2.)AMT Viro/Myco Quick Flashcards
Virus:
-either dna or rna not both
-obligate intracellular parasite
-no cell wall, no ribosomes, no growth on media
Capsid: Protein coating genome; made of capsomer
Capsomer: structural protein units make up capsid
Nucelocapsid:
-Nucleic acid and capsid
Envelope:
outer membrane around capsid, aids in attachement to host
Virion:
mature virus particle with a nucleic acid core surrounded by a protein coat, w/wout an envelope
Peplomer: spike protein
Bacteriophage, phage:
-virus that infects and replicates in bacteria/archaea
-proteins that encapsulate DNA/RNA, replicate in bacteria after injecting their genome in their cytoplasm
Viral Diseases
Respiratory:
-flu,RSV, parainflu
Gastroenteritis
-noro, rota, adeno
Vesicles/lesions
-HSV, VZV/shingles
Cervical
-HPV
Meningitis
-HSV, entero
Immunocompromised
-CMV, EBV, HSV,
Hepatitis
-HAV, HBV, HCV
HIV
Coronavirus
1.)MERs
-arabian, camels
-respiratory failure from contact
SARS
-china, EIA/molecular
SARS-CoV2
-bat, china
-respiratory droplet
nasopharygeal swab
-RNA molecular and antigen assay
-Ab detection
Viral diagnostic
1.)Direct detection:
-electron microscope
-light miscrope for inclusion bodies
-Fluorescent microscope, DFA(ab detects ag)
-PCR/nucleic acid probes
-Antigen/EIA: flu, rsv, rotavirus
2.)Virus isolation
-animal inoculation
-embryonated egg inoculation
-shell vial centrifugation
-in vitro cell culture: CPE
-cytopathic effects
-rounding, swelling, shrinking of cells
3.)Serology
-sera a week apart, 4fold rise in IgG diagnostic of infection
-ELISA: HepB blood donor
-EBV (heterophile, Monospot)
-Hep (ab markers)
-HIV, HTLV
Cell culture:
-Primary: from animals, isolates most viruses
-Diploid/finite: can only use one type of cell culture,
-Continuous: malignat/Hep2, HSV, RSV, adeno
Collect: 3 to 7 days w/in onset symp, viral shedding highest in early infection, decreases a few days after acute symptoms
-aspiration of secretions best
-swabs dacron/rayon
-VTM: Hanks balanced salt sln w/antibiotics
4C if not w/in 1 hr
(not blood)
-60C if not w/in 24hrs
tranport on dry ice
What is the most common format for viral isolation?
Tube monolayer cell culture is the most common format for viral isolation. Tissue is minced and treated with an enzyme to disperse individual cells further. The cells are seeded onto a surface to form a monolayer in a tube or flask. Leukocyte culture, organ culture and laboratory animals are primarily reserved for specialized and research laboratories.
Three potential viroterrism agents
echo viruses called
ebola
small pox
hanta (RNA, rodents)
Enteric cytopathic human orphan virus
Cause of gastroenteritis kids winter
Rotavirus
Infection can be reactivated with latent infection with
Herpesviridae
two ways to inactivate viruses
10% bleach, 3-10min
2% glutaraldehydge, 1-10min
DNA viruses
Adeno
HepB
Herpes 1/2
CMV
EBV
VZV
Parvo
Papillo (HPV)
Pox (small pox)
Herpes viruses are RNA or DNA?
name some
Herpes: DNA
HSV1/2,6/8
VZV
EBV
CMV
Hepadnavirus
Hep B
Papillomavirus
HPV
HSV 1 is oral or genital
HSV 2 is oral or genital
- oral
- genital
Common RNA
-Coronavirus
-Orthomyxovirus/flu ABC
-Picornavirus/Rhinovirus: cold
-Calicivirus/Noro: gastroenteritis in US
-Reovirus/Rotavirus gastroenterotis in kids
-Retrovirus: HIV, HTLV
-Hep A
-Paramyxo: Mumps/Measles, RSV kids
-Rhabdo/Rabies
…
orthomyxoviruses
flu a,b,c
Flavi-viruses
Arbovirus, dengue, yellow
WN, St.luis
HCV
Rhabdoviruses
Rabies
Retro viruses
HIV, HTLV
Reovirus
Rotavirus
Paramyxovirus mostly kids, elderly, immunocomp
Measures, mumps
Paraflue
RSV
HMPV
PCR
Ligase chain reaction
strand displacement amp all are nucleic acid amplification teq
not flow
Lipase chain reaction:
Nucleic acid amplification
The ligase chain reaction (LCR) is a method of DNA amplification. The ligase chain reaction (LCR) is an amplification process that differs from PCR in that it involves a thermostable ligase to join two probes or other molecules together which can then be amplified by standard polymerase chain reaction (PCR) cycling
Strand Displacement Amplification (SDA): Nucleic acid amp
Strand Displacement Amplification (SDA) is an isothermal, in vitro nucleic acid amplification technique
Histoplasma, Crypto, Cocci, Blasto, Geotrichum all produce this kind of mycoses
systemic
Dermatophytes, Microsporus produces this kind of mycoses
cutaneous/skin
Sporotrichum, Chromoblasto make this kind of mycoses
subcutaneous
Colorful bodies are found in which fungi
Chromoblastomycosis