Published Date: 2011-11-24 10:55:52
Subject: PRO/AH/EDR> Influenza (70): USA (IA) swine-origin H3N2 reassortant
Archive Number: 20111124.3438
INFLUENZA (70): USA (IOWA) SWINE-ORIGIN H3N2 REASSORTANT
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A ProMED-mail post
http://www.promedmail.orgProMED-mail is a program of the
International Society for Infectious Diseases
http://www.isid.orgDate: Wed 23 Nov 2011Source: CDC. MMWR Morb Mortal Wkly Rep 2011; 60 (dispatch); 1-3[edited]http://www.cdc.gov/mmwr/preview/mmwrhtml/mm60d1123a1.htm?s_cid=mm60d1123a1_e&source=govdelivery
Limited human-to-human transmission of novel influenza A (H3N2) virus
- Iowa
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On 20 Nov 2011 CDC confirmed 3 cases of swine-origin triple
reassortant influenza A (H3N2) (S-OtrH3N2) virus infection in children
in 2 counties in Iowa. None of the children were hospitalized, and
each has recovered from a mild episode of febrile respiratory illness.
All 2 were in contact with one another, and none had a known recent
exposure to swine. No additional human infections with this virus have
been detected in Iowa, and no evidence of sustained human-to-human
transmission of this S-OtrH3N2 virus exists; surveillance is ongoing.
In total, 18 human infections with swine-origin influenza A (H3N2)
viruses have been identified since 2009 (1,2). The most recent 10
cases, including the 3 Iowa cases described in this report, were
infections with S-OtrH3N2 viruses containing the matrix (M) gene from
the pandemic 2009 influenza A (H1N1) virus (pH1N1). These viruses are
considered reassortant viruses between a swine-origin influenza A
(H3N2) virus circulating in North American swine and a pH1N1 virus.
All cases of human infection with S-OtrH3N2 virus containing the M
gene from the pH1N1 virus have occurred in 2011 and have been reported
from 4 states: Pennsylvania (3 cases), Maine (2), Indiana (2), and
Iowa (3) (3).
Case reports
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Patient A: in the 2nd week of November 2011, patient A, a previously
healthy female child, experienced acute onset of influenza-like
illness (ILI). 3 days after her illness onset (illness day 4), she was
seen by a health-care provider, who obtained a respiratory specimen
and performed a rapid influenza diagnostic test, which was positive.
As part of routine influenza surveillance, the respiratory specimen
was forwarded to the University of Iowa State Hygienic Laboratory
(SHL) for further evaluation. Patient A's brother experienced onset of
ILI one day before patient A's date of illness onset. Patient A's
brother was not tested for influenza but was treated with oseltamivir
by a health-care provider and has recovered. During her illness days 2
and 3, patient A was in contact with her father, who subsequently
developed ILI 2 days after his most recent contact with patient A. He
was not tested for influenza. No other household member has reported
respiratory illness. No family member reported exposure to swine
before their illness onset. On her illness day one, patient A attended
a small gathering of children.
Patients B and C: patient B is a previously healthy male child who
developed ILI 2 days after patient A's 1st day of illness. He is the
sibling of patient C, a previously healthy male child who developed
ILI one day after patient B's illness onset. Both children were seen
by a health-care provider 2 days after patient B's illness onset;
rapid influenza diagnostic testing was positive for both patients. As
part of routine influenza surveillance, respiratory specimens were
forwarded to SHL for further evaluation. The mother of patients B and
C reported that no other household member had a respiratory illness
and none had been exposed to swine before patient B became ill. On
patient A's illness day one, patients B and C attended the same small
gathering of children as patient A.
Epidemiologic and laboratory investigations
-------------------------------------------
An investigation by the Iowa Department of Public Health (IDPH)
determined that the families of patients A, B, and C reported no
recent travel or attendance at community events. To date, the only
epidemiologic link among patients A, B, and C that has been identified
is attendance at a gathering of children on patient A's illness day
one. No illnesses were reported among adults or among the 5 other
children who were present at this gathering on that day. No swine
exposures have been identified among adults or children attending this
gathering. IDPH has detected no increase in absenteeism or reports of
respiratory illness in the community where patients A, B, and C reside
or in the schools in the community. Enhanced surveillance for ILI has
been implemented in health-care facilities in the communities where
patients A, B, and C reside. IDPH has instructed health-care providers
to obtain respiratory specimens from patients with ILI for influenza
diagnostic testing at SHL. Thus far, no additional cases of S-OtrH3N2
infection have been identified, and surveillance data from the state
have shown low levels of influenza activity currently and at the time
of all these patients' illnesses.
Eight days after patient A's illness onset, real-time reverse
transcription-polymerase chain reaction (rRT-PCR) testing of
respiratory specimens from patients A, B, and C at SHL indicated
possible S-OtrH3N2 influenza virus. At CDC, preliminary rRT-PCR
diagnostic results were inconclusive but indicated probable infection
with a swine-origin influenza A (H3N2) virus. Subsequent complete
genome sequencing at CDC confirmed all 3 specimens as S-OtrH3N2 with
the M gene from the pH1N1 virus. The viruses from these 3 patients are
resistant to amantadine and rimantadine but are expected to be
susceptible to the neuraminidase inhibitor drugs oseltamivir and
zanamivir based on their genetic sequence. Because these viruses carry
a unique combination of genes, little information currently is
available regarding the capacity of this virus to transmit efficiently
in swine, humans, or between swine and humans.
MMWR editorial note
-------------------
Since July 2011, a total of 10 cases of human infection with S-OtrH3N2
viruses have been identified in the United States, all containing the
M gene from the pH1N1 virus. Seven of these 10 cases resulted in mild
illness, but 3 of the infected persons were hospitalized for
influenza; all patients have recovered. In all 7 earlier cases,
exposure to swine was identified in the patient or in a close contact
of the patient (4). The lack of known exposure to swine in the 3 cases
described in this report, combined with the known epidemiologic links,
suggests that limited human-to-human transmission of this novel
influenza virus might have occurred. Transmission of swine-origin
influenza A (H3N2) viruses not containing the M gene from the pH1N1
virus to humans from close contact with an infected person has been
reported previously and has not resulted in sustained human-to-human
transmission (5). Preliminary evidence from the investigation of these
cases in Iowa shows no evidence of ongoing transmission among humans.
Swine influenza viruses are spread from pig to pig but are not known
to spread through human contact with pork or pork products.
Although the vast majority of human infections with animal influenza
viruses do not result in human-to-human transmission (6), each case
should be investigated fully to ascertain if these viruses are
transmitted among humans and to limit further exposure of humans to
infected animals, if infected animals are suspected. Such
investigations require close collaboration among state, local, and
federal public and animal health officials. As part of routine
preparedness measures to counter possible pandemic threats posed by
novel influenza viruses in the event that they gain the ability to
spread easily from person-to-person, CDC has developed a candidate
vaccine virus that could be used to produce a human influenza vaccine
against these S-OtrH3N2 viruses and has provided this candidate virus
to manufacturers.
Although swine exposure was not associated with the 3 cases described
in this report, because most previous cases of human infection with
S-OtrH3N2 viruses have occurred in patients who reported swine
exposure before illness onset, clinicians should consider swine-origin
influenza A virus infection in the differential diagnosis of patients
with febrile respiratory illness who have had contact with swine. It
is anticipated that commercially available diagnostic tests, including
point-of-care rapid tests, will detect infection with the S-OtrH3N2
virus; however, these tests will not differentiate S-OtrH3N2 from
seasonal influenza A viruses. Clinicians who suspect swine influenza
virus infections in humans should treat with oseltamivir when
indicated (7), obtain a nasopharyngeal swab from the patient, place
the swab in viral transport medium, and contact their state or local
health department to facilitate transport and timely diagnosis at a
state public health laboratory, using the CDC RT-PCR assay cleared by
the Food and Drug Administration. CDC requests that state public
health laboratories send all suspected novel influenza A specimens,
such as these S-OtrH3N2 viruses, to the CDC Influenza Division's Virus
Surveillance and Diagnostics Branch Laboratory.
The 2011-12 seasonal influenza vaccine is expected to provide limited
protection from this virus for adults but none for young children.
Enhanced surveillance, including surveillance for ILI and diagnostic
testing of respiratory specimens, is being conducted in Iowa and
surrounding states as part of the ongoing investigation of these
cases. Additional information about swine influenza is available at
http://www.cdc.gov/flu/swineflu.
References
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1. CDC. Update: influenza activity - United States, 2010-11 season,
and composition of the 2011-12 influenza vaccine. MMWR 2011; 60:
705-12. Available at
http://www.cdc.gov/mmwr/preview/mmwrhtm ... mm6021a5_w.
2. CDC. Update: influenza activity - United States, 2009-10 season.
MMWR 2010; 59: 901-8. Available at
http://www.cdc.gov/mmwr/preview/mmwrhtm ... mm5929a2_w.
3. CDC. FluView: 2011-2012 influenza season week 45 ending 12 Nov
2011. Available at
http://www.cdc.gov/flu/weekly. Accessed 23 Nov
2011.
4. CDC: Swine-origin influenza a (H3N2) virus infection in two
children - Indiana and Pennsylvania, July-August 2011. MMWR 2011; 60:
1213-5. Available at
http://www.cdc.gov/mmwr/preview/mmwrhtm ... mm6035a6_w.
5. Robinson JL, Lee BE, Patel J, et al: Swine influenza (H3N2)
infection in a child and possible community transmission, Canada.
Emerg Infect Dis 2007; 13(12): 1865-70. Available at
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2876760.
6. Myers KP, Olsen CW, Gray GC: Cases of swine influenza in humans: a
review of the literature. Clin Infect Dis 2007; 44(8): 1084-8.
Available at
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1973337.
7. CDC: Antiviral agents for the treatment and chemoprophylaxis of
influenza -- recommendations of the Advisory Committee on Immunization
Practices (ACIP). MMWR 2011 ;60(No. RR-1). Available at
http://www.cdc.gov/mmwr/preview/mmwrhtm ... rr6001a1_w.
--
Communicated by:
ProMED-mail
[In summary, this report describes the investigation of the 3
confirmed cases of human infection with S-OtrH3N2 virus in Iowa
associated with limited person-to-person transmission. It provides
details not available in the earlier reports, namely, the infections
occurred among children in contact with one another, and all cases
were mild and self-limited. No child had known exposure to swine. The
viruses identified are similar to 7 previous cases reported in 2011,
but these are the 1st cases reported from Iowa.
Swine influenza viruses have been reported sporadically to infect
humans. In the United States, 7 cases of swine-origin triple
reassortant influenza A (H3N2) (S-OtrH3N2) virus infection have been
reported in 2011. Cases have usually occurred after exposure to
swine.
Transmission of swine-origin influenza A (H3N2) viruses not containing
the M gene from the pH1N1 virus to humans from close contact with an
infected person has been reported previously and has not resulted in
sustained human-to-human transmission.
The 2011-12 seasonal influenza vaccine is expected to provide limited
protection from this virus for adults but none for young children. -
Mod.CP]
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