微生物學(xué)英文教學(xué)課件：chapter10 Microbial Taxonomy

1、PART IVThe Diversity of the Microbial WorldC H A P T E R 10Microbial Taxonomy10.1 General Introduction and Overview One of the most fascinating and attractive aspects of the microbial world is its extraordinary diversity. Because of the bewildering diversity of living organisms, it is desirable to c

2、lassify or arrange them into groups based on their mutual similarities. Taxonomy Greek taxis, arrangement or order, and nomos, law, or nemein, to distribute or govern is defined as the science of biological classification. In a broader sense it consists of three separate but interrelated parts: clas

3、sification, nomenclature, and identification. Classification is the arrangement of organisms into groups or taxa (s., taxon) based on mutual similarity or evolutionary relatedness. Nomenclature is the branch of taxonomy concerned with the assignment of names to taxonomic groups in agreement with pub

4、lished rules. Identification is the practical side of taxonomy, the process of determining that a particular isolate belongs to a recognized taxon. The term systematics often is used for taxonomy. However, many taxonomists define it in more general terms as “the scientific study of organisms with th

5、e ultimate object of characterizing and arranging them in an orderly manner.” Any study of the nature of organisms, when the knowledge gained is used in taxonomy, is a part of systematics. Thus it encompasses disciplines such as morphology, ecology, epidemiology, biochemistry, molecular biology, and

6、 physiology. Currently microbial taxonomy is in ferment because of the use of new molecular techniques in classifying microorganisms. Even though these new advances have generated much excitement and are drastically changing microbial taxonomy, more traditional approaches still have value and also w

7、ill be outlined.10.2 Microbial Evolution and Diversity It has been estimated that our planet is about 4.6 billion years old. Fossilized remains of procaryotic cells around 3.5 to 3.8 billion years old have been discovered in stromatolites and sedimentary rocks.形成于35億年前的微生物化石主要是些類似簡單桿狀細(xì)菌的原始生物形成于8.5億年

8、前的微生物化石20億年前以后的巖石中的微生物的化石形態(tài)多樣性明顯增多形成于10億年前的微生物化石形態(tài)上非常類似于現(xiàn)代的藍(lán)細(xì)菌，進(jìn)行不產(chǎn)氧光合作用的光能自養(yǎng)菌，及化能無機(jī)營養(yǎng)的硫細(xì)菌。形態(tài)上類似于現(xiàn)代的綠藻（真核生物） Thus procaryotic life arose very shortly after the earth cooled. Very likely the earliest procaryotes were anaerobic. Cyanobacteria and oxygen-producing photosynthesis probably developed 2.5

9、to 3.0 billion or more years ago. Microbial diversity increased greatly as oxygen became more plentiful. The studies of Carl Woese and his collaborators on rRNA sequences in procaryotic cells suggest that procaryotes divided into two distinct groups very early on. Figure 19.3 depicts a universal phy

10、logenetic tree that reflects these views. The tree is divided into three major branches representing the three primary groups: Bacteria, Archaea, and Eucarya.Carl Woese“Taxonomists counts suggest that insects dominate the diversity game, but new analyses reveal that microbes are the real winners.” T

11、he archaea and bacteria first diverged, then the eucaryotes developed. These three primary groups are called domains and placed above the phylum and kingdom levels (the traditional kingdoms are distributed among these three domains). The domains differ markedly from one another. Eucaryotic organisms

12、 with primarily glycerol fatty acyl diester membrane lipids and eucaryotic rRNA belong to the Eucarya. The domain Bacteria contains procaryotic cells with bacterial rRNA and membrane lipids that are primarily diacyl glycerol diesters. Procaryotes having isoprenoid glycerol diether or diglycerol tetr

13、aether lipids in their membranes and archaeal rRNA compose the third domain, Archaea.020406080100120140160180200 96999095before 90Papers about the horizontal gene transfer10.3 Taxonomic Ranks根據(jù)Carl Woese的理論，現(xiàn)在還在界界之上之上使用域域(domain) （把全部生物先分為古生菌域、細(xì)菌域和真核生物域，域下面再分界。）Glossary for Taxonomic Ranks Domain域,

14、Superkingdom 超/總界 Kingdom界 Subkingdom亞界 Division, Phylum門 Subdivision, Subphylum亞門 Class綱 Subclass亞綱 Order目 Suborder亞目 Family科 Subfamily亞科 Tribe族 Subtribe亞族 Genus屬 Subgenus亞屬 The basic taxonomic group in microbial taxonomy is the species. Taxonomists working with higher organisms define the term spe

15、cies differently than do microbiologists. Species of higher organisms are groups of interbreeding or potentially interbreeding natural populations that are reproductively isolated from other groups. This is a satisfactory definition for organisms capable of sexual reproduction but fails with many mi

16、croorganisms because they do not reproduce sexually. Procaryotic species are characterized by phenotypic and genotypic differences. A procaryotic species is a collection of strains that share many stable properties and differ significantly from other groups of strains. This definition is very subjec

17、tive and can be interpreted in many ways. The following more precise definition has been proposed by some bacterial taxonomists. A species (genomospecies) is a collection of strains that have a similar G +C composition and 70% or greater similarity as judged by DNA hybridization experiments. Ideally

18、 a species also should be phenotypically distinguishable from other similar species. A strain is a population of organisms that is distinguishable from at least some other populations within a particular taxonomic category. It is considered to have descended from a single organism or pure culture is

19、olate. Strains within a species may differ slightly from one another in many ways. Biovars are variant procaryotic strains characterized by biochemical or physiological differences, morphovars differ morphologically, and serovars have distinctive antigenic properties. One strain of a species is desi

20、gnated as the type strain. It is usually one of the first strains studied and often is more fully characterized than other strains; however, it does not have to be the most representative member. Microbiologists name microorganisms by using the binomial system of the Swedish botanist Carl von Linn.

21、The Latinized, italicized name consists of two parts. The first part, which is capitalized, is the generic name, and the second is the uncapitalized specific epithet (e.g., Escherichia coli). The specific epithet is stable; the oldest epithet for a particular organism takes precedence and must be us

22、ed.微生物的命名雙名法，由二個拉丁字或希臘字或拉丁化了的其它文字組成，一般用斜體表示一般用斜體表示屬名在前，一般用拉丁字名詞表示，字首字母大寫種名在后，常用拉丁文形容詞表示，全部小寫若所分離的菌株只鑒定到屬，而未鑒定到種，可用若所分離的菌株只鑒定到屬，而未鑒定到種，可用sp來表示，來表示，例如例如 Bacillus sp In contrast, a generic name can change if the organism is assigned to another genus because of new information. For example, the genus St

23、reptococcus has been divided to form two new genera, Enterococcus and Lactococcus based on rRNA analysis and other characteristics. Thus Streptococcus faecalis is now Enterococcus faecalis. Often the name will be shortened by abbreviating the genus name with a single capital letter, for example E. c

24、oli. Approved lists of bacterial names were published in 1980 in the International Journal of Systematic Bacteriology, and new valid names are published periodically. Bergeys Manual of Systematic Bacteriology contains the currently accepted system of procaryotic taxonomy.10.4 Major Characteristics U

25、sed in Taxonomy Many characteristics are used in classifying and identifying microorganisms. This section briefly reviews some of the most taxonomically important properties. For sake of clarity, characteristics have been divided into two groups: classical and molecular.1.Classical Characteristics C

26、lassical approaches to taxonomy make use of morphological, physiological, biochemical, ecological, and genetic characteristics. These characteristics have been employed in microbial taxonomy for many years. They are quite useful in routine identification and may provide phylogenetic information as w

27、ell.(1) Morphological Characteristics Morphological features are important in microbial taxonomy for many reasons. Morphology is easy to study and analyze, particularly in eucaryotic microorganisms and the more complex procaryotes. In addition, morphological comparisons are valuable because structur

28、al features depend on the expression of many genes, are usually genetically stable, and normally (at least in eucaryotes) these do not vary greatly with environmental changes. Thus morphological similarity often is a good indication of phylogenetic relatedness. Many different morphological features

29、are employed in the classification and identification of microorganisms. Although the light microscope has always been a very important tool, its resolution limit of about 0.2 m reduces its usefulness in viewing smaller microorganisms and structures. The transmission and scanning electron microscope

30、s, with their greater resolution, have immensely aided the study of all microbial groups.(2) Physiological and Metabolic Characteristics Physiological and metabolic characteristics are very useful because they are directly related to the nature and activity of microbial enzymes and transport protein

31、s. Since proteins are gene products, analysis of these characteristics provides an indirect comparison of microbial genomes. (3) Ecological Characteristics Many properties are ecological in nature since they affect the relation of microorganisms to their environment. Often these are taxonomically va

32、luable because even very closely related microorganisms can differ considerably with respect to ecological characteristics. Some examples of taxonomically important ecological properties are life cycle patterns; the nature of symbiotic relationships; the ability to cause disease in a particular host

33、; and habitat preferences such as requirements for temperature, pH, oxygen, and osmotic concentration. Many growth requirements are also considered physiological characteristics.(4) Genetic Analysis Because most eucaryotes are able to reproduce sexually, genetic analysis has been of considerable use

34、fulness in the classification of these organisms. Although procaryotes do not reproduce sexually, the study of chromosomal gene exchange through transformation and conjugation is sometimes useful in their classification. Transformation can occur between different procaryotic species but only rarely

35、between genera. The demonstration of transformation between two strains provides evidence of a close relationship since transformation cannot occur unless the genomes are fairly similar. Transformation studies have been carried out with several genera: Bacillus, Micrococcus, Haemophilus, Rhizobium,

36、and others. Despite transformations usefulness, its results are sometimes hard to interpret because an absence of transformation may result from factors other than major differences in DNA sequence. Plasmids are undoubtedly important in taxonomy because they are present in most bacterial genera, and

37、 many carry genes coding for phenotypic traits. Because plasmids could have a significant effect on classification if they carried the gene for a trait of major importance in the classification scheme, it is best to base a classification on many characters.2.Molecular Characteristics Some of the mos

38、t powerful approaches to taxonomy are through the study of proteins and nucleic acids. Because these are either direct gene products or the genes themselves, comparisons of proteins and nucleic acids yield considerable information about true relatedness. These more recent molecular approaches have b

39、ecome increasingly important in procaryotic taxonomy.(1) Comparison of Proteins The amino acid sequences of proteins are direct reflections of mRNA sequences and therefore closely related to the structures of the genes coding for their synthesis. For this reason, comparisons of proteins from differe

40、nt microorganisms are very useful taxonomically. There are several ways to compare proteins. The most direct approach is to determine the amino acid sequence of proteins with the same function. The sequences of proteins with dissimilar functions often change at different rates; some sequences change

41、 quite rapidly, whereas others are very stable. Nevertheless, if the sequences of proteins with the same function are similar, the organisms possessing them are probably closely related. The sequences of cytochromes and other electron transport proteins, histones, heat-shock proteins, transcription

42、and translation proteins, and a variety of metabolic enzymes have been used in taxonomic studies. Because protein sequencing is slow and expensive, more indirect methods of comparing proteins frequently have been employed. The electrophoretic mobility of proteins is useful in studying relationships

43、at the species and subspecies levels. Antibodies can discriminate between very similar proteins, and immunologic techniques are used to compare proteins from different microorganisms. The physical, kinetic, and regulatory properties of enzymes have been employed in taxonomic studies. Because enzyme

44、behavior reflects amino acid sequence, this approach is useful in studying some microbial groups, and group-specific patterns of regulation have been found.(2) Nucleic Acid Base Composition Microbial genomes can be directly compared, and taxonomic similarity can be estimated in many ways. The first,

45、 and possibly the simplest, technique to be employed is the determination of DNA base composition. DNA contains four purine and pyrimidine bases: adenine (A), guanine (G), cytosine (C), and thymine (T). In double-stranded DNA, A pairs with T, and G pairs with C. Thus the (G+C)/(A+T) ratio or G+C con

46、tent, the percent of G+C in DNA, reflects the base sequence and varies with sequence changes as follows: If two organisms differ in their G+C content by more than about 10%, their genomes have quite different base sequences. On the other hand, it is not safe to assume that organisms with very simila

47、r G+C contents also have similar DNA base sequences because two very different base sequences can be constructed from the same proportions of AT and GC base pairs. Only if two microorganisms also are alike phenotypically does their similar G+C content suggest close relatedness. G+C content data are

48、taxonomically valuable in at least two ways. First, they can confirm a taxonomic scheme developed using other data. If organisms in the same taxon are too dissimilar in G+C content, the taxon probably should be divided. Second, G+C content appears to be useful in characterizing procaryotic genera si

49、nce the variation within a genus is usually less than 10% even though the content may vary greatly between genera. For example, Staphylococcus has a G+C content of 30 to 38%, whereas Micrococcus DNA has 64 to 75% G+C; yet these two genera of gram-positive cocci have many other features in common.(3)

50、 Nucleic Acid Hybridization The similarity between genomes can be compared more directly by use of nucleic acid hybridization studies. If DNA molecules are very different in sequence, they will not form a stable, detectable hybrid. Therefore DNA-DNA hybridization is used to study only closely relate

51、d microorganisms.特異性的探針主要用于病原微生物的快速鑒定 More distantly related organisms are compared by carrying out DNA-RNA hybridization experiments using radioactive ribosomal or transfer RNA. Distant relationships can be detected because rRNA and tRNA genes represent only a small portion of the total DNA genome

52、and have not evolved as rapidly as most other microbial genes.(4) Nucleic Acid Sequencing Despite the usefulness of G+C content determination and nucleic acid hybridization studies, genome structures can be directly compared only by sequencing DNA and RNA. Techniques for rapidly sequencing both DNA

53、and RNA are now available; thus far RNA sequencing has been used more extensively in microbial taxonomy. Most attention has been given to sequences of the 16S rRNAs isolated from the 30S subunits of procaryotic ribosomes. The rRNAs are almost ideal for studies of microbial evolution and relatedness

54、since they are essential to a critical organelle found in all microorganisms. Their functional role is the same in all ribosomes. Furthermore, their structure changes very slowly with time, presumably because of their constant and critical role. Because rRNA contains variable and stable sequences, b

55、oth closely related and very distantly related microorganisms can be compared. This is an important advantage as distantly related organisms can be studied only using sequences that change little with time.10.5 Bergeys Manual of Systematic Bacteriology In 1923, David Bergey (1860-1937), professor of

56、 bacteriology at the University of Pennsylvania, and four colleagues published a classification of bacteria that could be used for identification of bacterial species, the Bergeys Manual of Determinative Bacteriology. This manual is now in its ninth edition.1.The First Edition of Bergeys Manual of S

57、ystematic Bacteriology Because it has not been possible in the past to classify procaryotes satisfactorily based on phylogenetic relationships, the system given in the first edition of Bergeys Manual of Systematic Bacteriology is primarily phenetic. Each of the 33 sections in the four volumes contai

58、ns procaryotes that share a few easily determined characteristics and bears a title that either describes these properties or provides the vernacular names of the procaryotes included. The characteristics used to define sections are normally features such as general shape and morphology, Gram-staini

59、ng properties, oxygen relationship, motility, the presence of endospores, the mode of energy production, and so forth. Procaryotic groups are divided among the four volumes in the following manner: (1) gram-negative bacteria of general, medical, or industrial importance; (2) gram-positive bacteria o

60、ther than actinomycetes; (3) gram-negative bacteria with distinctive properties, cyanobacteria, and archaea; (4) actinomycetes (gram-positive filamentous bacteria).2.The Second Edition of Bergeys Manual of Systematic Bacteriology There has been enormous progress in procaryotic taxonomy since 1984, t