黑胶虫污染 PPT课件.pptx

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1、Got black swimming dots in your cell culture?Identification of Achromobacter as a novel cell culture contaminantabstractCell culture model systems are utilized for their ease of use,relative inexpensiveness,and potentially limitless sample size.Reliable results cannot be obtained,however,when cultur

2、es contain contamination.This report discusses the observation and identification of mobile black specks移动的黑点observed in multiple cell lines.Cultures of the contamination were grown,and DNA was purified from isolated colonies分离菌.The 16S rDNA gene was PCR amplified using primers that will amplify the

3、 gene from many genera,and then sequenced.Sequencing results matched the members of the genus Achromobacter,bacteria common in the environment.Achromobacter species have been shown to be resistant to multiple antibiotics.Attempts to decontaminate the eukaryotic真核cell culture used multiple antibiotic

4、s at different concentrations.The contaminating chromobacter was eventually eliminated,without permanently harming the eukaryotic cells,using a combination of the antibiotics ciprofloxacin and piperacillin.环丙沙星、哌拉西林In the case of non-commercially经济 available lines,all attempts areusually taken to cl

5、ean up the culture by selectively killing thecontamination without harming the cell line.Often the culprits首因ofculture contamination is mycoplasma支原体,intracellular bacteria thatcan be almost undetectable in culture.Approximately 28%of 460human cell lines surveyed contained mycoplasma 1.Numerouscomme

6、rcial kits试剂盒are available to identify mycoplasma contamina-tion 2,3 and antibiotic solutions are commercially available to ridcultures of them.Additional culture contamination includes otherbacteria,mold,and fungiUnknown bacterial contamination can be transient.Contami-nation is common with poor as

7、eptic technique and can be devas-tating in a research setting 3.While many undesired organismsmay steal nutrients from cell lines in culture,they may also prey onthe cells themselves.Predatory bacteria have been shown to feedon other bacteria 5,6,particularly in a limited nutrient environ-ment7.Expe

8、rimental results mayalso be altered due to unwantedactivation of cells.Different cellular functions,including thosetriggered by Toll-like receptors,can be activated by a variety ofbacterial components.Several online science blogs discuss a cell culture contaminatethat looks like black specks in the

9、cell culture(http:/ researcherson these blogs describe black dots that fidget or swim and lookmore like rods than dots.Our laboratory has experienced sporadic cell culture contamination fitting this description.Here we reportthe identification of a bacterial cell culture contaminate,a memberof the A

10、chromobacter genus,matching anecdotal descriptions ofcell culture contaminants of multiple eukaryotic cell lines.Inaddition,we provide information regarding antibiotic resistanceand treatment effectiveness.Antibiotics and doses tested to treat Achromobacter contaminated cells.Antibiotic Dose(m g/ml)

11、Gentamicin庆大5002000Amikacin 502500Tobramycin妥布霉素妥布霉素50600Imipenem 264Erythromycin 25500Piperacillin哌拉西林哌拉西林0.51000Choramphenicol氯霉素氯霉素50500Ciprofloxacin环丙沙星环丙沙星10750Plasmocin 2562.5清除支原体污染Antibiotics were added to the complete media which was replaced every 35 days with fresh media and antibiotics.A

12、chromobacter can survive and multiply in water and moist soil.Sources have been identified as untreated well water,swimmingpools,dialysis fluids,distilled water,deionized water,tap water,disinfectants,water systems,ventilators,humidifiers,IV fluids,andinfant formula未经处理的水，游泳池、透析液、蒸馏水、去离子水、自来水，消毒剂、水系

13、统、风机、加湿器、静脉输液，和婴儿配方奶粉Initial attempts to lyse裂解the culture contamination were done inthe eukaryotic cell culture supernatant.Boiling(510 min at 95.C)and sonicating声波降解标本声波降解标本(1530 s at output power 4)did not result in available DNA for PCR.It is possible that the large amount of protein present in

14、eukaryotic真核culture media,primarily from the FBS,could have protected the bacterial cells.DNA was finally isolated using a commercial kit from Promega from isolated colonies grown on blood agar琼脂.The PCR products,about1400 base pairs in size,were isolated by ethanol乙醇precipitation沉淀and sent for sequ

15、encing.After the sequencing,the resulting sequences were checked for similarity to other known sequences using NCBIs BLAST and the Ribosomal Database Project(RDP).Sequence 1 shared 99%sequence identity with Alcaligenes and Achromobacter 16S rDNA gene sequences,asMembers of the Achromobacter and Alca

16、ligenesgenera have reclassified to and from these two genera,includingAchromobacter(Alcaligenes)xylosoxidans and Achromobacter(Alca-ligenes)denitrificans 22,23.It is unclear whether the similarity toboth members of the Achromobacter and Alcaligenes genera is dueto uncertainty in the nomenclature of

17、previously submittedsequences or due to the actual sequence of the contaminatingbacteria.RDP,a web-based program containing only 16S rDNAsequences,was utilized to confirm the contaminating bacteriasgenus.Results using SeqMatch from the RDP identified thesequences as belonging to the genus Achromobac

18、ter.Phylogenetictrees based on the BLASTand RDP results grouped the bacteriawithpredominantly Achromobacter 16S rDNA sequences(data notshown).Sequences 2,3,and 4 share 99%sequence identity withsequence 1Achromobacter 革兰氏阴性，氧化酶阳性，有鞭毛，在3742 C，pH为6.58.5生长良好In our This contaminant was cultured from FBS

19、and NCS,tap water,distilled water,the water bath(in the water and colony material onthe metal),phospho-buffered saline,and tris-buffered saline.FBSand NCS were suspected as the primary,but not only,sources ofcontamination for several reasons.First,cells thawed from cryo-storage(stored in 95%FBS or N

20、CS and 5%dimethyl sulfoxide),which had been previously uncontaminated,contained the bacteriaonce thawed解冻解冻.Second,multiple sources of FBS and NCS appeared tobe contaminated with the rod-like棒状棒状motile structures,presumed tobe bacteria,when samples were examined under a microscope.Third,this contami

21、nant morphology and motility has beenobserved in cells obtained from other labs using NCS from the samesource.Cultures of Achromobacter were visualized using microscopy.Cultures were mixed with an equal volume of agarose and placedon a slide.Fig.1A shows many bacterial cells while 1B showsIMCE大肠腺瘤,Y

22、AMC小鼠结肠上皮,MC38小鼠结肠癌,小鼠胚胎成纤维3T3-L1individual cells.Cells were approximately 45 m m and were rod-Shaped.One member of the genus,Achromobacter xylosoxidans木糖木糖has been found to be the causative agent病原体病原体in multiple cases of septicemia败血症败血症,mainly in immunocompromised individuals,and sometimes due to

23、 contaminated medical supplies 2530.Achromobacter is becoming a serious threat to the health of individuals with cystic fibrosis囊性纤维化囊性纤维化.Eukaryotic cells were killed at various concentrations of antibi-otics,depending on cell type.For example,a ciprofloxacinconcentration greater than 60 m g/ml kil

24、led both MC38 and YAMCcells.A combination of two antibiotics,piperacillin and cipro-floxacin哌拉西林、环丙沙星哌拉西林、环丙沙星,at a concentration of 10 m g/ml each,was best at selec-tively killing the Achromobacter contaminant without appearing to harm the eukaryotic cells.Achromobacter have been previously been sh

25、own to be susceptible to antibiotics administered together.A.xylosoxidans is resistant to ciprofloxacin,but susceptible to a combination of piperacillin and tazobactamInthis study,isolation of an unknown contaminantwas revealedas member of the genus Achromobacter.The bacteria in this genuscan surviv

26、e in a wide range of environments including tap water,the water bath,FBS,NCS,and many common laboratory solutions.In addition,commercial cells were found to contain this contami-nant.It is important that researchers utilizing cell culture forexperiments become aware of this multi-drug resistant bact

27、erialcontaminant.Selective killing of these bacteria in eukaryotic cellculture was successful only with a combination of two antibiotics,piperacillin and ciprofloxacin,both at a concentration of 10 m g/mleach.This report presents the novel identification of this cellculture contaminant and a possible way to remove the swimmingblack dots from cell culture.