Endospore staining

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Endospore stain on Bacillus subtilis. The spore is stained green and the vegetative cell is stained a pinkish red color. OSC Microbio 02 04 Endospores.jpg
Endospore stain on Bacillus subtilis . The spore is stained green and the vegetative cell is stained a pinkish red color.

Endospore staining is a technique used in bacteriology to identify the presence of endospores in a bacterial sample. [1] Within bacteria, endospores are protective structures used to survive extreme conditions, including high temperatures making them highly resistant to chemicals. [2] Endospores contain little or no ATP which indicates how dormant they can be. Endospores contain a tough outer coating made up of keratin which protects them from nucleic DNA as well as other adaptations. Endospores are able to regerminate into vegetative cells, which provides a protective nature that makes them difficult to stain using normal techniques such as simple staining and gram staining. Special techniques for endospore staining include the Schaeffer–Fulton stain and the Moeller stain.

Contents

History

Endospores were first studied in 1876 by scientists Cohn and Koch. [3] It was found that endospores could not be stained using simple stains such as methylene blue, safranin, and carbol fuchsin. These scientists, along with a few others, found out that spores were dormant and resistant to heat. In the early 1900s, researchers were trying to find alternative methods to improve disease and infection from these endospores. [3]

In 1922, Dorner published a method for staining endospores. He found a differential staining technique where endospores appear green and vegetative cells appear pinkish red. [4] Dorner used heat as a step in the process, but it was time-consuming, so in 1933, Schaeffer and Fulton modified his method.

Schaeffer and Fulton made the heating process a lot faster by using a Bunsen burner. Although this method was not the most beneficial, it was a lot more convenient than Dorner's method. This improved method provided a quicker and easier test and allowed for the spores to be more susceptible to the dyes. [4] To this day, the Schaeffer- Fulton stain is still performed to help identify bacteria.

Examples

Endospores are able to last for decades in multiple hard conditions, such as drying and freezing. This is because the DNA inside the endospore is able to survive over a long period of time. Most bacteria are unable to form endospores due to their high resistance, but some common species are the genera Bacillus ( over 100 species) and Clostridium (over 160 species). [2]

Shape and location

Types of endospores that can be identified include free endospores, central endospores( middle of the cell), subterminal( between the end and middle of the cell), and terminal ( end of the cell) endospores. There can also be a combination of terminal or subterminal. Endospores can be differentiated based on shape, either spherical or elliptical (oval), size relative to the cell, and whether they cause the cell to look swollen or not. [2]

Staining mechanism

In the Schaeffer-Fulton staining method, a primary stain containing malachite green is forced into the spore by steaming the bacteria. Malachite green can be left on the slide for 15 minutes or more to stain the spores. It takes a long time for the spores to stain due to their density, so heat acts as the mordant when performing this differential stain. Malachite green is water-soluble so vegetative cells and spore mother cells can be decolorized with distilled water and counterstained with 0.5% Safranin. [7] In the end, a proper smear would show the endospore as a green dot within either a red or pink-colored cell. [2]

Mycobacterium is one obstacle that is faced with this type of staining process because it will still stain green even though it does not produce any endospores. This is due to its waxy cell wall which retains the malachite green dye even after the decolorizing process. A different type of staining called acid-fast stain will have to be done in order to get further information about this particular type of bacterium.

Summary of Endospore Stain
Application ofReagentCell color
Vegetative cellEndospore
Primary Stain Malachite Green GreenGreen
MordantHeat( Steam)GreenGreen
Decolorizer Distilled Water ColorlessColorless with Green endospore
Counter Stain Safranin PinkPink with Green endospore

Staining procedure

Source: [2]

  1. Using aseptic technique, prepare and air dried heat fixed slide with the desired organism.
  2. Prepare a boiling water bath.
  3. Cover the slide with a piece of paper towel and place on staining rack over the water bath.
  4. Flood the paper towel on the slide with Malachite Green ( primary stain).
  5. Steam the slide for 5 to 7 minutes (mordant).
  6. After the time is up, carefully remove the slide from the water bath using forceps. Take off papertowel.
  7. Let the slide cool down, and then using the forceps over the staining rack, gently rinse with distilled water until the runoff is clear( decolorizer).
  8. Pour off any excess water and place slide on the staining rack and flood with Safranin ( counterstain) for one minute.
  9. Rinse off any excess safranin gently with distilled water and carefully blot dry both sides.
  10. When slide is dry, view slide under the microscope under the oil immersion objective (100X).

Related Research Articles

<i>Bacillus</i> Genus of bacteria

Bacillus is a genus of Gram-positive, rod-shaped bacteria, a member of the phylum Bacillota, with 266 named species. The term is also used to describe the shape (rod) of other so-shaped bacteria; and the plural Bacilli is the name of the class of bacteria to which this genus belongs. Bacillus species can be either obligate aerobes which are dependent on oxygen, or facultative anaerobes which can survive in the absence of oxygen. Cultured Bacillus species test positive for the enzyme catalase if oxygen has been used or is present.

<span class="mw-page-title-main">Gram stain</span> Investigative procedure in microbiology

Gram stain, is a method of staining used to classify bacterial species into two large groups: gram-positive bacteria and gram-negative bacteria. It may also be used to diagnose a fungal infection. The name comes from the Danish bacteriologist Hans Christian Gram, who developed the technique in 1884.

<span class="mw-page-title-main">Gram-positive bacteria</span> Bacteria that give a positive result in the Gram stain test

In bacteriology, gram-positive bacteria are bacteria that give a positive result in the Gram stain test, which is traditionally used to quickly classify bacteria into two broad categories according to their type of cell wall.

<i>Bacillus cereus</i> Species of bacterium

Bacillus cereus is a Gram-positive rod-shaped bacterium commonly found in soil, food, and marine sponges. The specific name, cereus, meaning "waxy" in Latin, refers to the appearance of colonies grown on blood agar. Some strains are harmful to humans and cause foodborne illness due to their spore-forming nature, while other strains can be beneficial as probiotics for animals, and even exhibit mutualism with certain plants. B. cereus bacteria may be anaerobes or facultative anaerobes, and like other members of the genus Bacillus, can produce protective endospores. They have a wide range of virulence factors, including phospholipase C, cereulide, sphingomyelinase, metalloproteases, and cytotoxin K, many of which are regulated via quorum sensing. B. cereus strains exhibit flagellar motility.

<span class="mw-page-title-main">Endospore</span> Protective structure formed by bacteria

An endospore is a dormant, tough, and non-reproductive structure produced by some bacteria in the phylum Bacillota. The name "endospore" is suggestive of a spore or seed-like form, but it is not a true spore. It is a stripped-down, dormant form to which the bacterium can reduce itself. Endospore formation is usually triggered by a lack of nutrients, and usually occurs in gram-positive bacteria. In endospore formation, the bacterium divides within its cell wall, and one side then engulfs the other. Endospores enable bacteria to lie dormant for extended periods, even centuries. There are many reports of spores remaining viable over 10,000 years, and revival of spores millions of years old has been claimed. There is one report of viable spores of Bacillus marismortui in salt crystals approximately 25 million years old. When the environment becomes more favorable, the endospore can reactivate itself into a vegetative state. Most types of bacteria cannot change to the endospore form. Examples of bacterial species that can form endospores include Bacillus cereus, Bacillus anthracis, Bacillus thuringiensis, Clostridium botulinum, and Clostridium tetani. Endospore formation is not found among Archaea.

<i>Clostridium</i> Genus of Gram-positive bacteria, which includes several significant human pathogens

Clostridium is a genus of anaerobic, Gram-positive bacteria. Species of Clostridium inhabit soils and the intestinal tract of animals, including humans. This genus includes several significant human pathogens, including the causative agents of botulism and tetanus. It also formerly included an important cause of diarrhea, Clostridioides difficile, which was reclassified into the Clostridioides genus in 2016.

<span class="mw-page-title-main">Staining</span> Technique used to enhance visual contrast of specimens observed under a microscope

Staining is a technique used to enhance contrast in samples, generally at the microscopic level. Stains and dyes are frequently used in histology, in cytology, and in the medical fields of histopathology, hematology, and cytopathology that focus on the study and diagnoses of diseases at the microscopic level. Stains may be used to define biological tissues, cell populations, or organelles within individual cells.

<i>Bacillus subtilis</i> Catalase-positive bacterium

Bacillus subtilis, known also as the hay bacillus or grass bacillus, is a Gram-positive, catalase-positive bacterium, found in soil and the gastrointestinal tract of ruminants, humans and marine sponges. As a member of the genus Bacillus, B. subtilis is rod-shaped, and can form a tough, protective endospore, allowing it to tolerate extreme environmental conditions. B. subtilis has historically been classified as an obligate aerobe, though evidence exists that it is a facultative anaerobe. B. subtilis is considered the best studied Gram-positive bacterium and a model organism to study bacterial chromosome replication and cell differentiation. It is one of the bacterial champions in secreted enzyme production and used on an industrial scale by biotechnology companies.

<span class="mw-page-title-main">Malachite green</span> Organic dye

Malachite green is an organic compound that is used as a dyestuff and controversially as an antimicrobial in aquaculture. Malachite green is traditionally used as a dye for materials such as silk, leather, and paper. Despite its name the dye is not prepared from the mineral malachite; the name just comes from the similarity of color.

<span class="mw-page-title-main">Ziehl–Neelsen stain</span> Bacteriological technique

The Ziehl-Neelsen stain, also known as the acid-fast stain, is a bacteriological staining technique used in cytopathology and microbiology to identify acid-fast bacteria under microscopy, particularly members of the Mycobacterium genus. This staining method was initially introduced by Paul Ehrlich (1854–1915) and subsequently modified by the German bacteriologists Franz Ziehl (1859–1926) and Friedrich Neelsen (1854–1898) during the late 19th century.

<span class="mw-page-title-main">Acid-fastness</span> Physical property of certain bacterial and eukaryotic cells

Acid-fastness is a physical property of certain bacterial and eukaryotic cells, as well as some sub-cellular structures, specifically their resistance to decolorization by acids during laboratory staining procedures. Once stained as part of a sample, these organisms can resist the acid and/or ethanol-based decolorization procedures common in many staining protocols, hence the name acid-fast.

<span class="mw-page-title-main">Counterstain</span>

A counterstain is a stain with colour contrasting to the principal stain, making the stained structure easily visible using a microscope.

The bacterium, despite its simplicity, contains a well-developed cell structure which is responsible for some of its unique biological structures and pathogenicity. Many structural features are unique to bacteria and are not found among archaea or eukaryotes. Because of the simplicity of bacteria relative to larger organisms and the ease with which they can be manipulated experimentally, the cell structure of bacteria has been well studied, revealing many biochemical principles that have been subsequently applied to other organisms.

Spore photoproduct lyase is a radical SAM enzyme that repairs DNA cross linking of thymine bases caused by UV-radiation. There are several types of thymine cross linking, but SPL specifically targets 5-thyminyl-5,6-dihydrothymine, which is also called spore photoproduct (SP). Spore photoproduct is the predominant type of thymine crosslinking in germinating endospores, which is why SPL is unique to organisms that produce endospores, such as Bacillus subtilis. Other types of thymine crosslinking, such as cyclobutane pyrimidine dimers (CPD) and pyrimidine (6-4) pyrimidone photoproducts (6-4PPs), are less commonly formed in endospores. These differences in DNA crosslinking are a function of differing DNA structure. Spore genomic DNA features many DNA binding proteins called small acid soluble proteins, which changes the DNA from the traditional B-form conformation to an A-form conformation. This difference in conformation is believed to be the reason why dormant spores predominantly accumulate SP in response to UV-radiation, rather than other forms of cross linking. Spores cannot repair cross-linking while dormant, instead the SPs are repaired during germination to allow the vegetative cell to function normally. When not repaired, spore photoproduct and other types of crosslinking can cause mutations by blocking transcription and replication past the point of the crosslinking. The repair mechanism utilizing spore photoproduct lyase is one of the reasons for the resilience of certain bacterial spores.

Moist heat sterilization describes sterilization techniques that use hot water vapor as a sterilizing agent. Heating an article is one of the earliest forms of sterilization practiced. The various procedures used to perform moist heat sterilization process cause destruction of micro-organisms by denaturation of macromolecules.

<i>Bacillus anthracis</i> Species of bacterium

Bacillus anthracis is a gram-positive and rod-shaped bacterium that causes anthrax, a deadly disease to livestock and, occasionally, to humans. It is the only permanent (obligate) pathogen within the genus Bacillus. Its infection is a type of zoonosis, as it is transmitted from animals to humans. It was discovered by a German physician Robert Koch in 1876, and became the first bacterium to be experimentally shown as a pathogen. The discovery was also the first scientific evidence for the germ theory of diseases.

<span class="mw-page-title-main">Dipicolinic acid</span> Chemical compound

Dipicolinic acid is a chemical compound which plays a role in the heat resistance of bacterial endospores. It is also used to prepare dipicolinato ligated lanthanide and transition metal complexes for ion chromatography.

<span class="mw-page-title-main">Schaeffer–Fulton stain</span> Endospore isolation technique

The Schaeffer–Fulton stain is a technique designed to isolate endospores by staining any present endospores green, and any other bacterial bodies red. The primary stain is malachite green, and the counterstain is safranin, which dyes any other bacterial bodies red.

Moeller staining involves the use of a steamed dye reagent in order to increase the stainability of endospores. Carbol fuchsin is the primary stain used in this method. Endospores are stained red, while the counterstain methylene blue stains the vegetative bacteria blue.

The Kinyoun method or Kinyoun stain, developed by Joseph J. Kinyoun, is a procedure used to stain acid-fast species of the bacterial genus Mycobacterium. It is a variation of a method developed by Robert Koch in 1882. Certain species of bacteria have a waxy lipid called mycolic acid, in their cell walls which allow them to be stained with Acid-Fast better than a Gram-Stain. The unique ability of mycobacteria to resist decolorization by acid-alcohol is why they are termed acid-fast. It involves the application of a primary stain, a decolorizer (acid-alcohol), and a counterstain. Unlike the Ziehl–Neelsen stain, the Kinyoun method of staining does not require heating. In the Ziehl–Neelsen stain, heat acts as a physical mordant while phenol acts as the chemical mordant. Since the Kinyoun stain is a cold method, the concentration of carbol fuschin used is increased.

References

  1. Microbiology An Introduction Tenth Edition; Tortora Funke Case
  2. 1 2 3 4 5 6 Leboffe, Michael (2015). Microbiology Laboratory Theory and Application. Englewood, CO: Morton Publishing. pp. |page=215. ISBN   978-1-61731-250-2.
  3. 1 2 Gould, G. W. (2006). "History of science – spores". Journal of Applied Microbiology. 101 (3): 507–513. doi: 10.1111/j.1365-2672.2006.02888.x . ISSN   1365-2672. PMID   16907801. S2CID   25322574.
  4. 1 2 Hussey, Marise; Zayaitz, Anne (2011-09-29). "Endospore Stain Protocol". American Society for Microbiology. Archived from the original on 2012-06-01. Retrieved 2012-03-06.
  5. 1 2 Nicholson, W. L. (2002-03-01). "Roles of Bacillus endospores in the environment". Cellular and Molecular Life Sciences. 59 (3): 410–416. doi: 10.1007/s00018-002-8433-7 . ISSN   1420-9071. PMID   11964119. S2CID   31150248.
  6. "2.4E: Endospores". Biology LibreTexts. 2016-03-02. Retrieved 2021-11-11.
  7. "UW System Authentication Redirector". wayf.wisconsin.edu. Retrieved 2021-11-11.