in European wild boar resistant to natural M. bovis infection . Pan et al.  proposed that Ipr1-related proteins may play a role in integrating signals generated by intracellular pathogens or viruses with host cell mechanisms that regulate gene expression and cell death, thus modulating host susceptibility to infection. However, recent publications have documented that polymorphisms in Sp110 gene are not associated with susceptibility to tuberculosis in humans [13–15]. These results suggest that Sp110 may have a different role during infection by intracellular bacterial pathogens in humans.
In the study reported herein, we hypothesized that Sp110 may be involved in the infection of human promyelocytic cells with A. phagocytophilum and used a combination of real-time RT-PCR and RNA interference (RNAi) to test this hypothesis.
Determination of Sp110 mRNA levels in uninfected and infected HL-60 cells
Human HL-60 cells were cultured and infected with A. phagocytophilum as previously described (multiplicity of infection, MOI = 2) . Uninfected and infected cultures were sampled at 0, 12, 24, 48, 72 and 96 hours post-infection (hpi) and Sp110 and major surface protein 4 (msp4) mRNA levels were determined by real-time RT-PCR using human Sp110 (Genbank accession number NM_004509) and msp4  sequence-specific primers (Sp110, forward: 5'-cttcctatgaacggcagagc; reverse: 5'-ggcgactcactcaggatctc; msp4, APMSP4RT5: 5'-tgacaggggaggatcttacg and APMSP4RT3: 5'-tctagctccgccaatagcat) and the QuantiTec SYBR Green RT-PCR kit (Qiagen, Valencia, CA, USA) in a Bio-Rad iQ5 thermal cycler (Hercules, CA, USA) following manufacturer's recommendations. mRNA levels were normalized against human β-actin (forward: 5'-tgatatcgccgcgctcgtcgtc; reverse: 5'-gccgatccacacggagtact)  and displayed in mRNA arbitrary units. Sp110 mRNA levels were compared between infected and uninfected cells by ANOVA test (P = 0.05).
RNA interference in HL-60 cells
Results and discussion
The Sp110 mRNA levels increased in HL-60 cells after 24 hpi with A. phagocytophilum and reached 2× induction at 96 hpi (Fig. 1). The increase in Sp110 mRNA levels coincided with pathogen multiplication and increasing infections (Fig. 1) and may reflect a protective cellular response to limit rickettsial infection or the result of the manipulation by A. phagocytophilum of host gene transcription to promote pathogen multiplication.
The studies of Sp110 function demonstrated that this protein has an important role in immunoprotective mechanisms against pathogens in humans . However, Sp110 is also used by some viruses such as Epstein-Barr virus, to enhance replication in infected cells . As shown here for A. phagocytophilum, Sp110 transcription is induced by some DNA viruses, suggesting that this mechanism may represent an evolutionary adaptation that facilitates pathogen replication .
In summary, we have shown that A. phagocytophilum increases Sp110 mRNA levels in infected human promyelocytic HL-60 cells. These results suggest a new mechanism by which A. phagocytophilum modulates gene expression through NB-associated proteins. Furthermore, silencing of Sp110 expression reduced pathogen infection/multiplication, thus suggesting that A. phagocytophilum can modulate the transcription of Sp110 to facilitate infection of human HL-60 cells. The mechanism by which A. phagocytophilum modulates the transcription of Sp110 to enhance infection of human HL-60 cells will require further study.
This work was supported by the Oklahoma Agricultural Experiment Station (project 1669), the Sitlington Endowed Chair for Food Animal Research to K.M.K. and the Ministry of Science and Education (MEC), Spain (project AGL2005-07401). Dr. Raúl Manzano-Roman was funded by Ministerio de Educación y Ciencia, Spain. V. Naranjo was founded by Consejería de Educación, JCCM, Spain.
- Dumler JS, Barbet AC, Bekker CPJ, Dasch GA, Palmer GH, Ray SC, Rikihisa Y, Rurangirwa FR: Reorganization of the genera in the families Rickettsiaceae and Anaplasmataceae in the order Rickettsiales: unification of some species of Ehrlichia with Anaplasma, Cowdria with Ehrlichia and Ehrlichia with Neorickettsia, descriptions subjective synonyms of Ehrlichia phagocytophila. Int J Sys Evol Microbiol. 2001, 51: 2145-2165.View ArticleGoogle Scholar
- Dumler JS, Choi KS, Garcia-Garcia JC, Barat NS, Scorpio DG, Garyu JW, Grab DJ, Bakken JS: Human granulocytic anaplasmosis and Anaplasma phagocytophilum. Emerg Infect Dis. 2005, 11: 1828-1834.View ArticlePubMedPubMed CentralGoogle Scholar
- Carlyon JA, Fikrig E: Invasion and survival strategies of Anaplasma phagocytophilum. Cell Microbiol. 2003, 5: 743-754. 10.1046/j.1462-5822.2003.00323.x.View ArticlePubMedGoogle Scholar
- de la Fuente J, Massung RF, Wong SJ, Chu FK, Lutz H, Meli M, von Loewenich FD, Grzeszczuk A, Torina A, Caracappa S, Mangold AJ, Naranjo V, Stuen S, Kocan KM: Sequence analysis of the msp4 gene of Anaplasma phagocytophilum strains. J Clin Microbiol. 2005, 43: 1309-1317. 10.1128/JCM.43.3.1309-1317.2005.View ArticlePubMedPubMed CentralGoogle Scholar
- de la Fuente J, Ayoubi P, Blouin EF, Almazán C, Naranjo V, Kocan KM: Gene expression profiling of human promyelocytic cells in response to infection with Anaplasma phagocytophilum. Cell Microbiol. 2005, 7: 549-559. 10.1111/j.1462-5822.2004.00485.x.View ArticlePubMedGoogle Scholar
- Pedra JH, Sukumaran B, Carlyon JA, Berliner N, Fikrig E: Modulation of NB4 promyelocytic leukemic cell machinery by Anaplasma phagocytophilum. Genomics. 2005, 86: 365-377. 10.1016/j.ygeno.2005.05.008.View ArticlePubMedGoogle Scholar
- Bloch DB, Nakajima A, Gulick T, Chiche JD, Orth D, de La Monte SM, Bloch KD: Sp110 localizes to the PML-Sp100 nuclear body and may function as a nuclear hormone receptor transcriptional coactivator. Mol Cell Biol. 2000, 20: 6138-6146. 10.1128/MCB.20.16.6138-6146.2000.View ArticlePubMedPubMed CentralGoogle Scholar
- Regad T, Chelbi-Alix MK: Role and fate of PML nuclear bodies in response to interferon and viral infections. Oncogene. 2001, 20: 7274-7286. 10.1038/sj.onc.1204854.View ArticlePubMedGoogle Scholar
- Roscioli T, Cliffe ST, Bloch DB, Bell CG, Mullan G, Taylor PJ, Sarris M, Wang J, Donald JA, Kirk EP, Ziegler JB, Salzer U, McDonald GB, Wong M, Lindeman R, Buckley MF: Mutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive disease. Nat Genet. 2006, 38: 620-622. 10.1038/ng1780.View ArticlePubMedGoogle Scholar
- Saito T, Ji G, Shinzawa H, Okumoto K, Hattori E, Adachi T, Takeda T, Sugahara K, Ito JI, Watanabe H, Saito K, Togashi H, Ishii K, Matsuura T, Inageda K, Muramatsu M, Kawata S: Genetic variations in humans associated with differences in the course of hepatitis C. Biochem Biophys Res Commun. 2004, 317: 335-341. 10.1016/j.bbrc.2004.03.056.View ArticlePubMedGoogle Scholar
- Pan H, Yan BS, Rojas M, Shebzukhov YV, Zhou H, Kobzik L, Higgins DE, Daly MJ, Bloom BR, Kramnik I: Ipr1 gene mediates innate immunity to tuberculosis. Nature. 2005, 434: 767-772. 10.1038/nature03419.View ArticlePubMedPubMed CentralGoogle Scholar
- Naranjo V, Ayoubi P, Vicente J, Ruiz-Fons F, Gortazar C, Kocan KM, de la Fuente J: Characterization of selected genes upregulated in non-tuberculous European wild boar as possible correlates of resistance to Mycobacterium bovis infection. Vet Microbiol. 2006, 116: 224-231. 10.1016/j.vetmic.2006.03.013.View ArticlePubMedGoogle Scholar
- Babb C, Keet EH, van Helden PD, Hoal EG: SP110 polymorphisms are not associated with pulmonary tuberculosis in a South African population. Hum Genet. 2007, 121: 521-522. 10.1007/s00439-007-0335-1.View ArticlePubMedGoogle Scholar
- Szeszko JS, Healy B, Stevens H, Balabanova Y, Drobniewski F, Todd JA, Nejentsev S: Resequencing and association analysis of the SP110 gene in adult pulmonary tuberculosis. Hum Genet. 2007, 121: 155-160. 10.1007/s00439-006-0293-z.View ArticlePubMedGoogle Scholar
- Thye T, Browne EN, Chinbuah MA, Gyapong J, Osei I, Owusu-Dabo E, Niemann S, Rusch-Gerdes S, Horstmann RD, Meyer CG: No associations of human pulmonary tuberculosis with Sp110 variants. J Med Genet. 2006, 43: e32-10.1136/jmg.2005.037960.View ArticlePubMedPubMed CentralGoogle Scholar
- Thomas V, Fikrig E: Anaplasma phagocytophilum specifically induces tyrosine phosphorylation of ROCK1 during infection. Cell Microbiol. 2007, 7: 1730-1737. 10.1111/j.1462-5822.2007.00908.x.View ArticleGoogle Scholar
- Nicklas JA, Buel E: Development of an Alu-based, real-time PCR method for quantitation of human DNA in forensic samples. J Forensic Sci. 2003, 48: 936-944.PubMedGoogle Scholar
- Nicewonger J, Suck G, Bloch D, Swaminathan S: Epstein-Barr virus (EBV) SM protein induces and recruits cellular Sp110b to stabilize mRNAs and enhance EBV lytic gene expression. J Virol. 2004, 78: 9412-9422. 10.1128/JVI.78.17.9412-9422.2004.View ArticlePubMedPubMed CentralGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/7/110/prepub
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