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Microbiology
- Gopagalla pranay (88a)
INTRODUCTION:-
1. Crimean-Congo haemorrhagic fever (CCHF) is a viral
infection described in parts of Africa, Asia, south-eastern
Europe,
2. The causative agent, CCHF virus, belongs to the genus
Nairovirus of the Bunyaviridae family
3. It causes severe disease in humans with a risk of
nosocomial transmission and a high fatality rate. The
occurrence of the disease is linked to the geographical
distribution of hard tick vectors, mostly from the
Hyalomma genus.
pathogenesis
Prevention methods
• Prevention and control of CCHF infection is achieved by avoiding or minimising exposure
to infected ticks by using tick repellents. Wearing protective clothing and early and
correct removal of ticks are recommended. Since nosocomial cases of CCHF are quite
common and often result in high mortality, strict universal precautions, including barrier
nursing, should be taken with hospitalised cases, as with other haemorrhagic fevers. A
vaccine derived from inactivated mouse brain is used in Bulgaria, but is not widely
available, and efficiency and safety have to be re-evaluated, as well as specific human
immunoglobulin used for post-exposure prophylaxis. In endemic areas, a measure of tick
control has been achieved by environmental sanitation of underbrush habitats.
Acaricides may be useful on domestic animals to control CCHF virus-infected ticks if
used 10–14 days prior to slaughter or to export of animals from enzootic regions.
Management and treatment
Since there is no validated specific antiviral therapy for
CCHF, treatment relies on supportive care, including the
administration of thrombocytes, fresh frozen plasma,
and erythrocyte preparations. Oral or intravenous
ribavirin has been used with reported success, although
with no confirmed benefit. The value of human
immunoglobulins from recovered patients for treatment
has to be re-evaluated.
Diagnosis
Direct diagnosis of CCHF is done by detection of viral
genome by RT-PCR up to 10–15 days post onset of illness.
Serological detection of specific IgM antibodies can be
done starting day five. Crimean-Congo haemorrhagic fever
IgG seroconversion or four-fold titer increase can help the
diagnosis, but it is delayed. As CCHF is considered a highly
hazardous pathogen, sample shipment and handling
require specific protocols.
MicroBio .pptx

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MicroBio .pptx

  • 2. INTRODUCTION:- 1. Crimean-Congo haemorrhagic fever (CCHF) is a viral infection described in parts of Africa, Asia, south-eastern Europe, 2. The causative agent, CCHF virus, belongs to the genus Nairovirus of the Bunyaviridae family 3. It causes severe disease in humans with a risk of nosocomial transmission and a high fatality rate. The occurrence of the disease is linked to the geographical distribution of hard tick vectors, mostly from the Hyalomma genus.
  • 4. Prevention methods • Prevention and control of CCHF infection is achieved by avoiding or minimising exposure to infected ticks by using tick repellents. Wearing protective clothing and early and correct removal of ticks are recommended. Since nosocomial cases of CCHF are quite common and often result in high mortality, strict universal precautions, including barrier nursing, should be taken with hospitalised cases, as with other haemorrhagic fevers. A vaccine derived from inactivated mouse brain is used in Bulgaria, but is not widely available, and efficiency and safety have to be re-evaluated, as well as specific human immunoglobulin used for post-exposure prophylaxis. In endemic areas, a measure of tick control has been achieved by environmental sanitation of underbrush habitats. Acaricides may be useful on domestic animals to control CCHF virus-infected ticks if used 10–14 days prior to slaughter or to export of animals from enzootic regions.
  • 5. Management and treatment Since there is no validated specific antiviral therapy for CCHF, treatment relies on supportive care, including the administration of thrombocytes, fresh frozen plasma, and erythrocyte preparations. Oral or intravenous ribavirin has been used with reported success, although with no confirmed benefit. The value of human immunoglobulins from recovered patients for treatment has to be re-evaluated.
  • 6. Diagnosis Direct diagnosis of CCHF is done by detection of viral genome by RT-PCR up to 10–15 days post onset of illness. Serological detection of specific IgM antibodies can be done starting day five. Crimean-Congo haemorrhagic fever IgG seroconversion or four-fold titer increase can help the diagnosis, but it is delayed. As CCHF is considered a highly hazardous pathogen, sample shipment and handling require specific protocols.