[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"$fxLN3MUwXCdr5RPjwZYIDpOj8CHyjOmngWTgoKXPtZbg":3,"$ftRsL60Qx_XnPg3KCqkEzWxuqDAZkaCmb7fzGG9Hzd4k":32,"$f3Ft0rKFJHppdzE-vuveecxx1BUcg9iOlMLtyzf_MJDg":153},[4,8,12,16,20,24,28],{"title":5,"slug":6,"path":7},"About Microbeonline.com","about-microbeonline-com","\u002Fabout-microbeonline-com\u002F",{"title":9,"slug":10,"path":11},"About Me","about-me","\u002Fabout-microbeonline-com\u002Fabout-me\u002F",{"title":13,"slug":14,"path":15},"Advertise with Us","advertise-us","\u002Fadvertise-us\u002F",{"title":17,"slug":18,"path":19},"Privacy Policy","privacy-policy","\u002Fprivacy-policy\u002F",{"title":21,"slug":22,"path":23},"Abbreviations","abbreviations","\u002Fabbreviations\u002F",{"title":25,"slug":26,"path":27},"Microbes","microbes","\u002Fmicrobes\u002F",{"title":29,"slug":30,"path":31},"Books","recommended-books","\u002Frecommended-books\u002F",{"type":33,"data":34},"blog",{"slug":35,"title":36,"description":36,"seoTitle":37,"seoDescription":37,"author":38,"createdDate":39,"lastUpdatedDate":40,"draft":41,"category":42,"image":37,"body":43,"faq":44,"tags":45,"related":47},"klebsiella-pneumoniae-properties-virulence-diseases-diagnosis","Klebsiella pneumoniae: Properties, Diseases, Lab Diagnosis",null,"Acharya Tankeshwar","2019-03-26","2026-07-18",false,"bacteriology","*Klebsiella pneumoniae* is a Gram-negative rod-shaped bacteria of the genus *Klebsiella* and the family Enterobacteriaceae. They are members of the normal intestinal flora of humans and animals and may be isolated from a variety of environmental sources.\n\n> K. pneumoniae was first isolated in the late 19th century and was initially known as Friedlander’s bacterium. Classic cases of pneumonia, characterized by production of brick-red or “currant jelly” sputum, were known to be caused by Friedlander’s bacillus (Klebsiella pneumoniae).\n\n*Klebsiella pneumoniae* causes infections in people of all age groups, especially in infants, the elderly, immunocompromised, and **alcoholics**. It is one of the leading causes of hospital-acquired (nosocomial) infections. The range of infections includes pneumonia *(it is a frequent cause of ventilator-associated pneumonia)*, urinary tract infection, [bloodstream infection (BSI),](\u002Fblood-culture-indications-timing-and-volume\u002F) and liver abscesses. Though *Klebsiella pneumoniae* accounts for a small percentage of pneumonia cases, the case fatality rates are high *(up to 90% in untreated cases)*.\n\n*Klebsiella pneumoniae* is a major threat to public health with the emergence of multidrug-resistant strains, rendering infection by these strains very challenging to treat. Strains of *K.pneumoniae* producing [extended-spectrum beta-lactamases (ESBLs)](\u002Fbetalactamase-classification\u002F)or carbapenemases are considered [global priority pathogens.](\u002Flist-antibiotic-resistant-priority-pathogens-according\u002F)\n\n## General Properties of Klebsiella pneumoniae\n\n![Mucoid colonies of Klebsiella pneumoniae - mucoid colonies](https:\u002F\u002Fassets.microbeonline.com\u002Fblogs\u002FKlebsiella-pneumoniae.jpg)Figure: mucoid colonies\n\n1. Gram–negative\n2. Non-spore-forming rods\n3. Facultative anaerobes\n4. Catalase Test: Positive\n5. Oxidase Test: Negative\n6. Lactose fermenter (forms pink-colored colonies on MacConkey Agar).\n7. Presence of polysaccharide capsule (in the culture plate mucoid colonies are seen).\n8. Non-motile (*Klebsiella* species are nonmotile and non-flagellated and thus have no H antigens).\n\n## Virulence Factors of Klebsiella pneumoniae\n\n- Capsule\n- Cell wall receptors\n- Lipopolysaccharide (endotoxin)\n- Fimbriae\n- Siderophores\n\nVirulence factors of *Klebsiella pneumoniae* will be discussed in-depth in another post.\n\n![ - Virulence factors ofK. pneumoniae(Source)](https:\u002F\u002Fassets.microbeonline.com\u002Fblogs\u002FVirulence-Factors.jpg)Figure: Virulence factors of *K. pneumoniae*\n\n## Laboratory diagnosis of K. pneumoniae infection\n\n**Sample**: Sputum *(Red currant-jelly sputum may be seen in a patient infected with K. pneumoniae)*, mid-stream urine, or blood (depending on the suspected illness\u002Fclinical presentation).\n\nColony characteristics of *Klebsiella pneumoniae*\n\n- **Blood Agar**: Mucoid, non-hemolytic colonies\n- **MacConkey Agar:** Mucoid, lactose-fermenting (pink colored) colonies\n\n| Test Name | Results |\n| --- | --- |\n| Catalase test | Positive |\n| Oxidase test | Negative |\n| Indole Production Test | Negative (*K. oxytoca* is indole positive) |\n| Methyl-Red Test | Negative |\n| Voges-Proskauer Test | Positive |\n| Citrate Utilization Test | Positive |\n| Hydrogen Sulfide (H2S) Production | Negative |\n| TSI test | Acid\u002FAcid, Gas (++), No  H₂SH₂S |\n| Urea Hydrolysis Test | Positive |\n| Lysine Decarboxylase Test | Positive |\n| Arginine Dihydrolase Test | Negative |\n| Ornithine decarboxylase test | Negative |\n| Motility at 36 °C | Non-motile |\n| D-Glucose (acid\u002Fgas) | Positive\u002FPositive |\n| D-mannitol fermentation | Positive |\n| Sucrose fermentation | Positive |\n| Lactose fermentation | Positive |\n| D-sorbitol fermentation | Positive |\n| Cellobiose | Positive |\n| Esculin hydrolysis | Positive |\n| Acetate Utilization Test | Positive |\n| ONPG Test | Positive |\n\nVarious biochemical tests using conventional methods or miniature commercial system (API-20E or Enterotube test) is done to identify the suspected colony as *Klebsiella pneumoniae*.  Some of the commonly used tests for the identification of *Klebsiella pneumoniae* are given below.\n\n**Note:** To minimize the cost and effort, some diagnostic\u002Fhospital laboratories perform only certain tests such as [Triple Sugar Iron Agar (TSI)](\u002Ftriple-sugar-iron-agar-tsi-principle-procedure-and-interpretation\u002F), sulfite indole motility (SIM) \u002F urease indole motility (UIM), and citrate utilization test to identify isolates of Enterobacteriaceae family, full panel\u002Fcommercially available miniature test system ([API-20E](\u002Fapi-20e-test-system-introduction-procedure-results-interpretations\u002F) and Enterotube test) is used only when the test results are inconclusive.\n\n**References**\n\n1. [Bailey & Scott’s Diagnostic Microbiology](https:\u002F\u002Famzn.to\u002F2WZxPHL), Forbes, 11th edition\n2. Ashurst JV, Dawson A. Klebsiella Pneumonia. \\[Updated 2023 Jul 20\\]. In: StatPearls \\[Internet\\]. Treasure Island (FL): StatPearls Publishing; 2023 Jan-. Available from: \u003Chttps:\u002F\u002Fwww.ncbi.nlm.nih.gov\u002Fbooks\u002FNBK519004\u002F>\n3. Qu, T. T., Zhou, J. C., Jiang, Y., Shi, K. R., Li, B., Shen, P., Wei, Z. Q., & Yu, Y. S. (2015). Clinical and microbiological characteristics of Klebsiella pneumoniae liver abscess in East China. *BMC infectious diseases*, *15*, 161. \u003Chttps:\u002F\u002Fdoi.org\u002F10.1186\u002Fs12879-015-0899-7>\n4. Madigan Michael T, Bender, Kelly S, Buckley, Daniel H, Sattley, W. Matthew, & Stahl, David A. (2018). [Brock Biology of Microorganisms](https:\u002F\u002Famzn.to\u002F2USOj0v) (15th Edition). Pearson.",[],[46],"enterobacteriaceae",[48,73,80,87,104,134,140,147],{"slug":49,"title":50,"description":51,"seoTitle":37,"seoDescription":37,"author":52,"createdDate":53,"lastUpdatedDate":54,"draft":41,"category":55,"image":37,"faq":56,"tags":72},"mixed-acid-fermentation","Mixed Acid Fermentation: The Pathway That Makes E. coli Methyl Red-Positive","Mixed acid fermentation splits glucose into a mixture of strong acids, lactate, acetate, formate, succinate, plus ethanol, in variable proportions. That flood of acid drops the pH below 4.4, which is exactly what the methyl red test detects. Here is the pathway, the enzymes, why \"mixed\" is the whole point, and how it differs from the 2,3-butanediol route that VP detects.","Ashma Shrestha","2023-08-21","2026-07-15","biochemical-tests",[57,60,63,66,69],{"question":58,"answer":59},"Why is E. coli methyl red-positive?","Because E. coli carries out mixed acid fermentation. When it ferments glucose anaerobically, it produces a mixture of strong acids, lactic, acetic, formic, and succinic, along with ethanol, all at once. These acids accumulate and drive the pH of the medium below 4.4. The methyl red test detects exactly this: methyl red turns red at pH 4.4 or below, so a mixed-acid fermenter like E. coli gives a positive (red) methyl red result. The test is essentially a readout of whether the organism ran mixed acid fermentation.",{"question":61,"answer":62},"What makes mixed acid fermentation different from other fermentations?","It produces several end products simultaneously in variable proportions, rather than one product in a fixed amount. Homolactic fermentation makes only lactate; alcoholic fermentation makes ethanol and CO2. Mixed acid fermentation makes a mixture, lactic, acetic, formic, and succinic acids plus ethanol and gas, and the exact proportions vary with the organism and conditions. This variable mixture is what the name refers to and is why it drives the pH low enough to be detected by the methyl red test.",{"question":64,"answer":65},"What is the difference between mixed acid fermentation and the 2,3-butanediol pathway?","They are the two roads enteric bacteria take from pyruvate. Mixed acid fermentation produces strong acids that lower the pH and is detected by the methyl red test; E. coli, Salmonella, Shigella, and Proteus take this road. The 2,3-butanediol pathway produces mostly neutral products (acetoin and 2,3-butanediol), spares the pH, and is detected by the Voges-Proskauer test; Klebsiella, Enterobacter, and Serratia take this road. The two are largely mutually exclusive, which is why the methyl red and VP tests usually give opposite results.",{"question":67,"answer":68},"Why do some mixed acid fermenters produce gas and others do not?","Gas production depends on a specific enzyme, formate hydrogen-lyase, which splits the formic acid made during mixed acid fermentation into carbon dioxide and hydrogen. A mixed-acid fermenter that has this enzyme produces gas, seen as a bubble in a Durham tube. One that lacks or has limited formate hydrogen-lyase, such as Shigella or Salmonella Typhi, still ferments glucose to acid but produces no gas, making it anaerogenic. So acid production and gas production are separate features.",{"question":70,"answer":71},"Why is mixed acid fermentation important in biotechnology?","Because its end products, ethanol, succinate, lactate, and acetate, are commercially valuable, and the pathway's flexibility makes it tunable. Since E. coli can be directed toward one product or another, strains have been metabolically engineered to over-produce specific end products, for example ethanol as a biofuel or succinate as a chemical feedstock. The same feature that makes the pathway produce a variable mixture makes it a useful target for metabolic engineering, with redox balance being the main constraint.",[46],{"slug":74,"title":75,"description":75,"seoTitle":37,"seoDescription":37,"author":52,"createdDate":76,"lastUpdatedDate":77,"draft":41,"category":42,"image":37,"faq":78,"tags":79},"klebsiella-oxytoca-properties-and-pathogenesis","Klebsiella oxytoca: Properties and Pathogenesis","2022-07-12","2026-07-05",[],[46],{"slug":81,"title":82,"description":82,"seoTitle":37,"seoDescription":37,"author":38,"createdDate":83,"lastUpdatedDate":84,"draft":41,"category":42,"image":37,"faq":85,"tags":86},"yersinia-pestis-properties-disease-diagnosis","Yersinia pestis: Properties, Disease, Lab Diagnosis","2020-04-24","2026-07-19",[],[46],{"slug":88,"title":89,"description":90,"seoTitle":37,"seoDescription":37,"author":38,"createdDate":91,"lastUpdatedDate":92,"draft":41,"category":55,"image":37,"faq":93,"tags":103},"kliglers-iron-agar-kia-principle-procedure-and-results","Kligler’s Iron Agar (KIA): Principle, Procedure, Results","A faint black line at the slant-butt junction is easy to overlook, and it's exactly the reaction that can point toward Salmonella Typhi. Full KIA principle, tube-reading rules, and the KIA\u002FTSI distinction explained.","2019-04-30","2026-07-12",[94,97,100],{"question":95,"answer":96},"Why does KIA give an alkaline slant\u002Facid butt (K\u002FA) result for glucose-only fermenters?","KIA contains glucose (0.1%) and lactose (1.0%) at a 10:1 concentration ratio. A glucose-only fermenter initially produces acid throughout the tube, turning both slant and butt yellow. However, glucose is quickly exhausted. The organism then shifts to aerobic oxidative metabolism on the slant surface, oxidatively deaminating peptone to produce alkaline amine compounds — the slant reverts to red\u002Falkaline. The anaerobic butt retains the acid from initial glucose fermentation. Result: K\u002FA. Organisms that ferment lactose (10x more concentrated) maintain sustained acid production throughout the tube, giving A\u002FA.",{"question":98,"answer":99},"What is the critical difference between Vibrio cholerae results on KIA vs TSI?","Vibrio cholerae ferments glucose and sucrose but NOT lactose. On KIA (which contains only glucose and lactose): the organism ferments glucose only, giving a K\u002FA result — identical to Salmonella or Shigella. On TSI (which contains glucose, lactose, AND sucrose): V. cholerae also ferments sucrose, giving an A\u002FA result. This distinction is diagnostically critical — in a cholera outbreak setting, a K\u002FA result on KIA alone could lead to V. cholerae being worked up as Salmonella. Always use TSI rather than KIA alone when V. cholerae is clinically suspected, and confirm with oxidase test, string test, and serology.",{"question":101,"answer":102},"If a KIA tube shows heavy black precipitate throughout, how should the butt colour be interpreted?","A heavily H₂S-positive KIA tube where black iron sulphide precipitate obscures the butt colour should always be interpreted as acid (A) in the butt — regardless of whether yellow colour is visible. H₂S is only produced in an acidic environment, so the presence of H₂S itself confirms the butt is acid. Never report an H₂S-positive tube as K\u002FK. The blackening in the butt indicates glucose fermentation (acid) plus H₂S production, making the full reading: K\u002FA + H₂S positive — consistent with Salmonella (non-Typhi) or Citrobacter.",[46],{"slug":105,"title":106,"description":107,"seoTitle":108,"seoDescription":109,"author":38,"createdDate":110,"lastUpdatedDate":40,"draft":41,"category":55,"image":37,"faq":111,"tags":133},"api-20e-test-system-introduction-procedure-results-interpretations","API 20E Test: Procedure, Reading the 21 Reactions, and the 7-Digit Profile Code","How to set up, incubate, and read the API 20E strip: which wells need oil, which need reagents, how to run the 21st test (oxidase), and how to build the 7-digit profile number for identification.","API 20E: Inoculation, Reading, Profile Number, and Identification","Prepare and inoculate an API 20E strip, add reagents, read biochemical reactions, calculate the profile number, and interpret organism identification.","2015-05-06",[112,115,118,121,124,127,130],{"question":113,"answer":114},"How many tests are in the API 20E, 20 or 21?","The strip has 20 wells, but a complete identification uses 21 reactions. The oxidase test is performed separately, off the strip, and fills the last position in the profile code.",{"question":116,"answer":117},"Which API 20E wells need a mineral oil overlay?","Five: ADH, LDC, ODC, URE, and H₂S. The oil creates the anaerobic conditions these reactions need. Without it, they read falsely.",{"question":119,"answer":120},"Which wells need reagents added after incubation?","Three: TDA (ferric chloride), IND (Kovács' reagent), and VP (KOH followed by α-naphthol). Add these only after reading every self-developing well.",{"question":122,"answer":123},"Why does the VP well take longer to read?","The pink-red color from acetoin detection can take up to 10 minutes to develop. Do not call VP negative before then. TDA and IND, by contrast, are read almost immediately.",{"question":125,"answer":126},"How is the 7-digit profile number generated?","The 21 reactions are grouped into seven triplets. Within each triplet the wells score 1, 2, and 4 from top to bottom; you add up only the positives, giving a digit from 0 to 7. The seven digits form the profile, which you look up in apiweb or the API catalog.",{"question":128,"answer":129},"What do I do if the profile gives a doubtful or low-confidence identification?","apiweb reports a %ID and a T-value; a low or non-discriminating result means you need supplementary tests (such as oxidase, nitrate reduction, or motility) or a repeat run, rather than accepting the closest match.",{"question":131,"answer":132},"Can API 20E identify organisms other than Enterobacteriaceae?","It is designed for Enterobacteriaceae and other non-fastidious Gram-negative rods. It is not suitable for fastidious organisms or non-fermenters outside its database scope, which need different panels.",[46],{"slug":135,"title":136,"description":136,"seoTitle":37,"seoDescription":37,"author":38,"createdDate":137,"lastUpdatedDate":40,"draft":41,"category":42,"image":37,"faq":138,"tags":139},"shigella-disease-properties-pathogenesis-and-laboratory-diagnosis","Shigella: Disease, Properties, Pathogenesis, Lab Diagnosis","2013-05-18",[],[46],{"slug":141,"title":142,"description":142,"seoTitle":37,"seoDescription":37,"author":38,"createdDate":143,"lastUpdatedDate":77,"draft":41,"category":144,"image":37,"faq":145,"tags":146},"e-coli-only-bacteria-that-wins-record-number-of-nobel-prizes","E. coli: Only bacterium that wins records number of Nobel Prizes","2013-05-04","general-microbiology",[],[46],{"slug":148,"title":149,"description":149,"seoTitle":37,"seoDescription":37,"author":38,"createdDate":150,"lastUpdatedDate":40,"draft":41,"category":42,"image":37,"faq":151,"tags":152},"e-coli-disease-properties-pathogenesis-and-laboratory-diagnosis","Escherichia coli: Properties and Identification","2013-04-27",[],[46],[154,160,166,171,175,179,184,189,193,197],{"slug":155,"name":38,"description":156,"image":157,"body":158,"postCount":159},"acharya-tankeshwar","Editor-in-chief","https:\u002F\u002Fassets.microbeonline.com\u002Fauthors\u002Ftankeshwar-acharya-author-microbeonline.jpg","***Tankeshwar Acharya, MSc (Medical Microbiology)***\n\n*Tankeshwar Acharya is an Assistant Professor in the Department of Microbiology at Patan Academy of Health Sciences (PAHS), Nepal, where he has been teaching and practicing clinical microbiology for over 14 years. He is the founder of Microbe Online, one of the leading free microbiology education resources on the web, covering bacteriology, mycology, parasitology, immunology, and clinical laboratory diagnostics written from direct experience in both the classroom and the diagnostic laboratory.*",433,{"slug":161,"name":52,"description":162,"image":163,"body":164,"postCount":165},"ashma-shrestha","SEO Copywriter and Science Communicator\nKathmandu, Nepal","https:\u002F\u002Fassets.microbeonline.com\u002Fauthors\u002Fashma-shrestha.png","Ashma Shrestha holds a Master of Science in Medical Microbiology from the Institute of Science and Technology (IOST), Tribhuvan University, Nepal, where she developed a strong foundation in virology, molecular biology, and diagnostic microbiology.\n\nShe now works as an SEO Copywriter at Resolution Digital, where she combines her scientific training with research-driven content strategy. She is certified in Google Analytics and Google Business Profile (GBP), and brings a data-informed approach to science communication writing content that is not only accurate but structured to reach and serve the students who need it most.\n\nAt microbeonline, Ashma contributes articles primarily in virology and molecular biology, areas she finds most compelling for their mechanistic depth and their growing clinical relevance. Her writing reflects the same standard the site is built on: factual rigor, clear explanation of the *why* behind microbiology concepts, and content that helps students move from memorization to genuine understanding.\n\nShe is passionate about making complex microbiological concepts accessible without sacrificing accuracy; a skill that sits at the intersection of her scientific training and her professional work in content and SEO.",81,{"slug":167,"name":168,"description":169,"image":37,"body":37,"postCount":170},"sushmita-baniya","Sushmita Baniya","Author \u002F Contributor",32,{"slug":172,"name":173,"description":169,"image":37,"body":37,"postCount":174},"samikshya-acharya","Samikshya Acharya",20,{"slug":176,"name":177,"description":169,"image":37,"body":37,"postCount":178},"alisha-tripathi","Alisha Tripathi",6,{"slug":180,"name":181,"description":182,"image":37,"body":37,"postCount":183},"aastha-shrestha","Aastha Shrestha"," Author \u002F Contributor",9,{"slug":185,"name":186,"description":187,"image":37,"body":37,"postCount":188},"guest-author","Guest Author","Guest Author \u002F Contributor",2,{"slug":190,"name":191,"description":169,"image":37,"body":37,"postCount":192},"srijana-khanal","Srijana Khanal",18,{"slug":194,"name":195,"description":187,"image":37,"body":37,"postCount":196},"dr-poonam-acharya","Dr. Poonam Acharya",1,{"slug":198,"name":199,"description":169,"image":37,"body":200,"postCount":201},"nisha-rijal","Nisha Rijal","**Nisha Rijal** is a microbiologist and quality assurance specialist. She served for nearly 12 years as a microbiologist at the National Public Health Laboratory (NPHL), Nepal's national reference laboratory, and continues to work as a consultant microbiologist in international public health organization. ",51]