INFECTIOUS DISEASE
DR. ROOPAM JAIN
PROFESSOR & HEAD,
DEPT. OF PATHOLOGY & BLOOD BANK
Routes of Microbial Infecton
Special Techniques for
Diagnosing Infectious Agents
Spectrum of Inflammatory
Responses to Infection
Classification of
Important Sexually
Transmitted
Diseases
Diseases caused by
bacteria, spirochaetes &
mycobacteria
STAPHYLOCOCCAL INFECTIONS
• gram-positive cocci
• present everywhere—in the skin, umbilicus, nasal vestibule,
stool etc.
• 3 species are pathogenic to human beings: Staph. aureus,
Staph. epidermidis and Staph. saprophyticus.
• Most staphylococcal infections are caused by Staph. aureus.
• Staphylococcal infections are among the commonest antibiotic
resistant hospital-acquired infection in surgical wounds
A wide variety of suppurative diseases are
caused by Staph. aureus which includes
• 1. Infections of skin
• 2. Infections of burns and surgical wounds
• 3. Infections of the upper and lower respiratory tract
• 4. Bacterial arthritis
• 5. Infection of bone (Osteomyelitis)
• 6. Bacterial endocarditis
• 7. Bacterial meningitis
• 8. Septicaemia
• 9. Toxic shock syndrome
STAPHYLOCOCCAL
INFECTIONS
Suppurative diseases
caused by
Staphylococcus aureus
STREPTOCOCCAL INFECTIONS
• gram-positive cocci
• more known for their non-suppurative autoimmune
complications than suppurative inflammatory responses.
• Streptococcal infections occur throughout the world
(underprivileged populations)
Implicated in different streptococcal diseases
• 1. Group A or Streptococcus pyogenes, also called b-haemolytic
streptococci - upper respiratory tract infection and cutaneous
infections (erysipelas).
• 2. Group B or Streptococcus agalactiae produces infections in the
newborn and is involved in non-suppurative poststreptococcal
complications such as RHD and acute glomerulonephritis.
• 3. Group C and G streptococci - respiratory infections.
Implicated in different streptococcal diseases
• 4. Group D or Streptococcus faecalis, also called enterococci are
important in causation of urinary tract infection, bacterial
endocarditis, septicaemia etc.
• 5. Untypable a-haemolytic streptococci such as Streptococcus
viridans constitute the normal flora of the mouth and may cause
bacterial endocarditis.
• 6. Pneumococci or Streptococcus pneumoniae - bacterial
pneumonias, meningitis and septicaemia
Diseases
caused by
streptococci
CLOSTRIDIAL DISEASES
• gram-positive spore-forming anaerobic microorganisms
• found in the GIT of herbivorous animals and man.
• undergo vegetative division under anaerobic conditions, and
sporulation under aerobic conditions.
• toxins responsible for the diseases:
• 1. Gas gangrene by C. perfringens
• 2. Tetanus by C. tetani
• 3. Botulism by C. botulinum
• 4. Clostridial food poisoning by C. perfringens
• 5. Necrotising enterocolitis by C. perfringens.
GAS GANGRENE
• rapidly progressive and fatal illness
• Myonecrosis due to elaboration of myotoxins
• In majority of cases (80-90%), the source of myotoxins is C.
perfringens Type A; others are C. novyi and C. septicum.
• Generally, traumatic wounds and surgical procedures are
followed by contamination with clostridia and become the site
of myonecrosis.
• The incubation period is 2 to 4 days.
• The most common myotoxin produced by C. perfringens Type A
is the alpha toxin which is a lecithinase.
• The prevention of gas gangrene lies in debridement of damaged
tissue in which the clostridia thrive.
• The lesion has serosanguineous discharge with odour and
contains gas bubbles.
• There is very scanty inflammatory reaction at the site of gas
gangrene
TETANUS
• ‘lock jaw’ is a severe acute neurologic syndrome
• caused by tetanus toxin, tetanospasmin, which is a neurotoxic exotoxin
elaborated by C. tetani.
• The spores of the microorganism present in the soil enter the body
through a penetrating wound.
• The degenerated microorganisms liberate the tetanus neurotoxin which
causes neuronal stimulation and spasm of muscles.
• The incubation period of the disease is 1-3 weeks.
• The earliest manifestation is lock-jaw or trismus.
• Rigidity of muscles of the back causes backward arching or opisthotonos.
• Death occurs due to spasm of respiratory and laryngeal muscles.
DISEASES
CAUSED BY
FUNGI
Diseases caused by fungi
MYCETOMA
• Chronic suppurative infection (limb, shoulder)
• characterised by draining sinuses (colonies of fungi or bacteria)
• Types:
 Caused by actinomyces (higher bacteria) also called
actinomycetoma comprises about 60%.
 ”
Eumycetoma caused by true fungi, Madurella mycetomatis or
Madurella grisea, comprises the remaining 40%.
• The organisms are inoculated directly from soil into bare feet,
from carrying of contaminated sacks on the shoulders, and into
the hands from infected vegetation.
MYCETOMA
MORPHOLOGIC FEATURES
• After several months of infection,
• The affected site, most commonly foot, is swollen -- ‘madura foot’.
• The lesions extend deeply into the subcutaneous tissues, along
the fascia and eventually invade the bones.
• They drain through sinus tracts which discharge purulent material
and black grains.
• Surrounding tissue shows granulomatous reaction.
Madura foot.
Brown granule lying in necrotic tissue in the discharging sinus
CANDIDIASIS
• an opportunistic fungal infection caused most commonly by
Candida albicans and occasionally by Candida tropicalis.
• Candida species are present as normal flora of the skin and
mucocutaneous areas, intestines and vagina.
• Various predisposing factors are: impaired immunity, prolonged
use of oral contraceptives, long-term antibiotic therapy,
corticosteroid therapy, diabetes mellitus, obesity, pregnancy etc.
CANDIDIASIS
MORPHOLOGIC FEATURES
• Candida produces superficial infections of the skin and
mucous membranes, or may invade deeper tissues.
1. Oral thrush
2. Candidal vaginitis
3. Cutaneous candidiasis
4. Systemic candidiasis
1. Oral thrush
• Commonest form of mucocutaneous candidiasis
• Fullfledged lesions consist of creamy white
pseudomembrane composed of fungi covering the tongue,
soft palate, and buccal mucosa
• In severe cases-ulceration
2. Candidal vaginitis
• Vaginal candidiasis or monilial vaginitis is characterised
clinically by thick, yellow, curdy discharge.
• The lesions form pseudomembrane of fungi on the vaginal
mucosa.
• They are quite pruritic and may extend to involve the vulva
(vulvovaginitis) and the perineum.
3. Cutaneous candidiasis
• Candidal involvement of nail folds - paronychia and colonisation in
the intertriginous areas of the skin, axilla, groin, infra- and inter-
mammary, intergluteal folds and interdigital spaces.
4. Systemic candidiasis
• Usually a terminal event
• The organisms gain entry into the body through an ulcerative
lesion on the skin and mucosa or may be introduced
• Most commonly encountered in kidneys as ascending
pyelonephritis and in heart as candidal endocarditis.
Candidiasis of the ulcer in the skin
CUTANEOUS SUPERFICIAL MYCOSIS
• Dermatophytes cause superficial mycosis of the skin, the
important examples - Microsporum, Trichophyton and
Epidermophyton.
• These superficial fungi are spread by direct contact or by
fomites and infect tissues such as the skin, hair and nails.
• Examples
”
. Tinea capitis - patchy alopecia affecting the scalp and eyebrows.
”
. Tinea barbae is acute folliculitis of the beard. ”
. Tinea corporis is dermatitis with erythematous papules.
• Diagnosis of dermatophytosis - light microscopic examination
of skin scrapings
Selected Human Viruses &
Viral Diseases
Mechanisms
by which
viruses cause
injury to cells
DISEASES CAUSED BY VIRUSES
VIRAL HAEMORRHAGIC FEVERS
• common features of causing haemorrhages, shock & sometimes
death.
• arthropod-borne (or arbo) viruses
• Classified - 4 groups:
1. Mosquito-borne (e.g. yellow fever, dengue fever, Rift Valley fever)
2. Tick-borne (e.g. Crimean haemorrhagic fever, Kyasanur Forest
disease)
3. Zoonotic (e.g. Korean haemorrhagic fever, Lassa fever)
4. Marburg virus disease & Ebola virus disease by unknown route.
• Mosquito-borne viral haemorrhagic fevers in which Aedes aegypti
mosquitoes are vectors.
• Two important examples of Aedes mosquito-borne viral
haemorrhagic fevers are yellow fever and dengue fever.
YELLOW FEVER
• Oldest known viral haemorrhagic fever
• restricted to some regions of Africa and South America.
• Monkeys carry the virus without suffering from illness and the
virus is transmitted from them to humans by Aedes aegypti as
vector.
Clinical features:
• Sudden onset of high fever, & chills,
• myalgia,
• headache,
• jaundice,
• hepatic failure,
• renal failure,
• bleeding disorders
• hypotension.
YELLOW FEVER
MORPHOLOGIC FEATURES
Liver. The characteristic changes include:
i) midzonal necrosis;
ii) Councilman bodies; and
iii) microvesicular fat.
Kidneys. The kidneys show the following changes:
i) coagulative necrosis of proximal tubules;
ii) accumulation of fat in the tubular epithelium; and
iii) haemorrhages.
DENGUE HAEMORRHAGIC FEVER
(DHF)
• The word dengue is derived from African word ‘denga’ meaning
fever with haemorrhages.
• Dengue is caused by virus transmitted by bites of mosquito Aedes
aegypti.
• DHF was first described in 1953 when it struck Philippines.
• regularly reported from tropics and subtropics—South East Asia,
Latin America
• Dengue occurs in two forms:
1. Dengue fever or break-bone fever in an uncomplicated
way is a self-limited febrile illness affecting muscles and
joints with severe back pain due to myalgia (and hence
the name ‘breakbone’ fever).
2. Dengue haemorrhagic fever (DHF), on the other hand, is
a severe and potentially fatal form of acute febrile illness
characterised by cutaneous and intestinal haemorrhages
d/t thrombocytopenia, haemoconcentration,
Hypovolaemic shock and neurologic disturbances.
• DHF is most common in children under 15 years of age.
• There are 4 types of dengue viruses
• These visruses infect blood monocytes, lymphocytes and
endothelial cells.
• If patient is treated appropriately at this stage, there is rapid and
dramatic recovery.
• But in untreated cases, dengue shock syndrome develops and
death occurs.
MORPHOLOGIC FEATURES :
i) Focal haemorrhages and congestion
ii) Increased vascular permeability resulting in oedema in different
organs
iii) Coagulopathy with thrombocytopenia
iv) Haemoconcentration.
Diagnosis of DHF:
1. Serologic testing for detection of antibodies
2. Detection of virus by immunofluorescence method & monoclonal
antibodies
3. Rapid methods such as reverse transcriptase-PCR and fluorogenic-
ELISA.
• Main abnormalities in investigations in DHF are as under:
i) Leucopenia with relative lymphocytosis,
ii) Thrombocytopenia
iii) Elevated haematocrit due to haemoconcentration
iv) X-ray chest showing bilateral pleural effusion
v) Deranged liver function tests (elevated transaminases,
hypoalbuminaemia and reversed A:G ratio)
vi) Prolonged coagulation tests (PT, APTT and TT)
• At autopsy:
i) Brain: Intracranial haemorrhages, cerebral oedema, dengue
encephalitis.
ii) Liver: Enlarged; necrosis of hepatocytes and Kupffer cells, Reye’s
syndrome in children.
iii) Kidneys: Petechial haemorrhages and features of renal failure.
iv) Muscles and joints: Perivascular mononuclear cell infiltrate.
CHIKUNGUNYA VIRUS
INFECTION
• The word chikungunya means “that which bends up”
• Primarily a disease in nonhuman primates but the
infection is transmitted to humans by A. aegypti
mosquito.
CHIKUNGUNYA VIRUS INFECTION
Clinically, the disease is characterised by
• abrupt onset of fever,
• severe arthralgia
• migratory polyarthritis affecting small joints,
• chills,
• headache,
• anorexia, nausea, abdominal pain,
• rash,
• Petechiae,
• ocular symptoms such as photophobia.
”
• Major laboratory findings
• leucopenia,
• mild thrombocytopenia,
• elevated transaminaseS
• raised CRP.
INFLUENZA VIRUS INFECTIONS
• Important and common form of communicable disease.
• General clinical features range from a mild afebrile illness
similar to common cold by appearance of sudden fever,
headache, myalgia, malaise, chills and respiratory tract
manifestations such as cough, soar throat to a more severe
form of acute respiratory illness and lymphadenopathy.
• Sometimes with alarming morbidity and mortality in the
world.
• Seasonal flu vaccine is administered to population at high
risk in developed countries.
ETIOLOGIC AGENT
• Influenza virus is a single-stranded RNA virus belonging to
coronaviruses.
• Depending upon its antigenic characteristics of the
nucleoprotein and matrix, 3 distinct types are known: A, B & C.
• Influenza type A is responsible for most serious and severe forms
of outbreaks in human beings while types B and C cause a milder
form of illness.
Type A influenza virus is further subtyped based on its 2 viral
surface features:
• Haemagglutinin (H) H antigen elicits host immune response by
antibodies and determines the future protection against
influenza A viruses.
• Neuraminidase (N) Antibody response against N antigen limits
the spread of viral infection and is responsible for reduction of
infection.
• Subtypes of influenza A viruses are designated by denoting
serial subtype numbers of H and N antigens as H1N1, H2N2
etc.
• Influenza A viruses infect human beings, birds, pigs & horses.
• Major antigenic variation in H or N antigens is called antigenic
shift while minor variation is termed antigenic drift.
• In general, population at high risk are immunosuppressed
patients, elderly individuals and infants.
• Two of the known subtypes of influenza A viruses which have
affected the human beings in recent times are as under:
 ”
Avian influenza virus A/H5N1 commonly called “bird flu”.
 ”
Swine influenza virus A/H1N1 commonly called “swine flu”.
BIRD FLU (INFLUENZA A/H5N1)
• H5N1 subtype of the influenza type A virus
infection causes severe acute respiratory
syndrome (SARS) which is the human form of bird
flu or avian influenza with having similar
symptomatology.
• Every year, there have been outbreaks in poultry
birds in different parts of the world resulting in
slaughtering of millions of infected chickens every
year.
• Every year there have been seasonal outbreaks in
the human form of the disease in high winter.
PATHOGENESIS
• SARS is caused by influenza type A/H5N1 respiratory
virus, also called SARS-associated coronaviruses (SARS-
CoV).
• Humans acquire infection through contaminated nasal,
respiratory and faecal material from infected birds.
• An individual who has human flu and also gets infected
with bird flu, then the hybrid virus so produced is
highly contagious and causes lethal disease.
• Humans do not have immune protection against avian
viruses.
INFECTIOUS DISEASE by DR. ROOPAM JAIN

INFECTIOUS DISEASE by DR. ROOPAM JAIN

  • 1.
    INFECTIOUS DISEASE DR. ROOPAMJAIN PROFESSOR & HEAD, DEPT. OF PATHOLOGY & BLOOD BANK
  • 2.
  • 3.
  • 5.
  • 6.
  • 8.
    Diseases caused by bacteria,spirochaetes & mycobacteria
  • 11.
    STAPHYLOCOCCAL INFECTIONS • gram-positivecocci • present everywhere—in the skin, umbilicus, nasal vestibule, stool etc. • 3 species are pathogenic to human beings: Staph. aureus, Staph. epidermidis and Staph. saprophyticus. • Most staphylococcal infections are caused by Staph. aureus. • Staphylococcal infections are among the commonest antibiotic resistant hospital-acquired infection in surgical wounds
  • 12.
    A wide varietyof suppurative diseases are caused by Staph. aureus which includes • 1. Infections of skin • 2. Infections of burns and surgical wounds • 3. Infections of the upper and lower respiratory tract • 4. Bacterial arthritis • 5. Infection of bone (Osteomyelitis) • 6. Bacterial endocarditis • 7. Bacterial meningitis • 8. Septicaemia • 9. Toxic shock syndrome
  • 13.
  • 14.
    STREPTOCOCCAL INFECTIONS • gram-positivecocci • more known for their non-suppurative autoimmune complications than suppurative inflammatory responses. • Streptococcal infections occur throughout the world (underprivileged populations)
  • 15.
    Implicated in differentstreptococcal diseases • 1. Group A or Streptococcus pyogenes, also called b-haemolytic streptococci - upper respiratory tract infection and cutaneous infections (erysipelas). • 2. Group B or Streptococcus agalactiae produces infections in the newborn and is involved in non-suppurative poststreptococcal complications such as RHD and acute glomerulonephritis. • 3. Group C and G streptococci - respiratory infections.
  • 16.
    Implicated in differentstreptococcal diseases • 4. Group D or Streptococcus faecalis, also called enterococci are important in causation of urinary tract infection, bacterial endocarditis, septicaemia etc. • 5. Untypable a-haemolytic streptococci such as Streptococcus viridans constitute the normal flora of the mouth and may cause bacterial endocarditis. • 6. Pneumococci or Streptococcus pneumoniae - bacterial pneumonias, meningitis and septicaemia
  • 17.
  • 18.
    CLOSTRIDIAL DISEASES • gram-positivespore-forming anaerobic microorganisms • found in the GIT of herbivorous animals and man. • undergo vegetative division under anaerobic conditions, and sporulation under aerobic conditions. • toxins responsible for the diseases: • 1. Gas gangrene by C. perfringens • 2. Tetanus by C. tetani • 3. Botulism by C. botulinum • 4. Clostridial food poisoning by C. perfringens • 5. Necrotising enterocolitis by C. perfringens.
  • 20.
    GAS GANGRENE • rapidlyprogressive and fatal illness • Myonecrosis due to elaboration of myotoxins • In majority of cases (80-90%), the source of myotoxins is C. perfringens Type A; others are C. novyi and C. septicum. • Generally, traumatic wounds and surgical procedures are followed by contamination with clostridia and become the site of myonecrosis. • The incubation period is 2 to 4 days. • The most common myotoxin produced by C. perfringens Type A is the alpha toxin which is a lecithinase.
  • 21.
    • The preventionof gas gangrene lies in debridement of damaged tissue in which the clostridia thrive. • The lesion has serosanguineous discharge with odour and contains gas bubbles. • There is very scanty inflammatory reaction at the site of gas gangrene
  • 22.
    TETANUS • ‘lock jaw’is a severe acute neurologic syndrome • caused by tetanus toxin, tetanospasmin, which is a neurotoxic exotoxin elaborated by C. tetani. • The spores of the microorganism present in the soil enter the body through a penetrating wound. • The degenerated microorganisms liberate the tetanus neurotoxin which causes neuronal stimulation and spasm of muscles. • The incubation period of the disease is 1-3 weeks. • The earliest manifestation is lock-jaw or trismus. • Rigidity of muscles of the back causes backward arching or opisthotonos. • Death occurs due to spasm of respiratory and laryngeal muscles.
  • 23.
  • 24.
  • 25.
    MYCETOMA • Chronic suppurativeinfection (limb, shoulder) • characterised by draining sinuses (colonies of fungi or bacteria) • Types:  Caused by actinomyces (higher bacteria) also called actinomycetoma comprises about 60%.  ” Eumycetoma caused by true fungi, Madurella mycetomatis or Madurella grisea, comprises the remaining 40%. • The organisms are inoculated directly from soil into bare feet, from carrying of contaminated sacks on the shoulders, and into the hands from infected vegetation.
  • 26.
    MYCETOMA MORPHOLOGIC FEATURES • Afterseveral months of infection, • The affected site, most commonly foot, is swollen -- ‘madura foot’. • The lesions extend deeply into the subcutaneous tissues, along the fascia and eventually invade the bones. • They drain through sinus tracts which discharge purulent material and black grains. • Surrounding tissue shows granulomatous reaction.
  • 27.
    Madura foot. Brown granulelying in necrotic tissue in the discharging sinus
  • 28.
    CANDIDIASIS • an opportunisticfungal infection caused most commonly by Candida albicans and occasionally by Candida tropicalis. • Candida species are present as normal flora of the skin and mucocutaneous areas, intestines and vagina. • Various predisposing factors are: impaired immunity, prolonged use of oral contraceptives, long-term antibiotic therapy, corticosteroid therapy, diabetes mellitus, obesity, pregnancy etc.
  • 29.
    CANDIDIASIS MORPHOLOGIC FEATURES • Candidaproduces superficial infections of the skin and mucous membranes, or may invade deeper tissues. 1. Oral thrush 2. Candidal vaginitis 3. Cutaneous candidiasis 4. Systemic candidiasis
  • 30.
    1. Oral thrush •Commonest form of mucocutaneous candidiasis • Fullfledged lesions consist of creamy white pseudomembrane composed of fungi covering the tongue, soft palate, and buccal mucosa • In severe cases-ulceration 2. Candidal vaginitis • Vaginal candidiasis or monilial vaginitis is characterised clinically by thick, yellow, curdy discharge. • The lesions form pseudomembrane of fungi on the vaginal mucosa. • They are quite pruritic and may extend to involve the vulva (vulvovaginitis) and the perineum.
  • 31.
    3. Cutaneous candidiasis •Candidal involvement of nail folds - paronychia and colonisation in the intertriginous areas of the skin, axilla, groin, infra- and inter- mammary, intergluteal folds and interdigital spaces. 4. Systemic candidiasis • Usually a terminal event • The organisms gain entry into the body through an ulcerative lesion on the skin and mucosa or may be introduced • Most commonly encountered in kidneys as ascending pyelonephritis and in heart as candidal endocarditis.
  • 32.
    Candidiasis of theulcer in the skin
  • 33.
    CUTANEOUS SUPERFICIAL MYCOSIS •Dermatophytes cause superficial mycosis of the skin, the important examples - Microsporum, Trichophyton and Epidermophyton. • These superficial fungi are spread by direct contact or by fomites and infect tissues such as the skin, hair and nails. • Examples ” . Tinea capitis - patchy alopecia affecting the scalp and eyebrows. ” . Tinea barbae is acute folliculitis of the beard. ” . Tinea corporis is dermatitis with erythematous papules. • Diagnosis of dermatophytosis - light microscopic examination of skin scrapings
  • 34.
    Selected Human Viruses& Viral Diseases
  • 37.
  • 38.
  • 39.
    VIRAL HAEMORRHAGIC FEVERS •common features of causing haemorrhages, shock & sometimes death. • arthropod-borne (or arbo) viruses • Classified - 4 groups: 1. Mosquito-borne (e.g. yellow fever, dengue fever, Rift Valley fever) 2. Tick-borne (e.g. Crimean haemorrhagic fever, Kyasanur Forest disease) 3. Zoonotic (e.g. Korean haemorrhagic fever, Lassa fever) 4. Marburg virus disease & Ebola virus disease by unknown route. • Mosquito-borne viral haemorrhagic fevers in which Aedes aegypti mosquitoes are vectors. • Two important examples of Aedes mosquito-borne viral haemorrhagic fevers are yellow fever and dengue fever.
  • 40.
    YELLOW FEVER • Oldestknown viral haemorrhagic fever • restricted to some regions of Africa and South America. • Monkeys carry the virus without suffering from illness and the virus is transmitted from them to humans by Aedes aegypti as vector. Clinical features: • Sudden onset of high fever, & chills, • myalgia, • headache, • jaundice, • hepatic failure, • renal failure, • bleeding disorders • hypotension.
  • 41.
    YELLOW FEVER MORPHOLOGIC FEATURES Liver.The characteristic changes include: i) midzonal necrosis; ii) Councilman bodies; and iii) microvesicular fat. Kidneys. The kidneys show the following changes: i) coagulative necrosis of proximal tubules; ii) accumulation of fat in the tubular epithelium; and iii) haemorrhages.
  • 42.
    DENGUE HAEMORRHAGIC FEVER (DHF) •The word dengue is derived from African word ‘denga’ meaning fever with haemorrhages. • Dengue is caused by virus transmitted by bites of mosquito Aedes aegypti. • DHF was first described in 1953 when it struck Philippines. • regularly reported from tropics and subtropics—South East Asia, Latin America
  • 43.
    • Dengue occursin two forms: 1. Dengue fever or break-bone fever in an uncomplicated way is a self-limited febrile illness affecting muscles and joints with severe back pain due to myalgia (and hence the name ‘breakbone’ fever). 2. Dengue haemorrhagic fever (DHF), on the other hand, is a severe and potentially fatal form of acute febrile illness characterised by cutaneous and intestinal haemorrhages d/t thrombocytopenia, haemoconcentration, Hypovolaemic shock and neurologic disturbances.
  • 44.
    • DHF ismost common in children under 15 years of age. • There are 4 types of dengue viruses • These visruses infect blood monocytes, lymphocytes and endothelial cells. • If patient is treated appropriately at this stage, there is rapid and dramatic recovery. • But in untreated cases, dengue shock syndrome develops and death occurs.
  • 45.
    MORPHOLOGIC FEATURES : i)Focal haemorrhages and congestion ii) Increased vascular permeability resulting in oedema in different organs iii) Coagulopathy with thrombocytopenia iv) Haemoconcentration.
  • 46.
    Diagnosis of DHF: 1.Serologic testing for detection of antibodies 2. Detection of virus by immunofluorescence method & monoclonal antibodies 3. Rapid methods such as reverse transcriptase-PCR and fluorogenic- ELISA.
  • 47.
    • Main abnormalitiesin investigations in DHF are as under: i) Leucopenia with relative lymphocytosis, ii) Thrombocytopenia iii) Elevated haematocrit due to haemoconcentration iv) X-ray chest showing bilateral pleural effusion v) Deranged liver function tests (elevated transaminases, hypoalbuminaemia and reversed A:G ratio) vi) Prolonged coagulation tests (PT, APTT and TT)
  • 48.
    • At autopsy: i)Brain: Intracranial haemorrhages, cerebral oedema, dengue encephalitis. ii) Liver: Enlarged; necrosis of hepatocytes and Kupffer cells, Reye’s syndrome in children. iii) Kidneys: Petechial haemorrhages and features of renal failure. iv) Muscles and joints: Perivascular mononuclear cell infiltrate.
  • 49.
    CHIKUNGUNYA VIRUS INFECTION • Theword chikungunya means “that which bends up” • Primarily a disease in nonhuman primates but the infection is transmitted to humans by A. aegypti mosquito.
  • 50.
    CHIKUNGUNYA VIRUS INFECTION Clinically,the disease is characterised by • abrupt onset of fever, • severe arthralgia • migratory polyarthritis affecting small joints, • chills, • headache, • anorexia, nausea, abdominal pain, • rash, • Petechiae, • ocular symptoms such as photophobia. ”
  • 51.
    • Major laboratoryfindings • leucopenia, • mild thrombocytopenia, • elevated transaminaseS • raised CRP.
  • 52.
    INFLUENZA VIRUS INFECTIONS •Important and common form of communicable disease. • General clinical features range from a mild afebrile illness similar to common cold by appearance of sudden fever, headache, myalgia, malaise, chills and respiratory tract manifestations such as cough, soar throat to a more severe form of acute respiratory illness and lymphadenopathy. • Sometimes with alarming morbidity and mortality in the world. • Seasonal flu vaccine is administered to population at high risk in developed countries.
  • 53.
    ETIOLOGIC AGENT • Influenzavirus is a single-stranded RNA virus belonging to coronaviruses. • Depending upon its antigenic characteristics of the nucleoprotein and matrix, 3 distinct types are known: A, B & C. • Influenza type A is responsible for most serious and severe forms of outbreaks in human beings while types B and C cause a milder form of illness. Type A influenza virus is further subtyped based on its 2 viral surface features: • Haemagglutinin (H) H antigen elicits host immune response by antibodies and determines the future protection against influenza A viruses. • Neuraminidase (N) Antibody response against N antigen limits the spread of viral infection and is responsible for reduction of infection.
  • 54.
    • Subtypes ofinfluenza A viruses are designated by denoting serial subtype numbers of H and N antigens as H1N1, H2N2 etc. • Influenza A viruses infect human beings, birds, pigs & horses. • Major antigenic variation in H or N antigens is called antigenic shift while minor variation is termed antigenic drift. • In general, population at high risk are immunosuppressed patients, elderly individuals and infants. • Two of the known subtypes of influenza A viruses which have affected the human beings in recent times are as under:  ” Avian influenza virus A/H5N1 commonly called “bird flu”.  ” Swine influenza virus A/H1N1 commonly called “swine flu”.
  • 55.
    BIRD FLU (INFLUENZAA/H5N1) • H5N1 subtype of the influenza type A virus infection causes severe acute respiratory syndrome (SARS) which is the human form of bird flu or avian influenza with having similar symptomatology. • Every year, there have been outbreaks in poultry birds in different parts of the world resulting in slaughtering of millions of infected chickens every year. • Every year there have been seasonal outbreaks in the human form of the disease in high winter.
  • 56.
    PATHOGENESIS • SARS iscaused by influenza type A/H5N1 respiratory virus, also called SARS-associated coronaviruses (SARS- CoV). • Humans acquire infection through contaminated nasal, respiratory and faecal material from infected birds. • An individual who has human flu and also gets infected with bird flu, then the hybrid virus so produced is highly contagious and causes lethal disease. • Humans do not have immune protection against avian viruses.