This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Adeolu M, Alnajar S, Naushad S, S Gupta R. Genome-based phylogeny and taxonomy of the ‘Enterobacteriales’: proposal for Enterobacterales ord. nov. divided into the families Enterobacteriaceae, Erwiniaceae fam. nov., Pectobacteriaceae fam. nov., Yersiniaceae fam. nov., Hafniaceae fam. nov., Morganellaceae fam. nov., and Budviciaceae fam. nov. Int J Syst Evol Microbiol. 2016;66(12):5575–5599. https://doi.org/10.1099/ijsem.0.001485AdeoluMAlnajarSNaushadSS GuptaR. Genome-based phylogeny and taxonomy of the ‘Enterobacteriales’: proposal for Enterobacterales ord. nov. divided into the families Enterobacteriaceae, Erwiniaceae fam. nov., Pectobacteriaceae fam. nov., Yersiniaceae fam. nov., Hafniaceae fam. nov., Morganellaceae fam. nov., and Budviciaceae fam. nov. 2016;66(12):5575–5599. https://doi.org/10.1099/ijsem.0.00148510.1099/ijsem.0.00148527620848Search in Google Scholar
Aspiotis A, Cullmann W, Dick W, Stieglitz M. Inducible beta-lactamases are principally responsible for the naturally occurring resistance towards beta-lactam antibiotics in Proteus vulgaris. Chemotherapy. 1986;32(3):236–246. https://doi.org/10.1159/000238420AspiotisACullmannWDickWStieglitzM. Inducible beta-lactamases are principally responsible for the naturally occurring resistance towards beta-lactam antibiotics in Proteus vulgaris. 1986;32(3):236–246. https://doi.org/10.1159/00023842010.1159/0002384203519112Search in Google Scholar
Behrendt U, Augustin J, Sproer C, Gelbrecht J, Schumann P, Ulrich A. Taxonomic characterisation of Proteus terrae sp. nov., a N2O-producing, nitrate-ammonifying soil bacterium. Antonie van Leeuwenhoek. 2015;108(6):1457–1468. https://doi.org/10.1007/s10482-015-0601-5BehrendtUAugustinJSproerCGelbrechtJSchumannPUlrichA. Taxonomic characterisation of Proteus terrae sp. nov., a N2O-producing, nitrate-ammonifying soil bacterium. 2015;108(6):1457–1468. https://doi.org/10.1007/s10482-015-0601-510.1007/s10482-015-0601-526437638Search in Google Scholar
Cremonesi P, Pisani LF, Lecchi C, Ceciliani F, Martino P, Bonastre AS, Karus A, Balzaretti C, Castiglioni B. Development of 23 individual TaqMan® real-time PCR assays for identifying common foodborne pathogens using a single set of amplification conditions. Food Microbiol. 2014 Oct;43:35–40. https://doi.org/10.1016/j.fm.2014.04.007CremonesiPPisaniLFLecchiCCecilianiFMartinoPBonastreASKarusABalzarettiCCastiglioniB. Development of 23 individual TaqMan® real-time PCR assays for identifying common foodborne pathogens using a single set of amplification conditions. 2014Oct;43:35–40. https://doi.org/10.1016/j.fm.2014.04.00710.1016/j.fm.2014.04.00724929880Search in Google Scholar
Drzewiecka D. Significance and roles of Proteus spp. bacteria in natural environments. Microb Ecol. 2016 Nov;72(4):741–758. https://doi.org/10.1007/s00248-015-0720-6DrzewieckaD. Significance and roles of Proteus spp. bacteria in natural environments. 2016Nov;72(4):741–758. https://doi.org/10.1007/s00248-015-0720-610.1007/s00248-015-0720-6508032126748500Search in Google Scholar
Garrity GM, Bell JA, Lilburn TG. Bergey’s Manual® of Systematic Bacteriology, Second edition. New York (USA): Springer-Verlag New York; 2004.GarrityGMBellJALilburnTG. , Second edition. New York (USA): Springer-Verlag New York; 2004.Search in Google Scholar
Gu W, Wang W, Tong P, Liu C, Jia J, Lu C, Jia J, Lu C, Han Y, Sun X, Kuang D, Li N, Dai J. Comparative genomic analysis of Proteus spp. isolated from tree shrews indicated unexpectedly high genetic diversity. PLoS One. 2020;15(2):e0229125. https://doi.org/10.1371/journal.pone.0229125GuWWangWTongPLiuCJiaJLuCJiaJLuCHanYSunXKuangDLiNDaiJ. Comparative genomic analysis of Proteus spp. isolated from tree shrews indicated unexpectedly high genetic diversity. 2020;15(2):e0229125. https://doi.org/10.1371/journal.pone.022912510.1371/journal.pone.0229125703487432084183Search in Google Scholar
Hamilton AL, Kamm MA, Ng SC, Morrison M. Proteus spp. as putative gastrointestinal pathogens. Clin Microbiol Rev. 2018 Jun 13;31(3):e00085-17. https://doi.org/10.1128/CMR.00085-17HamiltonALKammMANgSCMorrisonM. Proteus spp. as putative gastrointestinal pathogens. 2018Jun13;31(3):e00085-17. https://doi.org/10.1128/CMR.00085-1710.1128/CMR.00085-17605684229899011Search in Google Scholar
Ishiguro K, Sugimoto K. Purification and characterization of the Proteus vulgaris BlaA protein, the activator of the beta-lactamase gene. J Biochem. 1996 Jul 01;120(1):98–103. https://doi.org/10.1093/oxfordjournals.jbchem.a021399IshiguroKSugimotoK. Purification and characterization of the Proteus vulgaris BlaA protein, the activator of the beta-lactamase gene. 1996Jul01;120(1):98–103. https://doi.org/10.1093/oxfordjournals.jbchem.a02139910.1093/oxfordjournals.jbchem.a0213998864850Search in Google Scholar
Johnson JR. Foodborne illness acquired in the United States. Emerg Infect Dis. 2011 Jul;17(7):1338–1339, author reply 1339–1340. https://doi.org/10.3201/eid1707.110256JohnsonJR. Foodborne illness acquired in the United States. 2011Jul;17(7):1338–1339, author reply 1339–1340. https://doi.org/10.3201/eid1707.11025610.3201/eid1707.11025621762616Search in Google Scholar
Kralik P, Ricchi M. A basic guide to real time PCR in microbial diagnostics: definitions, parameters, and everything. Front Microbiol. 2017;8:108. https://doi.org/10.3389/fmicb.2017.00108KralikPRicchiM. A basic guide to real time PCR in microbial diagnostics: definitions, parameters, and everything. 2017;8:108. https://doi.org/10.3389/fmicb.2017.0010810.3389/fmicb.2017.00108528834428210243Search in Google Scholar
Liu Y, Cao Y, Wang T, Dong Q, Li J, Niu C. Detection of 12 common food-borne bacterial pathogens by TaqMan Real-Time PCR using a single set of reaction conditions. Front Microbiol. 2019 Feb 13;10:222. https://doi.org/10.3389/fmicb.2019.00222LiuYCaoYWangTDongQLiJNiuC. Detection of 12 common food-borne bacterial pathogens by TaqMan Real-Time PCR using a single set of reaction conditions. 2019Feb13;10:222. https://doi.org/10.3389/fmicb.2019.0022210.3389/fmicb.2019.00222638107230814987Search in Google Scholar
Mangal M, Bansal S, Sharma SK, Gupta RK. Molecular detection of foodborne pathogens: a rapid and accurate answer to food safety. Crit Rev Food Sci Nutr. 2016 Jul 03;56(9):1568–1584. https://doi.org/10.1080/10408398.2013.782483MangalMBansalSSharmaSKGuptaRK. Molecular detection of foodborne pathogens: a rapid and accurate answer to food safety. 2016Jul03;56(9):1568–1584. https://doi.org/10.1080/10408398.2013.78248310.1080/10408398.2013.78248325830555Search in Google Scholar
Matsubara N, Yotsuji A, Kumano K, Inoue M, Mitsuhashi S. Purification and some properties of a cephalosporinase from Proteus vulgaris. Antimicrob Agents Chemother. 1981 Jan 01;19(1): 185–187. https://doi.org/10.1128/AAC.19.1.185MatsubaraNYotsujiAKumanoKInoueMMitsuhashiS. Purification and some properties of a cephalosporinase from Proteus vulgaris. 1981Jan01;19(1): 185–187. https://doi.org/10.1128/AAC.19.1.18510.1128/AAC.19.1.1851813797018383Search in Google Scholar
Mobley HL, Chippendale GR, Swihart KG, Welch RA. Cytotoxicity of the HpmA hemolysin and urease of Proteus mirabilis and Proteus vulgaris against cultured human renal proximal tubular epithelial cells. Infect Immun. 1991;59(6):2036–2042. https://doi.org/10.1128/IAI.59.6.2036-2042.1991MobleyHLChippendaleGRSwihartKGWelchRA. Cytotoxicity of the HpmA hemolysin and urease of Proteus mirabilis and Proteus vulgaris against cultured human renal proximal tubular epithelial cells. 1991;59(6):2036–2042. https://doi.org/10.1128/IAI.59.6.2036-2042.199110.1128/iai.59.6.2036-2042.19912579622037363Search in Google Scholar
Mobley HL, Jones BD, Penner JL. Urease activity of Proteus penneri. J Clin Microbiol. 1987;25(12):2302–2305. https://doi.org/10.1128/JCM.25.12.2302-2305.1987MobleyHLJonesBDPennerJL. Urease activity of Proteus penneri. 1987;25(12):2302–2305. https://doi.org/10.1128/JCM.25.12.2302-2305.198710.1128/jcm.25.12.2302-2305.19872694753429622Search in Google Scholar
O’Hara CM, Brenner FW, Miller JM. Classification, identification, and clinical significance of Proteus, Providencia, and Morganella. Clin Microbiol Rev. 2000 Oct 01;13(4):534–546. https://doi.org/10.1128/CMR.13.4.534O’HaraCMBrennerFWMillerJM. Classification, identification, and clinical significance of Proteus, Providencia, and Morganella. 2000Oct01;13(4):534–546. https://doi.org/10.1128/CMR.13.4.53410.1128/CMR.13.4.5348894711023955Search in Google Scholar
Padaruth SK, Biranjia-Hurdoyal SD. Hygiene practices and faecal contamination of the hands of children attending primary school in Mauritius. Int Health. 2014. https://doi.org/10.1093/inthealth/ihu080PadaruthSKBiranjia-HurdoyalSD. Hygiene practices and faecal contamination of the hands of children attending primary school in Mauritius. 2014. https://doi.org/10.1093/inthealth/ihu08010.1093/inthealth/ihu08025424722Search in Google Scholar
Park SH, Hanning I, Jarquin R, Moore P, Donoghue DJ, Donoghue AM, Ricke SC. Multiplex PCR assay for the detection and quantification of Campylobacter spp., Escherichia coli O157:H7, and Salmonella serotypes in water samples. FEMS Microbiol Lett. 2011 Mar;316(1):7–15. https://doi.org/10.1111/j.1574-6968.2010.02188.xParkSHHanningIJarquinRMoorePDonoghueDJDonoghueAMRickeSC. Multiplex PCR assay for the detection and quantification of Campylobacter spp., Escherichia coli O157:H7, and Salmonella serotypes in water samples. 2011Mar;316(1):7–15. https://doi.org/10.1111/j.1574-6968.2010.02188.x10.1111/j.1574-6968.2010.02188.x21204924Search in Google Scholar
Qadripur SA, Schauder S, Schwartz P. [Black nails caused by Proteus mirabilis] (in German). Hautarzt. 2001 Jul 1;52(7):658–661. https://doi.org/10.1007/s001050170110QadripurSASchauderSSchwartzP. [Black nails caused by Proteus mirabilis] (in German). 2001Jul1;52(7):658–661. https://doi.org/10.1007/s00105017011010.1007/s00105017011011475651Search in Google Scholar
Smith SI, Opere B, Goodluck HT, Akindolire OT, Folaranmi A, Odekeye OM, Omonigbehin EA. Antibiotic susceptibility pattern of Staphylococcus species isolated from telephone receivers. Singapore Med J. 2009 Feb;50(2):208–211.SmithSIOpereBGoodluckHTAkindolireOTFolaranmiAOdekeyeOMOmonigbehinEA. Antibiotic susceptibility pattern of Staphylococcus species isolated from telephone receivers. 2009Feb;50(2):208–211.Search in Google Scholar
Wang Y, Zhang S, Yu J, Zhang H, Yuan Z, Sun Y, Zhang L, Zhu Y, Song H. An outbreak of Proteus mirabilis food poisoning associated with eating stewed pork balls in brown sauce, Beijing. Food Control. 2010 Mar;21(3):302–305. https://doi.org/10.1016/j.foodcont.2009.06.009WangYZhangSYuJZhangHYuanZSunYZhangLZhuYSongH. An outbreak of Proteus mirabilis food poisoning associated with eating stewed pork balls in brown sauce, Beijing. 2010Mar;21(3):302–305. https://doi.org/10.1016/j.foodcont.2009.06.00910.1016/j.foodcont.2009.06.009Search in Google Scholar
Wang Z, Zuo J, Gong J, Hu J, Jiang W, Mi R, Huang Y, Chen Z, Phouthapane V, Qi C, Wang C, Han X. Development of a multiplex PCR assay for the simultaneous and rapid detection of six pathogenic bacteria in poultry. AMB Express. 2019;9:185. https://doi.org/10.1186/s13568-019-0908-0WangZZuoJGongJHuJJiangWMiRHuangYChenZPhouthapaneVQiCWangCHanX. Development of a multiplex PCR assay for the simultaneous and rapid detection of six pathogenic bacteria in poultry. 2019;9:185. https://doi.org/10.1186/s13568-019-0908-010.1186/s13568-019-0908-0685625131728678Search in Google Scholar
Wu Y, Liu X, Chen Q, Liu H, Dai Y, Zhou Y, Wen J, Tang Z, Chen Y. Surveillance for foodborne disease outbreaks in China, 2003 to 2008. Food Control. 2018;84:382–388. https://doi.org/10.1016/j.foodcont.2017.08.010WuYLiuXChenQLiuHDaiYZhouYWenJTangZChenY. Surveillance for foodborne disease outbreaks in China, 2003 to 2008. 2018;84:382–388. https://doi.org/10.1016/j.foodcont.2017.08.01010.1016/j.foodcont.2017.08.010712594832288325Search in Google Scholar
Yatsunenko T, Rey FE, Manary MJ, Trehan I, Dominguez-Bello MG, Contreras M, Magris M, Hidalgo G, Baldassano RN, Anokhin AP, et al. Human gut microbiome viewed across age and geography. Nature. 2012 Jun;486(7402):222–227. https://doi.org/10.1038/nature11053YatsunenkoTReyFEManaryMJTrehanIDominguez-BelloMGContrerasMMagrisMHidalgoGBaldassanoRNAnokhinAP. Human gut microbiome viewed across age and geography. 2012Jun;486(7402):222–227. https://doi.org/10.1038/nature1105310.1038/nature11053337638822699611Search in Google Scholar