Information about Ciprofloxacin
Ciprofloxacin is the generic international name for the synthetic antibiotic manufactured and sold by Bayer Pharmaceutical under the brand names Cipro, Ciproxin and Ciprobay (and other brand names in other markets, e.g. veterinary drugs), belonging to a group called fluoroquinolones.
Ciprofloxacin is bactericidal. Its mode of action depends upon blocking bacterial DNA replication by binding itself to an enzyme called DNA gyrase, thereby causing double-stranded breaks in the bacterial choromosome.
In cell culture it is used to treat infection with mycoplasma.
Use against chlamydia and mycoplasma infections is now contraindicated; ciprofloxacin appears to be ineffective against these organisms, merely stopping their growth (and allowing them to resume growth after the antibiotic is withdrawn) rather than killing them. [1]
It is contraindicated in children, pregnancy, and in patients with epilepsy. Dose adjustment or avoidance may be necessary with liver or renal failure.
Ciprofloxacin can cause photosensitivity reactions and can elevate plasma theophylline levels to toxic values. It can also cause constipation and sensitivity to caffeine. Ciprofloxacin is also known to cause swelling of joints and cartilage, and cause tendon rupture and chronic pain.
Heavy exercise is discouraged, as achilles tendon rupture has been reported in patients taking ciprofloxacin. Achilles tendon rupture due to ciprofloxacin use is typically associated with renal failure.
The toxicity of drugs that are metabolised by the cytochrome P450 system is enhanced by concomitant use of some quinolones. They may also interact with the GABA A receptor and cause neurological symptoms; this is further augmented by certain non-steroidal anti-inflammatory drugs.[5]
Fluoroquinolones are increasingly contraindicated for patients who have been to S.E. Asia due to the growing prevalence of antibiotic resistance to the class of antibiotics in that region.[6]
The incidence of side effects for ciprofloxacin is acceptable and relatively safe. Approximately 9% of patients taking the medication experience side effects ranging from mild to moderate, with the vast majority of those relating to metabolic-nutritional problems and the central nervous system.[8] Compared to other Fluoroquinolones the incidence and severity of side effects from ciprofloxacin is low.[9]
Due to its elimination half-life, ciprofloxacin is administered twice daily. No dose adjustments are generally required for mild to moderate renal impairment.
Encouraged by the magnitude of this success, as well as the influx of cash, Bayer Pharmaceutical embarked on a plan to remake itself from a minor pharmaceutical manufacturer into a major player in the international pharmaceutical business, with a lock on the antibiotic field. Unfortunately, a combination of the tendency for antibiotics to be viewed as a commodity and prescribed on the basis of lowest cost, Bayer's inability to follow up with another 'blockbuster' discovery, and a general downturn in the international pharmaceutical business forced Bayer into a major downsizing in 2000-2001. Faced with the imminent expiry of its patent rights to ciprofloxacin in the early 2000s and the predictable loss of market share to generic ciprofloxacin, Bayer has resorted to the usual strategy of pharmaceutical companies in such a situation; focus on the development and patenting of new variations of the old drug (i.e. pediatric ciprofloxacin, intravenous ciprofloxacin, once-a-day ciprofloxacin, etc.), which will have the side effect of extending the patent on the original drug.
"Cipro" became a household word during the 2001 anthrax attacks.
The panic reactions after 9/11 led to mass deployment and may well be the most signifigant factor in the decreased effectiveness of ciproflaxin by promoting the survival of resistant strains of bacteria.
Generic ciprofloxacin is now available in many markets around the world including the USA. In addition two new once daily formulations have been launched in the USA. Bayer have marketed Cipro XR® which is an extended release formulation. Meanwhile Depomed have developed ProQuin XR® another once daily formulation of ciprofloxacin which uses a gastric retention polymer technology to slow the release of ciprofloxacin into the blood.
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Activity
Ciprofloxacin is a broad-spectrum antibiotic that is active against both Gram-positive and Gram-negative bacteria. It functions by inhibiting DNA gyrase, a type II topoisomerase, which is an enzyme necessary to separate replicated DNA, thereby inhibiting cell division.- Enterobacteriaceae
- Vibrio
- Haemophilus influenzae
- Haemophilus ducreyi
- Neisseria gonorrhoeae
- Neisseria meningitidis
- Moraxella catarrhalis
- Brucella
- Campylobacter
- Mycobacterium intracellulare
- Legionella sp.
- Pseudomonas aeruginosa
- Bacillus anthracis
- Escherichia coli
- Bacteroides
- Burkholderia cepacia
- Enterococcus faecium
- Ureaplasma urealyticum
- Streptococcus pyogenes
- and others
In cell culture it is used to treat infection with mycoplasma.
Use against chlamydia and mycoplasma infections is now contraindicated; ciprofloxacin appears to be ineffective against these organisms, merely stopping their growth (and allowing them to resume growth after the antibiotic is withdrawn) rather than killing them. [1]
Label information
The drug is available for oral, parenteral and topical use. It is used in lower respiratory infections (pneumonias), urinary tract infections, STDs, septicemias, Legionellosis and atypical Mycobacterioses. Dosage in respiratory infections is 500-1500 mg a day in 2 doses.It is contraindicated in children, pregnancy, and in patients with epilepsy. Dose adjustment or avoidance may be necessary with liver or renal failure.
Ciprofloxacin can cause photosensitivity reactions and can elevate plasma theophylline levels to toxic values. It can also cause constipation and sensitivity to caffeine. Ciprofloxacin is also known to cause swelling of joints and cartilage, and cause tendon rupture and chronic pain.
Interactions
Quercetin, a flavonoid occasionally used as a dietary supplement may interact with fluoroquinolones, as quercetin competitively binds to bacterial DNA gyrase. Some foods such as garlic and apples contain high levels of quercetin. Whether this inhibits or enhances the effect of fluoroquinolones is not entirely clear.[2]Contraindications
Metal cations such as aluminium, magnesium, calcium, ferrous sulphate, and zinc are thought to form chelation complexes with fluoroquinolone antibiotics and prevent the drugs from being absorbed. Because of this, avoid taking ciprofloxacin with antacids which contain aluminium, magnesium or calcium. Sucralfate, which has a high aluminium content, also reduces the bioavailability of ciprofloxacin to approximately 4%.[3] Ciprofloxacin may be taken with meals or on an empty stomach. Ciprofloxacin should not be taken with dairy products or calcium-fortified juices alone, but may be taken with a meal that contains these products.[4]Heavy exercise is discouraged, as achilles tendon rupture has been reported in patients taking ciprofloxacin. Achilles tendon rupture due to ciprofloxacin use is typically associated with renal failure.
The toxicity of drugs that are metabolised by the cytochrome P450 system is enhanced by concomitant use of some quinolones. They may also interact with the GABA A receptor and cause neurological symptoms; this is further augmented by certain non-steroidal anti-inflammatory drugs.[5]
Fluoroquinolones are increasingly contraindicated for patients who have been to S.E. Asia due to the growing prevalence of antibiotic resistance to the class of antibiotics in that region.[6]
Side Effects
In 2005 the FDA changed the package insert for Cipro [7] to acknowledge the tendon ruptures and the development of irreversable neurological conditions.The incidence of side effects for ciprofloxacin is acceptable and relatively safe. Approximately 9% of patients taking the medication experience side effects ranging from mild to moderate, with the vast majority of those relating to metabolic-nutritional problems and the central nervous system.[8] Compared to other Fluoroquinolones the incidence and severity of side effects from ciprofloxacin is low.[9]
Dosing
Ciprofloxacin is available in oral tablets (250, 500, 750, and 1000 mg), as well as ready-made infusion bottles (200 and 400 mg). A combination preparation of ciprofloxacin 500 mg and tinidazole 600 mg is marketed under the name Ciplox-TZ® for infections where anaerobes or protozoa together with ciprofloxacin-sensitive aerobes are likely.Due to its elimination half-life, ciprofloxacin is administered twice daily. No dose adjustments are generally required for mild to moderate renal impairment.
Business aspects
The discovery and development of ciprofloxacin is that rare case of an actual groundbreaking new drug development, opening up an entire new class of antibiotics for further research, development, and marketing. Even more remarkable, it seems to be a case where the first drug discovered of this class remains the 'gold standard' in terms of efficacy, with the other drugs developed by other pharmaceutical companies relegated to 'me-too' status and forced to compete on the basis of lower cost.Encouraged by the magnitude of this success, as well as the influx of cash, Bayer Pharmaceutical embarked on a plan to remake itself from a minor pharmaceutical manufacturer into a major player in the international pharmaceutical business, with a lock on the antibiotic field. Unfortunately, a combination of the tendency for antibiotics to be viewed as a commodity and prescribed on the basis of lowest cost, Bayer's inability to follow up with another 'blockbuster' discovery, and a general downturn in the international pharmaceutical business forced Bayer into a major downsizing in 2000-2001. Faced with the imminent expiry of its patent rights to ciprofloxacin in the early 2000s and the predictable loss of market share to generic ciprofloxacin, Bayer has resorted to the usual strategy of pharmaceutical companies in such a situation; focus on the development and patenting of new variations of the old drug (i.e. pediatric ciprofloxacin, intravenous ciprofloxacin, once-a-day ciprofloxacin, etc.), which will have the side effect of extending the patent on the original drug.
"Cipro" became a household word during the 2001 anthrax attacks.
The panic reactions after 9/11 led to mass deployment and may well be the most signifigant factor in the decreased effectiveness of ciproflaxin by promoting the survival of resistant strains of bacteria.
Generic ciprofloxacin is now available in many markets around the world including the USA. In addition two new once daily formulations have been launched in the USA. Bayer have marketed Cipro XR® which is an extended release formulation. Meanwhile Depomed have developed ProQuin XR® another once daily formulation of ciprofloxacin which uses a gastric retention polymer technology to slow the release of ciprofloxacin into the blood.
Footnotes
1. ^ Dreses-Werringloer U, Padubrin I, Jurgens-Saathoff B, Hudson AP, Zeidler H, Kohler L. Persistence of Chlamydia trachomatis Is Induced by Ciprofloxacin and Ofloxacin In Vitro. Antimicrob Agents Chemother 2000 Dec;44(12):3288-97. PMID 11083629
2. ^ Hilliard JJ, Krause HM, Bernstein JI, Fernandez JA, Nguyen V, Ohemeng KA, Barrett JF. 'A comparison of active site binding of 4-quinolones and novel flavone gyrase inhibitors to DNA gyrase.'' Adv Exp Med Biol. 1995;390:59-69. PMID 8718602.
3. ^ Spivey JM, Cummings DM, Pierson NR. Failure of prostatitis treatment secondary to probable ciprofloxacin-sucralfate drug interaction. Pharmacotherapy 1996;16:314-6. PMID 8820479.
4. ^ Drug effects of Ciprofloxacin
5. ^ Brouwers JR. Drug interactions with quinolone antibacterials. Drug Saf 1992;7:268-81. PMID 1524699.
6. ^ Fluoroquinolone Resistance in Neisseria gonorrhoeae -- Colorado and Washington, 1995 [1]
7. ^ Cipro package insert. Page 7 Warning of tendon ruptures and irreversable neurological conditions.
8. ^ Schacht P. (1989). Safety of oral ciprofloxacin. An update based on clinical trial results. American Journal of Medcine: Nov 30;87(5A):98S-102S.
9. ^ Rubinstein, E. (2001). History of Quinolones and Their Side Effects. Chemotherapy. 47:3-8 (DOI: 10.1159/000057838)
2. ^ Hilliard JJ, Krause HM, Bernstein JI, Fernandez JA, Nguyen V, Ohemeng KA, Barrett JF. 'A comparison of active site binding of 4-quinolones and novel flavone gyrase inhibitors to DNA gyrase.'' Adv Exp Med Biol. 1995;390:59-69. PMID 8718602.
3. ^ Spivey JM, Cummings DM, Pierson NR. Failure of prostatitis treatment secondary to probable ciprofloxacin-sucralfate drug interaction. Pharmacotherapy 1996;16:314-6. PMID 8820479.
4. ^ Drug effects of Ciprofloxacin
5. ^ Brouwers JR. Drug interactions with quinolone antibacterials. Drug Saf 1992;7:268-81. PMID 1524699.
6. ^ Fluoroquinolone Resistance in Neisseria gonorrhoeae -- Colorado and Washington, 1995 [1]
7. ^ Cipro package insert. Page 7 Warning of tendon ruptures and irreversable neurological conditions.
8. ^ Schacht P. (1989). Safety of oral ciprofloxacin. An update based on clinical trial results. American Journal of Medcine: Nov 30;87(5A):98S-102S.
9. ^ Rubinstein, E. (2001). History of Quinolones and Their Side Effects. Chemotherapy. 47:3-8 (DOI: 10.1159/000057838)
External links
- Data sheet for Cipro
- Fluoroquinolone Toxicity Research Foundation querying the overall safety of fluoroquinolones
- Fluoroquinolone-Induced Tendinopathy: What do we know? Richard M. Harrell, MD.
- Emergency Medicine Magzine a review of ciprofloxacin in relation to other fluoroquinolones
- How Stuff Works - Cipro
- MedlinePlus Drug Information: Ciprofloxacin
Antibacterials for systemic use: quinolones (J01M) | |
|---|---|
| Fluoroquinolones | Ciprofloxacin • Enoxacin • Fleroxacin • Gatifloxacin • Gemifloxacin • Grepafloxacin • Levofloxacin • Lomefloxacin • Moxifloxacin • Norfloxacin • Ofloxacin • Pefloxacin • Prulifloxacin • Rufloxacin • Sparfloxacin • Temafloxacin • Trovafloxacin • Sitafloxacin |
| Other quinolones | Cinoxacin • Flumequine • Nalidixic acid • Oxolinic acid • Pipemidic acid • Piromidic acid • Rosoxacin |
antibiotic is a chemotherapeutic agent that inhibits or abolishes the growth of micro-organisms, such as bacteria, fungi, or protozoans. The term originally referred to any agent with biological activity against living organisms; however, "antibiotic" now is used to refer to
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Bayer AG
Public (ISIN: DE0005752000 , NYSE: BAYRY.PK , TYO: 4863 )
Founded 1863
Headquarters Leverkusen, North Rhine-Westphalia, Germany
Key people N/A
Industry Pharmaceutical
Revenue €27.
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Public (ISIN: DE0005752000 , NYSE: BAYRY.PK , TYO: 4863 )
Founded 1863
Headquarters Leverkusen, North Rhine-Westphalia, Germany
Key people N/A
Industry Pharmaceutical
Revenue €27.
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quinolones are a family of broad-spectrum antibiotics. The parent of the group is nalidixic acid. The majority of quinolones in clinical use belong to the subset of fluoroquinolones, which have a fluoro group attached the central ring system, typically at the 6-position.
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A bactericide or bacteriocide is a substance that kills bacteria and, preferably, nothing else. Bactericides are either disinfectants, antiseptics or antibiotics.
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Important Functional Groups in a Bactericidal Substance
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In pharmacology, the term mechanism of action refers to the specific biochemical interaction through which a drug substance produces its pharmacological effect. A mechanism of action usually includes mention of the specific molecular targets to which the drug binds, such as an
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DNA replication is the process of copying a double-stranded DNA molecule. This process is important in all known life forms and the general mechanisms of DNA replication are not the same in prokaryotic and eukaryotic organisms.
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Enzymes are proteins that catalyze (i.e. accelerate) chemical reactions.[1] In enzymatic reactions, the molecules at the beginning of the process are called substrates, and the enzyme converts them into different molecules, the products.
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DNA gyrase, often referred to simply as gyrase, is a type II topoisomerase (EC 5.99.1.3 ) that introduces negative supercoils (or relaxes positive supercoils) into DNA by looping the template so as to form a crossing, then cutting one of the double helices and passing the
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The term broad-spectrum antibiotic refers to an antibiotic with activity against a wide range of disease-causing bacteria. This is in contrast to a narrow-spectrum antibiotic which is effective against only specific families of bacteria.
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Gram-positive bacteria are those that retain a crystal violet dye during the Gram stain process.[1] Gram-positive bacteria appear blue or violet under a microscope, while Gram-negative bacteria appear red or pink.
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Gram-negative bacteria are those that do not retain crystal violet dye in the Gram staining protocol.[1] Gram-positive bacteria will retain the dark blue dye after an alcohol wash.
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DNA gyrase, often referred to simply as gyrase, is a type II topoisomerase (EC 5.99.1.3 ) that introduces negative supercoils (or relaxes positive supercoils) into DNA by looping the template so as to form a crossing, then cutting one of the double helices and passing the
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Topoisomerases (type I: EC 5.99.1.2 , type II: EC 5.99.1.3 ) are isomerase enzymes that acts on the topology of DNA. It was first discovered by Harvard Professor James C. Wang.
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Enterobacteriales
Family: Enterobacteriaceae
Rahn, 1937
Genera
See text.
The Enterobacteriaceae are a large family of bacteria, including many of the more familiar pathogens, such as Salmonella
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Family: Enterobacteriaceae
Rahn, 1937
Genera
See text.
The Enterobacteriaceae are a large family of bacteria, including many of the more familiar pathogens, such as Salmonella
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Vibrio
Pacini 1854
Type species
Vibrio cholerae
Species
V. aerogenes
V. aestuarianus
V. agarivorans
V. albensis
V. alginolyticus
V. brasiliensis
V.
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Pacini 1854
Type species
Vibrio cholerae
Species
V. aerogenes
V. aestuarianus
V. agarivorans
V. albensis
V. alginolyticus
V. brasiliensis
V.
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Haemophilus influenzae
Classification & external resources
ICD-10 A 49.2
ICD-9 041.5
Haemophilus influenzae
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Classification & external resources
ICD-10 A 49.2
ICD-9 041.5
Haemophilus influenzae
H. influenzae on a blood agar plate.
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H. ducreyi
Binomial name
Haemophilus ducreyi
(Neveu-Lemaire 1921)
Bergey et al. 1923
Haemophilus ducreyi
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Binomial name
Haemophilus ducreyi
(Neveu-Lemaire 1921)
Bergey et al. 1923
Haemophilus ducreyi
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N. gonorrhoeae
Binomial name
Neisseria gonorrhoeae
Zopf, 1885
Neisseria gonorrhoeae (also known as Gonococci
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Binomial name
Neisseria gonorrhoeae
Zopf, 1885
Neisseria gonorrhoeae (also known as Gonococci
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N. meningitidis
Binomial name
Neisseria meningitidis
Albrecht & Ghon 1901
Neisseria meningitidis, also simply known as meningococcus
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Binomial name
Neisseria meningitidis
Albrecht & Ghon 1901
Neisseria meningitidis, also simply known as meningococcus
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M. catarrhalis
Binomial name
Moraxella catarrhalis
Moraxella catarrhalis is a gram-negative, aerobic, oxidase-positive diplococcus which may both colonise and cause respiratory
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Binomial name
Moraxella catarrhalis
Moraxella catarrhalis is a gram-negative, aerobic, oxidase-positive diplococcus which may both colonise and cause respiratory
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Brucella
Species
B. abortus
B. canis
B. melitensis
B. neotomae
B. ovis
B. suis
Brucella is a genus of Gram-negative bacteria.[1] They are small (0.5 to 0.
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Species
B. abortus
B. canis
B. melitensis
B. neotomae
B. ovis
B. suis
Brucella is a genus of Gram-negative bacteria.[1] They are small (0.5 to 0.
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Campylobacter
Sebald and Véron 1963
Species
C. coli
C. concisus
C. curvus
C. fetus
C. gracilis
C. helveticus
C. hominis
C. hyointestinalis
C.
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Sebald and Véron 1963
Species
C. coli
C. concisus
C. curvus
C. fetus
C. gracilis
C. helveticus
C. hominis
C. hyointestinalis
C.
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P. aeruginosa
Binomial name
Pseudomonas aeruginosa
(Schröter 1872)
Migula 1900
Type strain
ATCC 10145
CCUG 551
CFBP 2466
CIP 100720
DSM 50071
JCM 5962
LMG 1242
NBRC 12689
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Binomial name
Pseudomonas aeruginosa
(Schröter 1872)
Migula 1900
Type strain
ATCC 10145
CCUG 551
CFBP 2466
CIP 100720
DSM 50071
JCM 5962
LMG 1242
NBRC 12689
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B. anthracis
Binomial name
Bacillus anthracis
Cohn 1872
Bacillus anthracis is a Gram-positive, facultatively anaerobic, rod-shaped bacterium of the genus Bacillus.
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Binomial name
Bacillus anthracis
Cohn 1872
Bacillus anthracis is a Gram-positive, facultatively anaerobic, rod-shaped bacterium of the genus Bacillus.
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E. coli
Binomial name
Escherichia coli
(Migula 1895)
Castellani and Chalmers 1919
Escherichia coli (IPA: [ˌɛ.
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Binomial name
Escherichia coli
(Migula 1895)
Castellani and Chalmers 1919
Escherichia coli (IPA: [ˌɛ.
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S. pneumoniae
Binomial name
Streptococcus pneumoniae
(Klein 1884)
Chester 1901
Streptococcus pneumoniae, or pneumococcus
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Binomial name
Streptococcus pneumoniae
(Klein 1884)
Chester 1901
Streptococcus pneumoniae, or pneumococcus
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C. trachomatis
Binomial name
Chlamydia trachomatis
Busacca, 1935
Chlamydia trachomatis
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Binomial name
Chlamydia trachomatis
Busacca, 1935
Chlamydia trachomatis
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