This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Bannasch MJ, Foley JE. Epidemiologic evaluation of multiple respiratory pathogens in cats in animal shelters. J Feline Med Surg. 2005 Apr;7(2):109–119. https://doi.org/10.1016/j.jfms.2004.07.004BannaschMJFoleyJEEpidemiologic evaluation of multiple respiratory pathogens in cats in animal sheltersJ Feline Med Surg2005Apr72109119https://doi.org/10.1016/j.jfms.2004.07.004Search in Google Scholar
Barimani M, Mosallanejad B, Ghorbanpoor M, Esmaeilzadeh S. Molecular detection of Chlamydia felis in cats in Ahvaz, Iran. Arch Razi Inst. 2019 Jun;74(2):119–126. https://doi.org/10.22092/ari.2018.116617.1172BarimaniMMosallanejadBGhorbanpoorMEsmaeilzadehSMolecular detection of Chlamydia felis in cats in Ahvaz, IranArch Razi Inst2019Jun742119126https://doi.org/10.22092/ari.2018.116617.1172Search in Google Scholar
Cai Y, Fukushi H, Koyasu S, Kuroda E, Yamaguchi T, Hirai K. An etiological investigation of domestic cats with conjunctivitis and upper respiratory tract disease in Japan. J Vet Med Sci. 2002 Mar; 64(3):215–219. https://doi.org/10.1292/jvms.64.215CaiYFukushiHKoyasuSKurodaEYamaguchiTHiraiKAn etiological investigation of domestic cats with conjunctivitis and upper respiratory tract disease in JapanJ Vet Med Sci2002Mar643215219https://doi.org/10.1292/jvms.64.215Search in Google Scholar
Carlisle SS, Nahata MC.Chlamydia pneumoniae and coronary heart disease. Ann Pharmacother. 1999 May;33(5):615–622. https://doi.org/10.1345/aph.18169CarlisleSSNahataMCChlamydia pneumoniae and coronary heart diseaseAnn Pharmacother1999May335615622https://doi.org/10.1345/aph.18169Search in Google Scholar
Clarkson MJ, Philips HL. Isolation of faecal chlamydia from sheep in Britain and their characterization by cultural properties. Vet J. 1997 May;153(3):307–310. https://doi.org/10.1016/s1090-0233(97)80064-0ClarksonMJPhilipsHLIsolation of faecal chlamydia from sheep in Britain and their characterization by cultural propertiesVet J1997May1533307310https://doi.org/10.1016/s1090-0233(97)80064-0Search in Google Scholar
Gonsales FF, Brandão PE, Melville PA, Zuniga E, Benites NR.Chlamydia felis: Lack of association between clinical signs and the presence of the cryptic plasmid. Microb Pathog. 2016 Aug;97:14–18. https://doi.org/10.1016/j.micpath.2016.05.009GonsalesFFBrandãoPEMelvillePAZunigaEBenitesNRChlamydia felis: Lack of association between clinical signs and the presence of the cryptic plasmidMicrob Pathog2016Aug971418https://doi.org/10.1016/j.micpath.2016.05.009Search in Google Scholar
Grayston JT.Chlamydia pneumoniae and atherosclerosis. Clin Infect Dis. 2005 Apr;40(8):1131–1132. https://doi.org/10.1086/428739GraystonJTChlamydia pneumoniae and atherosclerosisClin Infect Dis2005Apr40811311132https://doi.org/10.1086/428739Search in Google Scholar
Helps C, Reeves N, Tasker S, Harbour D. Use of real-time quantitative PCR to detect Chlamydophila felis infection. J Clin Microbiol. 2001 Jul;39(7):2675–2676. https://doi.org/10.1128/JCM.39.7.2675-2676.2001HelpsCReevesNTaskerSHarbourDUse of real-time quantitative PCR to detect Chlamydophila felis infectionJ Clin Microbiol2001Jul39726752676https://doi.org/10.1128/JCM.39.7.2675-2676.2001Search in Google Scholar
Holst BS, Englund L, Palacios S, Renström L, Berndtsson LT. Prevalence of antibodies against feline coronavirus and Chlamydophila felis in Swedish cats. J Feline Med Surg. 2006 Jun;8(3):207–211. https://doi.org/10.1016/j.jfms.2005.12.004HolstBSEnglundLPalaciosSRenströmLBerndtssonLTPrevalence of antibodies against feline coronavirus and Chlamydophila felis in Swedish catsJ Feline Med Surg2006Jun83207211https://doi.org/10.1016/j.jfms.2005.12.004Search in Google Scholar
Horn M.Chlamydiae as symbionts in eukaryotes. Annu Rev Microbiol. 2008;62:113–131. https://doi.org/10.1146/annurev.micro.62.081307.162818HornMChlamydiae as symbionts in eukaryotesAnnu Rev Microbiol200862113131https://doi.org/10.1146/annurev.micro.62.081307.162818Search in Google Scholar
James A, Macdonald J. Recombinase polymerase amplification: Emergence as a critical molecular technology for rapid, low-resource diagnostics. Expert Rev Mol Diagn. 2015;15(11):1475–1489. https://doi.org/10.1586/14737159.2015.1090877JamesAMacdonaldJRecombinase polymerase amplification: Emergence as a critical molecular technology for rapid, low-resource diagnosticsExpert Rev Mol Diagn2015151114751489https://doi.org/10.1586/14737159.2015.1090877Search in Google Scholar
Larsen MM, Moern B, Fuller A, Andersen PL, Ostergaard LJ.Chlamydia pneumoniae and cardiovascular disease. Med J Aust. 2002 Nov;177(10):558–562. https://doi.org/10.5694/j.1326-5377.2002.tb04953.xLarsenMMMoernBFullerAAndersenPLOstergaardLJChlamydia pneumoniae and cardiovascular diseaseMed J Aust2002Nov17710558562https://doi.org/10.5694/j.1326-5377.2002.tb04953.xSearch in Google Scholar
Low HC, Powell CC, Veir JK, Hawley JR, Lappin MR. Prevalence of feline herpesvirus 1, Chlamydophila felis, and Mycoplasma spp DNA in conjunctival cells collected from cats with and without conjunctivitis. Am J Vet Res. 2007 Jun;68(6):643–648. https://doi.org/10.2460/ajvr.68.6.643LowHCPowellCCVeirJKHawleyJRLappinMRPrevalence of feline herpesvirus 1, Chlamydophila felis, and Mycoplasma spp DNA in conjunctival cells collected from cats with and without conjunctivitisAm J Vet Res2007Jun686643648https://doi.org/10.2460/ajvr.68.6.643Search in Google Scholar
McDonald M, Willett BJ, Jarrett O, Addie DD. A comparison of DNA amplification, isolation and serology for the detection of Chlamydia psittaci infection in cats. Vet Rec. 1998 Jul;143(4):97–101. https://doi.org/10.1136/vr.143.4.97McDonaldMWillettBJJarrettOAddieDDA comparison of DNA amplification, isolation and serology for the detection of Chlamydia psittaci infection in catsVet Rec1998Jul143497101https://doi.org/10.1136/vr.143.4.97Search in Google Scholar
Ohya K, Okuda H, Maeda S, Yamaguchi T, Fukushi H. Using CF0218-ELISA to distinguish Chlamydophila felis-infected cats from vaccinated and uninfected domestic cats. Vet Microbiol. 2010 Dec; 146(3–4):366–370. https://doi.org/10.1016/j.vetmic.2010.05.026OhyaKOkudaHMaedaSYamaguchiTFukushiHUsing CF0218-ELISA to distinguish Chlamydophila felis-infected cats from vaccinated and uninfected domestic catsVet Microbiol2010Dec1463–4366370https://doi.org/10.1016/j.vetmic.2010.05.026Search in Google Scholar
Pannekoek Y, Qi-Long Q, Zhang YZ, van der Ende A. Genus delineation of Chlamydiales by analysis of the percentage of conserved proteins justifies the reunifying of the genera Chlamydia and Chlamydophila into one single genus Chlamydia. Pathog Dis. 2016 Aug;74(6):ftw071. https://doi.org/10.1093/femspd/ftw071PannekoekYQi-LongQZhangYZvan der EndeAGenus delineation of Chlamydiales by analysis of the percentage of conserved proteins justifies the reunifying of the genera Chlamydia and Chlamydophila into one single genus ChlamydiaPathog Dis2016Aug746ftw071https://doi.org/10.1093/femspd/ftw071Search in Google Scholar
Rampazzo A, Appino S, Pregel P, Tarducci A, Zini E, Biolatti B. Prevalence of Chlamydophila felis and feline herpesvirus 1 in cats with conjunctivitis in northern Italy. J Vet Intern Med. 2003 Nov–Dec; 17(6):799–807. https://doi.org/10.1111/j.1939-1676.2003.tb02517.xRampazzoAAppinoSPregelPTarducciAZiniEBiolattiBPrevalence of Chlamydophila felis and feline herpesvirus 1 in cats with conjunctivitis in northern ItalyJ Vet Intern Med2003Nov–Dec176799807https://doi.org/10.1111/j.1939-1676.2003.tb02517.xSearch in Google Scholar
Rodolakis A, Yousef Mohamad K. Zoonotic potential of Chlamydophila. Vet Microbiol. 2010 Jan;140(3–4):382–391. https://doi.org/10.1016/j.vetmic.2009.03.014RodolakisAYousef MohamadKZoonotic potential of ChlamydophilaVet Microbiol2010Jan1403–4382391https://doi.org/10.1016/j.vetmic.2009.03.014Search in Google Scholar
Sachse K, Bavoil PM, Kaltenboeck B, Stephens RS, Kuo CC, Rosselló-Móra R, Horn M. Emendation of the family Chlamydiaceae: proposal of a single genus, Chlamydia, to include all currently recognized species. Syst Appl Microbiol. 2015 Mar;38(2):99–103. https://doi.org/10.1016/j.syapm.2014.12.004SachseKBavoilPMKaltenboeckBStephensRSKuoCCRosselló-MóraRHornMEmendation of the family Chlamydiaceae: proposal of a single genus, Chlamydia, to include all currently recognized speciesSyst Appl Microbiol2015Mar38299103https://doi.org/10.1016/j.syapm.2014.12.004Search in Google Scholar
von Bomhard W, Polkinghorne A, Lu ZH, Vaughan L, Vögtlin A, Zimmermann DR, Spiess B, Pospischil A. Detection of novel chlamydiae in cats with ocular disease. Am J Vet Res. 2003 Nov; 64(11):1421–1428. https://doi.org/10.2460/ajvr.2003.64.1421von BomhardWPolkinghorneALuZHVaughanLVögtlinAZimmermannDRSpiessBPospischilADetection of novel chlamydiae in cats with ocular diseaseAm J Vet Res2003Nov641114211428https://doi.org/10.2460/ajvr.2003.64.1421Search in Google Scholar
Wons J, Meiller R, Bergua A, Bogdan C, Geißdörfer W. Follicular conjunctivitis due to Chlamydia felis – Case report, review of the literature and improved molecular diagnostics. Front Med. 2017 Jul;4:105. https://doi.org/10.3389/fmed.2017.00105WonsJMeillerRBerguaABogdanCGeißdörferWFollicular conjunctivitis due to Chlamydia felis – Case report, review of the literature and improved molecular diagnosticsFront Med2017Jul4105https://doi.org/10.3389/fmed.2017.00105Search in Google Scholar
Wu K, Zhang Y, Zeng S, Liu X, Li Y, Li X, Chen W, Li Z, Qin Y, Chen J, et al. Development and application of RAA nucleic acid test strip assay and double RAA gel electrophoresis detection methods for ASFV and CSFV. Front Mol Biosci. 2022 Jan;8:811824. https://doi.org/10.3389/fmolb.2021.811824WuKZhangYZengSLiuXLiYLiXChenWLiZQinYChenJDevelopment and application of RAA nucleic acid test strip assay and double RAA gel electrophoresis detection methods for ASFV and CSFVFront Mol Biosci2022Jan8811824https://doi.org/10.3389/fmolb.2021.811824Search in Google Scholar
Xue G, Li S, Zhang W, Du B, Cui J, Yan C, Huang L, Chen L, Zhao L, Sun Y, et al. Reverse-transcription recombinase-aided amplification assay for rapid detection of the 2019 novel coronavirus (SARS-CoV-2). Anal Chem. 2020 Jul;92(14):9699–9705. https://doi.org/10.1021/acs.analchem.0c01032XueGLiSZhangWDuBCuiJYanCHuangLChenLZhaoLSunYReverse-transcription recombinase-aided amplification assay for rapid detection of the 2019 novel coronavirus (SARS-CoV-2)Anal Chem2020Jul921496999705https://doi.org/10.1021/acs.analchem.0c01032Search in Google Scholar
Yao XH, Hu DH, Fu SH, Li F, He Y, Yin JY, Yin QK, Xu ST, Liang GD, Li XD, Nie K, Wang HY. A Reverse-Transcription Recombinase-Aided Amplification Assay for the rapid detection of the Wuxiang virus. Biomed Environ Sci. 2022;35(8):746–749. https://doi.org/10.3967/bes2022.096YaoXHHuDHFuSHLiFHeYYinJYYinQKXuSTLiangGDLiXDNieKWangHYA Reverse-Transcription Recombinase-Aided Amplification Assay for the rapid detection of the Wuxiang virusBiomed Environ Sci2022358746749https://doi.org/10.3967/bes2022.096Search in Google Scholar