出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2014/04/23 23:24:01」(JST)
| Haemophilus influenzae | |
|---|---|
| H. influenzae on a blood agar plate. | |
| Scientific classification | |
| Domain: | Bacteria |
| Kingdom: | Eubacteria |
| Phylum: | Proteobacteria |
| Class: | Gammaproteobacteria |
| Order: | Pasteurellales |
| Family: | Pasteurellaceae |
| Genus: | Haemophilus |
| Species: | H. influenzae |
| Binomial name | |
| Haemophilus influenzae (Lehmann & Neumann 1896) |
|
Haemophilus influenzae (formerly called Pfeiffer's bacillus or Bacillus influenzae) is a Gram-negative, coccobacillary, facultatively anaerobic bacterium belonging to the Pasteurellaceae family. H. influenzae was first described in 1892 by Richard Pfeiffer during an influenza pandemic.[1] The bacterium was mistakenly considered to be the cause of influenza until 1933 when the viral etiology of influenza became apparent, and is still colloquially known as 'bacterial influenza'. H. influenzae is responsible for a wide range of localized and invasive infections. This species was the first free-living organism to have its entire genome sequenced. The sequencing project was completed and published in 1995.
In 1930, two major categories of H. influenzae were defined: the unencapsulated strains and the encapsulated strains. Encapsulated strains were classified on the basis of their distinct capsular antigens. There are six generally recognized types of encapsulated H. influenzae: a, b, c, d, e, and f.[2] Genetic diversity among unencapsulated strains is greater than within the encapsulated group. Unencapsulated strains are termed nontypable (NTHi) because they lack capsular serotypes; however, they can be classified by multilocus sequence typing. The pathogenesis of H. influenzae infections is not completely understood, although the presence of the capsule in encapsulated type b (Hib), a serotype causing conditions such as epiglottitis, is known to be a major factor in virulence. Their capsule allows them to resist phagocytosis and complement-mediated lysis in the nonimmune host. The unencapsulated strains are almost always less invasive; they can, however, produce an inflammatory response in humans, which can lead to many symptoms. Vaccination with Hib conjugate vaccine is effective in preventing Hib infection, but does not prevent infection with NTHi strains.[3]
| Haemophilus influenzae infection | |
|---|---|
| Classification and external resources | |
| ICD-10 | A49.2 |
| ICD-9 | 041.5 |
| DiseasesDB | 5570 |
| MedlinePlus | 000612 (Meningitis) |
| eMedicine | topic list |
Most strains of H. influenzae are opportunistic pathogens; that is, they usually live in their host without causing disease, but cause problems only when other factors (such as a viral infection, reduced immune function or chronically inflamed tissues, e.g. from allergies) create an opportunity. They infect the host by sticking to the host cell using Trimeric Autotransporter Adhesins (TAA).
Naturally acquired disease caused by H. influenzae seems to occur in humans only. In infants and young children, H. influenzae type b (Hib) causes bacteremia, pneumonia, epiglottitis and acute bacterial meningitis. On occasion, it causes cellulitis, osteomyelitis, and infectious arthritis.
Due to routine use of the Hib conjugate vaccine in the U.S. since 1990, the incidence of invasive Hib disease has decreased to 1.3/100,000 in children. However, Hib remains a major cause of lower respiratory tract infections in infants and children in developing countries where the vaccine is not widely used. Unencapsulated H. influenzae strains are unaffected by the Hib vaccine and cause ear infections (otitis media), eye infections (conjunctivitis), and sinusitis in children, and are associated with pneumonia.
Clinical features may include initial symptoms of an upper respiratory tract infection (URTI) mimicking a viral infection, usually associated with fevers, often low grade. The URTI then may progresses to a LRTI in a few days with features often resembling a wheezy bronchitis. Sputum may be difficult to expectorate and is often grey to creamy in colour. The cough may persist for weeks without appropriate treatment. Be suspicious of patients with symptoms of a chest infection with wheezing who do not respond to penicillins or 1st generation cephalosporins.
Clinical diagnosis of H. influenzae is typically performed by bacterial culture or latex particle agglutinations. Diagnosis is considered confirmed when the organism is isolated from a sterile body site. In this respect, H. influenzae cultured from the nasopharyngeal cavity or sputum would not indicate H. influenzae disease, because these sites are colonized in disease-free individuals.[5] However, H. influenzae isolated from cerebrospinal fluid or blood would indicate H. influenzae infection.
Bacterial culture of H. influenzae is performed on agar plates, the preferable one being chocolate agar, with added X (hemin) and V (nicotinamide adenine dinucleotide) factors at 37°C in a CO2-enriched incubator.[6] Blood agar growth is only achieved as a satellite phenomenon around other bacteria. Colonies of H. influenzae appear as convex, smooth, pale, grey or transparent colonies.
Gram-stained and microscopic observation of a specimen of H. influenzae will show Gram-negative, rod shaped, with no specific arrangement. The cultured organism can be further characterized using catalase and oxidase tests, both of which should be positive. Further serological testing is necessary to distinguish the capsular polysaccharide and differentiate between H. influenzae b and nonencapsulated species.
Although highly specific, bacterial culture of H. influenzae lacks in sensitivity. Use of antibiotics prior to sample collection greatly reduces the isolation rate by killing the bacteria before identification is possible.[7] Beyond this, H. influenzae is a finicky bacterium to culture, and any modification of culture procedures can greatly reduce isolation rates. Poor quality of laboratories in developing countries has resulted in poor isolation rates of H. influenzae.
H. influenzae will grow in the hemolytic zone of Staphylococcus aureus on blood agar plates; the hemolysis of cells by S. aureus releases factor V which is needed for its growth. H. influenzae will not grow outside the hemolytic zone of S. aureus due to the lack of nutrients such as factor V in these areas. Fildes agar is best for isolation. In Levinthal medium capsulated strains show distinctive iridescence.
The latex particle agglutination test (LAT) is a more sensitive method to detect H. influenzae than culture.[8] Because the method relies on antigen rather than viable bacteria, the results are not disrupted by prior antibiotic use. It also has the added benefit of being much quicker than culture methods. However, antibiotic sensitivity testing is not possible with LAT alone, so a parallel culture is necessary.
Polymerase chain reaction (PCR) assays have been proven to be more sensitive than either LAT or culture tests, and highly specific.[8] However, PCR assays have not yet become routine in clinical settings. Countercurrent immunoelectrophoresis has been shown to be an effective research diagnostic method, but has been largely supplanted by PCR.
Both H. influenzae and S. pneumoniae can be found in the upper respiratory system of humans. In an in vitro study of competition, S. pneumoniae always overpowered H. influenzae by attacking it with hydrogen peroxide and stripping off the surface molecules H. influenzae needs for survival.[9]
When both bacteria are placed together into a nasal cavity, within 2 weeks, only H. influenzae survives. When either is placed separately into a nasal cavity, each one survives. Upon examining the upper respiratory tissue from mice exposed to both bacteria species, an extraordinarily large number of neutrophils (immune cells) was found. In mice exposed to only one bacterium, the cells were not present.
Lab tests showed neutrophils exposed to dead H. influenzae were more aggressive in attacking S. pneumoniae than unexposed neutrophils. Exposure to dead H. influenzae had no effect on live H. influenzae.
Two scenarios may be responsible for this response:
It is unclear why H. influenzae is not affected by the immune response.[10]
Haemophilus influenzae produces beta-lactamases, and it is also able to modify its penicillin-binding proteins, so it has gained resistance to the penicillin family of antibiotics. In severe cases, cefotaxime and ceftriaxone delivered directly into the bloodstream are the elected antibiotics, and, for the less severe cases, an association of ampicillin and sulbactam, cephalosporins of the second and third generation, or fluoroquinolones are preferred. (Fluoroquinolone-resistant Haemophilus influenzae has been observed.)[11]
Macrolide antibiotics (e.g., clarithromycin) may be used in patients with a history of allergy to beta-lactam antibiotics.[citation needed] Macrolide resistance has also been observed.[12]
Effective vaccines for Haemophilus influenzae Type B have been available since the early 1990s, and is recommended for children under age 5 and asplenic patients. The World Health Organization recommends a pentavalent vaccine, combining vaccines against diphtheria, tetanus, pertussis, hepatitis B and Hib. There is not yet sufficient evidence on how effective this pentavalent vaccine is in relation to the individual vaccines.[13]
Hib vaccines cost about seven times the total cost of vaccines against measles, polio, tuberculosis, diphtheria, tetanus, and pertussis. Consequently, whereas 92% of the populations of developed countries was vaccinated against Hib as of 2003, vaccination coverage was 42% for developing countries, and only 8% for least-developed countries.[14]
H. influenzae was the first free-living organism to have its entire genome sequenced. Completed by Craig Venter and his team, Haemophilus was chosen because one of the project leaders, Nobel laureate Hamilton Smith, had been working on it for decades and was able to provide high-quality DNA libraries. The genome consists of 1,830,140 base pairs of DNA in a single circular chromosome that contains 1740 protein-coding genes, 2 transfer RNA genes, and 18 other RNA genes. The sequencing method used was whole-genome shotgun, which was completed and published in Science in 1995 and conducted at The Institute for Genomic Research.[15]
Unencapsulated H. influenzae is often observed in the airways of patients with chronic obstructive pulmonary disease (COPD). Neutrophils are also observed in large numbers in sputum from patients with COPD. The neutrophils phagocytize H. influenzae, thereby activating an oxidative respiratory burst.[16] However instead of killing the bacteria the neutrophils are themselves killed (though such an oxidative burst likely causes DNA damage in the H. influenzae cells). The lack of killing of the H. influenzae appears to explain the persistence of infection in COPD.[16]
H. influenzae mutants defective in the rec1 gene (a homolog of recA) are very sensitive to killing by the oxidizing agent hydrogen peroxide.[17] This finding suggests that rec1 expression is important for H. influenzae survival under conditions of oxidative stress. Since it is a homolog of recA, rec1 likely plays a key role in recombinational repair of DNA damage. Thus H. influenzae may protect its genome against the reactive oxygen species produced by the host’s phagocytic cells through recombinational repair of oxidative DNA damages.[18] Recombinational repair of a damaged site of a chromosome requires, in addition to rec1, a second homologous undamaged DNA molecule. Individual H. influenzae cells are capable of taking up homologous DNA from other cells by the process of transformation. Transformation in H. influenzae involves at least 15 gene products,[15] and is likely an adaptation for repairing DNA damages in the resident chromosome (as suggested in Transformation (genetics)#Transformation, as an adaptation for DNA repair).
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| リンク元 | 「髄膜炎」「Haemophilus influenzae」「ヒブワクチン」「AciHIB vaccine」「pedvaxHIB vaccine」 |
| 関連記事 | 「Haemophilus influenzae」「B」「type」「typed」「bed」 |
| 4ヶ月未満 | B群溶連菌(50%) | 大腸菌(25%) | インフルエンザ菌(20%) | リステリア菌(1%) | |
| 4ヶ月～6歳未満 | インフルエンザ菌(70%) | 肺炎球菌(25%) | |||
| 6歳～50歳未満 | 肺炎球菌(65%) | インフルエンザ菌(10%) | 髄膜炎菌 | ||
| 50歳以上 | 肺炎球菌(80%) | 黄色ブドウ球菌 | |||
| 免疫不全者 | クレブシエラ | 連鎖球菌 | 緑膿菌 | 黄色ブドウ球菌 | 真菌 |
| Newborn (0–6 mos) | Children (6 mos–6 yrs) | 6–60 yrs | 60 yrs + |
| Streptococcus agalactiae | Streptococcus pneumoniae | Neisseria meningitidis | Streptococcus pneumoniae |
| Escherichia coli | Neisseria meningitidis | Enteroviruses | Gram-negative rods |
| Listeria | Haemophilus influenzae type B | Streptococcus pneumoniae | Listeria |
| Enteroviruses | HSV |
| 1位 | 2位 | 3位 | |
| 新生児 | 大腸菌 | B群溶連菌 | リステリア菌 |
| 小児期(6歳以下) | インフルエンザ菌 | 肺炎球菌 | |
| 成人 | 肺炎球菌 | 髄膜炎菌 |
| 年齢 | 病原体 | ||
| 3ヶ月未満 | B群溶連菌 | 大腸菌 | リステリア菌 |
| 3ヶ月以上の乳小児 | インフルエンザ菌 | 肺炎球菌 | |
| 成人 | 肺炎球菌 | 髄膜炎菌 | |
| 高齢者 | 肺炎球菌 | グラム陰性桿菌 | リステリア菌 |
| 細菌性髄膜炎 | ウイルス性髄膜炎 | 結核性髄膜炎 | 真菌性髄膜炎 | 癌性髄膜炎 | |
| 外観 | 混濁 | clear | 水様～ キサントクロミー 日光微塵 |
clear～ 日光微塵 |
clear～ キサントクロミー |
| 圧 70-180 (mmH2O) |
↑↑ 200～800以上 |
↑ 200～300 |
↑ 200～800 |
↑ 200～800 |
↑ 200～300 |
| 細胞 0-5 (/mm3) |
500～数百万 | 10～1,000 | 25～1,000 | 25～1,000 | 25～500 |
| 好中球 | リンパ球 | リンパ球 | リンパ球 | 好中球 | |
| タンパク 15-45 mg/dl |
↑↑ 50～1,500 |
↑ 正常～100 |
↑ 50～500 |
↑ 100～500 |
↑ 50～500 |
| 糖 50-80 mg/dl |
↓↓ 0～40 |
→ 正常 |
↓↓ ～40 |
↓↓ ～40 |
↓ ～40 |